国际肿瘤学杂志 ›› 2018, Vol. 45 ›› Issue (11): 665-669.doi: 10.3760/cma.j.issn.1673-422X.2018.11.006

• 论著 • 上一篇    下一篇

胃肠间质瘤术后伊马替尼辅助治疗停止后复发、转移的诊治分析

万文泽,张睿智,李承果,杨文昶,王涛,曾祥宇,蔡明 ,王国斌,张鹏,陶凯雄   

  1. 430022 武汉,华中科技大学同济医学院附属协和医院胃肠外科
  • 出版日期:2018-11-08 发布日期:2018-12-21
  • 通讯作者: 陶凯雄,Email: kaixiongtao@hust.edu.cn E-mail:kaixiongtao@hust.edu.cn
  • 基金资助:
    国家自然科学基金(81572413、81702386);华中科技大学自主创新基金(2017KFYXJJ230、2017KFYXJJ256)

Analysis of diagnosis and treatment of gastrointestinal stromal tumor recurrence and metastasis after postoperative adjuvant imatinib treatment

Wan Wenze, Zhang Ruizhi, Li Chengguo, Yang Wenchang, Wang Tao, Zeng Xiangyu, Cai Ming, Wang Guobin, Zhang Peng, Tao Kaixiong   

  1. Department of Gastrointestinal Surgery, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430022, China
  • Online:2018-11-08 Published:2018-12-21
  • Contact: Tao Kaixiong, Email: kaixiongtao@hust.edu.cn E-mail:kaixiongtao@hust.edu.cn
  • Supported by:
    National Natural Science Foundation of China (81572413, 81702386); Independent Innovation Fund of Huazhong University of Science and Technology (2017KFYXJJ230, 2017KFYXJJ256)

摘要: 目的 探讨原发胃肠间质瘤(GIST)完整切除术后伊马替尼辅助治疗停止后复发、转移的临床特点、治疗策略及疗效,分析其相关危险因素。方法 回顾性分析2005年1月至2017年12月华中科技大学同济医学院附属协和医院诊治的80例完整切除肿瘤后,接受伊马替尼辅助治疗1年以上并已停药的原发GIST患者,收集其人口学特征、相关临床指标、病理及随访资料。采用Kaplan-Meier法进行生存分析,采用log-rank检验进行单因素分析,采用Cox回归模型进行多因素分析。结果 80例患者中17例出现停药后复发、转移,中位复发时间为12个月,患者无特异性临床表现,复发、转移部位分别为肝脏转移9例、腹膜转移5例、局部复发3例。本组17例复发、转移患者9例接受单纯伊马替尼治疗,其中6例部分缓解,3例疾病稳定,随访期间7例继发耐药,中位无进展生存时间为35个月(95%CI为15~55个月),中位总生存时间为49个月(95%CI为30~68个月);7例接受手术联合伊马替尼治疗,随访期间4例继发耐药,疾病控制良好,中位无进展生存时间为31个月(95%CI为6~56个月),中位总生存时间未达到;剩余1例放弃治疗。单因素分析结果显示肿瘤部位(χ2=4.120,P=0.042)、术前中性粒细胞与淋巴细胞比值(NLR)(χ2=7.513,P=0.006)和术前血小板与淋巴细胞比值(PLR)(χ2=6.575,P=0.010)是影响GIST伊马替尼辅助治疗停止后复发、转移的相关危险因素;多因素分析显示肿瘤部位(HR=3.787,95%CI为1.126~12.732,χ2=4.631,P=0.031)是伊马替尼辅助治疗停止后复发、转移的独立危险因素。结论 GIST患者在伊马替尼辅助治疗停止后发生肿瘤复发、转移无特异临床表现。较之胃来源GIST,非胃来源的GIST停药后复发风险更高。单纯伊马替尼或手术联合伊马替尼治疗对停药后复发患者均有可靠疗效。

关键词: 胃肠道间质肿瘤, 肿瘤复发, 局部, 肿瘤转移, 伊马替尼

Abstract: Objective To investigate the clinical characteristics, treatment strategies and curative effect of recurrence and metastasis of primary gastrointestinal stromal tumor (GIST) after complete resection along with adjuvant therapy with imatinib, and to analyze the risk factors of recurrence and metastasis after adjuvant therapy. Methods The demographic data, clinicopathological characteristics and follow-up data of 80 primary GIST patients who received adjuvant therapy with imatinib for at least 1-year duration and had already stopped taking imatinib from January 2005 to December 2017 in Union Hospital, Tongji Medical College, Huazhong University of Science and Technology were analyzed retrospectively. The survival analysis was performed using Kaplan-Meier approach. Univariate analysis was conducted using log-rank test. Multivariate analysis was produced by Cox regression model. Results Of the enrolled 80 patients, recurrence and metastasis were detected in 17 cases after completion of postoperative adjuvant therapy with imatinib, with a median recurrence time of 12 months. All the 17 patients showed no specific clinical manifestations. Liver metastasis, peritoneum metastasis and local recurrence were found in 9, 5 and 3 cases, respectively. In the 17 patients with recurrence and metastasis, 9 patients received imatinib monotherapy. Among the 9 patients, 6 achieved partial responses, while 3 demonstrated stable disease, and secondary drug resistance was found in 7 patients during the follow-up period, with a median progression-free survival of 35 months (95%CI: 15-55 months) and median overall survival of 49 months (95%CI: 30-68 months). A total of 7 patients with recurrence and metastasis were treated with imatinib after operation and achieved satisfying tumor control, and secondary drug resistance was found in 4 patients during the follow-up period, with a median progression-free survival of 31 months (95%CI: 6-56 months) and fell short of median overall survival. The remaining 1 patient gave up treatment. Univariate analysis showed that tumor location (χ2=4.120, P=0.042), preoperative neutrophil-to-lymphocyte ratio (NLR) (χ2=7.513, P=0.006) and preoperative platelet-to-lymphocyte ratio (PLR) (χ2=6.575, P=0.010) were associated with recurrence and metastasis of GIST patients after completion of adjuvant therapy. Multivariate analysis revealed that tumor location (HR=3.787, 95%CI: 1.126-12.732, χ2=4.631, P=0.031) was an independent prognostic factor for those patients. Conclusion GIST patients who are identified recurrence and metastasis after completion of adjuvant imatinib treatment show no specific clinical manifestations after stopping andjuvant therapy with imatinib. Compared with gastric GIST, non-gastric origin GIST has a higher risk of recurrence. Imatinib monotherapy and surgery combined with imatinib therapy are both effective in treating this subgroup of patients.

Key words: Gastrointestinal stromal tumor, Neoplasm recurrence, local, Neoplasm metastasis, Imatinib