Belantamab Mafodotin for the Treatment of Multiple Myeloma: An Overview of the Clinical Efficacy and Safety.

Despite the introduction of immunomodulatory drugs (IMiDs), proteasome inhibitors (PIs), and, more recently, monoclonal antibodies (mAbs), in the chemotherapy regimens for newly diagnosed (NDMM) and relapsed/refractory MM (RRMM), the occurrence of drug resistance remains a challenge in MM patients. This is mainly in the advanced stage of the disease when treatments are limited, and the prognosis is abysmal. Nevertheless, novel molecules and therapeutic approaches are rapidly moving through the several phases of drug development and could address the need for new treatment options. The recent innovative B-cell maturation antigen (BCMA) targeted immunotherapies, such as belantamab mafodotin, the first-in-class monoclonal antibody-drug conjugate (ADC), induce an effective and durable response in triple-class refractory disease and to be approved in MM. In contrast with the other BCMA-targeted therapies as CAR T cells with a complex manufacturing process, and bispecific antibodies, both requiring inpatient hospitalization to monitor the occurrence of severe adverse events, belantamab mafodotin is an "off-the-shelf" drug that can be administered in an outpatient setting. Many belantamab mafodotin-based combinations are under evaluation in Phase I, II, and III clinical trials either late or in early RRMM patients. Ocular toxicity represents a peculiar side effect of belantamab mafodotin. This toxicity is generally manageable with adequate dose reductions or delays since most patients who developed keratopathy recovered on treatment and discontinued ADC are rare. Here, we described the most recent clinical data of belantamab mafodotin and discussed the possible leading role of this intriguing agent in the near future of MM treatment.

Introduction

Multiple Myeloma (MM), the second most frequent hematological neoplasm,1 is characterized by aberrant proliferation of plasma cells, which commonly produce a large number of monoclonal immunoglobulins leading to organ damage, such as osteolytic bone lesions and renal impairment, as well as bone marrow failure symptoms like anemia or recurrent infection due to immune-paresis.2 Although MM remains incurable, it is a biologically very heterogeneous disease with median survival ranging from 2 to 10 years.3,4

The therapeutic landscape of MM has outstandingly changed in the last 20 years with the introduction of proteasome inhibitors (PIs: bortezomib, carfilzomib, ixazomib), immunomodulatory agents (IMiDs: thalidomide, lenalidomide, pomalidomide), and, more recently, monoclonal antibodies (mAbs: elotuzumab, daratumumab, isatuximab), which has led to an unprecedented improvement of the outcome either in patients eligible (TE) or not-eligible for transplantation (NTE). Currently, therapeutic approaches including triplet induction combinations, high-dose therapy (HDT) followed by autologous transplantation (ASCT), and consolidation-maintenance, results in a 10-years survival probability of 60% in TE patients.5 In elderly patients, triplet or doublet combinations with PIs or IMiDs allowed achieving a median survival of 5 years.6 Perhaps the addition of daratumumab, mAb targeting CD38 molecule, to regimens used in the upfront setting could further improve survival both in TE and NTE patients. However, the course of MM is characterized by periods in which the disease is in remission and by phases of relapse until MM becomes resistant to therapies. At this point, MM is complicated to treat since the several drug combinations used in earlier lines of treatment further reduce the availability of subsequent effective treatments.7 Patients who become refractory to PIs, IMiDs, and monoclonal antibodies have an inferior outcome with a median OS of 5.6 months8, so there is a significant unmet need for effective, innovative therapies to be offered to these patients. Among novel immunotherapies, belantamab mafodotin (Belamaf) is the first antibody-drug conjugate targeting B-cell maturation antigen (BCMA) to be approved for the treatment of multiple myeloma. This review will focus on Belamaf, describing its mechanism of action, pharmacokinetics, and available clinical data on their safety and efficacy.

Methods

To perform this review, we searched the database of PubMed using the terms “multiple myeloma”, “relapsed”, “refractory”, “B-cell maturation antigen”, “antibody-drug conjugate”, “belantamab mafodotin”. Available data included in abstracts presented at the ASH, ASCO, EHA, and other International Meetings were also used. Moreover, the clinicaltrials.gov database was searched using “multiple myeloma” and “belantamab mafodotin”.

Results

Emerging Therapies for RRMM

After the therapeutic success of using mAbs to treat other hematologic malignancies,9,10 this approach became available for MM.

Elotuzumab, a humanized IgG1 mAb binding to SLAMF7 (signaling lymphocytic activation molecule 7) expressed both on MM and NK cells, is the first one to be explored in the treatment of MM11 and to demonstrate, in combination with lenalidomide and dexamethasone (Elo-Rd), a significant OS benefit in relapsed/refractory MM (RRMM) compared to lenalidomide plus dexamethasone (Rd) in Phase III ELOQUENT-2 trial.12 Triplets Elo-Rd and Elo-Pd (elotuzumab, pomalidomide, and dexamethasone), assessed in phase III ELOQUENT-3 study13 have been approved for the treatment of RRMM.

Daratumumab is the first fully human IgG1κ targeting CD38 eliciting cell death through complement-dependent cytotoxicity (CDC), antibody-dependent cell-mediated cytotoxicity (ADCC), antibody-dependent cellular phagocytosis (ADCP), induction of apoptosis, and modulation of CD38 enzyme activities.14 After GEN50115 and SIRIUS16 studies demonstrated the efficacy of daratumumab monotherapy; it has been approved in combinations with lenalidomide and dexamethasone (DRd) or Bortezomib and dexamethasone (DVd) for treatment of RRMM who have received at least one prior line of therapy, based on the results of phase III POLLUX17 and CASTOR18 trials. More recently, daratumumab has been evaluated in combination with pomalidomide and dexamethasone (DPd) vs Pd or combination with Carfilzomib and dexamethasone (DKd) vs Kd in phase III APOLLO19 and CANDOR20 trials. Both studies met their primary endpoint of improved PFS, and these combinations are starting to become the new standard in RRMM patients. However, with daratumumab combination regimens now increasingly utilized in the front-line setting based on phase III CASSIOPEIA,21 ALCYONE22, and MAIA23 trials, the role of daratumumab-containing therapies in the relapse setting is uncertain, in the absence of clear evidence that rechallenging with daratumumab can overcome prior daratumumab refractoriness.

Another mAb targeting CD38 is isatuximab, a chimeric IgG1κ mAb targeting a specific epitope on CD38. This mechanism of action is different from that of daratumumab since it induces direct apoptosis in MM cells, inhibits CD38 enzymatic activity more effectively than daratumumab, and is less able to induce CDC. Moreover, isatuximab exerts an immunomodulatory effect since it inhibits the suppressive function of Tregs by reducing their number, decreasing immune inhibitory cytokine production, including IL-10, and blocking their trafficking. All these activities improved NK- and T-cell-mediated antitumor immune responses.24 Isatuximab in combination with pomalidomide and dexamethasone (Isa-Pd) can be used in RRMM patients who have received at least two prior lines of therapy after approval based on results of phase III ICARIA trial.25

However, as with other agents, resistance to daratumumab is a possible event leading to a poor outcome, as showed in the retrospective MAMMOTH study8 including 275 patients among whom those penta-refractory (refractory to 1 CD38 mAb + 2 PIs + 2 IMiDs) had a median OS of 5.6 months. Hence, there is a need for developing and introducing novel therapies in clinical practice. Among more advanced emerging treatments, selinexor, melfuflen, cerebron E3 ligase modulators (CELMoDs), and venetoclax were found very promising. Selinexor is the first-in-class oral selective inhibitor Nuclear Export (SINE) compound targeting XPO-1 (exporting-1) to be explored in MM.26 Recently, it has been approved in combination with Bortezomib and dexamethasone (SVd) for treatment of RRMM patients who have received at least one prior therapy, based on results of phase III BOSTON trial.27 In patients treated with one to three previous lines of treatment, SVd allowed a median PFS of 13.9 months vs 9.5 months in patients treated with Vd. Besides grade 3–4, thrombocytopenia and neutropenia occurring in 39% and 6% of patients, respectively, about 25% of patients experienced gastrointestinal toxicity. In 2019 selinexor had received approval in combination with dexamethasone in advanced disease.28 Melfuflen (melfuflen-flufenamide) is the first-in-class peptide-drug conjugate targeting aminopeptidases and releasing alkylating agents into tumor cells29 which demonstrated in combination with dexamethasone efficacy in triple-class refractory MM patients in the Phase II HORIZON, showing in RRMM patients with a median of 5 prior lines of therapy a median PFS of 4.2 months.30 Combined with dexamethasone, it has been recently approved by FDA in patients who have received at least four previous lines of therapy. CELMoDs starting from iberdomide represent the next-generation IMiDs and exert more potent immunomodulation than lenalidomide and pomalidomide.31 Venetoclax, an oral BCL-2 targeted therapy, approved for CLL and AML, demonstrated remarkable efficacy in RRMM harboring t(11;14) or with high BCL-2 expression.32

Novel immunotherapies, including bispecific antibodies, antibody-drug conjugates, and CAR T cells, human genetically modified T cells, are the new frontiers of MM therapy and great hope in more advanced and refractory diseases in which these treatments can induce high-quality and durable responses.33,34 In the recently published KarrMMa study,35 idecabtagene vicleucel at the dose of 450×106 CAR T cells induced responses in 81% of patients who had received a median of 6 prior lines of therapies and median PFS was 12.1 months. As regard BCMA targeting bispecific antibodies, preliminary results from teclistamab given subcutaneously showed a promising ORR of 73% in patients with a median of 5 previous lines of therapy, being ORR 75% in penta-refractory patients.36

The availability of all these therapeutic options in the near future will make the choice of treatment in RRMM a very complex process.

Chemistry and Mechanisms of Action of Belantamab Mafodotin

As mentioned above, naked mAbs eliminate target MM cells by activating host defense mechanisms regulated by Fcγ receptor-expressing effector cells.37 However, in MM patients, immune dysregulation involving B cells and T cells, dendritic cells (DC), and natural killer cells (NK) has been demonstrated.38 Daratumumab was found to induce expansion of T-cells and increase T-cell clonality. Still, in patients who become resistant to this mAb, an increase of exhausted T cells with upregulation of the checkpoint inhibitors lymphocyte-activation gene 3 (LAG3) and T cell immunoreceptor with Ig and ITIM domains (TIGIT) was observed.39 Moreover, NK cell depletion has been documented following daratumumab administration and may reduce the efficacy of this mAb.40 An evolution of naked mAbs is represented by antibody-drug conjugates (ADC), a payload delivery system is consisting of a monoclonal antibody directed against a tumor-specific antigen and a cytotoxic agent inducing cell death (payload) covalently conjugated through chemical linkers41 (Figure 1). An ideal antigen for effective immunotherapy with ADC should be a highly expressed molecule on the membrane of MM plasma cells, and BCMA, a member of the TNF receptor superfamily 17, represents an excellent candidate since it has been found on the surface of late-stage of normal B lymphocytes and malignant plasma cells.42 For BCMA, two ligands have been identified: a proliferation-inducing ligand (APRIL) and B-cell activating factor (BAFF).43 Activation of BCMA enhances expression of genes critical for the survival of plasma cell growth, adhesion, osteoclast activation, angiogenesis, metastasis, and immunosuppression.44 Soluble BCMA (sBCMA) derives from the ectodomain shedding of the membrane receptor by gamma-secretase activity. The levels of sBCMA have prognostic value;45 correlate with the phase of MM’s natural history, increasing through the progression from MGUS to smoldering myeloma and then to active MM;46 they can also be helpful to monitor clinical response to ongoing therapy.45,47

Figure 1

Structure of an antibody-drug conjugate.

The choice of the antibody is crucial and, based on experience with naked mAbs as elotuzumab and daratumumab, the most commonly used antibody is a fully human or humanized antibody immunoglobulin G subtype (IgG) for long-circulating half-life in the human bloodstream (up to three weeks) and minimal immunogenicity. Probably, the most complex aspect of ADC development is the chemistry of the linker requiring several requirements: the linker has to be strong enough to withstand degradation in the plasma since instability of linker causes premature liberation of toxic payload with damage to non-target healthy cells; in the same time, it has to be vulnerable enough for degradation and release of the payload in the endosome/lysosome once the ADC is internalized into the target tumor cell.41,48 Linkers can be categorized into two classes according to the payload release mechanism: cleavable linkers are designed to respond to a specific environmental condition (pH, lysosomal protease, or glutathione) which assesses the linkers to enable chemical or biochemical reactions as hydrolyzation or proteolysis. Non-cleavable linkers rely on the monoclonal antibody degradation by cytosolic and lysosomal proteases after ADC internalization with the liberation of payload molecule linked with an amino acid residue of degraded antibody.41 It is also necessary to pay attention to the choice of the killing molecule that requires several requirements as substantial cell toxicity, possessing the appropriate modified site from where the conjugate releases the original drug in the tumor cell, and a definite mechanism of action.49 The commonly used payloads are microtubule inhibitor agents as maytansinoids and auristatin (including monomethyl auristatin E and F), able to bind to tubulin, causing G2/M arrest and apoptosis50 and DNA-modifying drugs as calicheamicin, inducing cell death by DNA double-strand breaking.51 In the next future, payloads will probably be less potent but more targeted against a specific tumor cell. In Table 1, we summarized the main antibody-drug conjugates in development.

Table 1

Main Antibody Drug Conjugates Targeting BCMA

Agent	Target	Type	Phase
AMG224	BCMA	Mertansine ADC	I
MEDI2228	BCMA	Pyrrolobenzodiazepine ADC	I
CC-99,712	BCMA	Undisclosed ADC	I
HDP-101	BCMA	Amanitin ADC	Preclinical
STRO-001	CD74	Maytansinoid ADC	I
FOR46	CD46	monomethyl auristatin-F ADC	I
ABBV-838	SLAMF7	monomethyl auristatin-E ADC	I/Ib

Belantamab mafodotin (Belamaf, GSK2587916) is a first-in-class humanised IgG1 ADC developed to treat MM. This afucosylated Fc-engineered ADC includes an antibody targeting BCMA covalently linked via a cysteine linker to the microtubule inhibitor monomethyl auristatin F (MMAF). Therefore, the most important characteristics of Belamaf structure are the highly potent cytotoxic agent; the afucosylation significantly increasing the binding affinity of the Fc domain to the FcγR (FcγRIIIa) expressed on effector cells; the uncleavable maleimidocaproyl (mc) cysteine linker region, which makes the ADC stable in circulation.52 Several are the mechanism of action of Belamaf, and the main one is binding to BCMA on tumor plasma cell, internalization, and release of MMAF, which binds to tubulin and inhibits its polymerization resulting in G2/M arrest and caspase 3 dependent apoptosis (Figure 2).53 Due to afucosylation of antibody, Belamaf significantly improves the potency and efficacy of ADCC activity against MM cells. Importantly, in vitro studies showed that ADCC was enhanced by the addition of lenalidomide, providing the basis for a possible combination of Belamaf with IMiDs.

Figure 2

Mechanisms of action of belantamab mafodotin.

Moreover, Belamaf exerts anti-myeloma activity inducing ADCP. A dose of 4 mg/kg was found in mouse xenograft models to induce a complete tumor eradication for the entire 60-day study.53 More recently, in vitro and in vivo studies demonstrated that durable antitumor activity of Belamaf is characterized by T, NK, and dendritic cell infiltration and increased markers of immunogenic cell death (ICD) and is abrogated upon depletion of CD8+ T cells.54 Therefore, these mechanisms represent a rationale for combination with various immunomodulatory therapies.

Clinical Studies

DREAMM-1 Study

Phase I DREAMM-155 was the first-in-human study to explore Belamaf as monotherapy in RRMM. This international study comprised a Part 1, a dose-escalation phase assessing the safety and tolerability of Belamaf and recommended phase II dose (RP2D) and a Part 2, dose-expansion phase, evaluating safety and tolerability pharmacokinetics, and clinical activity. In part 1, patients received Belamaf at doses ranging from 0.03 mg/kg to 4.6 mg/kg, administered in 1 h intravenous infusion every three weeks until progression, unacceptable toxicity, or completion of 16 doses of treatment. To evaluate the incidence and severity of infusion-related reactions (IRRs), prophylaxis was not permitted for the first infusion but only for subsequent ones. From 2014 to 2017, 73 patients were enrolled, 38 in Part 1 and 35 in Part 2. Among patients included in the dose-escalation phase, 76% had received at least five prior lines of therapy and the median time from diagnosis was 5.3 years. The most common grade 3–4 adverse events were thrombocytopenia (34%) and anemia (16%). However, 53% of patients receiving Belamaf developed ocular toxicity, which is a well-known side effect with other MMAF-linked antibody-drug56 and will be described in more detail in a chapter below. No maximal tolerated dose was established, so 3.4 mg/kg was the RP2D to treat patients in Part 2 of the study, chosen based on pharmacokinetics, activity, and safety data. Regarding characteristics of 35 patients enrolled in Part 2,57 40% had received more than five prior lines of therapy, 97% were refractory to PIs, 94% to IMiDs, 40% to daratumumab. The most common grade 3–4 adverse events were thrombocytopenia (35%), anemia (17/%), pneumonia (6%), and IRRs (6%). Corneal events were seen in 69% of patients, most commonly blurred vision (51%), dry eye (37%), and photophobia (29%), whose median duration was 35 days. Regarding efficacy data, 60% of patients achieved a PR or better, and 54% achieved at least VGPR. In patients without and with prior daratumumab exposure, ORR was 71.4% and 42.9%, respectively. In contrast, ORR was 38.5% in triple-refractory (daratumumab + 1 PI + 1 IMiD), 70% in patients who had received ≤ 3 prior therapies and 50% in > 5 prior therapies. The median time to first response was 1.2 months, and responses deepened over time. After over a year of additional follow-up from the previous interim analyses performed with a median follow-up of 12.5 months, the median duration of response was 14.3 months and median PFS 12 months. In patients with prior daratumumab treatment and refractory disease to PIs and IMiDs, the median PFS was 6.2 months. In patients without daratumumab treatment, median PFS was 15.7 months.57

DREAMM-2 Study

The most important study leading to Belamaf approval for RRMM treatment is the international, open-label, two-arm, phase II DREAMM-2 study58 which explored the safety and efficacy of two doses of belantamab mafodotin in RRMM patients who were refractory to an IMiDs (lenalidomide or pomalidomide), a PI (Bortezomib, Carfilzomib or ixazomib) and refractory or intolerant to an anti-CD38 mAb. Dosing regimens explored were Belamaf 2.5 mg/kg or 3.4 mg/kg, selected based on results of the DREAMM-1 study. The trial’s primary endpoint was ORR, defined as the percentage of patients achieving at least PR as per IMWG 2016 criteria.59 In contrast, secondary outcomes were duration of response (DoR), time to response, PFS, OS, and safety, including keratopathy. One hundred ninety-six patients were randomly allocated to receive Belamaf 2.5 mg/kg (n=97) and 3.4 mg/kg (n=99) intravenously over 30 min, every three weeks until disease progression or unacceptable toxicity. Patients had received a median of 7 (range 3–21) and 6 (range 3–21) prior lines of therapy in the 2.5 mg/kg and 3.4 mg/kg cohort, respectively. As per inclusion criteria, all patients were refractory to an IMiD, to a PI and 100% and 92% of patients were refractory to previous therapies including daratumumab in the 2.5 mg/kg and 3.4 mg/kg cohort, respectively, with 34% and 37% of patients receiving daratumumab as the last prior therapy. Patients with ISS stage III, extramedullary disease, and high-risk cytogenetics were well represented in both groups. At a median follow-up of 13 months, ORR was 31% in the 2.5 mg/kg cohort and 34% in the 3.4 mg/kg cohort. Belamaf monotherapy was found to induce deep responses since 19% and 23% (58% and 66% of patients achieving at least PR) in the 2.5 and 3.4 groups, respectively, achieved at least VGPR. The median DoR and PFS were 11 months and 2.8 months in the 2.5 mg/kg group vs 6.2 months and 3.9 months in the 3.4 mg/kg group. Median OS was 13.7 months in the 2.5 mg/kg cohort and 13.8 months in the 3.4 mg/kg cohort with the estimated 1-year survival of approximately 57% in both groups.60

The median number of treatment cycles administered was 3 (range 1–17), and the median time on treatment was 9.3 weeks.61 Serious adverse events (SAEs) occurred in 42% and 47% in the 2.5 mg/kg and 3.4 mg/kg group, and they were considered study-treatment-related in 12% and 20% of patients, respectively. Main hematologic grade 3–4 adverse events were thrombocytopenia developing in 22% of patients receiving Belamaf 2.5 mg/kg vs 32% in those 3.4 mg/kg, anemia in 21% vs 27%, neutropenia in 11% vs 17%. Among nonhematologic toxicities, keratopathy (MECs) was the most common adverse event in 72% of patients in the 2.5 mg/kg group and 77% in the 3.4 mg/kg group. The median time to first MEC was 37 days vs 22.5 days, majority of patients experienced the first event by dose 4 and 48% and 47% of patients treated with 2.5 mg/kg and 3.4 mg/kg, respectively, recovered from the last events at the last follow-up of 13 months. Other ocular events included blurred vision (any grade: 25% in 2.5 mg/kg group and 33% in 3.4 mg/kg group; grade 3–4: 4% in both groups); dry eye occurring in 15% vs 25% (mostly grade 1–2); changes in visual acuity (18% vs 20%), with first episode resolving in 82% vs 100% of patients after a median of 21.5 or 23.5 days in 2.5 mg/kg cohort and 3.4 mg/kg cohort, respectively. Keratopathy was the main toxicity requiring Belamaf dose delays (47% in 2.5 mg/kg cohort and 53% in the 3.4 mg/kg cohort) and dose reduction (25% vs 30%). In contrast, only 1% vs 3% of patients permanently discontinued treatment due to ocular toxicities. Other nonhematologic adverse events were not common, and grade 3–4 infections were seen in 7% and 13% of patients receiving lower and higher Belamaf dose. The 2.5 mg/kg was selected as the recommended dose to use in future clinical studies based on similar efficacy data compared with 3.4 mg/kg but a better safety profile. As regards IRRs, after a median follow-up of 13 months, they occurred in 21% of patients receiving dose regimen of 2.5 mg/kg and were mostly of grade 1–2, with no patients developing grade 4–5 IRR. Most patients (90%) developed the complication during the first cycle, and the incidence of these events declined after that.62 Analysis of symptoms and HRQoL of patients enrolled in the DREAMM-2 and receiving the 2.5 mg/kg dose showed improved pain, physical functioning, and disease symptoms from baseline over time. Of note, improvement in fatigue was seen in 30% of patients at week 25.63

Based on the results of the DREAMM-2 study, belantamab mafodotin was approved by FDA an EMA on August 2020 for the treatment with RRMM who have received at least four prior therapies, including an anti CD38 mAb, a PI, and an IMiD. The recommended dosage is 2.5 mg/kg every three weeks until progression or unacceptable toxicity.

At the last EHA, ASCO, and ASH meetings, post-hoc analyses of specific subpopulations of the DREAMM-2 study have been presented. Patients with mild (defined as eGFR ≥ 60 ≤ 90 mL/min/1.73 m2) or moderate (eGFR ≥ 30 ≤ 60) renal impairment achieved a similar ORR compared to patients with normal renal function. However, despite a similar incidence of keratopathy, grade 3–4 thrombocytopenia was more frequent in patients with renal impairment, particularly in patients receiving 3.4 mg/kg.64 Efficacy of Belamaf monotherapy was documented in either standard-risk or high-risk cytogenetics patients with DoR, PFS and probability of a durable response similar in the two groups of patients.65 Belamaf was found efficacy in very advanced MM disease as showed by a retrospective analysis comparing the outcome of patients receiving Belamaf 2.5 mg/kg with 3–6 prior therapies v.s ≥ 7 prior therapies. ORR was 34% and 30% in the first and second group, respectively; median DoR was 11 months vs 13.1 months, median PFS 2.9 vs 2.2 months. No differences in keratopathy, dose delay or dose reduction were reported between the two groups of patients.66 Moreover, a recent post-hoc analysis showed that among patients with prolonged treatment interruptions (> 63 days), mainly due to keratopathy, 76% maintained or deepened their response during the delay.67

Although the DREAMM-2 study demonstrated the ability of belantamab mafodotin to induce a durable response in heavily pretreated RRMM patients, the company was requested to design a trial comparing Belamaf with another available treatment in this setting of patients, so the ongoing phase III DREAMM-3 trial (Table 2) is evaluating Belamaf vs Pd in approximately in 320 RRMM patients with ≥2 prior lines of therapy. Results from this clinical trial are expected by July 2024.61

Table 2

Ongoing Clinical Trial with Belantamab Mafodotin

Trial	Phase	Population	Intervention	Trial ID
DREAMM-3	III	RRMM with ≥2 lines including PI and lenalidomide	Belamaf vs Pd	NCT04162210
DREAMM-4	I/II	RRMM with ≥3 lines including PI, IMiD, and anti CD38 mAb	Belamaf + pembrolizumab	NCT03848845
DREAMM-5	I/II	RRMM with ≥3 lines including PI, IMiD, and anti CD38 mAb	Belamaf + innovative drugs	NCT04126200
DREAMM-6	I/II	RRMM with ≥1 prior therapy	Belamaf-Rd or Belamaf-Vd	NCT03544281
DEAMM-7	III	RRMM with ≥1 prior therapy	Belamaf-Vd vs DVd	NCT042246047
DEAMM-8	III	RRMM with ≥1 prior therapy including lenalidomide	Belamaf-Pd vs PVd	NCT04484623
DREAMM-9	I	Transplant ineligible NDMM	Belamaf-VRd followed by Belamaf-Rd	NCT04091126
DREAMM-12	I	Renal impairmentRRMM with ≥2 lines including PI and IMiD,	Belamaf	NCT04398745
DREAMM-13	I	Hepatic impairmentRRMM with ≥2 lines including PI and IMiD,	Belamaf	NCT04398680
Study of belamaf as pre-and post-autologous stem cell transplant and maintenance for MM	I	Transplant eligible NDMM	Belamaf pre- (day −42) and post- ASCT for 2 years	NCT04680468
Blmf, lenalidomide, and dexamethasone in transplant-ineligible patients with newly diagnosed multiple myeloma (BelaRd)	I/II	Transplant ineligible NDMM	BelaRd	NCT04808037
Belantamab mafodotin in newly diagnosed transplant eligible multiple myeloma patients	II	Transplant eligible NDMM	Bela-VRd followed by ASCT, consolidation with Belamaf and VRd, maintenance with lenalidomide and Belamaf	NCT04802356
Characterization of corneal epithelial changes in participants treated with belantamab mafodotin	III	RRMM who have received or are receiving belamaf and with keratopathy	Impression cytology or superficial keratectomy	NCT045549363

Abbreviations: Pd, pomalidomide, dexamethasone; Rd, lenalidomide, dexamethasone; Vd, bortezomib, dexamethasone; DVd, daratumumab, bortezomib, dexamethasone; PVd, pomalidomide, bortezomib, dexamethasone; VRd, bortezomib, lenalidomide, dexamethasone; RRMM, relapsed/refractory multiple myeloma; NDMM, newly diagnosed multiple myeloma.

Pharmacokinetics and Metabolism

The pharmacokinetics of belantamab mafodotin was assessed by measuring Belamaf, total mAb (with and without the cytotoxic payload MMAF), and cys-mcMMAF in plasma collected at cycle 1 and 3 of all patients enrolled in the DREAMM-155 and DREAMM-258 studies. After administration of Belamaf at dose of 2.5 mg/kg, maximal serum concentration (Cmax) was 42.5 μg/mL after a median of 0.78 h (tmax), mean AUC of 4666 μg.h/mL and mean Ctrough of 2.4 mg/mL. The mean steady-state volume of distribution of Belamaf was 10.8 L, and it was cleared slowly with a total plasma clearance of 0.92 L/day and a terminal t1/2 of 12 days. Over time, clearance was reduced, and t1/2 was 14 days.68

An analysis of population pharmacokinetics and exposure-response for critical endpoints from the DREAMM-2 study showed that time to response but not time to best response was inversely related to Belamaf Ctrough. Safety endpoints were strongly associated with exposure, so higher Ctrough was related to the probability of developing ocular exam finding (OEF) and inversely correlated to time to onset. Higher cys-mcMMAF maximum concentration and lower platelet count at baseline were associated with an increased probability of grade 3–4 thrombocytopenia, whereas no factors were found to impact neutropenia and IRRs. Increased likelihood of ocular toxicity and severe thrombocytopenia with higher exposure or dose was not associated with a commensurate improvement in efficacy in the DREAMM-2 study, supporting a monotherapy dose of 2.5 mg/kg every three weeks in RRMM patients.69

ALGONQUIN Study

The peculiar mechanism of action of Belamaf provides a rationale for combining this ADC with other active agents used for the treatment of MM as IMiDs, which have shown to exert a pleiotropic effect on a wide range of immune cells as NK cells activation and T cells co-stimulation.70 The multicenter, nonrandomized, ALGONQUIN phase I study,71 performed by Canadian Myeloma Research Group, explored safety and efficacy of Belamaf in combination with pomalidomide and dexamethasone in RRMM who had received ≥1 prior line of therapy, lenalidomide refractory, PIs exposed or refractory, and pomalidomide naïve. In Part 1, dose-finding patients received pomalidomide 4 mg days 1–21, dexamethasone 40 mg weekly (20 mg in patients older than 75 years), and belamaf single (1.92 or 2.5 mg/kg day 1) or split (2.5 or 3.4 mg/kg spit on days 1 and 8) every four weeks. The primary endpoint of this part was to identify the MTD and RP2D to use in Part 2, which aimed to evaluate the ORR of the combination. At the presentation of the study at the last ASH meeting, the number of patients enrolled in the dose-finding phase was 35 with a median age of 64 years (range 36–81) and a median of 3 prior lines of therapy (range 1–5). Seventy-three percent of patients were lenalidomide and PIs refractory, whereas 35% were triple-refractory (lenalidomide, PIs, and daratumumab). MTD was established to be Belamaf 2.5 mg/kg (day 1) and 2.5 mg/kg split-dosing (1,25 mg/kg days 1 and 8) every four weeks in combination with standard doses of pomalidomide and dexamethasone (Pd). Grade 3–4 hematologic adverse events consisted of neutropenia (40.5%) and thrombocytopenia (32.4%). Grade 3–4 keratopathy occurred in 51% of patients and decreased visual acuity in 16%. IRRs developed in 29% of patients, but they were mainly of grade 1–2. Overall, at least 88% of patients achieved at least PR (≥ VGPR = 68%; CR = 20.6%) and, after a median follow-up of 7.8 months, median PFS was not reached. Efficacy was also documented in triplet refractory MM patients since ORR was 100%, with 72% of patients obtaining at least VGPR. However, a single dose of 1.92 mg/kg in combination with Pd was found to be the best in terms of efficacy and safety profile since ORR was 82%, at least VGPR 64%, median PFS 14.1 months, and grade 3–4 keratopathy 25%, showing that Belamaf-Pd compares favorably to other pomalidomide-based triplets as pomalidomide, Bortezomib, dexamethasone (PVd: median PFS 11.2 months),72 elotuzumab, pomalidomide, dexamethasone (Elo-Pd: median PFS 10.3 months),13 daratumumab, pomalidomide, dexamethasone (DPd: median PFS 12.4 months),19 isatuximab, pomalidomide, dexamethasone (Isa-Pd: median PFS 11.5 months)25 and, finally, selinexor-Pd (median PFS 10.4 months).73

DREAMM-4 Study

Belamaf was evaluated in association with pembrolizumab in the phase I/II DREAMM-4 study74 in RRMM patients with ≥3 prior lines of therapy, including anti-CD38 mAb. The rationale of this combination is that PD-1 inhibitors may augment immune responses to Belamaf-induced immunogenic cell death. In the dose-escalation part of the study, patients received Belamaf 2.5 mg/kg or 3.4 mg/kg plus pembrolizumab 200 mg iv every three weeks. A total of 13 patients with a median age of 71 years (range 50–81) and a median number of prior therapies of 5 (3–13) were enrolled in this study phase. The ORR was 67% and 43% in the 2.5 mg/kg and 3.4 mg/kg cohort, respectively. Ocular toxicity represented the most common AEs: any grade keratopathy (with or without symptoms) was reported in 83% and 57%, being of grade 3–4 in 33% and 0 patients, respectively. Both blurred vision and dry eye were seen in 50% of patients in the 2.5 mg/kg group, whereas they were 14% in 3.4 mg/kg. Of note, adding pembrolizumab to Belamaf increased the incidence of grade 3–4 pneumonia, occurring in 17% of patients receiving Belamaf 2.5 mg/kg and 29% in those 3.4 mg/kg. Based on the results of Part 1 dose-escalation, patients enrolled in the Part 2 cohort expansion are receiving Belamaf at the dose of 2.5 mg/kg every three weeks.

Other Ongoing Clinical Trials with Belantamab Mafodotin

In the DREAMM-5 Platform trial,75 Belamaf has been evaluated in combination with other anti-myeloma agents in RRMM patients with ≥3 prior lines of therapy. The sub-studies currently open or opening soon to enrollment include Belamaf combined with GSK3174998, a humanized wild-type IgG1 anti-OX40 agonist antibody, binding to co-stimulatory OX40 receptor expressed on activated CD4+ and CD8+ cells enhancing immune-mediated anti-cancer activity (sub-study 1); in the sub-study 2, Belamaf is evaluated with feladilimab (GSK3359609) a humanized anti-ICOS agonist antibody binding to ICOS-expressing T cells; nirogacestat, a selective γ-secretase inhibitor able to increase the cell-surface level and availability of BCMA, is under evaluation with Belamaf in the sub-study 3; sub-study 4 assesses Belamaf with dostarlimab, a humanized anti-PD-1 antibody and, finally, sub-study 5 evaluates Belamaf pus isatuximab.

DREAMM-676 is an ongoing, two-part, two-arm, open-label, phase I/II study of Belamaf in combination with lenalidomide-dexamethasone (Rd) (arm A) or bortezomib-dexamethasone (Vd) (arm B) in patients with ≥1 prior line of therapy (bortezomib-refractory patients are not excluded). At the last ASH Meeting, preliminary results of 18 patients enrolled in arm B have been presented. Patients had received a median of 3 prior lines of therapy (range 1–11) and received Belamaf 2.5 mg/kg on day 1, bortezomib 1.3 mg/m2 on days 1, 4, 8, 11 of cycles 1–8, and dexamethasone 20 mg on days 1, 2, 4, 5, 8, 9, 11, 12. After eight cycles, patients could receive Belamaf monotherapy until progression or unacceptable toxicity. All patients experienced keratopathy, being of grade 3 in 61% of them, whereas any grade blurred vision and dry eye were seen in 67% and 22% of patients, respectively. Grade 3–4 thrombocytopenia occurred in 78% and peripheral neuropathy, grade 1–2, in 33% of patients. As regard activity, ORR was 78% and ≥ VGPR 67%, and, after a median of 18.2 weeks on treatment, median DoR was not reached.

DREAMM-777 is an ongoing phase III trial comparing Belamaf, Bortezomib, dexamethasone (B-Vd) to daratumumab, Bortezomib, dexamethasone (D-Vd) in RRMM patients with ≥1 prior lines of therapy. The primary endpoint is PFS. The key secondary endpoint is MRD, as assessed by next-generation sequencing. As of November 2020, 108 patients have been enrolled.

Another phase III trial (DREAMM-8)78 is studying Belamaf, pomalidomide, dexamethasone (B-Pd) vs pomalidomide, Bortezomib, dexamethasone (PVd) in RRMM patients with ≥1 prior lines of therapy (including lenalidomide). The primary objective is PFS, and the key secondary is MRD negativity rate. The trial started in October 2020 and aimed to enroll 450 patients worldwide.

In Table 2, we summarized ongoing clinical trials with belantamab mafodotin.

Toxicities of Belantamab Mafodotin

Ocular toxicity is the most important AE of Belamaf: ocular events included keratopathy (microcyst-like epithelial changes [MECs]: an eye exam finding with/without symptoms), best-corrected visual acuity (BCVA) changes, and symptoms (blurred vision and dry eye). ADC toxicities could be explained by on-target or off-target mechanisms: given the majority of the proteins targeted by these agents are not expressed in the cornea (eg, BCMA), the MECs may primarily represent an off-target mechanism. Farroq et al79 hypothesized that Belamaf could reach corneal cells through vascularized part of the limbus or through the tear film because Belamaf has been detected in rabbit tears. Belamaf can be internalized through the process called micropinocytosis in the limbal epithelial stem cells, inducing their apoptosis and starting the migration of the still alive epithelial cells toward the peripheral cornea. As long as these corneal cells are in the peripheral zone of the cornea, MECs can be identified at the slit lamp images but without any ocular symptoms. When the migration reaches the central cornea and crosses the visual axis, blurred vision and BCVA changes are reported. Over time, the migration of new corneal epithelial cells to replace dead cells that are extruded, allows the resolution of MECs and symptoms. Median timing of resolution reflects the timing of corneal proliferation, from 14 days to several weeks. These migrating Belamaf-containing cells can be visualized by IVCM (in vivo confocal microscopy) as hyperreflective opacities.79

Published results of Phase 2 DREAMM-2 study58 showed that the most common grade 3–4 AE was keratopathy (27% and 21% in the two cohorts, respectively). In patients receiving Belamaf single-agent 2.5 mg/kg, 72% of patients experienced MECs, but fewer patients (56%) had symptoms and/or a ≥ 2 lines BCVA decline. Events led to treatment discontinuation in 3% of patients: 1% each due to MECs, blurred vision, and reduced BCVA. The median time to the onset of ocular AEs with Belamaf 2.5 mg/kg were 37 days for MECs, 64 for BCVA changes, 52 for blurred vision, and 42 for dry eyes. The median time to the duration of these were 87 days for MECs, 33 for BCVA changes, 43 for blurred vision, and 39 for dry eyes. The examination of the outcome of ocular events at the first occurrence showed that 77% of patients recovered from their MEC event, and 82% of patients recovered from their BCVA decline (measured as the change in BCVA worse than 20/50 in the better-seeing eye). Data from the last follow-up showed that 48% of patients recovered from their MEC event, and 82% of them recovered from their BCVA decline.58,80,81

Ferron-Brady et al82 demonstrated that higher Belamaf Ctrough (the predicted concentration on day 21 at the end of the first cycle) was associated with great probability of grade ≥ 2 or ≥ 3 corneal events or with an earlier onset of them, but not with the probability of blurred vision, dry eye or decline of BCVA than 20/50. History of dry eye was associated with a higher probability of any grade blurred vision, while the initial presence of keratopathy increased the probability of grade ≥ 2 blurred vision. It is not recommended to administer Belamaf to patients with keratopathy at baseline.

As for the management of ocular toxicity, the ocular sub-study of DREAMM-283 demonstrated that prophylaxis with corticosteroid tears was ineffective in preventing ocular toxicity. The use of cooling eye mask or vasoconstrictors are recommended to minimize ocular exposure to the drug, but their benefit is unclear. The only helpful intervention to block ocular toxicity is dose delay or dose reductions to allow time for replacement of corneal epithelial cells. Ongoing studies are evaluating alternative dose reduction strategies, including split dosing or less frequent dosing. Cohen et al67 showed that treatment delay > 63 days did not negatively impact the response to therapy: they examined 16 patients in the DREAMM-2 trial who experienced dose delay > 63 days. Fourteen of them (88%) continued to experience a clinical benefit during the first prolonged delay: 38% deepened their response during the delay, 38% maintained the same response, and 13% had increasing paraprotein without criteria for disease progression. Popat et al63 demonstrated that patients showed a general improvement in fatigue during the treatment period and, despite ocular AEs, their quality of life did not worsen over time. Lin et al84 studied imipramine as a new potential drug against micropinocytosis in cellular and biological systems, and it could be a new approach to fight against ocular toxicity of Belamaf. Given the process of micropinocytosis could also be involved in Belamaf-related thrombocytopenia, the identification of useable micropinocytosis inhibitors should be an active research topic.

Overall, given the frequency of ocular AEs with Belamaf, it is very important to better understand its pathogenetic mechanisms and clinical features in order to make the most suitable treatment judgments. Multidisciplinary management of Belamaf therapy is crucial and ophthalmologic evaluation, at baseline (including visual acuity measurement and slit-lamp microscopy) up to 3 weeks before the first Belamaf administration, prior to each cycle (up to 2 weeks before) and then whenever clinically recommended, is mandatory.

The targeted delivery of chemotherapy with ADCs should have reduced toxicities compared to systemic chemotherapy, but auristatin is associated with haematological toxicity when attached to non-cleavable linkers. Toxicity can occur due to the expression of antigens on normal tissues (on-target), inadequate linker stability leading to systemic release of the payload, or off-target uptake of the linker-payload compound. Apart from ocular toxicity, thrombocytopenia was the most relevant side effect, explained through the same pathogenetic mechanism as the corneal toxicity via the apoptosis of megakaryocyte progenitor cells. In DREAMM-1 trial55 grade, 3–4 thrombocytopenia and anemia were 35% and 17%, respectively. Grade 3–4 thrombocytopenia occurred in 22% of patients receiving Belamaf 2.5 mg/kg vs 32% in the 3.4 mg/kg group of DREAMM-258 study (anemia 21% and 27%, respectively). Thrombocytopenia was reported in 78% of patients in the DREAMM-6 trial,76 leading to dose discontinuation in 33% of patients and dose delay in 39%.

IRRs occurred in 21% of patients in the 2.5 mg/kg cohort and 16% in the 3.4 mg/kg group of the DREAMM-2 trial.58 Most of them were limited to the first infusion, and nearly all were grade 1–2. Grade ≥3 IRRs during the first dose were 3%. Premedication was not required by the protocol, and when it was used (1/4 of all patients), it did not proportionately decrease the incidence of IRRs of these patients compared to the overall study population. Grade 2 IRRs were reported in 17% of patients in the DREAMM-6 trial without any dose modifications or discontinuations.

Other minor toxicities were pneumonia, hypertension, GGT increase, AST increase, hypercalcemia, and fatigue.

Discussion

Several drugs are now available for the treatment of MM, making treatment selection and sequencing of compounds a complex process. Clonal heterogeneity and complexity of MM require multiple drug associations through all disease phases to eliminate all clonal cells and long-term or continuous therapy to keep tumor cells under control. Therefore, most patients quickly become refractory to multiple drugs in their disease history, so agents with novel mechanisms of action are needed for these patients. Belamaf is the first-in-class anti-BCMA ADC approved for RRMM with a peculiar mechanism of action that makes it unique in the therapeutic landscape of MM. DREAMM-155,57 and, even more, DREAMM-258 study established that a single drug with these characteristics can be effective in patients with very advanced MM patients in whom deep response (20% VGPR) and long-term remission duration (around one year) were achieved. The higher response rates observed in the dose-expansion DREAMM-157 study can be attributed to the lower percentage of patients refractory to daratumumab (40% vs 100% in the 2.5 mg/kg group of DREAMM-2 study58) as well as to fewer patients with more than four prior lines of therapy, a very difficult-to-treat population (57% vs 84%).These results would have never been achieved with conventional chemotherapies or more recent therapies such as selinexor that, combined with dexamethasone, led to a similar response rate but with a shorter duration (median five months).28 Moreover, despite better ORR and median PFS, 84% of patients in the SVd arm of BOSTON trial27 had received 1 or 2 prior lines of therapy, and only 6% had been exposed to daratumumab. The response with Belamaf was maintained or improved in patients who hold therapy for toxicity, suggesting a disease control by the immune system and the possibility of dose-intensity reduction or alternative schedules. The same group of triple- or penta-refractory patients is the population on active investigation for other immunotherapies as bispecific antibodies and CAR T cell therapies with which an impressive rate of deep response has been obtained.33,34 ORRs obtained with bispecific antibodies as teclistamab, and CAR T cell therapy as idecabtagene vicleucel in triple-refractory MM patients are very impressive, but longer follow-up is required to see whether the response can last over time, so Belamaf, besides selinexor, represents now one of the most appropriate therapeutic options in very advanced MM as suggested by the most recent EHA-ESMO guidelines.85 Moreover, the activity of CAR T cells and bispecific antibodies depend on T-cell “fitness”, and it could be reduced with the loss of BCMA expression due to prior BCMA-directed therapy such as Belamaf. Both bispecific antibodies and CAR T cell therapies require hospitalization in accredited centers with ICU and neurology services due to possible life-threatening toxicity such as CRS (cytokine release syndrome) and ICANS (immune effector cell-associated neurotoxicity syndrome), never seen with Belamaf. In contrast with CAR T cells and bispecific antibodies, Belamaf could be prescribed in the elderly. In fact, among patients enrolled in the DREAMM-2 trial,58 59% were 65 years or older, whereas, in the KarMMa trial,35 using idecabtagene vicleucel, a CAR T cell therapy, 35% of patients were ≥ 65 years old. As shown above, grade 3–4 neutropenia, thrombocytopenia, and infections occurred in 22%, 11%, and 7%, respectively, of patients receiving Belamaf 2.5 mg/kg vs 89%, 52%, and 22% seen in patients treated with CAR T cell therapy. Moreover, 84% of patients receiving idecabtagene vicleucel developed CRS and 18% neurologic effects. CAR T cell therapies require conditioning chemotherapy and a personalized manufacturing process that could be prohibitive for rapid progression disease, whereas Belamaf and bispecific antibodies are “off-the-shelf” and immediately available. Belamaf, due to its targeted cytotoxicity, acts independently on T cells fitness. In contrast, the outcome of patients treated with both bispecific antibodies and CAR T cells are strictly dependent on host immune system performance, that has deteriorated in the elderly population. Moreover, subgroups analyses of patients treated with Belamaf monotherapy did not demonstrate excessive toxicity in patients with renal or hepatic insufficiency, high-risk or extramedullary disease, although activity seems to be lower in patients refractory to daratumumab. Several studies with Belamaf in combination with IMiDs, PIs, and other compounds are ongoing in late and early disease relapse since Belamaf toxicity seems to be not cumulative with other drugs while increasing effectiveness is expected. The combination of Belamaf with pomalidomide and dexamethasone showed good response in advanced RRMM71, but ongoing trials (Table 2) are assessing Belamaf in combination with Rd, Pd, or Vd in the first relapse or in NDMM in combination with VRD, and they could establish the role of this agent in the management of early MM.

Unfortunately, treatment with Belamaf may cause very peculiar toxicity. Ocular toxicity, until now an unknown side effect in MM therapy, can be seen after therapy with Belamaf. Corneal toxicity is very common, although it is mild and has no consequences for the patients in most cases. However, about a quarter of cases have significant, albeit reversible, visual disturbances that require reduction or discontinuation of therapy, rarely definitive discontinuation. This side effect is little known by haematologists. Therefore, when it occurs, it requires active collaboration with ophthalmologists to timely diagnose corneal/MEC changes and intervene in a timely fashion, which could be just dose delay or reduction and does not necessarily need an ophthalmic procedure. This issue will become even more important when Belamaf is used earlier in the course of MM rather than in patients with very advanced disease for whom alternatives are certainly fewer. However, Belamaf-associated ocular toxicity is the subject of very active research that tends to better understand the mechanism that induces toxicity leading to the discovery of possible antidotes, but at the moment, reduction of dose-intensity or alternative schedules are the main ways of research.

Conclusion

Belantamab mafodotin is the first BCMA-targeted immunotherapy to be approved for the treatment of advanced RRMM, representing hope for patients who have become refractory to all available classes of drugs. It showed efficacy as a single agent, but several ongoing trials are evaluating Belamaf in combination with all available agents and also with experimental molecules. Ocular toxicity is of concern, but further multidisciplinary cooperation will help to likely make this adverse event predictable and easy to manage.