Tajik Fatemeh, Eyob Belain, Khan Aaqil M, Radhakrishnan Vinodh Kumar, Senthil Maheswari
Department of Surgery, University of California Irvine Medical Center, Orange, CA 92868, USA.
Division of Surgical Oncology, Department of Surgery, University of California Irvine Medical Center, Orange, CA 92868, USA.
Cancers (Basel). 2025 Jan 17;17(2):289. doi: 10.3390/cancers17020289.
Despite the incremental improvement of survival with systemic therapy in metastatic gastric cancer (GC), the outcomes of patients with peritoneal carcinomatosis (PC) remain poor. The limited effectiveness of systemic therapy is attributed to the blood-peritoneal barrier and anarchic intra-tumoral circulation, which reduce the penetration of systemic therapy. Approaches that incorporate intraperitoneal (IP) chemotherapy, in addition to systemic therapies, may be a viable alternate strategy. Therefore, we provide a review of biology of gastric cancer peritoneal metastasis and evidence for bidirectional iterative IP chemotherapy in GCPC. A comprehensive search in PubMed, Scopus, Embase, Web of Science, Google Scholar, and ClinicalTrials.gov was performed to find the relevant articles and ongoing phase II/III clinical trials in iterative IP chemotherapy in GCPC. Intraperitoneal (IP) chemotherapy leverages the blood-peritoneal barrier to allow for the administration of high concentrations of chemotherapy directly to the peritoneal metastases, with a significant reduction in the systemic toxicity and enhanced drug efficacy against peritoneal metastasis. This pharmacokinetic advantage of IP chemotherapy can be further enhanced by additional measures such as heat or aerosolization. There are three IP chemotherapy approaches, namely, heated intraperitoneal chemotherapy (HIPEC), pressurized intraperitoneal aerosolized chemotherapy (PIPAC), and normothermic intraperitoneal chemotherapy (NIPEC). Recent evidence suggests that iterative IP chemotherapy combined with systemic therapy may offer significant survival benefits for patients with peritoneal metastasis. Furthermore, bidirectional treatment approaches may also increase the chances of surgical resection and survival. IP chemotherapy plays a pivotal role in the management of gastric carcinomatosis, particularly in combination with cytoreduction in highly selected patients. The combination of systemic and regional control may increase the chances of surgical resection and may ultimately lead to significant survival benefits.
尽管转移性胃癌(GC)患者经全身治疗后的生存率有所提高,但伴有腹膜癌转移(PC)的患者预后仍然较差。全身治疗效果有限归因于血腹屏障和肿瘤内紊乱的循环,这降低了全身治疗的穿透性。除全身治疗外,采用腹腔内(IP)化疗的方法可能是一种可行的替代策略。因此,我们综述了胃癌腹膜转移的生物学特性以及GCPC中双向迭代IP化疗的证据。我们在PubMed、Scopus、Embase、Web of Science、Google Scholar和ClinicalTrials.gov进行了全面检索,以查找GCPC中迭代IP化疗的相关文章和正在进行的II/III期临床试验。腹腔内(IP)化疗利用血腹屏障,可将高浓度化疗药物直接给药至腹膜转移灶,显著降低全身毒性,并增强对腹膜转移的药物疗效。IP化疗的这种药代动力学优势可通过加热或雾化等额外措施进一步增强。IP化疗有三种方法,即热腹腔内化疗(HIPEC)、加压腹腔内雾化化疗(PIPAC)和常温腹腔内化疗(NIPEC)。最近的证据表明,迭代IP化疗联合全身治疗可能为腹膜转移患者带来显著的生存益处。此外,双向治疗方法也可能增加手术切除和生存的机会。IP化疗在胃癌腹膜转移的治疗中起关键作用,特别是在高度选择的患者中与肿瘤细胞减灭术联合应用时。全身和局部控制相结合可能增加手术切除的机会,并最终带来显著的生存益处。