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 2.8 4区 医学 Q2 ONCOLOGY
Masayuki Shinkai, Motohiro Imano, Masaki Yokokawa, Jin Matsuyama, Yutaka Kimura, Toshio Shimokawa, Hisato Kawakami, Taroh Satoh, Takushi Yasuda, Hiroshi Furukawa
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引用次数: 0

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.

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。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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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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