Shimomura Akihiko, Fujiwara Yutaka, Kondo Shunsuke, Kodaira Makoto, Iwasa Satoru, Kitano Shigehisa, Tanabe Yuko, Tamura Kenji, Yamamoto Noboru
Department of Experimental Therapeutics, National Cancer Center Hospital, 5-1-1 Tsukiji, Chuo-ku, Tokyo, 104-0045, Japan.
Department of Breast & Medical Oncology, National Cancer Center Hospital, 5-1-1 Tsukiji, Chuo-ku, Tokyo, 104-0045, Japan.
Immunotherapy. 2016;8(1):9-15. doi: 10.2217/imt.15.89. Epub 2015 Oct 2.
The human IgG2 monoclonal antibody tremelimumab is an immune checkpoint inhibitor that blocks cytotoxic T lymphocyte-associated antigen-4 (CTLA-4). The therapeutic response of anti-CTLA-4 monoclonal antibodies possess unique kinetics, in that antitumor responses are often observed after initial short-term disease progression, in some cases as long as 6-12 months after anti-CTLA-4 treatment initiation. Here, we report two cases: one of bile duct cancer and the other of squamous cell carcinoma of unknown primary, both of which demonstrated initial rapid disease progression followed by dramatic tumor shrinkage after one or two doses of tremelimumab, without any immune-related adverse events. This delayed, yet dramatic antitumor response suggests that tremelimumab may hold promise in the treatment of solid tumors.
人源化IgG2单克隆抗体曲美木单抗是一种免疫检查点抑制剂,可阻断细胞毒性T淋巴细胞相关抗原4(CTLA-4)。抗CTLA-4单克隆抗体的治疗反应具有独特的动力学特点,即通常在初始短期疾病进展后观察到抗肿瘤反应,在某些情况下,抗CTLA-4治疗开始后长达6至12个月才出现。在此,我们报告两例病例:一例胆管癌,另一例原发灶不明的鳞状细胞癌,两例均在初始疾病快速进展后,经一或两剂曲美木单抗治疗后肿瘤显著缩小,且未出现任何免疫相关不良事件。这种延迟但显著的抗肿瘤反应表明曲美木单抗在实体瘤治疗中可能具有前景。