Skin/nail infections with the addition of pertuzumab to trastuzumab-based chemotherapy.

We report a series of breast cancer patients with invasive skin and nail infections with Staphylococcus species that we attribute to the addition of pertuzumab to trastuzumab-based therapy. With the suspicion of an increased incidence of cutaneous infection in patients treated with pertuzumab and trastuzumab-based chemotherapy, treating medical oncologists identified patients receiving therapy who experienced infection. Between March and October 2014, 18 patients treated with pertuzumab and trastuzumab-based chemotherapy were found to have 21 separate skin/nail infections. Treatment was administered as neoadjuvant therapy in 12 (67%) patients, adjuvant therapy in four (22%) patients, and for metastatic disease in two (11%) patients. Granulocyte growth factors were administered in 11 (61%) patients and no patients were documented to be neutropenic. New skin and nail lesions developed as early as cycle 1 and as late as 8 months from initial therapy. The 21 separate infections documented were folliculitis and "bite-like" lesions (10), abscess (6), paronychia (3), and cellulitis (2). The appearance of these lesions was distinct from typical EGFR-associated skin changes. When cultures were obtained, Staphylococcus species were isolated. Quantitative immunoglobulins were assessed in 14 (78%) patients and were abnormally low in six (43%) of these patients. The skin infections resulted in treatment delay in two (11%) patients and premature discontinuation of therapy in one patient. We believe that the skin/nail infections reported here in patients treated with the combination of pertuzumab and trastuzumab represent a previously unrecognized toxicity of adding pertuzumab to trastuzumab-based therapies.

RCT Entities:   Population Interventions Outcomes

Introduction

The HER2 protein is an important target for new drug development. Since the approval of trastuzumab in 1998, three additional HER2-directed therapies have been added to the armamentarium— lapatinib, ado-trastuzumab emtansine, and pertuzumab [1]. Lapatinib is known to produce skin and gastrointestinal toxicities that have been attributed to its dual blockade of HER2 and EGFR signaling [2]. When lapatinib is combined with trastuzumab to treat metastatic HER2-positive breast cancer, objective responses are observed even in patients who have previously been treated with trastuzumab-containing regimens. The toxicities observed with this combination are consistent with an additive effect of the two agents. Skin rashes and gastrointestinal toxicities are common, but no increase in cardiac toxicity or unanticipated side effects have been reported [3]. As second-line therapy, ado-trastuzumab emtansine results in superior disease outcomes and less toxicity than the combination of lapatinib and capecitabine [4]. Recently, the addition of pertuzumab to trastuzumab and docetaxel (PTH) has resulted in an improved objective response rate and significant improvements in both progression-free survival (PFS) and overall survival without increased toxicity [5, 6].

The benefit of adding pertuzumab to trastuzumab-based neoadjuvant chemotherapy was tested in the NEOSPHERE and TRYPHAENA trials. At the time of surgery, higher pathologic complete response rates were reported with the addition of pertuzumab [7, 8]. As a result, the FDA expanded the indications for pertuzumab to include both the metastatic and neoadjuvant settings. The NCCN guideline panel also recommended the addition of pertuzumab as adjuvant therapy [9, 10]. With these expanded indications, more women with HER2-positive breast cancers are receiving treatments that combine pertuzumab and trastuzumab with chemotherapy.

Over the past 12 months, our clinical breast cancer team became aware that women treated with trastuzumab and pertuzumab were developing severe Staphylococcus skin reactions, not previously recognized in the pivotal trials or evident in the FDA briefing documents [10]. We report the natural history of what we believe is a previously unrecognized toxicity of these regimens.

Methods

In March 2014, a treating Medical Oncologist identified unusual and severe Staphylococcus infections in two patients receiving neoadjuvant PTH (patients 1 and 2). At the weekly Breast Cancer Research Conference, the cases were discussed in the context that these skin infections were potentially related to the addition of pertuzumab to the conventional regimen of a taxane, with or without carboplatin, and trastuzumab. The clinicians agreed to be attentive and report other patients who developed severe Staphylococcus skin infections. The clinical workup of these patients was not defined; however, the faculty was encouraged to take photographs of the skin lesions, and many photographs were provided by patients as they became concerned about new skin eruptions. With the identification of hypoglobulinemia in an early patient, quantitative immunoglobulins were collected on many of the subsequent patients. Antimicrobial treatment was provided on a case-by-case basis and the Departments of Infectious Disease and/or Dermatology were involved in most cases. Attribution of the infection to the combination of pertuzumab and trastuzumab was made by the Infectious Disease team.

To rule out the possibility of an institutional outbreak of Staphylococcus infections, we enlisted the help of the hospital’s Infection Control team. After an extensive review, we found no increase in Staphylococcus infections since the approval of pertuzumab or since the identification of the first patient reported at City of Hope. Furthermore, some of the patients we reported were treated at different locations within the hospital, and two of the patients received therapy at a community practice site, 15 miles from the main City of Hope Duarte campus. The lot numbers for the agents administered were also documented to be different.

Approval from the IRB was obtained in order to characterize and report what appears to be a previously unrecognized toxicity of the combination of pertuzumab and trastuzumab with chemotherapy.

Results

Between March and October 2014, 18 patients with 21 separate skin/nail infections were identified. Their characteristics are summarized in Table 1. The median age was 51 years (range 33–67 years). Twelve (67 %) patients were treated in the neoadjuvant setting, four (22 %) in the adjuvant setting, and two (11 %) for metastatic disease. Ten (56 %) patients were treated with pertuzumab, trastuzumab, carboplatin, and docetaxel (PTCH); four (22 %) with PTH; two (11 %) with pertuzumab, trastuzumab, and nab-paclitaxel (nabPT); and pertuzumab was added to maintenance trastuzumab (PH) in the adjuvant setting for one patient. One patient (patient 12) who was initially treated with nabPT subsequently received PTCH; folliculitis developed while on PTCH. One patient (patient 2) developed three distinct infections. Of the 21 infectious episodes, seven developed after cycle 1, four after cycle 2, two after cycle 3, one after cycle 4, and seven after cycle 6.

Table 1

Patient Characteristics

Pt.	Age	Setting	Regimen	Cyclenumber	Skin reaction	Organism	Total Protein/Ig levels
1	51	Neoadjuvant	PTH	C6D12	Folliculitis—buttocks Abscess—thumb	MSSA	Total protein: 4.7 g/dL (6.3–8.2 g/dL); C6 Ig: normal; C6D28
2	48	Neoadjuvant	PTH	C2D6	Abscess—breast	–	–
				C3D6	Abscess—buttocks and shoulder	MRSA	Total protein: 6.2 g/dL (6.3–8.2 g/dL); C4D10
				C4-6	Paronychia	–	Ig: normal; C5D8 IgG: 661 (700–1,600); C6D17
3	56	Adjuvant	PTCH	C1D17	Folliculitis—scalp	–	Ig: normal; C3D1, C6D34 Total protein: 6.1 g/dL (6.3–8.2 g/dL); C6D23
4	53	Neoadjuvant	PTCH	C1D15	Folliculitis—scalp	–	Ig: normal; C4D1
5	49	Adjuvant	PTCH	C1D20	Folliculitis—abdomen	MRSA	Total protein: normal IgM: 38 (38–271); C3D1
6	64	Neoadjuvant	PTCH	C3D13	Abscess—shoulder “Bite-like” lesions	MRSA	Total protein: normal IgG: 707 (700–1,600); C4D6
7	47	Adjuvant	PTCH	C1D15	Folliculitis—scalp	–	–
8	57	Neoadjuvant	PTH	C2D17	Abscess—buttocks	–	–
9	46	Neoadjuvant	PTCH	C6D15	Paronychia—16 nails	–	IgG: 691 (806–1,813) IgM: 51 (104-522); C6D38
10	52	Neoadjuvant	nabPT	C1D2	Abscess—port day 2	MRSA	Ig: normal; C3D15
11	51	Metastatic	PTH	C1D2	“Bite-like” lesions	–	IgM: 26 (38–271); C2D1
12	33	Metastatic	nabPT; PTCH	C12D1	Folliculitis—arm	MSSA	Ig: normal; C12D1
13	36	Adjuvant	PH	C2D14	Folliculitis—face	–	Ig: normal; C4D38
14	50	Neoadjuvant	PTCH	C6D25	Paronychia	–	Ig: normal; C6D28
15	54	Neoadjuvant	PTCH	C2D14	Folliculitis—scalp	–	Ig: normal; C2D15
16	67	Neoadjuvant	PTCH	C6D46	Seroma with cellulitis	–	Total protein: 6.1 g/dL; C5D1 IgG: 579 (700–1,600); C6D46
17	38	Neoadjuvant	PTCH	C1D9	Folliculitis—face	–	–
18	56	Neoadjuvant	nabPT	C6D65	Cellulitis	MSSA	IgG: 556 (700–1,600); C6D65

PTCH pertuzumab, trastuzumab, carboplatin, and docetaxel; PTH pertuzumab, trastuzumab, and docetaxel; nabPT nab-paclitaxel, pertuzumab, and trastuzumab; PH pertuzumab and trastuzumab; MRSA methicillin-resistant Staphylococcus aureus; MSSA methicillin-sensitive Staphylococcus aureus; C cycle; D day; Pt patient

Most patients (12; 67 %) received granulocyte growth factors within 24–48 h of chemotherapy. No patients were documented to be neutropenic at the time of presentation with skin lesions. Cultures were performed on seven (39 %) patients; methicillin-sensitive Staphylococcus aureus (MSSA) was identified in three (43 %) of these patients and methicillin-resistant Staphylococcus aureus (MRSA) in four (57 %) of these patients. The development of skin lesions resulted in treatment delay in two (11 %) patients. Of the 12 neoadjuvant patients, eight (67 %) underwent definitive surgery and six (75 %) of these patients achieved a pathologic complete response.

Folliculitis involving the face or scalp was identified in six (33 %) patients with four (22 %) additional patients experiencing folliculitis and “bite-like” lesions on the arm, legs, abdomen, and buttocks. Abscesses were identified in five (28 %) patients, two of whom required incision and drainage, and one required removal of the portacath. Severe paronychial infections were seen in three (17 %) patients and one patient underwent surgical removal of two nails to facilitate healing. Two patients treated with neoadjuvant therapy developed cellulitis following their definitive local surgery. They are included in this series because of the rapid and severe nature of the infection and the documentation of hypogammaglobulinemia. Both were on maintenance trastuzumab, but had not received pertuzumab for 45 and 65 days, respectively. The clinical appearance was not typical of lapatinib-related skin rashes. Representative images of skin infections from five patients are shown in Fig. 1.

Fig. 1

Skin/nail infections a Buttocks folliculitis and b wrist abscess (patient 1); c Early precursor lesions and d buttock cellulitis (patient 2); e Early precursor lesions (patient 11); f Paronychia (patient 14); g Typical scalp folliculitis (patient 4)

Quantitative immunoglobulins were assessed in 14 (78 %) patients and were abnormally low in six (43 %) of these patients; four after cycle 6 of therapy. Multiple assessments of quantitative immunoglobulin levels were performed in three patients and became abnormal over time in all.

The following cases are representative of the unique natural history of this process.

Patient 1 is a 51-year-old East Indian woman who presented with inflammatory breast cancer involving the left breast, axilla, and supraclavicular lymph nodes. Treatment with PTH was initially well tolerated until cycle 6, day 7 when she complained of redness of the nose and a cough. She was not cytopenic and was empirically treated with a 10-day course of cephalexin and her symptoms resolved within 3 days. On cycle 6, day 14 while on cephalexin, she complained of new skin eruptions on the breast and buttocks that looked like “insect bites.” Over the subsequent 3 days these lesions increased in size, became erythematous, pus-filled, and exquisitely painful. She was seen on day 22 of cycle 6 as she was starting “maintenance trastuzumab.” On that clinic visit, she received a dose of intravenous vancomycin and trimethoprim/sulfamethoxazole was initiated. Three days later, she was admitted to the hospital with worsening skin lesions. Cultures from the buttocks and wrist (Fig. 1a, b) grew Staphylococcus aureus that was sensitive to vancomycin. Skin biopsies of a new “bite” area and the abscess on the left wrist demonstrated “severe acute superficial dermatitis with interface activity, ulceration and involvement of the adnexal glands with no evidence of vasculitis.” She was well-nourished; total protein was 4.7 g/dL (6.3–8.2 g/dL). No further workup was performed and she was discharged on intravenous vancomycin. All lesions completely resolved. At mastectomy, 6 mm of residual cancer was identified in the breast; the skin and all lymph nodes were without evidence of cancer. Her postoperative course was uneventful and she continues on maintenance trastuzumab without recurrence of the skin lesions.

Patient 2 is a 48-year-old African-American woman who presented with locally advanced breast cancer on the left with pathologic confirmation of axillary node involvement. On cycle 2, day 1 of PTCH she noted a pimple on the contralateral breast. By cycle 2, day 6 the area had increased in size (Fig. 1c). Although she was afebrile and had a normal white blood count, cephalexin was prescribed and the lesion resolved. Following cycle 4, she noted erythema and swelling on the shoulder and buttocks. She was prescribed cephalexin on day 3. By cycle 4, day 6 both lesions had increased in size and she was admitted to the hospital for intravenous vancomycin. The shoulder lesion was incised and drained. The buttocks lesion was consistent with cellulitis (Fig. 1d) and no surgical intervention was required. Skin biopsy of the buttocks demonstrated “superficial dermatitis and no evidence of vasculitis.” Cultures from the shoulder abscess grew MRSA and treatment was switched from vancomycin to daptomycin. Her total protein on admission was 6.2 g/dL (6.3–8.2 g/dL). Both lesions resolved and she completed six cycles of chemotherapy without dose or schedule modification. After cycle 6, she noted pain in her finger and toenails. Quantitative immunoglobulins were performed on cycle 5, day 8 and were normal. However, reassessment on cycle 6, day 17 was abnormal with IgG 661 (700–1,600).

The patient was taken to the operating room where she was found to have no evidence of tumor. The discomfort in the finger and toenails continued to worsen postoperatively and she was able to express pus-like fluid with pressure on the nail bed. One nail spontaneously fell off; others have cracked and broken off mid-nail bed. She is tolerating maintenance trastuzumab and the nails are slowly healing.

Skin biopsies were obtained in four patients. The pathologic findings are summarized in Table 2 and representative biopsies from two patients are shown in Fig. 2. Although the clinical appearance was atypical of EGFR inhibitor rashes, the biopsy results are consistent with findings seen with other EGFR inhibitor cutaneous toxicities. However, since these results are not specific or pathognomonic, additional biopsies were not obtained in subsequent patients. The epidermis in all four biopsy specimens demonstrated areas of compact orthokeratosis and/or parakeratosis, suggesting altered keratinocyte differentiation. Additionally, the inflammation was primarily periadnexal, which is consistent with other EGFR inhibitor reactions [11, 12]. Biopsies from patient 1 showed vacuolar degeneration of the basal layer that has also been seen with acneiform reactions to EGFR inhibitors (Fig. 2a) [13].

Table 2

Biopsy findings

Patient	Site of biopsy	Pathologic finding
1	Left thigh	Vacuolar degeneration of basal layer; dense mixed inflammatory infiltrate involving the follicles and adnexal structures
	Left breast	Ulceration with vacuolar degeneration of the basal layer; periadnexal abscess with predominantly neutrophilic infiltrate and some giant cells
2	Left hip	Hypergranulosis; compact orthokeratosis; mild superficial perivascular, perineural, and periadnexal infiltrates consisting of primarily monocytes and lymphocytes
12	Left upper arm	Focal areas of compact keratosis and parakeratosis; epidermal spongiosis; intra-epidermal pustule; abscess within pilosebaceous unit with dense mixed infiltrate with numerous neutrophils
15	Scalp	Focal compact and orthokeratosis; vacuolar degeneration of the basal layer; periadnexal and perifollicular lymphocytic infiltrate with sparse neutrophils

Fig. 2

Skin biopsies a high-power view of an H&E-stained section from patient 1 showing mild acute inflammation associated with spongiosis, vacuolar degeneration, and parakeratosis; b H&E-stained section from patient 12 showing superficial mild acute periadnexal inflammation with concurrent involvement of a hair follicle (folliculitis) and sweat glands

Patient 12 presented with erythematous papules and pustules on her left arm and abdomen following her eleventh cycle of PTCH. Culture from one of the pustules revealed MSSA and she completely cleared with oral doxycycline. The lesions recurred several weeks later and biopsy of a new lesion was performed. It demonstrated focal parakeratosis with periadnexal inflammation and a hypoplastic pilosebaceous unit (Fig. 2b). Although non-specific, these biopsy results are consistent with altered keratinocyte differentiation seen with EGFR inhibitors.

Discussion

The FDA approval of new agents is made on the basis of randomized clinical trials where the primary endpoints are tumor regression or improved PFS and overall survival. Toxicity is an important component of the approval process. However, the toxicity data are generally collected during the study conduct and are limited by the sample size. In response to patient demand, the approval process for new treatments of advanced cancers is shortening [14, 15]. As these agents become available to more patients, additional side effects become apparent. In fact, half of all serious adverse events are recognized more than seven years after FDA approval [16].

This is the first series to report the association of pertuzumab, trastuzumab, and chemotherapy with severe cutaneous staphylococcal infections. In CLEOPATRA, the median number of cycles of docetaxel administered was eight in both arms and the frequency of all adverse effects was noted to decrease once the docetaxel was discontinued. However diarrhea, rash, dry skin, neutropenic fever, pruritus, and mucosal inflammation appeared to be more common in patients assigned to pertuzumab [6]. Nail disorders were reported in 22.9 % of patients in both arms, but the incidence of grade 3/4 toxicity was higher in patients receiving pertuzumab, 1.2 % versus 0.3 % [10]. We believe that severe skin and nail infections with Staphylococcus species are unique side effects resulting from the addition of pertuzumab to trastuzumab-based chemotherapy. This toxicity may have gone unrecognized for a number of reasons. The pertuzumab safety data are derived from three large randomized clinical trials—CLEOPATRA, NEOSPHERE, and TRYPHAENA—that enrolled patients from many institutions worldwide (Table 3). The 808 patients in CLEOPATRA were enrolled from 205 sites and 25 countries. NEOSPHERE enrolled 417 patients from 59 sites and 16 countries, and TRYPHAENA enrolled 225 patients from 44 sites and 19 countries [5, 7, 8]. It would be difficult for an investigator to appreciate a safety signal with so few patients treated at any one site.

Table 3

Summary of randomized trials leading to FDA approval of pertuzumab

Docetaxel

Trastuzumab

Pertuzumab

Fluorouracil, epirubicin, cyclophosphamide

Paclitaxel

Carboplatin

Pts Patients, No Number, Pert Pertuzumab, Tras Trastuzumab

The clinical trial designs for the randomized trials are summarized in Table 3. Three of the four arms in the NEOSPHERE trial combined trastuzumab with pertuzumab, but each administered only four cycles of therapy. All three arms of the TRYPHAENA trial utilized pertuzumab and trastuzumab, but delivered only three cycles in one arm and six cycles in two arms. In our series, folliculitis was observed early, however, the more severe infections and nail infections developed after cycles 3 and 4. In total, the toxicity data for the combination of pertuzumab and trastuzumab are based on 846 patients, 556 of whom received six cycles, 215 four cycles, and 75 three cycles. Because the addition of lapatinib to trastuzumab results in a synergistic anti-tumor effect with predictable normal tissue toxicities, synergistic toxicities from adding pertuzumab to trastuzumab were not anticipated [3, 17, 18].

The majority of new agents are first tested in patients with metastatic disease, and it may be difficult to distinguish drug toxicity from symptoms of advanced disease. The musculoskeletal pains that occur with the aromatase inhibitors were only recognized as a toxicity of the drug class when they were used in the adjuvant setting [19]. Side effects that occur in the adjuvant versus neoadjuvant settings are less likely to be attributed to the underlying disease and safety signals are more apparent. The ongoing adjuvant APHINITY trial (Table 3) is likely to clarify new side effects related to the combined antibody therapy.

The development of pustular skin lesions may have been attributed to the steroid premedication routinely administered in patients receiving taxane-based therapies. The skin lesions described here are not typical of “steroid acne.” Steroid-induced acne generally presents as monomorphic papules distributed on the upper trunk, arms and less commonly on the face [20]. Although steroid use is generally immunosuppressive, the number and severity of these reactions are unlikely to be attributed to short-course steroid use alone. Additionally, the prevalence of staphylococcal infections in this population suggests that there is a specific underlying mechanism. Although the precise pathogenesis of these reactions is unknown, we propose several overlapping and synergistic mechanisms.

Both trastuzumab and pertuzumab target HER2, an epidermal growth factor receptor overexpressed in breast cancer cells and present in keratinocytes [21]. Although these agents do not induce the classic acneiform rash seen with other EGFR inhibitors such as cetuximab and erlotinib, the combination therapy is clearly disrupting epidermal differentiation in the patients who had biopsies [13]. These results suggest that the combination of trastuzumab and pertuzumab induces a reaction that is histologically similar to other EGFR inhibitors, though clinically distinct. The difference in the morphologies of the reactions is most likely due to the variability of HER kinase expression in the skin, nails, and follicles [22, 23]. Similar to other EGFR inhibitors, this altered epidermal differentiation predisposes to infection, primarily by staphylococcal species. In one study of 221 patients on EGFR inhibitor therapy, 38 % of the patients had clinical evidence of infection and over 50 % of these were culture positive for staphylococci [24]. The rash and infectious disease complications with these patients were managed prophylactically with oral antibiotics (usually doxycycline or minocycline) plus a topical steroid to treat the inflammatory component. It may be beneficial to treat breast cancer patients on combined therapy with prophylactic measures as well, especially if we can determine which patients are at the highest risk of developing infectious complications. Patients who develop rash with EGFR inhibitor therapy also tend to have better outcomes [25]. It will be interesting to determine if there is a similar correlation between pertuzumab and trastuzumab treatment. The complete pathologic response rate in this small series suggests that skin/nail infections were neither a favorable nor an unfavorable predictor or response.

Recent studies have demonstrated that the immunosuppressive effect of IVIG may be related to a small percentage of glycosylated IgG-Fc present in the preparations rather than a direct effect of antigen-specific binding [26]. It may be possible that the monoclonal antibodies themselves contribute to the immunosuppression seen in these patients. We did document hypoglobulinemia in six of the patients. However, many of the affected patients had normal immunoglobulins at the time of infection and other patients became hypoglobulinemic with continuation of therapy. Nonetheless, hypoglobulinemia alone does not explain the mechanism of infection.

The data presented here was derived from cases identified prospectively only after the patient developed an infection. We do not have data on the patients who did not experience any skin reaction. Amongst the group of physicians who identified the patients with skin infections reported here, the incidence was 30 %. To minimize any bias in assigning toxicity to pertuzumab and trastuzumab, we enlisted the help of specialists in Infectious Disease and Dermatology, and in three instances, the occurrence of a skin complication was deemed unrelated to treatment. Although this was not a prospective clinical trial, we are convinced that the occurrence of staphylococcal infections of the skin and nails is a unique toxicity observed when pertuzumab is added to trastuzumab. We are initiating a prospective trial to address cutaneous and immunologic changes in women undergoing treatment with this combined antibody therapy.