奥沙利铂、卡培他滨、曲妥珠单抗联合放化疗辅助治疗her2阳性胃或胃食管结癌手术患者的II期研究(TOXAG研究):土耳其肿瘤组研究。

Huseyin Abali, Suayib Yalcin, Huseyin C Onal, Faysal Dane, Berna Oksuzoglu, Nuriye Ozdemir, Huseyin Mertsoylu, Mehmet Artac, Celaletdin Camci, Bulent Karabulut, Fatma B Basal, Burcin Budakoglu, Mehmet A N Sendur, Burce Goktas, Fatih Ozdener, Arzu Baygul
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引用次数: 0

摘要

背景:曲妥珠单抗联合化疗可延长人表皮生长因子受体2 (HER2)过表达的晚期胃癌患者的总生存期。在这项II期开放标签前瞻性研究中,研究了曲妥珠单抗联合化疗和放化疗对治愈性切除的her2阳性胃癌患者的耐受性和安全性。方法:选取胃切除术加D2夹层后her2阳性的胃或胃食管交界处腺癌患者为研究对象。他们接受奥沙利铂3个周期(第1天静脉注射100 mg/m2)加卡培他滨(第1至14天口服850 mg/m2),曲妥珠单抗(第1周期第1天静脉注射8 mg/kg,此后6 mg/kg),每21天进行一次放化疗。曲妥珠单抗治疗1年。结果:在筛选的212例患者中,35例符合条件,34例接受治疗。中位年龄为56岁(最小至最大35 ~ 75岁),男性患者占73.5% (n=25), 33例(97.1%)为胃腺癌。30例(88.2%)行R0切除。大多数(26,61.7%)为III期疾病。大多数不良事件为I/II级,最常见的III级副作用是恶心(3,8.8%)、呕吐(3,8.8%)、腹泻(2,5.9%)和体重减轻(n= 2,5.9%)。2例患者在化疗和放化疗前3个周期死亡;一例继发于肺血栓栓塞,另一例由于脑缺血。在排除2例早期进展和1例同意退出后,剩余的31例患者中,28例(90.3%)能够完成试验的化疗和放化疗部分。25个月随访后,21例患者(61.8%)存活。12和24个月的总生存率分别为75.0%和58.0%,而12和24个月的无病生存率分别为65.7%和55.0%。结论:曲妥珠单抗联合卡培他滨、奥沙利铂在放化疗后作为胃或胃食管交界处腺癌的辅助治疗是安全且耐受的。HER2在治愈性切除患者中的过表达频率与转移性疾病患者相当(试验注册:clinicaltrials.gov,标识符:NCT01748773, 2012年12月13日,https://clinicaltrials.gov/ct2/show/NCT01748773)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A Phase II Study of the Combination of Oxaliplatin, Capecitabine, and Trastuzumab and Chemoradiotherapy in the Adjuvant Setting in Operated Patients With HER2-positive Gastric or Gastroesophageal Junction Cancer (TOXAG Study): A Turkish Oncology Group Study.

Background: Trastuzumab prolonged the overall survival in patients with advanced gastric cancer with human epidermal growth factor receptor 2 (HER2) overexpression in combination with chemotherapy. In this phase II open-label prospective study, the tolerability and safety of trastuzumab with chemotherapy, and chemoradiotherapy for curatively resected patients with HER2-positive gastric carcinoma was investigated.

Methods: The patients with HER2-positive gastric, or gastroesophageal junction adenocarcinoma, after gastrectomy plus D2 dissection, were included. They received 3 cycles of oxaliplatin (100 mg/m2 intravenously day 1) plus capecitabine (850 mg/m2 orally days 1 to 14), trastuzumab (8 mg/kg intravenously day 1 in cycle 1, 6 mg/kg thereafter) every 21 days, followed by chemoradiotherapy. Trastuzumab was given for 1 year.

Results: Of the 212 patients screened, 35 were eligible, and 34 were treated. The median age was 56 years (minimum to maximum: 35 to 75 y), male patients constituted 73.5% (n=25), and 33 (97.1%) had gastric adenocarcinoma. R0 resection was performed in 30 (88.2%). The majority (26, 61.7%) were in stage III disease. Most of the adverse events were grade I/II, the most frequent grade III side effects were nausea (3, 8.8%), vomiting (3, 8.8%), diarrhea (2, 5.9%), and weight loss (n=2, 5.9%). Two patients died during the first 3 cycles of chemotherapy and chemoradiotherapy; 1 secondary to pulmonary thromboembolism, and the other due to cerebral ischemia. After excluding 2 with early progression and 1 consent withdrawal, of the remaining 31 patients, 28 (90.3%) were able to complete the chemotherapy and chemoradiotherapy part of the trial. After the 25 months follow-up period, 21 patients (61.8%) were alive. Overall survival at 12 and 24 months was 75.0% and 58.0%, while disease-free survival at 12 and 24 months was 65.7% and 55.0%, respectively.

Conclusions: Trastuzumab in combination with capecitabine, oxaliplatin following chemoradiotherapy as the adjuvant therapy for gastric or gastroesophageal junction adenocarcinoma was considered as safe and tolerable. The frequency of HER2 overexpression in curatively resected patients is comparable to that in patients with metastatic disease (trial registration: clinicaltrials.gov the identifier: NCT01748773, December 13, 2012, https://clinicaltrials.gov/ct2/show/NCT01748773).

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