Nishikawa Kazuhiro, Koizumi Wasaburo, Tsuburaya Akira, Suzuki Motoko, Morita Satoshi, Fujitani Kazumasa, Akamaru Yusuke, Shimada Ken, Hosaka Hisashi, Nishimura Ken, Yoshikawa Takaki, Tsujinaka Toshimasa, Sakamoto Junichi
Cancer Treatment Center, Osaka International Medical & Science Center, Osaka Keisatsu Hospital, 10-31 Kitayama-cho, Tennoji-ku, Osaka, 543-0035, Japan.
Kitasato University, 1-15-3, Kitasato, Minami-ku, Sagamihara, Kanagawa, 252-0374, Japan.
Int J Clin Oncol. 2025 Feb;30(2):320-329. doi: 10.1007/s10147-024-02661-6. Epub 2024 Nov 25.
Biweekly irinotecan plus cisplatin combination therapy (BIRIP) and irinotecan monotherapy (IRI) are both expectable second-line chemotherapy (SLC) options for treating advanced gastric cancer (AGC). Although many patients receiving SLC have undergone gastrectomy, the impact of gastrectomy on SLC remains unclear, and the impact of gastrectomy may vary from regimen to regimen.
A total of 290 eligible patients registered in two randomized phase III trials evaluating BIRIP (IRI, 60 mg/m; CDDP, 30 mg/m, q2w) or IRI (150 mg/m, q2w) for patients with AGC was classified into the prior gastrectomy subgroup (PGG) or the no gastrectomy subgroup (NGG). We performed a subgroup analysis to evaluate the impact of gastrectomy on second-line BIRIP and IRI.
The BIRIP demonstrated significantly longer OS (11.1 vs. 6.8 months; HR 0.64; P = 0.026) and PFS (3.7 vs. 2.3 months; HR 0.54; P = 0.003) than the IRI, as well as better ORR (23.5% vs. 7.1%, P = 0.046) and DCR (74.5% vs. 47.6%, P = 0.010) in NGG. Although in PGG, the BIRIP failed to demonstrate differences in OS (13.8 vs. 13.8 months; HR 0.94; P = 0.722), PFS (4.9 vs. 4.5 months; HR 0.82; P = 0.194), ORR (18.3% vs. 20.5%) and DCR (70.4% vs. 65.1%). The incidence of grade 3 or worse adverse events did not differ except for a high incidence of anemia in the BIRIP group in PGG.
BIRIP was an effective treatment option that may improve survival outcomes among patients with AGC without previous gastrectomy.
UMIN000025367.
每两周一次的伊立替康联合顺铂联合疗法(BIRIP)和伊立替康单药疗法(IRI)都是治疗晚期胃癌(AGC)的二线化疗(SLC)的预期选择。尽管许多接受二线化疗的患者已经接受了胃切除术,但胃切除术对二线化疗的影响仍不清楚,并且胃切除术的影响可能因治疗方案而异。
在两项评估BIRIP(伊立替康,60mg/m²;顺铂,30mg/m²,每两周一次)或IRI(150mg/m²,每两周一次)用于AGC患者的随机III期试验中登记的290例符合条件的患者被分为先前胃切除亚组(PGG)或未行胃切除亚组(NGG)。我们进行了亚组分析,以评估胃切除术对二线BIRIP和IRI的影响。
在NGG中,BIRIP的总生存期(OS)(11.1个月对6.8个月;风险比[HR]0.64;P = 0.026)和无进展生存期(PFS)(3.7个月对2.3个月;HR 0.54;P = 0.003)显著长于IRI,客观缓解率(ORR)(23.5%对7.1%,P = 0.046)和疾病控制率(DCR)(74.5%对47.6%,P = 0.010)也更好。尽管在PGG中,BIRIP在OS(13.8个月对13.8个月;HR 0.94;P = 0.722)、PFS(4.9个月对4.5个月;HR 0.82;P = 0.194)、ORR(18.3%对20.5%)和DCR(70.4%对65.1%)方面未显示出差异。3级或更严重不良事件的发生率除了PGG中BIRIP组贫血发生率较高外没有差异。
BIRIP是一种有效的治疗选择,可能改善未接受过胃切除术的AGC患者的生存结局。
UMIN000025367。