Tomisaki Ikko, Harada Mirii, Sakano Shigeru, Terado Michikazu, Hamasuna Ryoichi, Harada Shuji, Matsumoto Hiroomi, Akasaka Soichiro, Nagata Yujiro, Minato Akinori, Harada Ken-Ichi, Fujimoto Naohiro
Department of Urology, University of Occupational and Environmental Health, Kitakyushu, Japan;
Department of Urology, University of Occupational and Environmental Health, Kitakyushu, Japan.
Anticancer Res. 2023 Jan;43(1):269-274. doi: 10.21873/anticanres.16159.
BACKGROUND/AIM: We aimed to clarify the association between body mass index (BMI) and clinical outcomes of pembrolizumab treatment for advanced urothelial cancer (UC).
We retrospectively reviewed the records of patients with advanced UC who received pembrolizumab after chemotherapy between March 2018 and December 2021. Patients were divided according to BMI into the non-overweight group (BMI <25 kg/m) and the overweight group (BMI ≥25 kg/m). We compared the two groups' tumour response, survival rates, and incidence of immune-related adverse events (irAEs) and investigated the factors predicting survival.
Of 84 eligible patients, 63 (75%) and 21 (25%) were in the non-overweight and overweight groups, respectively. Although the objective response rate was higher in the overweight group (55%) than that in the non-overweight group (29%), the difference was not significant. Progression-free survival (PFS) was significantly longer in the overweight group (median 15.2 months) than that in the non-overweight group (median 4.8 months; p=0.01). Overall survival was also longer in the overweight group (median 36.1 months) compared to that in the non-overweight group (13.4 months), but the difference was not significant (p=0.11). Multivariable analysis showed that overweight was significantly associated with favourable PFS. Any and severe (grade 3) irAEs were observed in 15 (24%) and 5 (7.9%) patients in the non-overweight group, respectively, and in 8 (38%) and 2 (9.5%) patients in the overweight group, respectively, but the differences were not significant.
BMI was associated with oncological outcomes in patients with advanced UC who received pembrolizumab but not with the development of irAEs.
背景/目的:我们旨在阐明体重指数(BMI)与派姆单抗治疗晚期尿路上皮癌(UC)临床结局之间的关联。
我们回顾性分析了2018年3月至2021年12月期间接受化疗后使用派姆单抗治疗的晚期UC患者的记录。根据BMI将患者分为非超重组(BMI<25kg/m²)和超重组(BMI≥25kg/m²)。我们比较了两组的肿瘤反应、生存率以及免疫相关不良事件(irAEs)的发生率,并研究了预测生存的因素。
84例符合条件的患者中,非超重组63例(75%),超重组21例(25%)。尽管超重组的客观缓解率(55%)高于非超重组(29%),但差异无统计学意义。超重组的无进展生存期(PFS)显著长于非超重组(中位值15.2个月对4.8个月;p=0.01)。超重组的总生存期也长于非超重组(中位值36.1个月对13.4个月),但差异无统计学意义(p=0.11)。多变量分析显示超重与良好的PFS显著相关。非超重组分别有15例(24%)和5例(7.9%)患者发生任何级和严重(3级)irAEs,超重组分别有8例(38%)和2例(9.5%)患者发生,但差异无统计学意义。
BMI与接受派姆单抗治疗的晚期UC患者的肿瘤学结局相关,但与irAEs的发生无关。