Yuto Terashima1†
Masaru Matsumoto1*†Saeko Ozaki2†Michiko Nakagawa2Shun Nakagome3†Yasuhiro Terasaki4†Hiroki Iida1Ryotaro Mitsugi1Eri Kuramochi1Naoko Okada1Tomoyasu Inoue1Satoru Matsuki1Shingo Kitagawa1†Aya Fukuizumi1†Naomi Onda1Susumu Takeuchi1†
Akihiko Miyanaga1†Kazuo Kasahara1†Masahiro Seike1†- 1Department of Pulmonary Medicine and Oncology, Graduate School of Medicine, Nippon Medical School, Tokyo, Japan
- 2Department of Dermatology, Graduate School of Medicine, Nippon Medical School, Tokyo, Japan
- 3Department of Gastroenterology, Graduate School of Medicine, Nippon Medical School, Tokyo, Japan
- 4Department of Analytic Human Pathology, Graduate School of Medicine, Nippon Medical School, Tokyo, Japan
A 73-year-old man with lung squamous cell carcinoma was administered carboplatin + nab-paclitaxel + pembrolizumab for four cycles. Subsequently, he presented with multiple purpuras on his extremities, joint swelling on his fingers, abdominal pain, and diarrhea, accompanied by acute kidney injury (AKI), increased proteinuria, hematuria, and elevated C-reactive protein levels. Skin biopsy showed leukocytoclastic vasculitis as well as IgA and C3 deposition in the vessel walls. Based on these findings, the patient was diagnosed with IgA vasculitis as an immune-related adverse event (irAE) induced by carboplatin + nab-paclitaxel + pembrolizumab. After discontinuation of pembrolizumab and glucocorticoids, the symptoms immediately resolved. Regular monitoring of skin, blood tests, and urinalysis are necessary, and the possibility of irAE IgA vasculitis should be considered in cases of purpura and AKI during treatment with immune checkpoint inhibitors.
Introduction
Standard therapeutic options for lung cancer have recently expanded with the development of immune checkpoint inhibitors (ICIs) (1). ICIs can enhance T lymphocytes activity and promote anti-tumor responses by blocking immune checkpoints (2). However, due to these mechanisms, ICIs can cause various side effects, which are known as immune-related adverse events (irAEs). IrAEs can develop in organs throughout the body, such as dermatitis, thyroid dysfunction, colitis, nephritis and pneumonitis. On the other hand, irAE vasculitis is rare (3). We herein report a case of irAE IgA vasculitis induced by carboplatin + nab-paclitaxel + pembrolizumab, an ICI.
Case report
A 73-year-old Japanese man presented with cough and dyspnea. Computed tomography (CT) showed a tumor in the left lower lobe, with lymph node enlargement at the left hilum and metastasis to the sacrum and left adrenal gland. We performed a transbronchial lung biopsy with bronchoscopy. Based on these findings and the result of biopsy, he was diagnosed with lung squamous cell carcinoma, cT4N2M1c stage IVB. The Oncomine™ Dx Target Test revealed no mutation of cancer-relevant genes, and PD-L1 expression was 10%–24% in the 22C3 assay. Before chemotherapy, the patient developed obstructive pneumonia and had an Eastern Cooperative Oncology Group Performance Status (ECOG-PS) score of 2. After antibacterial therapy for obstructive pneumonia, carboplatin and nab-paclitaxel were administered as first-line therapy. In the second treatment course, pembrolizumab was added as the patient’s ECOG-PS score improved. Five days after four cycles of treatment, the patient presented with fever and elevated C-reactive protein (CRP) levels. This led to the suspicion of recurrent obstructive pneumonia; thus, oral antibacterial therapy was initiated. Due to limited improvements in symptoms, the patient was admitted to our hospital. However, he developed multiple purpuras on his extremities and joint swelling on his fingers (Figures 1A–C). Purpura was observed not only on the lower legs but also on the thighs and abdomen. Therefore, we suspected irAEs and performed skin biopsy on the lower leg. Furthermore, additional symptoms of diarrhea and abdominal pain occurred. Laboratory analysis showed elevated white blood cells (11300/µL), CRP (17.66 mg/dL), blood urea nitrogen (30.3 mg/dL), and creatinine (3.35 mg/dL) levels as well as proteinuria and hematuria (Figure 2). In addition, serum IgA levels increased to 396 mg/dL. CT revealed intestinal edema and ascites (Figure 1D). A skin biopsy specimen exhibited neutrophil-dominated inflammatory cell infiltration from the small vessel walls into the surrounding tissues, suggestive of leukocytoclastic vasculitis (Figures 3A, B). Immunofluorescence staining showed granular IgA and C3 deposition in the vessel walls (Figures 3C, D). Therefore, the patient was diagnosed with irAE IgA vasculitis. We considered that symptoms such as purpura, joint swelling, acute kidney injury, and ascites were due to irAE IgA vasculitis. He was treated with intravenous methylprednisolone (1000 mg/day) followed by prednisolone (1 mg/kg/day) for 3 days. After the treatment initiation, the symptoms immediately resolved and creatinine levels improved (Figures 1E, 2). Subsequently, we tapered prednisolone from 60 mg/day to 30 mg/day by reducing the dose by 10 mg/day each week. After that, we continued to taper the dose by 5 mg/day every two weeks. Currently, the patient is maintaining a dose of 5 mg/day of prednisolone, and there has been no exacerbation of symptoms. Moreover, for lung cancer, we are currently on a watchful waiting approach without chemoimmunotherapy, including pembrolizumab, and the disease has been stable for four months.
Figure 1. (A–C) The patient developed multiple purpuras on his extremities. (D) CT revealed intestinal edema and ascites. (E) The purpura improved immediately after glucocorticoid treatment.
Figure 2. Clinical course of the patient and transition of creatinine levels after four cycles of carboplatin + nab-paclitaxel + pembrolizumab treatment, and diagnosed with irAE IgA vasculitis. Abbreviations: Cre, creatinine; CBDCA, carboplatin; nab-PTX, nab-paclitaxel; Pembro, pembrolizumab; AMPC/CVA, amoxicillin–clavulanate; ABPC/SBT, ampicillin–sulbactam; CTRX, ceftriaxone; mPSL, methylprednisolone; PSL, prednisolone.
Figure 3. Skin biopsy findings on the lower leg. (A, B) Hematoxylin and eosin staining showed neutrophil-dominated inflammatory cell infiltration from the small vessel walls into the surrounding tissues (scale bar [A] = 400 µm, [B] = 90 µm). (C) Immunofluorescence staining revealed granular IgA deposition in the vessel walls (×200). (D) Immunofluorescence staining revealed granular C3 deposition in the vessel walls (×200).
Discussion
ICIs, including pembrolizumab, enhances T cell activity against tumors and leads to improved clinical outcomes in various cancers by blocking inhibitory pathways like PD-1/PD-L1. The restoration of immune activity can lead to irAEs, such as colitis, hepatitis, endocrinopathies, pneumonitis, and vasculitis (2). In previous reports, most cases of irAE vasculitis were large vessel vasculitis (3). Thus, small vessel vasculitis, such as IgA vasculitis, is rare. IrAE IgA vasculitis was reported in patients with advanced melanoma as well as hepatocellular, renal cell, and squamous cell lung carcinomas, as in our study (Table 1) (4–9). These cases were induced by nivolumab, ipilimumab and durvalumab. To the best of our knowledge, this is the first report of irAE IgA vasculitis induced by chemoimmunotherapy, including pembrolizumab.
Table 1. Previous cases of irAE IgA vasculitis and the present case.
IgA vasculitis commonly occurs in children and is triggered by infections, tumors, drugs, and food (10, 11). In the present case, infections such as group A streptococcus or parvovirus, which are the frequent causes, were ruled out as antistreptolysin O antibody and parvovirus B19 were negative. Furthermore, the test results were negative for urinary tract, fungal, and other viral infections as well as tuberculosis. There was also no evidence of cancer progression. Obstructive pneumonia and administered antibiotics were suspected as causes. The patient had been previously treated with the same antibiotics (amoxicillin/clavulate and ampicillin/sulbactam), and he had never developed irAE IgA vasculitis. Moreover, a previous report suggested that the alteration of the PD-L1/PD-1 axis might be associated with the regulation of T-cell activation in the skin and peripheral blood of patients with vasculitis (12). Thus, although there is a possibility that the symptoms of irAE IgA vasculitis became apparent due to the concurrent administration of chemoimmunotherapy and antibiotics, we diagnosed the patient irAE IgA vasculitis induced by carboplatin + nab-paclitaxel + pembrolizumab.
In general, irAE has been managed with ICI discontinuation and systemic corticosteroid administration. If improvement is limited, immunosuppressive agents may be administered as the next treatment (13, 14). In previous reports, four out of six cases achieved remission with only discontinuation of ICIs and systemic corticosteroids (Table 1). In half of the reports, the treatment started with intravenous administration of methylprednisolone (500-1000 mg/day), followed by tapering to prednisolone (0.5-1 mg/kg/day). Our patient also rapidly improved with these treatments. Therefore, immunosuppressive agents were not administered. Further studies are warranted to establish the treatment strategy for irAE IgA vasculitis, which is relatively rare.
The clinical benefit of ICI readministration in patients with irAE IgA vasculitis remains unclear. In general, it is often not recommended in cases of grade 3 or higher irAEs (15). In previous reports, ICIs were not readministered in five of six cases after treatment for irAE IgA vasculitis (Table 1). In one case of ICI readministration, the treatment was conducted under prednisolone therapy, and no recurrence of irAEs was observed. Our patient developed grade 3 irAE IgA vasculitis and we determined that readministration of ICIs carries a high risk, even under steroid therapy. Furthermore, CT revealed no evidence of cancer progression. Thus, we did not readminister pembrolizumab. If the lung cancer progresses in the future, we plan to administer non-ICI drugs such as docetaxel.
In summary, we present a case of irAE IgA vasculitis induced by carboplatin + nab-paclitaxel + pembrolizumab. Regular monitoring of skin, blood tests, and urinalysis are necessary, and the possibility of irAE IgA vasculitis should be considered in cases of purpura and acute kidney injury during ICI treatment.
Data availability statement
The original contributions presented in the study are included in the article/supplementary material. Further inquiries can be directed to the corresponding author.
Ethics statement
Written informed consent was obtained from the individual(s) for the publication of any potentially identifiable images or data included in this article.
Author contributions
YT: Investigation, Validation, Visualization, Writing – original draft, Writing – review & editing. MM: Conceptualization, Investigation, Supervision, Writing – review & editing. SO: Resources, Writing – review & editing. MN: Resources, Writing – review & editing. SN: Resources, Writing – review & editing. YT: Resources, Writing – review & editing. HI: Writing – review & editing. RM: Writing – review & editing. EK: Writing – review & editing. NOk: Writing – review & editing. TI: Writing – review & editing. SM: Writing – review & editing. SK: Writing – review & editing. AF: Writing – review & editing. NOn: Writing – review & editing. ST: Writing – review & editing. AM: Writing – review & editing. KK: Conceptualization, Writing – review & editing. MS: Supervision, Writing – review & editing.
Funding
The author(s) declare that no financial support was received for the research, authorship, and/or publication of this article.
Acknowledgments
The authors would like to thank the patient and his family for their cooperation and understanding of this case report and medical staff for their sincere care for the patient. We thank Enago (https://www.enago.jp) for editing a draft of this manuscript.
Conflict of interest
AM has received honoraria from AstraZeneca, Nippon Kayaku, Merck, Kyowa Kirin, and Pfizer. KK has received honoraria Chugai Pharmaceutical, Eli Lilly, and Bristol-Myers Squibb. MS has received grants and contracts from any entity from Taiho Pharmaceutical, Chugai Pharmaceutical, Eli Lilly, Nippon Boehringer Ingelheim, Nippon Kayaku, and Kyowa Hakko Kirin; honoraria from AstraZeneca, MSD K.K, Chugai Pharmaceutical, Taiho Pharmaceutical, Eli Lilly, Ono Pharmaceutical, Bristol-Myers Squibb, Nippon Boehringer Ingelheim, Pfizer, Novartis, Takeda Pharmaceutical, Kyowa Hakko Kirin, Nippon Kayaku, Daiichi-Sankyo Company, Merck Biopharma, and Amgen.
The remaining authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
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Keywords: IgA vasculitis, immune-related adverse event, immune checkpoint inhibitor, pembrolizumab, non-small-cell lung cancer
Citation: Terashima Y, Matsumoto M, Ozaki S, Nakagawa M, Nakagome S, Terasaki Y, Iida H, Mitsugi R, Kuramochi E, Okada N, Inoue T, Matsuki S, Kitagawa S, Fukuizumi A, Onda N, Takeuchi S, Miyanaga A, Kasahara K and Seike M (2024) IgA vasculitis induced by carboplatin + nab-paclitaxel + pembrolizumab in a patient with advanced lung squamous cell carcinoma: a case report. Front. Immunol. 15:1370972. doi: 10.3389/fimmu.2024.1370972
Received: 15 January 2024; Accepted: 30 July 2024;
Published: 14 August 2024.
Edited by:
Benjamin Frey, University Hospital Erlangen, GermanyCopyright © 2024 Terashima, Matsumoto, Ozaki, Nakagawa, Nakagome, Terasaki, Iida, Mitsugi, Kuramochi, Okada, Inoue, Matsuki, Kitagawa, Fukuizumi, Onda, Takeuchi, Miyanaga, Kasahara and Seike. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Masaru Matsumoto, czcwNjJAbm1zLmFjLmpw
†ORCID: Yuto Terashima, orcid.org/0000-0002-1797-9708
Masaru Matsumoto, orcid.org/0000-0001-6647-6624
Saeko Ozaki, orcid.org/0000-0002-4430-3535
Shun Nakagome, orcid.org/0000-0003-0607-0803
Yasuhiro Terasaki, orcid.org/0000-0003-4495-7982
Shingo Kitagawa, orcid.org/0009-0005-0828-5025
Aya Fukuizumi, orcid.org/0000-0001-5993-157X
Susumu Takeuchi, orcid.org/0000-0002-0617-0962
Akihiko Miyanaga, orcid.org/0000-0003-2026-9181
Kazuo Kasahara, orcid.org/0000-0001-5551-1543
Masahiro Seike, orcid.org/0000-0002-1572-5472