Li S, Xue K, Dai H M, Wang Y K, Shan F, Li Z Y, Ji J F
Department of Gastrointestinal Cancer Center, Ward I, Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education), Peking University Caner Hospital & Institute, Beijing 100142, China.
Zhonghua Wei Chang Wai Ke Za Zhi. 2023 May 25;26(5):442-447. doi: 10.3760/cma.j.cn441530-20230302-00062.
To investigate the efficacy of laparoscopic hyperthermic intraperitoneal perfusion chemotherapy combined with intraperitoneal and systemic chemotherapy (HIPEC-IP-IV) in the treatment of peritoneal metastases from gastric cancer (GCPM). This was a descriptive case series study. Indications for HIPEC-IP-IV treatment include: (1) pathologically confirmed gastric or esophagogastric junction adenocarcinoma; (2) age 20-85 years; (3) peritoneal metastases as the sole form of Stage IV disease, confirmed by computed tomography, laparoscopic exploration, ascites or peritoneal lavage fluid cytology; and (4) Eastern Cooperative Oncology Group performance status 0-1. Contraindications include: (1) routine blood tests, liver and renal function, and electrocardiogram showing no contraindications to chemotherapy; (2) no serious cardiopulmonary dysfunction; and (3) no intestinal obstruction or peritoneal adhesions. According to the above criteria, data of patients with GCPM who had undergone laparoscopic exploration and HIPEC from June 2015 to March 2021 in the Peking University Cancer Hospital Gastrointestinal Center were analyzed, after excluding those who had received antitumor medical or surgical treatment. Two weeks after laparoscopic exploration and HIPEC, the patients received intraperitoneal and systemic chemotherapy. They were evaluated every two to four cycles. Surgery was considered if the treatment was effective, as shown by achieving stable disease or a partial or complete response and negative cytology. The primary outcomes were surgical conversion rate, R0 resection rate, and overall survival. Sixty-nine previously untreated patients with GCPM had undergone HIPEC-IP-IV, including 43 men and 26 women; with a median age of 59 (24-83) years. The median PCI was 10 (1-39). Thirteen patients (18.8%) underwent surgery after HIPEC-IP-IV, R0 being achieved in nine of them (13.0%). The median overall survival (OS) was 16.1 months. The median OS of patients with massive or moderate ascites and little or no ascites were 6.6 and 17.9 months, respectively (<0.001). The median OS of patients who had undergone R0 surgery, non-R0 surgery, and no surgery were 32.8, 8.0, and 14.9 months, respectively (=0.007). HIPEC-IP-IV is a feasible treatment protocol for GCPM. Patients with massive or moderate ascites have a poor prognosis. Candidates for surgery should be selected carefully from those in whom treatment has been effective and R0 should be aimed for.
探讨腹腔镜热灌注化疗联合腹腔及全身化疗(HIPEC-IP-IV)治疗胃癌腹膜转移(GCPM)的疗效。这是一项描述性病例系列研究。HIPEC-IP-IV治疗的适应证包括:(1)病理确诊为胃或食管胃交界腺癌;(2)年龄20-85岁;(3)经计算机断层扫描、腹腔镜探查、腹水或腹腔灌洗细胞学检查确诊为IV期疾病的唯一形式为腹膜转移;(4)东部肿瘤协作组体能状态0-1。禁忌证包括:(1)血常规、肝肾功能及心电图检查显示无化疗禁忌证;(2)无严重心肺功能障碍;(3)无肠梗阻或腹膜粘连。根据上述标准,对2015年6月至2021年3月在北京大学肿瘤医院胃肠中心接受腹腔镜探查和HIPEC治疗的GCPM患者的数据进行分析,排除接受过抗肿瘤药物或手术治疗的患者。腹腔镜探查和HIPEC术后两周,患者接受腹腔及全身化疗。每两至四个周期进行评估。如果治疗有效,即达到疾病稳定、部分缓解或完全缓解且细胞学检查阴性,则考虑手术。主要结局指标为手术转化率、R0切除率和总生存期。69例既往未接受治疗的GCPM患者接受了HIPEC-IP-IV治疗,其中男性43例,女性26例;中位年龄59(24-83)岁。中位腹膜癌指数(PCI)为10(1-39)。13例(18.8%)患者在HIPEC-IP-IV治疗后接受了手术,其中9例(13.0%)实现了R0切除。中位总生存期(OS)为16.1个月。大量或中度腹水患者与少量或无腹水患者的中位OS分别为6.6个月和17.9个月(<0.001)。接受R0手术、非R0手术和未手术患者的中位OS分别为32.8个月、8.0个月和14.9个月(=0.007)。HIPEC-IP-IV是一种治疗GCPM可行的治疗方案。大量或中度腹水患者预后较差。应从治疗有效的患者中仔细选择手术候选者,并应以R0为目标。