Department of Surgery, City of Hope National Medical Center, Duarte, CA, USA.
Computation and Quantitative Medicine, City of Hope National Medical Center, Duarte, CA, USA.
Ann Surg Oncol. 2024 Nov;31(12):7998-8007. doi: 10.1245/s10434-024-15980-9. Epub 2024 Sep 13.
Pressurized intraperitoneal aerosolized chemotherapy (PIPAC) is a novel, minimally invasive, safe, and repeatable method to treat carcinomatosis. Evidence regarding the clinical benefit (quality of life and survival) of PIPAC compared with that of conventional standard therapy (ST) is lacking.
This is the secondary analysis of the phase 1 US-PIPAC trial for refractory colorectal and appendiceal carcinomatosis. A PIPAC cohort was compared with a retrospective cohort of consecutive patients receiving ST. The primary outcome was number of good days (number of days alive and out of the hospital). The secondary outcomes were overall survival (OS), progression-free survival (PFS), health-related quality of life (HRQoL), and objective functional recovery (daily step count).
The study included 32 patients (PIPAC, 12; ST, 20) with similar baseline characteristics. Compared with the ST cohort, the PIPAC cohort had lower median inpatient hospital stays (> 24 h) within 6 months (0 vs 1; p = 0.015) and 1 year (1 vs 2; p = 0.052) and higher median good days at 6 months (181 vs 131 days; p = 0.042) and 1 year (323 vs 131 days; p = 0.032). There was no worsening of HRQoL after repeated PIPACs. Step counts diminished immediately after PIPAC but returned to baseline within 2-4 weeks. Kaplan-Meier analysis demonstrated a favorable association between receipt of PIPAC and OS (median, 11.3 vs 5.1 months; p = 0.036).
Compared with ST, PIPAC was associated with higher number of good days, reduced hospitalization burden, and longer OS without a negative impact on HRQoL with repeated PIPACs. These findings are foundational for evaluation of PIPAC in a randomized clinical trial.
加压腹腔内气溶胶化疗(PIPAC)是一种新颖的、微创的、安全的、可重复的治疗癌性腹膜转移的方法。与传统标准治疗(ST)相比,PIPAC 的临床获益(生活质量和生存)的证据尚缺乏。
这是美国 PIPAC 试验的 1 期临床试验的二次分析,该试验针对难治性结直肠和阑尾癌性腹膜转移。将 PIPAC 队列与接受 ST 的连续患者回顾性队列进行比较。主要结局是良好天数(存活和出院天数)的数量。次要结局是总生存期(OS)、无进展生存期(PFS)、健康相关生活质量(HRQoL)和客观功能恢复(日常步数)。
该研究纳入了 32 名患者(PIPAC 组 12 名,ST 组 20 名),具有相似的基线特征。与 ST 组相比,PIPAC 组在 6 个月内(0 对 1;p = 0.015)和 1 年内(1 对 2;p = 0.052)的中位住院时间更短,6 个月时的中位良好天数更高(181 对 131 天;p = 0.042),1 年时更高(323 对 131 天;p = 0.032)。重复 PIPAC 治疗后 HRQoL 没有恶化。PIPAC 后立即步数减少,但在 2-4 周内恢复到基线。Kaplan-Meier 分析显示,接受 PIPAC 与 OS 之间存在有利关联(中位数,11.3 对 5.1 个月;p = 0.036)。
与 ST 相比,PIPAC 与更高的良好天数、减少的住院负担和更长的 OS 相关,而不会对重复 PIPAC 治疗后的 HRQoL 产生负面影响。这些发现为 PIPAC 在随机临床试验中的评估奠定了基础。