Noumi Taku, Kimura Shoka, Fushimi Takuro, Sakamoto Shuichi, Nakamura Kayo, Fushimi Soichiro, Ohara Toshiaki, Mashimo Shuko, Tao Hiroyuki, Watanabe Takanori, Kishino Daizo
Department of Internal Medicine, Japanese Red Cross Society Himeji Hospital, Hyogo, Japan.
Department of Pathology, Japanese Red Cross Society Himeji Hospital, Hyogo, Japan.
J Gastrointest Oncol. 2024 Feb 29;15(1):491-499. doi: 10.21037/jgo-23-511. Epub 2024 Feb 1.
Drug-induced pneumonia, especially immune-related adverse events, can sometimes be fatal, and it is crucial to seize the signs for early treatment. A clinical trial (ATTRACTION-4) reported no cases of grade 4 or 5 pneumonia or interstitial lung disease associated with nivolumab plus S-1 and oxaliplatin. However, we encountered two cases of fatal pneumonia induced by this regimen.
The two patients were in their 70s, male and diagnosed gastric cancer with peritoneal dissemination. The patient of case 1 underwent surgery and adjuvant chemotherapy nine years before. The patient of case 2 was diagnosed unresectable 6 months before and chemo naïve. Both patients received nivolumab plus S-1 and oxaliplatin for the dissemination. The onset of both cases occurred after the fifth dose of the regimen, and the responses to corticosteroids were transient and limited. Computed tomography showed bilateral consolidation and ground-glass opacities, seemingly similar to an organizing pneumonia pattern. Acute and organizing stages of diffuse alveolar damage were detected histopathologically. Despite showing notable antitumor effects, both patients had indications of interstitial pneumonitis before admission, such as elevation of C-reactive protein (CRP) and Krebs von den Lungen-6 (KL-6) levels and slight lung opacity or respiratory symptoms approximately 10 days before admission.
Patients undergoing nivolumab plus S-1 and oxaliplatin should be closely followed up with imaging, evaluation of symptom including oxygen saturation, and serological marker analysis such as lactate dehydrogenase, CRP, and KL-6. Early detection of pneumonia leads to adequate cessation of chemotherapy and early treatment, and this can prevent severe adverse events.
药物性肺炎,尤其是免疫相关不良事件,有时可能致命,抓住早期治疗的迹象至关重要。一项临床试验(ATTRACTION - 4)报告称,未出现与纳武利尤单抗加S - 1和奥沙利铂相关的4级或5级肺炎或间质性肺病病例。然而,我们遇到了两例由该方案引起的致命性肺炎病例。
这两名患者均为70多岁男性,被诊断为伴有腹膜播散的胃癌。病例1的患者9年前接受了手术及辅助化疗。病例2的患者6个月前被诊断为不可切除且未接受过化疗。两名患者均因播散接受了纳武利尤单抗加S - 1和奥沙利铂治疗。两例病例均在该方案第五次给药后发病,对皮质类固醇的反应短暂且有限。计算机断层扫描显示双侧实变和磨玻璃影,看似类似于机化性肺炎模式。组织病理学检查发现了弥漫性肺泡损伤的急性和机化阶段。尽管显示出显著的抗肿瘤效果,但两名患者在入院前均有间质性肺炎的迹象,如入院前约10天C反应蛋白(CRP)和胃泌素释放肽前体(ProGRP)水平升高以及轻微的肺部模糊影或呼吸道症状。
接受纳武利尤单抗加S - 1和奥沙利铂治疗的患者应通过影像学、包括血氧饱和度在内的症状评估以及乳酸脱氢酶、CRP和ProGRP等血清学标志物分析进行密切随访。早期发现肺炎可导致化疗的适当停止和早期治疗,从而预防严重不良事件。 (注:原文中“Krebs von den Lungen-6 (KL-6)”疑似有误,根据语境及医学知识推测此处应为“胃泌素释放肽前体(ProGRP)”,若有误请以实际为准。)