Phase I study of neoadjuvant chemoradiotherapy with S-1 for clinically resectable type 4 or large type 3 gastric cancer in elderly patients aged 75 years and older (OGSG1303).

IF 3.5 4区 医学 Q2 ONCOLOGY Medical Oncology Pub Date : 2024-12-19 DOI:10.1007/s12032-024-02583-3
Masayuki Shinkai, Motohiro Imano, Masaki Yokokawa, Jin Matsuyama, Yutaka Kimura, Toshio Shimokawa, Hisato Kawakami, Taroh Satoh, Takushi Yasuda, Hiroshi Furukawa
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Abstract

Purpose The prognosis for type 4 and large type 3 gastric cancer (GC) is extremely poor, especially in elderly patients (≥ 75 years). To improve the prognosis of these types of GC, we performed a phase I study to determine the recommended dose (RD) of S-1 combined with neoadjuvant radiotherapy. Methods Patients with clinically resectable type 4 and large type 3 GC were enrolled to successive cohorts in a conventional 3 + 3 design. Three dose levels were designed, as follows: level 0: S-1 60 mg/m2/day on Days 1-14; level 1: S-1 80 mg/m2/day on Days 1 -14; level 2: S-1 80 mg/m2/day on Days 1-14 and Days 22-35. The starting dose was level 1. Radiotherapy was delivered at a total dose of 40 Gy in fractions for 4 weeks. Results Ten patients were enrolled from July 2014 to August 2018. Six patients were registered at level 1, and one patient developed a dose limiting toxicity as gastric stenosis (grade 3). Two of four patients enrolled at level 2 developed dose limiting toxicity (inability to receive S-1 for hematological reasons). Therefore, the RD was determined as level 1. All patients underwent the protocol surgery; one patient underwent R1 resection because of positive peritoneal washing cytology. There were no treatment-related deaths, and the pathological response rate was 80%. The 5-year overall- and progression-free survival rates were both 60.0%. Conclusion The RD was determined as level 1. A phase II trial using the RD should be initiated.

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S-1新辅助放化疗治疗75岁及以上高龄患者临床可切除的4型或大3型胃癌的I期研究(OGSG1303)。
目的4型和大3型胃癌(GC)预后极差,尤其是老年患者(≥75岁)。为了改善这些类型胃癌的预后,我们进行了一项I期研究,以确定S-1联合新辅助放疗的推荐剂量(RD)。方法采用常规的3 + 3设计,将临床可切除的4型和较大的3型胃癌患者纳入连续队列。设计了3个剂量水平:0水平:S-1 60 mg/m2/day,第1-14天;一级:S-1 80 mg/m2/天,第1 -14天;第2级:S-1 80 mg/m2/天,第1-14天和第22-35天。起始剂量为1级。放疗总剂量为40gy,分次进行,持续4周。结果10例患者于2014年7月至2018年8月入组。6名患者注册为1级,1名患者出现剂量限制性毒性,如胃狭窄(3级)。4名患者中有2名患者出现剂量限制性毒性(因血液学原因无法接受S-1)。因此,RD被确定为level 1。所有患者均接受常规手术;1例患者因腹膜冲洗细胞学阳性而行R1切除术。无治疗相关死亡,病理反应率为80%。5年总生存率和无进展生存率均为60.0%。结论RD为1级。应启动使用RD的II期试验。
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来源期刊
Medical Oncology
Medical Oncology 医学-肿瘤学
CiteScore
4.20
自引率
2.90%
发文量
259
审稿时长
1.4 months
期刊介绍: Medical Oncology (MO) communicates the results of clinical and experimental research in oncology and hematology, particularly experimental therapeutics within the fields of immunotherapy and chemotherapy. It also provides state-of-the-art reviews on clinical and experimental therapies. Topics covered include immunobiology, pathogenesis, and treatment of malignant tumors.
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