Prevention and management of adverse events of novel agents in multiple myeloma: a consensus of the European Myeloma Network.

During the last few years, several new drugs have been introduced for treatment of patients with multiple myeloma, which have significantly improved the treatment outcome. All of these novel substances differ at least in part in their mode of action from similar drugs of the same drug class, or are representatives of new drug classes, and as such present with very specific side effect profiles. In this review, we summarize these adverse events, provide information on their prevention, and give practical guidance for monitoring of patients and for management of adverse events.

Introduction

During the last years, options for multiple myeloma have increased substantially with the introduction of several immunomodulatory agents (IMiDs), proteasome inhibitors (PIs), monoclonal antibodies (mAbs), and a histone deacetylase inhibitor (HDACi). Inclusion of novel drugs in myeloma therapy resulted in an increased depth of responses, improved progression-free and overall survival with substantial gains in transplant-eligible patients, and more moderate improvements in elderly patients. The new drugs differ not only in their mode of action, but importantly, also in their toxicity profile from previous standard treatments. Here, we present the most relevant side effects of the novel drugs reported in pivotal clinical studies and discuss strategies for their prevention and management.

Methods

Pivotal trials leading to drug approval, and references of all regimens recommended by the National Comprehensive Cancer Network (NCCN) clinical practice guidelines on multiple myeloma, version 1.2018 [1], served as a basis for the summaries of treatment-emergent adverse events (AEs). Table S1 of the online supplemental material summarizes the indications approved in the United States (US) and the European Union (EU) valid at the time of writing. Tables 1 and S3 summarize the special warnings and precautions with regard to toxicities of novel agents and common backbone agents as per US prescribing information (USPI) and EU summary of medicinal product characteristics (EU SmPC). These form a patient monitoring guide for complications potentially associated with the approved regimens. All grade ≥3 AEs reported in the pivotal trials leading to US and/or EU approval and published at the time of writing are summarized in Table S2A–D. Where clearly identified in the drug labels, a distinction was made between AEs, defined as “…any untoward medical occurrence in a patient administered a medicinal product and which does not necessarily have to have a causal relationship with this treatment” and adverse drug reactions (ADRs), defined as “…all noxious and unintended responses to a medicinal product related to any dose…” [2]. When a clear classification was not available, the event was listed by the term used in the source document or generally as AE.

Table 1

Special warnings and precautions with regards to toxicities of novel agents as per USPI/EU SmPC

DVT deep vein thrombosis, PML progressive multifocal leukoencephalopathy, PRES posterior reversible encephalopathy syndrome, SPM second primary malignancy

aIncreased HIV viral load

bOnly a low incidence of peripheral neuropathy has been observed in patients treated with lenalidomide, however, the EU SmPC has a warning because of its structural similarity to thalidomide

cPatients with pre-existing peripheral neuropathy grade ≥2 have been excluded from pivotal trials, and caution should be exercised in treating such patients

dHerpes zoster and hepatitis B virus

eIncludes venous thromboembolism and thrombotic microangiopathy

The AEs that are discussed in the management section were selected based on their clinical importance rather than their incidence. Management recommendations were taken from available guidelines, such as those developed by the International Myeloma Working Group [3-5], the European Myeloma Network [6], the NCCN [1, 7], the British Committee for Standards in Hematology/United Kingdom Myeloma Forum [8], from literature referenced in the respective sections, and from the USPIs and EU SmPCs. These recommendations are subject to the treating physician’s best clinical judgment.

Incidence of adverse events

Multiple myeloma shows a wide range of tumor-related co-morbidities [4, 9] and the majority of patients receive a number of anti-myeloma drugs and medication to ameliorate tumor-associated or other co-morbidities. Thus, it is frequently impossible to clearly attribute a specific side effect to an individual drug. The AEs listed below therefore should be interpreted in the context of complications of the disease, of specific drugs or drug combinations administered, and of supportive or prophylactic measures. Of note, uniform reporting standards for AEs, such as the Medical Dictionary for Regulatory Activities (MedDRA, www.meddra.org) or the Common Terminology Criteria for Adverse Events (CTCAE, https://ctep.cancer.gov/protocoldevelopment/electronic_applications/ctc.htm), are not yet consistently used throughout studies, leading to a substantial variation in the documentation of quality, incidence, and grade of AEs (Table S2A–D).

Warnings and precautions for use of individual drugs as listed in the respective USPIs and EU SmPCs are shown in Table 1 (novel agents) and Table S3 (backbone agents) and provide guidance for patient monitoring during treatment.

Immunomodulatory agents (IMiDs)

The overall incidence of AEs reported in pivotal trials employing IMiD-based regimens is shown in Table S2A. All IMiDs are structural analogs of thalidomide and thus teratogenic. Adequate patient education and contraceptive measures are therefore mandatory for all three drugs of this class [10-15].

Thalidomide

In the United States, thalidomide (T)-based therapies are no longer widely used. In Europe, thalidomide is part of the VTD regimen for induction therapy before ASCT and remains an essential element of myeloma therapy in major regions of the world, like South America, parts of Asia, and several Eastern European countries. The incidence and severity of thalidomide-related AEs is dose and treatment duration dependent and influenced by potential comorbidities and toxicities of co-medications. Susceptibility for thalidomide-induced peripheral neuropathy (PNP) has been linked to polymorphism of genes governing repair mechanisms and inflammation in the peripheral nervous system [16]. A systematic review revealed somnolence, constipation, neuropathy, rash, cardiac events, and venous thromboembolism as the most frequent grade 3 or 4 AEs of thalidomide single-agent therapy, particularly with doses >200 mg/day in relapsed/refractory multiple myeloma (RRMM) [17]. In clinical trials using melphalan and prednisone in combination with thalidomide (MPT), hematological events, infections, other neurological toxicities, PNP, deep vein thrombosis, and dermatological toxicity were predominant [18, 19]. In addition, arterial thromboembolism, drowsiness, dizziness, orthostatic hypotension, neutropenia, thrombocytopenia, increased HIV viral load, bradycardia, serious dermatological reactions (Stevens–Johnson syndrome and toxic epidermal necrolysis), seizures, tumor lysis syndrome, and complications that are more frequent while on contraceptives, hypersensitivity, and increased risk for secondary primary malignancies were reported [13].

Patients should be monitored for thromboembolic complications, PNP, rash/skin reactions, bradycardia, arrhythmia, syncope, somnolence, neutropenia, thrombocytopenia, and others (Table 1) [10, 13].

Lenalidomide

The toxicity profile of lenalidomide (R), although structurally very similar to thalidomide, differs remarkably from the originator compound (Table S2A). Notably, neuropathy, constipation, and somnolence are rare, while hematologic AEs are more frequent [20]. Grade ≥3 neutropenia was reported in 26% of patients treated with lenalidomide–dexamethasone (Rd) for 18 cycles and in 28% of those on continuous Rd in the FIRST trial [21]. Grade ≥3 thrombocytopenia occurred in 8% of patients in either arm. The most frequent non-hematological grade ≥3 side effects occurring in the Rd 18 arm in more than 5% were infections (22%), fatigue (9%), cardiac disorders (7%), venous thromboembolism (6%), and asthenia (6%). Long-term lenalidomide therapy may be associated with chronic diarrhea [22]. Side effects observed with MPR and MPR followed by R maintenance in the MM015 trial [23] were similar to those reported for the FIRST trial and are listed in Table S2A. Lenalidomide therapy is associated with an increased risk for second primary malignancies, especially in the post-transplantation setting [24-26], or after a melphalan-containing regimen [27], and after an IMiD-based induction therapy [28]. Data from the latter study show a cumulative incidence of 0.7, 2.3, and 3.8% after 1, 2, and 3 years, with the highest incidence in elderly patients. Lenalidomide is to a substantial degree excreted by the kidney and the dose has to be adapted to glomerular filtration rate [29]. Dose modifications are indicated for grade 3 or 4 neutropenia or thrombocytopenia, and for grade 2 to 3 skin rash.

Table 2

Risk assessment model for the management of venous thromboembolism in multiple myeloma patients (adapted from Palumbo 2008 [46])

Risk factor	Recommendation for prophylaxis
Patient-related risk factor
Obesitya
History of VTE
Central-venous catheter or pacemaker	For patient-, myeloma- and other medication-related risk factors:
Comorbiditiesb
Inherited thrombophilia or blood clotting disorders	If one risk factor, aspirin 81-325 mg, once daily;
Surgical proceduresc	if two or more risk factors are present, LMWH
Myeloma-related risk factors	(equivalent of enoxaparin 40 mg once daily) or
Active uncontrolled disease	full-dose warfarin (target INR 2–3)
Hyperviscosity
Other medication-related risk factors
Erythropoietin
Myeloma medication-related risk factors	For myeloma medication-related risk factors:
IMiDs
High-dose dexamethasoned	LMWH (equivalent of enoxaparin 40 mg once daily)
Doxorubicin	or full-dose warfarin (target INR 2–3)
Multiagent chemotherapy

LMWH low molecular weight heparin, IMiDs immunomodulatory agents, INR international normalized ratio, VTE venous thromboembolism

aDefined as a body mass index ≥30 kg/m2

bComorbidities include diabetes, infections, cardiac diseases, chronic renal disease, and immobilization

cSurgical procedures include general surgery, any anesthesia, trauma, vertebroplasty, and kyphoplasty

d≥480 mg/month

Patients should be monitored for hematological events, thromboembolic complications, PNP, infections, severe skin reactions, diarrhea, secondary malignancies, allergic reactions, cataracts, and others (Table 1) [11, 14].

Pomalidomide

The most frequently reported grade 3 or 4 ADRs reported in heavily pretreated patients receiving pomalidomide were hematological ADRs, including neutropenia, anemia, and thrombocytopenia (Table S2A). Other severe ADRs included infections, fatigue, pyrexia, peripheral edema, and venous thromboembolic events. Cases of PNP were non-serious, although it is of note that patients with ongoing grade ≥2 PNP were excluded from clinical trials with pomalidomide. Modifications of pomalidomide dose are indicated for grade 3 or 4 neutropenia or thrombocytopenia, and for grade 2 to 3 skin rash.

Patients should be monitored for hematological events, thromboembolic complications, skin rash, infections, PNP, diarrhea, secondary malignancies, allergic reactions, dizziness, confusion, and others (Table 1) [12, 15].

Proteasome inhibitors (PIs)

The overall incidence of AEs reported in published pivotal trials employing PI-based regimens is shown in Table S2B.

Bortezomib

The most commonly reported ADRs occurring during treatment with bortezomib were neutropenia, thrombocytopenia, anemia, PNP (including sensory), herpes zoster, nausea, diarrhea, constipation, vomiting, fatigue, pyrexia, headache, paresthesia, decreased appetite, dyspnea, rash, and myalgia (Table S2B). Dose modifications are indicated in response to hematological AEs as well as PNP. Viral prophylaxis is mandatory and will be discussed in the prevention and management section.

Patients should be monitored for viral re-activation, PNP, constipation, diarrhea, progressive multifocal leukoencephalopathy, seizures, hypotension, posterior reversible encephalopathy syndrome, heart failure, pulmonary disorders, and others (Table 1) [30, 31].

Carfilzomib

Carfilzomib is generally very well tolerated. The most commonly reported ADRs were anemia, fatigue, diarrhea, thrombocytopenia, nausea, pyrexia, dyspnea, respiratory tract infection, cough, and peripheral edema (Table S2B). Other, less frequent, but possibly serious ADRs include cardiac toxicity, pulmonary toxicities, pulmonary hypertension, hypertension including hypertensive crises, venous thrombosis, hemorrhage, acute renal failure, tumor lysis syndrome, infusion reactions, hepatic toxicity, posterior reversible encephalopathy syndrome, thrombotic thrombocytopenic purpura and hemolytic uremic syndrome (TTP/HUS), and embryo-fetal risk. Cardiac toxicity and dyspnea typically occurred early in the course of carfilzomib therapy, predominantly in patients with pre-existing cardiac impairment. Dose modifications are warranted in response to hematological AEs or any other severe or life-threatening non-hematologic toxicity, as well as in patients with impaired renal function [32, 33].

Patients should be monitored for pre- and postinfusional hypertension, cardiac, renal and pulmonary toxicities, diarrhea, tumor lysis syndromes, neutropenia, and thrombocytopenia, and others (Table 1) [32, 33].

Ixazomib

Experience with AEs occurring with ixazomib is limited. The most frequent AEs found to be associated with ixazomib include thrombocytopenia, gastrointestinal toxicities, PNP, peripheral edema, cutaneous reactions, and hepatotoxicity (Table S2B). Dose modifications are recommended in response to thrombocytopenia, neutropenia, rash, PNP, and for other non-hematological toxicities at the physician’s discretion when they reach grade 3 or higher [34, 35].

Patients should be monitored for thrombocytopenia, neutropenia, nausea, vomiting, diarrhea, constipation, dry eye, conjunctivitis, and others (Table 1) [34, 35].

Histone deacetylase inhibitors (HDACis)

The overall incidence of AEs reported with panobinostat in combination with bortezomib and dexamethasone (Pano-Vd, PANORAMA trial) is shown in Table S2C. The most frequent hematological AEs included thrombocytopenia, anemia, neutropenia, and lymphopenia. Non-hematological AEs included diarrhea, sometimes with significant impairment of patients’ well-being, electrolyte imbalances, increased creatinine, fatigue, decreased appetite, peripheral edema, pyrexia, nausea, and vomiting. Grade ≥3 PNP was reported relatively frequently in this combination (18% in Pano-Vd versus 15% in placebo-Vd) [36], but the frequency of this complication would be reduced, if bortezomib was given by the subcutaneous route, the present standard of care [36], or if another PI was used. Dose modifications are recommended in response to thrombocytopenia, gastrointestinal toxicities, neutropenia, and hepatic impairment.

Patients should be monitored for diarrhea, nausea, infections, cardiac toxicities, blood cell counts, blood electrolytes, liver and thyroid function, hemorrhage, and others (Table 1) [37, 38].

Monoclonal antibodies (mAbs)

The overall incidence of AEs reported in published pivotal trials for mAb-based regimens is shown in Table S2D. The most frequent AEs are infusion-related reactions (IRR), usually during the first administration, which disappear thereafter and rarely lead to treatment discontinuation.

Elotuzumab

Apart from IRR, which occurred in 10% of patients receiving elotuzumab in combination with lenalidomide and dexamethasone, the most common ADRs were fatigue, pyrexia, constipation, PNP, diarrhea, herpes zoster, nasopharyngitis, cough, pneumonia, upper respiratory tract infections, lymphopenia, decreased appetite, and weight loss. Elotuzumab is a humanized IgGk antibody and interferes with response assessment in patients with IgGk M-component. The most serious ADR was pneumonia.

Patients should be monitored for infusion reactions, infections, diarrhea, fever, cough, constipation, hepatotoxicity, and others (Table 1) [39, 40].

Daratumumab

The most commonly reported ADRs were IRR, which occurred in approximately half of patients (mostly grade 1 or 2); the majority (95%) of IRR occurred at the first infusion. Other commonly reported ADRs were anemia, neutropenia, thrombocytopenia, dyspnea, fatigue, pyrexia, cough, nausea, back pain, pneumonia, and upper respiratory tract infections (Table S2D). Daratumumab interferes with blood group serological testing, as it binds to CD38 on red blood cells and results in a positive indirect antiglobulin test (indirect Coombs test) [41, 42]. Due to its nature as an IgGk antibody, it may interfere with response assessment in patients with an IgGk M-component [43] and also with minimal residual disease assessment, because it binds to CD38-positive residual myeloma cells thus precluding detection of CD38-positive cells by diagnostic anti-CD38 antibodies as recommended by EUROFLOW for conventional flow cytometry [44]. A subcutaneous preparation is in clinical testing and will allow much faster administration with significantly reduced incidence of side effects.

Patients should be monitored for IRR, nausea, fever, cough, upper respiratory tract infection, neutropenia, thrombocytopenia, and others (Table 1) [41, 42].

Backbone agents

Backbone agents frequently used in doublet or triplet combinations with novel agents are dexamethasone, cyclophosphamide, prednisone, doxorubicin, and melphalan. Table S3 shows potentially occurring toxicities of these chemotherapy and corticosteroid backbone agents as per USPI/EU SmPC. The NCCN does no longer consider melphalan-containing regimens as the standard of care to treat patients with multiple myeloma, because of their potential to induce significant cytopenias and subsequently limit the use of novel agents [1], but melphalan continues to be a valuable backbone in non-US countries to which novel agents are added.

Prevention and management of adverse events

In multiple myeloma, it is not always possible to discriminate whether complications occur as a consequence of drug treatment, of the disease itself, or due to a combination of both. Furthermore, a combination of drugs is usually administered. AEs therefore need to be considered in the context of this complex situation. Nevertheless, it is critical to carefully monitor patients regarding possible side effects (Table 1 and Tables S2A–D and S3) to avoid early complications that may compromise therapeutic outcome. Hematological toxicities are commonly observed with most novel agents, but as their prevention and management is quite similar independent of the drugs used, we will not discuss this in detail here [3, 6].

Thromboembolic complications

Treatment-, patient-, and myeloma-specific risk factors for thromboembolic complications, which are quite frequent in multiple myeloma [8, 45], are shown in Table 2. Thromboembolic events occur more frequently during the initial phase of treatment and less commonly during episodes of well-controlled disease, in remission, or at relapse [46]. IMiDs alone and particularly in combination with dexamethasone and other drugs, such as carfilzomib [32, 33], erythropoietin, or adriamycin, are associated with an increased risk of thromboembolic events [10-15].

Modifiable risk factors should be minimized if possible. Patients with one patient-specific risk factor for thromboembolism should receive thromboprophylaxis with aspirin at a dose of 81–325 mg [1, 4, 8, 46], while those with two patient-specific or one treatment-specific risk factors should be treated either with low molecular weight heparins (LMWH) or warfarin, (Table 2) [1, 4, 8, 10–15, 46]. However, there is currently no robust evidence on the optimal duration of thromboprophylaxis, especially in active uncontrolled disease as well as in lenalidomide maintenance therapy. Concomitant administration of erythropoietic agents or other drugs known to increase the risk of thrombosis, such as hormone replacement therapy, should be used with caution [11]. If a patient experiences thromboembolic complications, anti-myeloma treatment may temporarily be discontinued and anticoagulation therapy started using adjusted dose warfarin or LMWH, and appropriate monitoring should be applied. The appropriate initial therapy in the outpatient setting is therapeutic doses of LMWH. In hospitalized patients, unfractionated heparin for a minimum of 5 days may be preferred [8]. Treatment with LMWH or coumarin should be continued for several months with lower doses of LMWH. In patients started on intravenous heparin, therapy should be resumed until the patient’s partial thromboplastin time (PPT) has increased by 1.5–2.0-fold compared to control for two consecutive days and then switched to oral warfarin or coumarin. Once the acute thromboembolic event has stabilized, anti-myeloma therapy can be restarted depending upon a benefit-risk assessment with continued anticoagulation therapy with warfarin or LMWH. Alternatively, anti-myeloma therapy should be changed to a regimen with lower risk of thromboembolic complications. Renal failure with GFR <30 ml/min limits the use of LMWH, since these drugs depend on renal clearance for drug elimination and increased blood levels increase the risk of bleeding [47].

Whether the occurrence of thromboembolic complications is associated with increased mortality in multiple myeloma is still controversial. Shorter survival was reported in patients with early thrombotic events (within 6 months after start of initial therapy or within the first 2 years) while in another study no difference in mortality was noted, neither in newly diagnosed nor in relapsed/refractory myeloma. New oral anticoagulants (NOACs), which include dabigatran, rivaroxaban, apixaban, and edoxaban, have been shown to be useful for initial and extended VTE treatment [48]. These drugs have not systematically been studied in myeloma as yet, therefore specific recommendations cannot be made at this point in time.

Peripheral neuropathy

PNP is defined as any form of damage, inflammation, or degeneration of peripheral nerves [49] and can be induced by IMiDs, some PIs, and HDACis (Table 1 and Table S2A–C). Thalidomide can cause severe, mostly irreversible PNP, with higher risk in patients with pre-existing PNP [10–14, 50]. Among PIs, bortezomib was shown to induce severe PNP [30, 31]. Bortezomib-induced neurodegeneration occurs via a proteasome-independent mechanism and therefore is not considered a group effect of PIs [51].

The incidence of thalidomide-induced PNP (TiPNP) is dependent on dose, treatment duration, and patient-specific factors, and presents as a sensory neuropathy with prominent symptoms of paresthesia in the hands and feet (glove-and-stocking distribution) [49, 52, 53]. TiPNP also includes numbness, and mild motor involvement with muscle cramps and weakness [49]. Dose reductions are recommended in patients with grade 1 TiPNP with no loss of function, dose reduction, or treatment interruption in patients with grade 2, interfering with function but not with activities of daily living, and treatment discontinuation in patients where lower-grade TiPNP does not resolve upon dose modifications and in patients with grade 3 or 4 TiPNP (Table 3) [10, 13, 54]. Recommendations include patient monitoring at a monthly interval for the first 3 months of treatment to detect early signs of TiPNP and to continue regular monitoring during the entire treatment duration.

Table 3

Dose adjustment rules for thalidomide- and bortezomib-induced peripheral neuropathy [10, 30] and management of active neuropathic pain [3, 4, 8, 54, 56, 57]

Severity of neuropathy	Thalidomide dose adjustment	Bortezomib dose adjustmenta	Management of PN symptoms and pain
Grade 1 (asymptomatic; paresthesia, weakness and/or loss of reflexes) with no pain or loss of function	Continue to monitor the patient with clinical examination. Consider reducing dose if symptoms worsen. However, dose reduction is not necessarily followed by improvement of symptoms	None; consider SC administration
Grade 1 with pain or grade 2 (moderately symptomatic; interfering with function but not with activities of daily living)	Reduce dose or interrupt treatment and continue to monitor the patient with clinical and neurological examination. If no improvement or continued worsening of the neuropathy, discontinue treatment. If the neuropathy resolves to Grade 1 or better, the treatment may be restarted, if the benefit/risk is favorable	Reduce dose to 1.0 mg/m2 twice weekly or change treatment schedule to 1.3 mg/m2 once per week; use SC administration	Anti-epileptic agents, tricyclic antidepressants; topical pain medications (lidocaine, capsaicin); analgesics according to WHO three-step “ladder”:1. non-opioids (aspirin and paracetamol)2. mild opioids (codeine)3. strong opioids (morphine)Pain medication should be given at a fixed schedule every 3–6 h, rather than “on demand”
Grade 2 with pain or grade 3 (severely symptomatic; interfering with activities of daily living)	Discontinue treatment	Withhold treatment until symptoms of toxicity have resolved. When toxicity resolves re-initiate treatment, and reduce dose to 0.7 mg/m2 once per week
Grade 4 (neuropathy which is disabling) and/or severe autonomic neuropathy	Discontinue treatment	Discontinue treatment

PN peripheral neuropathy, SC subcutaneous, WHO World Health Organization

aSubcutaneous administration of bortezomib was reported to be associated with a significantly lower rate of peripheral neuropathy [55]

Bortezomib-induced PNP (BiPNP) is predominantly sensory, with symptoms of paresthesia and numbness in distal areas, particularly in the lower limbs. BiPNP characteristically shows prominent small fiber involvement, characterized by sharp, burning pain in the toes and soles of the feet. Damage of the autonomic nervous system, including orthostatic hypotension, suppressed heart rate variability, and delayed gastric emptying, may occur. Motor neuropathy is uncommon [53]. There are clear guidelines for the treatment of BiPNP (Table 3) [54]. In case of BiPNP grade 1 with pain or grade 2, the bortezomib dose should be reduced to 1.0 mg/m2 twice weekly or the treatment interval should be extended to 1.3 mg/m2 once per week. In case of grade 2 with pain or grade 3 BiPNP treatment should be withheld until symptoms have resolved, then treatment can be re-initiated at a dose of 0.7 mg/m2 once per week. In the case if BiPNP of grade 4 treatment must be discontinued [30, 31]. Intravenous administration of bortezomib leads to 10-fold higher peak plasma levels and to higher rates of BiPNP than subcutaneous administration. Subcutaneous administration therefore reduces the incidence of BiPNP, particularly BiPNP of grade 3 or 4, without compromising the anti-myeloma effect and thus should be the preferred mode of administration [55].

Treatment of symptoms of PNP and neuropathic pain remains unsatisfactory and includes anti-convulsive agents (gabapentin and pergabalin) and antidepressants [3, 4, 8]. Other agents, such as acetyl-l-carnitine and alphalipoic acid, have shown activity in treatment of chemotherapy-emergent PNP of other cancers [54]. In case of neuropathic pain, the three-step ladder of pain management in cancer patients issued by the World Health Organization (WHO) should be followed [56]. These recommend an escalating analgesic therapy that includes opioids, such as tapentadol for very severe neuropathic pain. Topical pain medications include lidocaine and capsaicin [57]. Both, TiPN and BiPN, can also be associated with autonomic symptoms induced by damage to small fibers. These include orthostatic hypotension, sexual dysfunction, constipation, and bradycardia [49]. In rare cases, the insertion of a pacemaker should be considered [58, 59]. Recommendations for orthostatic dysregulation consist of a combination of vasoconstrictor drugs, volume expansion, compression garments, and postural adjustment, together with reduction or discontinuation of any concomitant blood pressure lowering medication. Drugs such as midodrine, pyridostigmine, and fludrocortisone can be administered, and physical inactivity should be avoided [60].

Muscle cramps and seizures

Several drugs such as lenalidomide, thalidomide, PIs, and dexamethasone can induce subtle perturbations of muscle fibers and/or of neurogenic structures, but the detailed pathogenesis of muscle cramps is still unknown [49]. Presently, specific treatment recommendations are not available. General suggestions include fluid hydration, normalizing magnesium and potassium levels, use of muscle relaxants, and moving and stretching the affected areas. However, the efficacy of these measures has not been ascertained in clinical trials.

Prophylaxis and treatment of infections

Recommendations on antimicrobial prophylaxis and vaccination are summarized in Tables 4 and 5.

Table 4

Recommendations on antimicrobial prophylaxis in multiple myeloma patients (adapted from NCCN Guidelines “Prevention and Treatment of Cancer-Related Infections” Version 1.2017 [7])

Risk factor	Microbial infection type	Prophylaxis recommendation	Details
Multiple myeloma diagnosisaAutologous or allogeneicbHSCT, Proteasome inhibitors	Viral	Consider prophylaxis during neutropenia and for sometime thereafter depending on risk	HSV or VZV infection or reactivation: acyclovir, famcyclovir, valaciclovir;Consider VZV prophylaxis after autologous HSCTProteasome inhibitor therapy: VZV prophylaxis during active therapy including periods of neutropenia;CMV: prophylaxis in selected cases with repeated reactivation valgancyclovir or ganciclovir; in case of resistance or intolerance: foscarnet or cidofovir
	Bacterial	Consider prophylaxis	Trimethoprim–sulfamethoxazole, amoxicillin, quinolone
	Parasites	Consider prophylaxis	Trimethorpim–sulfamethoxazole, pentamidine-inhalation in allogeneic transplantation
	Fungal	Consider prophylaxis during neutropenia; consider pneumocystis pneumonia prophylaxis	Fluconazolec or micafungind

CMV cytomegalovirus, HSCT hematopoietic stem cell transplantation, HSV herpes simplex virus, VZV varicella zoster virus

aInfection risk varies depending on treatment modality, disease biology, and patient’s age and fitness

bFor allogeneic HSCT additional prophylactic measures have been recommended [93]

cItraconazole, voriconazole, and posaconazole are more potent inhibitors of cytochrome P450 3A4 isoenzymes than fluconazole and may significantly decrease the clearance of several agents used to treat cancer

dAll three agents in the class (micafungin, caspofungin, and anidulafungin) are considered by many to be interchangeable

Table 5

Recommendations on vaccination in multiple myeloma patientsa

Vaccine	Recommendation	Number of doses	Timing after ASCT	Comment
Influenza [7, 67, 94, 95]	Vaccination using trivalent vaccine (life vaccines should be avoided)	1, annually	4–6 mo.	Trivalent (or quadrivalent) vaccine preferable; vaccination should be repeated in case of insufficient response
Pneumococci [7, 62, 75]	NDMM: PCV13	3	6–12 mo.	Newly diagnosed, pneumococcal vaccine-naive patients
	Followed by: PPSV 23	1	≥12 mo.	>8 weeks after completion of PCV13 series; response rate with doubling of titer only in about 60%
Herpes zoster [7]	Vaccination after ASCT (life vaccines should be avoided)	1	May be considered at ≥24 mo. (if no ongoing immunosuppression)	Attenuated vaccine presently in clinical evaluation [63]; a varicella-zoster virus glycoprotein E subunit vaccine candidate was shown to be highly effective in controls [96]
Haemophilus influenzae type b [6, 7]	Vaccination	3	6–12 mo.
Hepatitis A [7, 62, 97]	Vaccination of patients and nonimmune close contacts living or traveling to endemic areas	2	6–12 mo.	All patients should be tested for hepatitis A, in case of negative results vaccination is recommended
Hepatitis B [7, 62, 97]	Vaccination of patients and nonimmune close contacts living or traveling to endemic areas and in those with end stage renal disease	3	6–12 mo.	Patients should be tested for hepatitis B, in case of negative results vaccination is recommended
Meningococcal conjugate [7, 62]	Recommended in high-risk patients	1–2	6–12 mo.	Consider in high-risk patients with splenectomy or complement deficiency
Live vaccines [7]	Not recommended		May be considered at ≥24 mo. (if no ongoing immunosuppression)	Measles, mumps, and rubella (MMR), varicella zoster, Bacillus Calmette-Guerin, oral typhoid and yellow fever, life influenza virus (intranasal live) and oral polio (live)

ASCT autologous stem cell transplantation, GVHD graft-versus-host disease, NDMM newly diagnosed multiple myeloma, PCV13 13-valent polysaccharide conjugated pneumococcal vaccine, PPSV23 polysaccharide pneumococcal vaccine

aVaccination may be postponed in patients receiving >20 mg of prednisone

Viruses

Almost all people harbor latent virus infections that normally are effectively controlled by the host’s immune surveillance system. Bortezomib, other PIs, high-dose dexamethasone or chemotherapy, and autologous stem cell transplantation inhibit specific T cell functions important for curbing latent virus infections enabling their reactivation, which may result in severe clinical complications [61]. Caregivers and patients should be aware of the increased risks inferred by immunosuppression and install appropriate prophylactic measures, if available.

Vaccination

Patients should be vaccinated against several pathogens (Table 4). The most important are influenza virus, pneumococci, and haemophilus influenzae. A trivalent or quadrivalent influenza vaccine should be used in patients, partners, and caregivers. Vaccination against pneumococci should be started with a 13-valent vaccine (PCV13) and followed at least 8 weeks later by a dose of PCV23 (23 valent polysaccharide conjugate) [62]. A herpes zoster vaccine is currently being studied in patients with multiple myeloma, but results have not been made available to date [63]. Present herpes zoster vaccines are live vaccines and controversy exists whether they can be offered to patients with well-controlled disease. As an alternative to live-attenuated vaccines, which are contraindicated for immunocompromised individuals, heat-inactivated varicella zoster vaccines, and recombinant subunit vaccines have been studied [64-66]. Patients and nonimmune close contacts traveling or living in areas of high endemicity of hepatitis B and hepatitis A should receive recombinant hepatitis B and A vaccine. Response to vaccines frequently is suboptimal in multiple myeloma, making it desirable to evaluate the efficacy of the vaccination. An individual report shows that repeated vaccinations with the same influenza vaccine enhances anti-vaccine antibody production [67]. Ideally, patients should already be vaccinated in the premalignant state, namely when presenting with high-risk MGUS or SMM or, when feasible, during periods of optimal disease control.

Hepatitis B and C

Patients living in regions with high prevalence of hepatitis as well as those with increased alanine transaminase should be screened using serologic tests (HBsAg, anti-HBc, and anti-HBs) for previous exposure, or ongoing infection, and/or reactivation. Preemptive antiviral prophylaxis with nucleoside/nucleotide analogs should be considered in patients with latent or previous HBV infection [68]. Formal recommendation for those with a high risk of HCV infection or with previous infections are not available, but it seems reasonable to screen the high-risk group (anti-HCV and/or HCV RNA) and to treat those with evidence of active infection with modern direct-acting antivirals.

Herpes zoster

Pain, scarring, and post-herpetic neuralgia are the most common morbidities associated with herpes zoster reactivation. In pivotal trials, herpes zoster infection occurred in 3–13% of patients receiving bortezomib monotherapy (Table S2B) [30, 31]. Therefore, antiviral prophylaxis during the entire duration of treatment with any of the available PIs, but also during treatment with mAbs, is mandatory [7]. Antiviral agents such as acyclovir, valaciclovir, and penciclovir can be used; valaciclovir and penciclovir have greater bioavailability than acyclovir making them particularly suitable for outpatient treatment [69]. Valaciclovir was shown to significantly reduce the incidence of post-herpetic neuralgia [70], but randomized controlled trials comparing the efficacy of the various agents are not available. In the case of overt viral disease, anti-myeloma therapy should be interrupted and antiviral therapy be intensified. Upon symptom relieve, anti-myeloma therapy can be continued, but a risk of renewed virus reactivation remains [7].

Cytomegalovirus

PIs and high-dose therapy increase the risk for cytomegalovirus (CMV) reactivation or infection. Such infections not rarely remain unrecognized. For diagnosis of CMV infection, polymerase chain reaction (PCR) technology should be used, because antibody testing may fail due to impaired antibody production. CMV prophylaxis is generally not recommended in multiple myeloma [71], but may be considered in selective cases with repeated CMV reactivation. In case of active infection, therapy is typically initiated with intravenous ganciclovir. For second-line treatment or in case of poor tolerance or resistance to ganciclovir, foscarnet and cidofovir can be used [7]. Several new drugs (maribavir, brincidofovir, and letermovir) are undergoing clinical trials. Oral valgancyclovir is convenient, usually well tolerated and an option for initial therapy in very fit patients and for prevention of recurrence of infections during periods of aggressive therapy. Treatment should be continued at minimum until a negative PCR test result.

Bacteria and fungi

The risk for bacterial infections is significantly higher compared to the normal population [72], and particularly high in patients with active disease after start of initial therapy [73], and in those with a history of frequent infections and in elderly frail patients. Grade 3 and 4 infections were noted in 29% of patients treated with continuous lenalidomide–dexamethasone [21] and in 16.5% of relapsed/refractory myeloma exposed to carfilzomib–lenalidomide–dexamethasone [74]. Hence, antibiotic prophylaxis with either trimethoprim–sulfamethoxazole, amoxicillin, or a quinolone should be considered for the first months after start of therapy in selected patients with high risk for bacterial infections such as very elderly patients, those with a history of several previous infections, and those exposed to regimes with a high risk of infectious complications.

Intravenous immunoglobulin is an additional option, but evidence from randomized studies supporting its efficacy is scarce. Chapel et al. showed a significant benefit with fewer infections and no sepsis by administration of 400 mg/kg intravenous immunoglobulin in patients with plateau phase [75]. A meta-analysis including nine small studies on intravenous immunoglobulins in patients with chronic lymphocytic leukemia (CLL) or multiple myeloma revealed a 55% decrease in major infections with active therapy, but no effect on overall survival [76]. Taken together, intravenous immunoglobulin prophylaxis may be considered in selected patients with a history of frequent bacterial infections independent on whether they present with humoral immunoparesis, and in patients with an ongoing severe bacterial infection with no or slow response to standard antibiotic therapy.

Data on the incidence of pneumocystis jirovecii infections during treatment with novel drugs are scarce. The risk increases with severe suppression of T cell immunity. In case of established infection, the treatment of choice is trimethoprim–sulfamethoxazole. Other options are dapsone, atovaquone, or pentamidine [1].

Severe skin reactions

Monitoring patients for severe skin reactions is recommended in patients receiving thalidomide, lenalidomide, pomalidomide, or ixazomib (Table S2A–D). For limited, localized rash, antihistamines or topical steroids are recommended. In case of mild but extensive rash, a short course of low-dose prednisone should be considered [77]. In patients with grade 2 or 3 skin rash, treatment should be interrupted or discontinued and reinstated in case of complete resolution. Rarely, severe skin reactions such as Steven–Johnson syndrome or even toxic dermal necrolysis have been reported [10, 11, 13, 14, 34]. In such severe cases, treatment should be permanently discontinued. For lenalidomide, a desensitization scheme with progressively increased doses and dosing frequencies to reach a target dose of 10 mg/day over the course of 6 weeks has been proposed [78]. Patients having experienced skin reactions during previous courses of thalidomide treatment should not receive lenalidomide [11, 14] or in case of limited alternatives should be started at a low dose and carefully be monitored. For patients developing grade 2 or 3 rash during therapy with ixazomib in combination with lenalidomide, lenalidomide should be withheld until recovery or improvement of rash to grade 1. Lenalidomide treatment can be resumed at the next lower dose. If grade 2 or 3 reappears, withhold both until rash recovers to grade 1 or lower. Following recovery, resume ixazomib at the next lower dose and resume lenalidomide at the last dose. In case of grade 4 toxicity discontinue both drugs [34].

Diarrhea

Diarrhea is a common side effect of novel drugs, and more frequently observed during exposure with bortezomib, lenalidomide, and panobinostat. Diarrhea in general was rare in patients exposed to continuous Rd (4%) or Rd18 (3%) in the FIRST study [22]. However, long-term therapy with lenalidomide may, after a long asymptomatic period, induce a specific form of diarrhea, the so-called bile salt malabsorption syndrome, which seems to result from damage of the intestinal mucosa. Increased accumulation of bile acids in the small bowel may lead to debilitating episodes of diarrhea that may severely impair the patients’ quality of life [22]. The diagnosis can be established by non-invasive selenium homocholic acid taurine (SeHCAT) scanning or is supported when treatment with bile acid binders such as colesevelam results in improvement of symptoms [79]. Following the diagnosis, dietary fat intake should be reduced (to 20% of total calories) and/or colesevelam prescribed. Usually, up to 6 × 625 mg in split doses with food per day lead to rapid improvement in bowel movements and diarrhea if bile acid malabsorption is the underlying cause [79].

Panobinostat was also shown to induce gastrointestinal side effects, particularly diarrhea, which is observed in up to 40% of patients. These events should be managed with liberal use of antidiarrheal medication, proper hydration, and antiemetics, if accompanied by emesis and nausea. The frequency of diarrhea may also be improved through appropriate dose modifications of panobinostat and/or bortezomib [36] or by combining the drug with other PIs.

Pharmacological treatment of diarrhea resulting from anti-myeloma treatment is based primarily on the empirical use of locally active opioids, such as loperamide, deodorized tincture of opium, and a combination of diphenoxylate plus atropine [80, 81]. Octreotide, a long-acting somatostatin analog, is generally reserved for use in complicated cases or as a second-line treatment for persistent diarrhea after loperamide [81]. In addition, existent dehydration and/or mineral loss should be compensated.

Renal toxicity

The renal toxicities that have been reported for lenalidomide, pomalidomide, bortezomib, carfilzomib, and elotuzumab are summarized in Table 6. Presently, there is insufficient data for panobinostat to provide evidence-based information on its renal toxicity and required dose adjustments in patients with pre-existing renal impairment. For lenalidomide and ixazomib dosing, recommendations have been issued for different levels of renal impairment. Lenalidomide should be dosed at 5 mg/day in end stage renal failure, at 15 every other day (or 7.5 mg/day) in patients with GFR <30 ml/min and at 10 mg/day in those with GFR 30–50 ml/min [11, 14]. Ixazomib should be used at a dose of 3 mg/week in patients with creatinine clearance of <30 ml/min [34, 35]. Pomalidomide can be administered without dose reduction to patients with moderate and severe renal impairment [82].

Table 6

Known renal toxicities and dosing recommendations according to USPI/EU SmPC

	Published toxicitiesa	CKD dose adjustment	ESRD dose adjustment
IMiDs
Thalidomide	TLS	No	No
Lenalidomide	AKI, AIN, Fanconi syndrome, minimal change disease, TLS	30 to < 50 ml/min CrCl: 10 mg daily	<30 ml/min CrCl (HD): 5 mg daily after HD
		<30 ml/min CrCl (NOD): 7.5 mg/day or 15 mg every 48 h
		End stage renal failure: 5 mg/day (on dialysis days after dialysis)
Pomalidomide	AKI, crystal nephropathy, TLS	No	Dose after dialysis
PIs
Bortezomib	TMA, TLS	No	Dose after dialysis
Carfilzomib	TMA, TLS, ATN	No	Dose after dialysis
Ixazomib	TLS	None in mild to moderate CKD, if < 30 ml/min CrCl (NOD): 3 mg/week	<30 ml/min CrCl (HD) including ESRD: 3 mg/week
HDACis
Panobinostat	None reported	No	Insufficient data
mAbs
Elotuzumab	AKI	No	No
Daratumumab	None reported	No	No

AIN acute interstitial nephritis, AKI acute kidney injury, ATN acute tubular necrosis, TMA thrombotic microangiopathy, CKD chronic kidney disease, CrCl creatinine clearance, ESRD end-stage renal disease, GFR glomerular filtration rate, HD hemodialysis, NOD not on dialysis, TLS tumor lysis syndrome

aAdapted from Wanchoo et al. [98]

Cardiac and vascular toxicities

Cardiac toxicity has been reported with IMiDs and PIs. Carfilzomib is associated with a higher risk for cardiotoxic adverse events, including hypertension, shortly after drug infusion. The exact mechanism has not yet been clarified, but an effect of carfilzomib on endothelial cells and a common acute rise in NT-proBNP has been reported [83]. A decline in ejection fraction in few patients was shown [83, 84]. In the ENDEAVOR study, events of heart failure and pulmonary hypertension were more frequently reported in Kd versus Vd patients and similar findings were also reported in the CLARION study comparing KMP with VMP [85]. Reported reductions in left ventricular ejection fraction were mostly reversible. The utility of echocardiography as a tool to identify patients at risk of reduced left or right ventricular function was found to be limited in patients receiving carfilzomib [86].

Important cardiopulmonary risk factors and recommendations for patient monitoring, as well as the prevention and management of such events are shown in Table 7. Patients with pre-existing cardiac disease and those aged 75 years or older are at higher risk for carfilzomib-induced cardiac toxicity. They should be subjected to a comprehensive medical assessment prior to carfilzomib initiation [32, 33, 87]. Before administration of carfilzomib, their blood pressure should be tightly controlled and should not exceed systolic levels above 140 mm Hg. In addition, adherence to 30-min infusion time is recommended. Shortening the infusion time to 10 min after 1–2 cycles can be considered, if there were no cardiac or pulmonary symptoms [88]. In case of grade 3 or 4 cardiac events, carfilzomib should be interrupted until recovery. Carfilzomib may be restarted at reduced dose after a thorough benefit/risk assessment [32, 33] and the patient should be assessed for fluid overload [87, 88]. A cardiologist should be involved to address the clinical issue [87, 88]. Currently, a clear dose effect of cardiac toxicity has not been demonstrated, but it seems prudent to start with a lower dose in elderly patients (aged >75 years) and in those with a history of mild cardiac disease. Patients with more severe heart disease have been excluded from clinical studies.

Table 7

Carfilzomib-related cardiopulmonary adverse events: Table 7A. Recommendations for patient monitoring, Table 7B. Recommendations for their prevention and management

7A. Patient monitoring	7B. Prevention and management [87, 88]
Life style risk factors	Control blood pressure
SmokingObesitySedentary habit	Before carfilzomib therapy to <140/90 mm Hg. RAAS inhibitors (ACE or angiotensin receptor 2 inhibitors) preferred, if needed combine with calcium channel blockers and/or diuretics, and, thirdly, beta blockers
Age	Monitor fluid intake
Biological age ≥75 years	Appropriate hydration prior carfilzomib dosing in cycle 1 as preventive measure of tumor lysis syndrome or renal toxicity. If high risk for cardiotoxic AEs, volume may be reduced to 250 ml even at first dose and thereafter
Comorbidity
HypertensionPeripheral vascular diseaseDiabetesHypercholesterolemia
	Thromboprophylaxis
	Use thromboprophylaxis, if carfilzomib is given in combination with IMiDs or at doses >27 mg/m2
Cardiac risk factors	Monitor cardiovascular function
Heart failure (with/without reduced LVEF)	Blood pressure (24 h monitoring in special cases), heart rate (ECG), signs of cardiac failure, ischemia, dyspnea, volume overload
Coronary artery disease (angina, previous MCI or interventions for CAD)Valvular heart disease with LV impairment or LV hypertrophy Hypertrophic, dilated, or restrictive cardiomyopathy Uncontrolled cardiac arrhythmia (AF or ventricular tachyarrhythmia)Pretreatment with cardiotoxic agents (anthracyclines), concurrent treatment with high dose dexamethasone or other anti-myeloma drugs	Intervention in case of cardiac AEs
	If grade ≥3 cardiovascular events, withhold carfilzomib Stop fluid administrationConsider restarting carfilzomib therapy at 1 dose level reduction (KRd: 27 mg/m2 → 20 mg/m2 → 15 mg/m2, Kd: 56 mg/m2 → 45 mg/m2 → 36 mg/m2 → 27 mg/m2) based on a benefit/risk assessment, particularly if non- or less cardiotoxic alternatives are not availableWhen resuming therapy, consider follow-up echocardiograms (predictive value uncertain [86], but treatment should be withheld in case of decrease in LVEF) and of biomarkers such as BNP or NT-pro-BNP (transient increase frequent after carfilzomib, if permanent significant increase, withhold carfilzomib)An infusion duration of at least 30 min is highly recommended for carfilzomib independent of dose [88]

ACE angiotensin-converting-enzyme, AEs adverse events, AF arterial fibrillation, BNP brain natriuretic peptide, CAD coronary artery disease, ECG electrocardiogram, Hg mercury, hr hour, IMiDs immunomodulatory drugs, LV left ventricular, LVEF left ventricular ejection fraction, MCI myocardial infarction, NT-pro-BNP N-terminal BNP precursor, RAAS renin angiotensin aldosterone system

Infusion-related reactions

Both approved monoclonal antibodies, elotuzumab and daratumumab, are of IgG1κ isotype, the former being humanized and the latter being fully human. In spite of their similarity with human IgG, treatment with these antibodies may results in infusion reactions that mostly are seen during the first and less so during following infusions. Lonial et al. reported infusion-related AEs in only 10% of patients receiving 20 mg/kg of elotuzumab, all of grade 1 or 2 [89]. Single-agent daratumumab resulted in higher rates of infusion-related AEs of 45% as reported in a phase II study, with only few being classified as grade 3 [90].

For both drugs, prophylactic measures are recommended. Forty-five to 90 min before start of elotuzumab infusion, dexamethasone (8 mg, IV), diphenhydramine (25–50 mg orally or IV) or equivalent, ranitidine (50 mg IV or 150 mg orally) or equivalent, and paracetamol/acetaminophen (650–1000 mg orally) should be administered. A similar regimen should be used ~1 h before daratumumab infusion, consisting of 100 mg of IV methylprednisolone or equivalent (may be reduced to 60 mg thereafter), oral antipyretic (paracetamol 650–1000 mg), oral or IV antihistamine (diphenhydramine 25–50 mg) or equivalent. All patients should receive post-infusion treatment with 20 mg methylprednisolone or equivalent on each of the 2 days following infusion. Special precautions need to be taken in patients with pre-existing chronic obstructive pulmonary disease (COPD). Premedication with 10 mg montelukast, an oral leukotriene receptor antagonist, 30 min before daratumumab should be considered as well as post-infusion therapy with short- and long-term bronchodilators and inhaled corticosteroids; patients with COPD stage IV disease should be excluded from daratumumab therapy [91]. An early report showed that an SC preparation of daratumumab can be safely administered within 30 min with a significantly lower rate of daratumumab-related IRRs [92]. Details of dilution volume of the drugs, infusion rates, increments in rates, and maximum speed are listed in Table 8.

Table 8

Prevention and treatment of monoclonal antibody-related infusion reactions

	Elotuzumab [39, 40]	Daratumumab [41, 42]
Timing	45–90 min prior to infusion	Approx. 1 hr. prior to infusion
Premedication	Dexamethasone (8 mg IV)H1 blocker: diphenhydramine (25–50 mg orally or IV) or equivalentH2 blocker: ranitidine (50 mg IV or 150 mg orally) or equivalentParacetamol/acetaminophen (650–1000 mg orally)	IV corticosteroid (methylprednisolone 100 mg) or equivalent dose of an intermediate-acting or long-acting corticosteroidOral antipyretic (paracetamol 650–100 mg)Oral or IV antihistamine (diphenhydramine 25–50 mg) or equivalentConsider montelukast prior to first infusion [91]Following the second infusion, the dose of IV corticosteroid may be reduced (methylprednisolone 60 mg)
Post-infusion medication		Oral corticosteroid (methylprednisolone 20 mg) or equivalent on each of the 2 days following all infusions. If daratumumab is used in combination with other drugs, a corticosteroid dose should be considered on the day after infusion. In those receiving a corticostreoid dose on day plus one, subsequent dosing may be omitted.In patients with a history of obstructive pulmonary disorder: use post infusion medication including short- and long-acting bronchodilators and inhaled corticosteroids
Treatment	If grade ≥2 IRR occurs, infusion must be interruptedMonitor vital signs every 30 min for 2 hr.Upon resolution to grade ≤1, restart administration at 0.5 mL/min with gradual increase at a rate of 0.5 mL/min every 30 min as tolerated to the rate at which IRR occurred; if no recurrence of IRR, escalation can be resumedGrade ≥3 IRR may require permanent discontinuation and emergency treatment	For IRRs of any grade/severity immediately interrupt infusionIf grade 1–2 IRR occurs, once patient is stabilized, resume infusion at half the rate at which the IRR occurred; if no recurrence of IRR, escalation can be resumedIf grade 3 IRR occurs, once IRR decreases to grade ≤2, restart infusion at no more than half the rate at which IRR occurred; if no recurrence of IRR, escalation can be resumedPermanently discontinue in the event of life-threatening (grade 4) IRRs at first or at any subsequent infusion

hr. (s) hour(s), IRR infusion-related reaction, IV intravenous, min minutes

In case of occurrence of infusion-related AEs of grade ≥2 during elotuzumab infusion, the infusion must be interrupted and can be restarted at lower infusion rate (0.5 ml/min) with gradual increase by 0.5 ml/min every 30 min as tolerated to the rate at which the IRR occurred. If this is well tolerated, escalation of the infusion rate can be resumed. Patients with a grade ≥3 IRR may require emergency treatment and permanent discontinuation. A similar procedure is recommended for daratumumab-induced IRR. The infusion should be interrupted at any grade/severity. If grade 1–2 IRR occurs, the infusion may be resumed at half the rate at which it occurred, provided the patient is stabilized; in case of no recurrence of IRR, escalation can be resumed. If grade 3 IRR occurs, once IRR decreases to grade ≤2, the infusion may be restarted at no more than half the rate at which the IRR occurred. If no recurrence of IRR, escalation can be resumed. Patients have to discontinue daratumumab therapy in case of grade 4 (life threatening) IRRs at first or subsequent infusion.

Teratogenicity

Almost all novel agents and backbone agents showed a certain embryo-fetal risk, especially the thalidomide analogs of the IMiD group (Table 1 and S2A). Pregnancy must be excluded before start of treatment. Women of reproductive potential and their partners should be informed about the embryo-fetal risk of the respective drugs and about adequate contraceptive measures. To prevent pregnancy, continuous abstinence from heterosexual intercourse or two reliable methods of contraception must be used. The respective USPIs and EU SmPCs have detailed instructions suited to the agents used.

Conclusions

A number of novel drugs have recently been introduced in the treatment of multiple myeloma. These drugs differ in their mode of action and their side effect and safety profile. Knowledge of their potential risks and of established measures to prevent occurrence of complications is essential for preventing severe symptoms, dose reductions, and/or treatment discontinuations and in some patients even mortality. In case of emergence of drug reactions, optimal management is key for optimizing treatment outcome.

Supplementary information 1

Supplementary information 2