Desmond Brendan, Alukaidey Lobna, Allan Zexi, Cabalag Carlos, Clemons Nicholas J, Michael Michael, Tie Jeanne, Tebbutt Niall, Duong Cuong P, Liu David S
Division of Cancer Surgery, Peter MacCallum Cancer Centre, 305 Grattan Street, Melbourne, Victoria, 3000, Australia.
Upper Gastrointestinal Surgery Unit, Division of Surgery, Anaesthesia and Procedural Medicine, Austin Hospital, 145 Studley Road, Heidelberg, Victoria, 3084, Australia.
Surg Oncol. 2025 Aug;61:102237. doi: 10.1016/j.suronc.2025.102237. Epub 2025 May 23.
Gastric cancer has a risk of early transcoelomic spread. Despite perioperative chemotherapy and surgery, peritoneal recurrence is a frequent contributor to mortality. The addition of neoadjuvant normothermic intraperitoneal chemotherapy (IPC) allows early treatment of microscopic disease. Our study aims to systematically evaluate the safety and efficacy of neoadjuvant IPC in patients with gastric cancer who are at high risk of peritoneal recurrence.
A systematic review was conducted according to the PRISMA guidelines. Embase, PubMed, Web of Science and Scopus were searched for relevant papers. The primary outcomes were the rates of disease-free (DFS) and overall survival (OS) among patients treated with neoadjuvant IPC. Secondary outcomes focused on adverse effects and toxicity.
Overall, 562 manuscripts were screened and 7 papers were included, totalling 158 patients. For cytology-positive patients, the addition of IPC led to a conversion to negative cytology and radical surgery in 78-89 %. This was associated with relatively high DFS and OS. Peritoneal-specific recurrence was higher in cohorts who initially had cytology-positive disease (63-69 %) compared to those who did not (0-29 %). Our data suggest that OS is lower in patients who were initially cytology-positive compared to cytology-negative disease. Importantly, neoadjuvant IPC did not appear to significantly increase treatment-related adverse events.
Our results suggest that the neoadjuvant IPC has efficacy and is safe, with high rates of cytology conversion (in cytology-positive disease), low rates of peritoneal recurrence (in locally advanced disease). This was associated with substantial improvements in DFS and OS, compared to current standard treatment regimens.
胃癌存在早期腹腔内播散的风险。尽管进行了围手术期化疗和手术,但腹膜复发仍是导致死亡的常见原因。新辅助常温腹腔内化疗(IPC)的加入可实现对微小病灶的早期治疗。我们的研究旨在系统评估新辅助IPC对腹膜复发高危胃癌患者的安全性和疗效。
根据PRISMA指南进行系统评价。检索Embase、PubMed、Web of Science和Scopus数据库以获取相关论文。主要结局是接受新辅助IPC治疗患者的无病生存率(DFS)和总生存率(OS)。次要结局聚焦于不良反应和毒性。
总体而言,共筛选了562篇手稿,纳入7篇论文,共计158例患者。对于细胞学阳性患者,加入IPC后78%-89%的患者实现了细胞学转阴并接受了根治性手术。这与相对较高的DFS和OS相关。初始细胞学阳性的队列腹膜特异性复发率(63%-69%)高于非阳性队列(0%-29%)。我们的数据表明,与细胞学阴性疾病患者相比,初始细胞学阳性患者的OS较低。重要的是,新辅助IPC似乎并未显著增加治疗相关不良事件。
我们的结果表明,新辅助IPC具有疗效且安全,细胞学转阴率高(细胞学阳性疾病),腹膜复发率低(局部进展期疾病)。与当前标准治疗方案相比,这与DFS和OS的显著改善相关。