Kawada Junji, Sakai Daisuke, Kimura Yutaka, Hirao Motohiro, Nishikawa Kazuhiro, Sugimoto Naotoshi, Oka Yoshio, Endo Shunji, Isozaki Yutaka, Matsuyama Jin, Kawabata Ryohei, Kawase Tomono, Fujitani Kazumasa, Kurokawa Yukinori, Kawakami Hisato, Shimokawa Toshio, Satoh Taroh
Department of Gastroenterological Surgery, Osaka General Medical Center, Osaka, Japan;
Department of Gastroenterological Surgery, Nippon Life Hospital, Osaka, Japan.
Anticancer Res. 2025 Mar;45(3):1077-1085. doi: 10.21873/anticanres.17495.
BACKGROUND/AIM: Irinotecan is a key drug for patients with advanced gastric cancer. We assessed the efficacy and safety of combination chemotherapy with trastuzumab and irinotecan in patients with advanced human epidermal growth factor receptor type 2 (HER2)-positive chemotherapy-refractory gastric cancer.
Eligibility criteria included unresectable or recurrent HER2-positive gastric cancer patients who were refractory to at least one regimen of chemotherapy. Irinotecan was administered at a dose of 150 mg/m every 2 weeks, and trastuzumab at a dose of 8 mg/kg on day 1 of the first cycle, followed by 6 mg/kg every 3 weeks. The primary endpoint was the disease control rate (DCR). The secondary endpoints were adverse events (AEs), overall response rate (ORR), time-to-treatment failure (TTF), progression-free survival (PFS), and overall survival (OS).
Thirty patients were enrolled, of whom 18 previously received a single chemotherapy regimen whereas 12 received two or more regimens. As one patient withdrew before the study treatment, 29 patients were assessable for efficacy and safety. The DCR was 65.5%, and the ORR was 20.7%. The median PFS and OS were 3.7 and 7.5 months, respectively. The major grade 3/4 AEs were neutropenia (24%), anemia (24%), leukopenia (21%), anorexia (11%), fatigue (14%), hypoalbuminemia (24%), and hypokalemia (14%). One treatment-related death occurred.
These findings indicate that irinotecan plus trastuzumab is feasible with modest potential efficacy against chemotherapy-refractory advanced HER2-positive gastric cancer.
背景/目的:伊立替康是晚期胃癌患者的关键药物。我们评估了曲妥珠单抗联合伊立替康治疗晚期人表皮生长因子受体2(HER2)阳性化疗难治性胃癌患者的疗效和安全性。
入选标准包括不可切除或复发的HER2阳性胃癌患者,且对至少一种化疗方案耐药。伊立替康每2周以150mg/m的剂量给药,曲妥珠单抗在第一个周期的第1天以8mg/kg的剂量给药,随后每3周以6mg/kg的剂量给药。主要终点是疾病控制率(DCR)。次要终点是不良事件(AE)、总缓解率(ORR)、治疗失败时间(TTF)、无进展生存期(PFS)和总生存期(OS)。
共纳入30例患者,其中18例曾接受单一化疗方案,12例接受两种或更多方案。由于1例患者在研究治疗前退出,29例患者可评估疗效和安全性。DCR为65.5%,ORR为20.7%。中位PFS和OS分别为3.7个月和7.5个月。主要的3/4级不良事件为中性粒细胞减少(24%)、贫血(24%)、白细胞减少(21%)、厌食(11%)、疲劳(14%)、低白蛋白血症(24%)和低钾血症(14%)。发生1例与治疗相关的死亡。
这些结果表明,伊立替康联合曲妥珠单抗对于化疗难治性晚期HER2阳性胃癌是可行的,且有一定的潜在疗效。