Department of Surgery, Yonsei University College of Medicine, Seoul, Republic of Korea; Gastric Cancer Center, Yonsei Cancer Center, Yonsei University Health System, Seoul, Republic of Korea.
Gastric Cancer Center, Yonsei Cancer Center, Yonsei University Health System, Seoul, Republic of Korea; Division of Medical Oncology, Department of Internal Medicine, Yonsei University College of Medicine, Seoul, Republic of Korea.
J Gastrointest Surg. 2024 Jul;28(7):1095-1103. doi: 10.1016/j.gassur.2024.04.030. Epub 2024 May 3.
In gastric cancer, peritoneal metastasis is the most common form of metastasis and leads to dismal prognosis. We aimed to evaluate the safety and efficacy of combining perioperative intraperitoneal (IP) plus systemic chemotherapy, cytoreductive surgery (CRS), and hyperthermic intraperitoneal chemotherapy (HIPEC) for patients with gastric cancer with limited peritoneal metastasis or even after reducing peritoneal tumor burden by upfront IP chemotherapy.
Patients were enrolled in phase Ib in a 3 + 3 dose escalation of IP paclitaxel plus a fixed dose of IP cisplatin and oral S-1. In phase II, patients were managed according to the peritoneal cancer index (PCI) by diagnostic laparoscopy. For patients with a PCI of >12, upfront IP and systemic chemotherapy were given. Patients with a PCI of ≤12 or reduced to ≤12 after upfront chemotherapy underwent CRS with HIPEC. The primary endpoints were safety and the recommended phase II dose (RP2D) confirmation for phase Ib and the 1-year overall survival rate for phase II.
The RP2D was defined as IP 175 mg/m paclitaxel and 60 mg/m cisplatin and oral 70 mg/m/day S-1 for 14 days. A total of 22 patients were included. After CRS with HIPEC, there were no grade 3 or higher complications. The median hospital stay was 7 days (range, 6-11). The median overall and progression-free survival were 27.3 months (95% CI, 14.4 to not estimable) and 12.6 months (95% CI, 7.7-14.5), respectively. One-year overall and progression-free survival rates were 81.0% (95% CI, 65.8-99.6) and 54.5% (95% CI, 37.2-79.9), respectively.
A combination of IP plus systemic chemotherapy, CRS, and HIPEC was safe and resulted in good survival outcomes.
在胃癌中,腹膜转移是最常见的转移形式,导致预后不良。我们旨在评估联合围手术期腹腔(IP)加全身化疗、细胞减灭术(CRS)和腹腔内热化疗(HIPEC)治疗局限性腹膜转移或甚至通过前期 IP 化疗降低腹膜肿瘤负担的胃癌患者的安全性和疗效。
患者在 3+3 剂量递增的 IP 紫杉醇加固定剂量的 IP 顺铂和口服 S-1 中入组 Ib 期。在 II 期,根据诊断腹腔镜检查的腹膜癌指数(PCI)对患者进行管理。对于 PCI>12 的患者,给予前期 IP 和全身化疗。PCI≤12 或前期化疗后降至≤12 的患者接受 CRS 加 HIPEC。Ib 期的主要终点是安全性和确认 II 期推荐剂量(RP2D),II 期的主要终点是 1 年总生存率。
RP2D 定义为 IP 175mg/m 紫杉醇和 60mg/m 顺铂和口服 70mg/m/天 S-1,连用 14 天。共纳入 22 例患者。CRS 加 HIPEC 后无 3 级或更高的并发症。中位住院时间为 7 天(范围,6-11 天)。中位总生存期和无进展生存期分别为 27.3 个月(95%CI,14.4 至不可估计)和 12.6 个月(95%CI,7.7-14.5)。1 年总生存率和无进展生存率分别为 81.0%(95%CI,65.8-99.6)和 54.5%(95%CI,37.2-79.9)。
IP 联合全身化疗、CRS 和 HIPEC 是安全的,并且生存结果良好。