Kunimatsu Yusuke, Kano Yukari, Tsutsumi Rei, Sato Izumi, Tanimura Mai, Tanimura Keiko, Takeda Takayuki
Department of Respiratory Medicine Japanese Red Cross Kyoto Daini Hospital Kyoto Japan.
Respirol Case Rep. 2023 Mar 13;11(4):e01122. doi: 10.1002/rcr2.1122. eCollection 2023 Apr.
The incidence rate of pseudoprogression during immune checkpoint inhibitor monotherapy for non-small cell lung cancer is reportedly 3.6%-6.9%, while pseudoprogression during chemoimmunotherapy is rare. Reports on pseudoprogression during dual immunotherapy combined with chemotherapy are lacking. Herein, a 55-year-old male with invasive mucinous adenocarcinoma (cT2aN2M1c [OTH, PUL], stage IVB, and programmed death-ligand 1 expression <1%), renal dysfunction, and disseminated intravascular coagulation was treated with carboplatin, solvent-based paclitaxel, nivolumab, and ipilimumab. After treatment initiation, computed tomography (CT) on day 14 showed disease progression. The patient was diagnosed with pseudoprogression because of a lack of symptoms, improved platelet count, and decreased fibrin/fibrinogen degradation product levels. CT on day 36 showed a reduction in the primary lesion size, multiple lung metastases, and mesenteric metastases. Therefore, pseudoprogression should be considered during dual immunotherapy with chemotherapy.
据报道,在非小细胞肺癌免疫检查点抑制剂单药治疗期间,假性进展的发生率为3.6%-6.9%,而在化疗免疫治疗期间假性进展很少见。关于双重免疫治疗联合化疗期间假性进展的报道较少。在此,一名55岁男性,患有浸润性黏液腺癌(cT2aN2M1c[OTH,PUL],IVB期,程序性死亡配体1表达<1%)、肾功能不全和弥散性血管内凝血,接受了卡铂、溶剂型紫杉醇、纳武单抗和伊匹木单抗治疗。治疗开始后,第14天的计算机断层扫描(CT)显示疾病进展。由于缺乏症状、血小板计数改善以及纤维蛋白/纤维蛋白原降解产物水平降低,该患者被诊断为假性进展。第36天的CT显示原发灶大小减小、多发肺转移和肠系膜转移。因此,在双重免疫治疗联合化疗期间应考虑假性进展。