{"title":"Fourteen-year follow-up results of imatinib therapy in patients with unresectable and metastatic gastrointestinal stromal tumors.","authors":"Tatsuo Kanda, Hiroshi Ichikawa, Takashi Ishikawa, Yusuke Muneoka, Yosuke Kano, Tetsuya Naito, Satoshi Suzuki, Toshifumi Wakai","doi":"10.1007/s10147-024-02631-y","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Imatinib therapy is the gold standard for the treatment of unresectable and metastatic gastrointestinal stromal tumors (GISTs). However, few studies have reported the long-term outcomes of the treatment.</p><p><strong>Methods: </strong>Seventy patients who underwent imatinib therapy for unresectable and metastatic GISTs were enrolled between 2001 and 2009, and follow-up data were collected until October 2023. One hundred and sixty-eight months had passed since the final enrollment. The outcome measures were patient survival and the status of GIST and imatinib therapy. The cumulative incidence of disease progression (PD) and the chronological changes in PD hazard rate (HR) were also analyzed.</p><p><strong>Results: </strong>The 5-, 10-, 15-, and 20-year overall survival rates were 64.3%, 30.0%, 16.8%, and 12.2%, respectively. Sixty of the 70 enrolled patients died before the data cutoff date: 47 (78.3%) patients died of GIST progression while the remaining 13 (21.7%) died of diseases other than GISTs. The cumulative incidence of PD logarithmically increased, and PD continued even after 10 years of treatment. PD HR decreased over time to reach the lowest value at 9.6 years after the initiation of treatment (HR 0.00027; 95% CI 0.00007-0.00174) and after that formed a small peak at 13 years (HR 0.00144; 95% CI 0.00043-0.00436).</p><p><strong>Conclusions: </strong>Imatinib therapy showed high clinical efficacy in terms of long-term survival in GIST patients. However, patients undergoing imatinib therapy were at continuous risk of PD even after the 10-year treatment. Long-term treatment and follow-up beyond 10 years are necessary for unresectable and metastatic GIST patients.</p>","PeriodicalId":13869,"journal":{"name":"International Journal of Clinical Oncology","volume":" ","pages":"1870-1877"},"PeriodicalIF":2.4000,"publicationDate":"2024-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"International Journal of Clinical Oncology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1007/s10147-024-02631-y","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/9/30 0:00:00","PubModel":"Epub","JCR":"Q3","JCRName":"ONCOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Background: Imatinib therapy is the gold standard for the treatment of unresectable and metastatic gastrointestinal stromal tumors (GISTs). However, few studies have reported the long-term outcomes of the treatment.
Methods: Seventy patients who underwent imatinib therapy for unresectable and metastatic GISTs were enrolled between 2001 and 2009, and follow-up data were collected until October 2023. One hundred and sixty-eight months had passed since the final enrollment. The outcome measures were patient survival and the status of GIST and imatinib therapy. The cumulative incidence of disease progression (PD) and the chronological changes in PD hazard rate (HR) were also analyzed.
Results: The 5-, 10-, 15-, and 20-year overall survival rates were 64.3%, 30.0%, 16.8%, and 12.2%, respectively. Sixty of the 70 enrolled patients died before the data cutoff date: 47 (78.3%) patients died of GIST progression while the remaining 13 (21.7%) died of diseases other than GISTs. The cumulative incidence of PD logarithmically increased, and PD continued even after 10 years of treatment. PD HR decreased over time to reach the lowest value at 9.6 years after the initiation of treatment (HR 0.00027; 95% CI 0.00007-0.00174) and after that formed a small peak at 13 years (HR 0.00144; 95% CI 0.00043-0.00436).
Conclusions: Imatinib therapy showed high clinical efficacy in terms of long-term survival in GIST patients. However, patients undergoing imatinib therapy were at continuous risk of PD even after the 10-year treatment. Long-term treatment and follow-up beyond 10 years are necessary for unresectable and metastatic GIST patients.
背景:伊马替尼疗法是治疗不可切除和转移性胃肠道间质瘤(GIST)的金标准。然而,很少有研究报告该疗法的长期疗效:方法:2001年至2009年间,70名接受伊马替尼治疗的不可切除和转移性胃肠道间质瘤患者被纳入研究,随访数据收集至2023年10月。最终入组至今已过去了168个月。结果指标为患者生存期、GIST和伊马替尼治疗情况。此外,还分析了疾病进展(PD)的累积发生率和PD危险率(HR)的时序变化:5年、10年、15年和20年总生存率分别为64.3%、30.0%、16.8%和12.2%。70名入组患者中有60人在数据截止日期前死亡:47人(78.3%)死于GIST进展,其余13人(21.7%)死于GIST以外的疾病。PD的累积发生率呈对数增长,甚至在治疗10年后PD仍在继续。随着时间的推移,PD HR下降,在治疗开始后9.6年达到最低值(HR 0.00027;95% CI 0.00007-0.00174),之后在13年形成一个小高峰(HR 0.00144;95% CI 0.00043-0.00436):结论:就GIST患者的长期生存而言,伊马替尼治疗显示出较高的临床疗效。结论:就GIST患者的长期生存而言,伊马替尼疗法显示出较高的临床疗效,然而,接受伊马替尼疗法的患者即使在10年治疗后仍有持续的PD风险。对于无法切除和转移的GIST患者,有必要进行10年以上的长期治疗和随访。
期刊介绍:
The International Journal of Clinical Oncology (IJCO) welcomes original research papers on all aspects of clinical oncology that report the results of novel and timely investigations. Reports on clinical trials are encouraged. Experimental studies will also be accepted if they have obvious relevance to clinical oncology. Membership in the Japan Society of Clinical Oncology is not a prerequisite for submission to the journal. Papers are received on the understanding that: their contents have not been published in whole or in part elsewhere; that they are subject to peer review by at least two referees and the Editors, and to editorial revision of the language and contents; and that the Editors are responsible for their acceptance, rejection, and order of publication.