Department of Gastroenterological Surgery, Osaka University Graduate School of Medicine, 2-2-E2, Yamadaoka, Suita, Osaka, 565-0871, Japan.
Japan Clinical Oncology Group Data Center/Operations Office, National Cancer Center Hospital, Tokyo, Japan.
Gastric Cancer. 2024 Mar;27(2):366-374. doi: 10.1007/s10120-023-01453-7. Epub 2024 Jan 5.
The prognosis for marginally resectable gastric cancer with extensive lymph node metastasis (ELM) remains unfavorable, even after R0 resection. To assess the safety and efficacy of preoperative docetaxel, oxaliplatin, and S-1 (DOS), we conducted a multicenter phase II trial.
Eligibility criteria included histologically proven HER2-negative gastric adenocarcinoma with bulky nodal (bulky N) involvement around major branched arteries or para-aortic node (PAN) metastases. Patients received three cycles of docetaxel (40 mg/m, day 1), oxaliplatin (100 mg/m, day 1), and S-1 (80-120 mg/body, days 1-14), followed by gastrectomy with D2 plus PAN dissection. Subsequently, patients underwent postoperative chemotherapy with S-1 for 1 year. The primary endpoint was major (grade ≥ 2a) pathological response rate (pRR) according to the Japanese Classification of Gastric Carcinoma criteria.
Between October 2018 and March 2022, 47 patients (bulky N, 20; PAN, 17; both, 10) were enrolled in the trial. One patient was ineligible. Another declined any protocol treatments before initiation. Among the 45 eligible patients who initiated DOS chemotherapy, 44 (98%) completed 3 cycles and 42 (93%) underwent R0 resection. Major pRR and pathological complete response rates among the 46 eligible patients, including the patient who declined treatment, were 57% (26/46) and 24% (11/46), respectively. Common grade 3 or 4 toxicities were neutropenia (24%), anorexia (16%), febrile neutropenia (9%), and diarrhea (9%). No treatment-related deaths occurred.
Preoperative chemotherapy with DOS yielded favorable pathological responses with an acceptable toxicity profile. This multimodal approach is highly promising for treating gastric cancer with ELM.
即使进行了 R0 切除,广泛淋巴结转移(ELM)的边缘可切除胃癌的预后仍然不佳。为了评估术前多西紫杉醇、奥沙利铂和 S-1(DOS)的安全性和有效性,我们进行了一项多中心 II 期试验。
入选标准包括组织学证实的 HER2 阴性胃腺癌,主要分支动脉周围或腹主动脉旁淋巴结(PAN)转移有大块淋巴结(bulky N)受累。患者接受三个周期的多西紫杉醇(40mg/m,第 1 天)、奥沙利铂(100mg/m,第 1 天)和 S-1(80-120mg/体,第 1-14 天)治疗,随后进行胃切除术加 D2 加 PAN 解剖。随后,患者接受 S-1 辅助化疗 1 年。主要终点是根据日本胃癌分类标准的主要(≥2a 级)病理性缓解率(pRR)。
2018 年 10 月至 2022 年 3 月期间,共有 47 名患者(bulky N,20 名;PAN,17 名;两者均有,10 名)入组该试验。1 名患者不符合条件。另一名患者在开始前拒绝了任何方案治疗。在开始 DOS 化疗的 45 名合格患者中,44 名(98%)完成了 3 个周期,42 名(93%)接受了 R0 切除。包括拒绝治疗的患者在内的 46 名合格患者的主要 pRR 和病理完全缓解率分别为 57%(26/46)和 24%(11/46)。常见的 3 级或 4 级毒性为中性粒细胞减少症(24%)、厌食症(16%)、发热性中性粒细胞减少症(9%)和腹泻(9%)。无治疗相关死亡。
DOS 术前化疗产生了良好的病理反应,且毒性可接受。这种多模式方法对治疗广泛淋巴结转移的胃癌具有很大的潜力。