日本胃癌、食管胃交界处癌或食管腺癌患者围手术期FLOT方案的安全性和有效性:单机构经验

S. Takei , A. Kawazoe , A. Jubashi , M. Komatsu , K. Sato , S. Mishima , D. Kotani , M. Yura , N. Sakamoto , S. Sakashita , T. Kuwata , T. Kojima , T. Fujita , T. Kinoshita , K. Shitara
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引用次数: 0

摘要

背景虽然在日本,局部胃癌的常见治疗策略是胃切除术后辅助化疗,但在非日本人群中进行的几项随机研究已将围手术期化疗确立为局部胃癌或胃食管交界处腺癌的标准治疗方法。患者和方法我们回顾性地查看了2020年2月至2023年2月期间接受围手术期FLOT(5-氟尿嘧啶+多西他赛+奥沙利铂+亮菌甲素)治疗的可切除胃癌、胃食管交界处癌和食管腺癌患者的病历。结果本研究共分析了91例患者,中位年龄为70岁(范围:29-82岁)。确诊时,83 名患者(91.2%)的原发病灶为 T3 或更高级别,85 名患者(93.4%)有淋巴结转移。共有 10 名患者在完成四个周期的术前化疗前接受了切除术,91 名患者中有 77 名(84.6%)完成了四个周期的化疗,其中 74 名接受了根治性切除术。FLOT 后进行根治性切除的 84 例患者中,82 例(97.6%)实现了 R0 切除,其中 8 例(9.5%)获得病理完全反应。切除术后,60名患者(65.9%)接受了至少一个周期的术后FLOT治疗,47名患者(51.6%)完成了八个周期的FLOT治疗。60名患者(65.9%)在术前和术后FLOT治疗期间发生了3级或3级以上的化疗相关不良事件,包括白细胞减少(30.8%)、中性粒细胞减少(50.5%)、发热性中性粒细胞减少(5.5%)和厌食(7.7%)。结论这些结果与 FLOT 4 关键试验的结果相当,表明 FLOT 方案在日本临床实践中具有可接受的可行性。
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Safety and efficacy of perioperative FLOT regimen in Japanese patients with gastric, esophagogastric junction, or esophageal adenocarcinoma: a single-institution experience

Background

Although the common treatment strategy for localized gastric cancer in Japan is gastrectomy followed by adjuvant chemotherapy, several randomized studies in non-Japanese populations have established perioperative chemotherapy as the standard treatment of localized gastric or gastroesophageal junction adenocarcinoma. Therefore, we have implemented this strategy in our institution.

Patients and methods

We retrospectively reviewed the medical records of patients with resectable gastric cancer, gastroesophageal junction cancer, and esophageal adenocarcinoma who had received perioperative FLOT (5-fluorouracil plus docetaxel plus oxaliplatin plus leucovorin) from February 2020 to February 2023.

Results

In this study, a total of 91 patients were analyzed, with a median age of 70 years (range: 29-82). At the time of diagnosis, 83 patients (91.2%) had T3 or higher-grade primary lesions, and 85 (93.4%) had lymph node metastasis. A total of 10 patients had resection before completing four cycles of preoperative chemotherapy, and 77 of 91 (84.6%) completed four cycles with 74 of them receiving radical resection. Among the 84 patients who had radical resection after FLOT, 82 (97.6%) achieved R0 resection, including 8 (9.5%) with a pathological complete response. After resection, 60 patients (65.9%) received at least one cycle of post-operative FLOT, and 47 (51.6%) completed eight cycles of FLOT treatment. Chemotherapy-related adverse events of grade 3 or higher occurred during the pre- and post-operative FLOT in 60 patients (65.9%), including leukopenia (30.8%), neutropenia (50.5%), febrile neutropenia (5.5%), and anorexia (7.7%). No treatment-related deaths occurred.

Conclusions

These findings were comparable to those in the pivotal FLOT 4 trial, suggesting acceptable feasibility of the FLOT regimen in Japanese clinical practice.

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