Unit of Infectious Diseases, Division of Immunology, Transplantation and Infectious Diseases, IRCCS San Raffaele Scientific Institute, Milan, Italy.
Department of Infectious Diseases, San Raffaele Scientific Institute, via Stamira d'Ancona 20, 20127, Milan, Italy.
Mycopathologia. 2019 Feb;184(1):181-185. doi: 10.1007/s11046-018-0291-4. Epub 2018 Aug 13.
The widespread use of T lymphocyte-associated antigen-4 (CTLA-4) and programmed death (PD)-1 and PD ligand-1 (PDL1)-targeted agents in cancer patients as immunotherapy has raised some issues on their safety profile. Regarding infectious complications, it has emerged that these compounds do not intrinsically increase susceptibility to opportunistic infections, which mainly correlate with the co-administration of systemic immunosuppressive therapy (high-dose corticosteroids and anti-tumor necrosis factors inhibitors) to cure immune-related adverse events (colitis, hepatitis, pneumonitis and pancreatitis), well-known complications of these targeted drugs. These observations lead experts' opinion to suggest primary anti-Pneumocystis prophylaxis in patients undergoing CTLA-4 and PD-1/PDL1 agents who will receive prednisone 20 mg daily for ≥ 4 weeks. Few data on invasive fungal infections in this context are available. We report here a case of probable invasive pulmonary aspergillosis (p-IPA) complicating first-line immunotherapy with pembrolizumab for metastatic lung cancer that was further aggravated by multidrug-resistant Pseudomonas aeruginosa superinfection of fungal cavities; the patient received concurrent systemic corticosteroid therapy as anti-edema treatment for cerebral metastases. Reviewing literature about Aspergillus diseases in subjects receiving CTLA-4 and PD-1 and PDL1-targeted agents, we found three cases of invasive aspergillosis and one case of exacerbation of chronic progressive pulmonary aspergillosis after nivolumab treatment; to the best of our knowledge, this is the first report of p-IPA complicating pembrolizumab immunotherapy. Briefly, in this new setting of biological/targeted drugs, waiting for growing clinical experience, we recommend a high level of alertness in diagnosing any infectious complications.
癌症患者的免疫疗法中广泛使用 T 淋巴细胞相关抗原-4(CTLA-4)和程序性死亡(PD)-1 和 PD 配体-1(PDL1)靶向药物,这引起了人们对其安全性的关注。关于感染性并发症,这些化合物本身并不会增加对机会性感染的易感性,这主要与全身免疫抑制治疗(大剂量皮质类固醇和抗肿瘤坏死因子抑制剂)联合使用以治疗免疫相关不良事件(结肠炎、肝炎、肺炎和胰腺炎)有关,这些靶向药物的常见并发症。这些观察结果使专家们认为,对于正在接受 CTLA-4 和 PD-1/PDL1 药物治疗且将每天接受 20 毫克泼尼松治疗≥4 周的患者,应进行原发性抗肺囊虫病预防。目前在这种情况下关于侵袭性真菌感染的数据很少。我们在此报告了一例可能的侵袭性肺曲霉病(p-IPA)病例,该病例是由转移性肺癌一线免疫治疗用帕博利珠单抗引起的,由于真菌空洞的多重耐药铜绿假单胞菌合并感染而进一步加重;该患者因脑转移接受了全身性皮质类固醇治疗以减轻水肿。我们回顾了接受 CTLA-4 和 PD-1 和 PDL1 靶向药物治疗的患者中关于曲霉病的文献,发现了三例侵袭性曲霉病和一例在接受纳武利尤单抗治疗后慢性进行性肺曲霉病恶化的病例;据我们所知,这是首例与帕博利珠单抗免疫治疗相关的 p-IPA 病例。简而言之,在这种新的生物/靶向药物治疗环境中,在等待更多的临床经验的同时,我们建议高度警惕任何感染性并发症的诊断。