Abstract P5-21-14: Long-term survival in HER2-positive metastatic breast cancer treated with first-line trastuzumab: Real-life results from the Curie ESME database

IF 16.6 1区 医学 Q1 ONCOLOGY Cancer research Pub Date : 2018-02-15 DOI:10.1158/1538-7445.SABCS17-P5-21-14
E. Kaczmarek, C. Saint-Martin, J. Pierga, E. Brain, R. Rouzier, C. Dubot, A. Savignoni, E. Mouret‐Fourme, G. Simon, M. Carton, F. Lerebours
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Abstract

Background About 20% of breast cancer (BC) patients will develop distant metastases. HER2-positive (HER2+) disease is associated with poorer prognosis. However, outcome of HER2+ BC patients has dramatically improved since the use of trastuzumab. Although most HER2+ metastatic BC (MBC) patients will eventually develop progressive disease within one year of trastuzumab-based treatment, some are long-term responders (LTR). Few data on these patients are available. Methods The primary objective was to assess overall survival (OS) of HER2+ MBC patients treated with trastuzumab as 1st-line at the Institut Curie, based on institution-specific data included in the French Epidemiological Strategy and Medical Economics (ESME) program for MBC patients established in 2014 by Unicancer. Long-term responders (LTR) were defined as having a non-progressive disease for at least 2 years under 1st-line trastuzumab. Secondary objectives included progression-free survival (PFS), disease-free interval (DFI), prediction factors for LTR status by univariate and multivariate analysis: characteristics of patients (age, BMI, menopausal status), of primary tumour (e.g. hormone receptor (HR) status), of treatment (e.g. endocrine therapy, partner for trastuzumab combination), number and type of metastases. Results From 2008 to 2014, 2990 MBC patients were identified in the Curie-ESME MBC database. Of these, 460 had HER2+ disease. Sixteen patients with second primary malignancy were excluded. Of the 444 remaining patients, 340 received 1st-line trastuzumab and could be analyzed. With a 42.5-month median follow-up time, the mean age at metastatic diagnosis was 55.7 years, 59.4% had a HR-positive disease and 43.2% had de novo metastases or occurring within 6 months after adjuvant treatment. DFI was >24 months in 47.9% of patients, and 78.5% received 1st-line trastuzumab combined with taxane-based chemotherapy (CT). In 87 patients (25.6%) classified as LTR, median PFS was 56.2 months (CI95% 41.53-not reached) vs. 10.9 months in non-LTR (CI95% 9.46-11.8). Median OS in LTR is not reached versus 44.3 months in non-LTR (CI95% 37.9-49.1). Median age, menopausal status, BMI, pathological characteristics and treatment for primary BC were similar in both groups. The following factors were predictive of LTR status by univariate analysis: number of metastatic sites ( 3, p=0.022); endocrine treatment for metastatic disease (p=0.002); absence of central nervous system metastases (p=0.035); and taxane-based 1st- line CT (p=0.032). In multivariate analysis, only number of metastatic sites and taxane-based 1st-line CT were predictive of LTR status. In contrast, age, DFI, visceral disease, and adjuvant trastuzumab-based treatment did not influence outcome. Although not statistically significant, HR+ status was more frequent in LTR versus non-LTR patients (66.7% versus 56.9%). Conclusions With a median follow-up of 42.5 months, we found that more than 95% of LTR to 1st-line trastuzumab were still alive and could achieve a median PFS longer than 4.6 years. Although some clinical factors are clearly associated with better outcome, further investigations are needed to identify the mechanisms of resistance or sensitivity to trastuzumab. Citation Format: Kaczmarek E, Saint-Martin C, Pierga J-Y, Brain E, Rouzier R, Dubot C, Savignoni A, Mouret-Fourme E, Simon G, Carton M, Lerebours F. Long-term survival in HER2-positive metastatic breast cancer treated with first-line trastuzumab: Real-life results from the Curie ESME database [abstract]. In: Proceedings of the 2017 San Antonio Breast Cancer Symposium; 2017 Dec 5-9; San Antonio, TX. Philadelphia (PA): AACR; Cancer Res 2018;78(4 Suppl):Abstract nr P5-21-14.
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摘要P5-21-14:一线曲妥珠单抗治疗HER2阳性转移性癌症的长期生存率:居里ESME数据库的实时结果
背景癌症约20%的患者会发生远处转移。HER2阳性(HER2+)疾病与较差的预后相关。然而,自从使用曲妥珠单抗后,HER2+BC患者的预后显著改善。尽管大多数HER2+转移性BC(MBC)患者最终会在曲妥珠单抗治疗的一年内发展为进行性疾病,但有些患者是长期反应者(LTR)。关于这些患者的数据很少。方法主要目的是根据联合国癌症基金会于2014年建立的法国MBC患者流行病学战略和医学经济学(ESME)计划中的机构特定数据,评估在居里研究所接受曲妥珠单抗一线治疗的HER2+MBC患者的总生存率(OS)。长期应答者(LTR)被定义为在一线曲妥珠单抗治疗下患有至少2年的非进展性疾病。次要目标包括无进展生存期(PFS)、无病间隔期(DFI)、通过单变量和多变量分析预测LTR状态的因素:患者特征(年龄、BMI、更年期状态)、原发肿瘤特征(如激素受体(HR)状态)、治疗(如内分泌治疗、曲妥珠单抗联合用药的伴侣)、转移的数量和类型。结果2008年至2014年,居里ESME MBC数据库中共发现2990名MBC患者。其中460人患有HER2+疾病。16例第二原发性恶性肿瘤患者被排除在外。在剩下的444名患者中,340人接受了曲妥珠单抗一线治疗,可以进行分析。中位随访时间为42.5个月,诊断为转移的平均年龄为55.7岁,59.4%的患者患有HR阳性疾病,43.2%的患者有新的转移或发生在辅助治疗后6个月内。47.9%的患者DFI>24个月,78.5%的患者接受了曲妥珠单抗一线联合紫杉烷化疗(CT)。在87名被归类为LTR的患者(25.6%)中,中位PFS为56.2个月(CI95%41.53未达到),而非LTR为10.9个月(CI 95%9.46-11.8)。LTR的中位OS未达到,而非LTER为44.3个月(CI95%37.9-49.1)。两组的中位年龄、更年期状态、BMI、病理特征和原发性BC的治疗相似。通过单因素分析,以下因素可预测LTR状态:转移部位数(3,p=0.022);转移性疾病的内分泌治疗(p=0.002);无中枢神经系统转移(p=0.035);在多变量分析中,只有转移部位的数量和基于紫杉烷的一线CT可以预测LTR状态。相反,年龄、DFI、内脏疾病和以曲妥珠单抗为基础的辅助治疗并不影响结果。尽管没有统计学意义,但与非LTR患者相比,LTR患者的HR+状态更常见(66.7%对56.9%)。结论通过42.5个月的中位随访,我们发现95%以上的一线曲妥珠单抗LTR患者仍然存活,中位PFS可达到4.6年以上。尽管一些临床因素显然与更好的结果有关,但还需要进一步的研究来确定对曲妥珠单抗的耐药性或敏感性的机制。引用格式:Kaczmarek E、Saint-Martin C、Pierga J-Y、Brain E、Rouzier R、Dubot C、Savignoni A、Mouret-Fourme E、Simon G、Carton M、Lerebours F.一线曲妥珠单抗治疗的HER2阳性转移性癌症的长期生存率:居里ESME数据库的真实生活结果[摘要]。在:2017年圣安东尼奥癌症研讨会论文集;2017年12月5日至9日;德克萨斯州圣安东尼奥。费城(PA):AACR;癌症研究2018;78(4增刊):摘要编号P5-21-14。
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来源期刊
Cancer research
Cancer research 医学-肿瘤学
CiteScore
16.10
自引率
0.90%
发文量
7677
审稿时长
2.5 months
期刊介绍: Cancer Research, published by the American Association for Cancer Research (AACR), is a journal that focuses on impactful original studies, reviews, and opinion pieces relevant to the broad cancer research community. Manuscripts that present conceptual or technological advances leading to insights into cancer biology are particularly sought after. The journal also places emphasis on convergence science, which involves bridging multiple distinct areas of cancer research. With primary subsections including Cancer Biology, Cancer Immunology, Cancer Metabolism and Molecular Mechanisms, Translational Cancer Biology, Cancer Landscapes, and Convergence Science, Cancer Research has a comprehensive scope. It is published twice a month and has one volume per year, with a print ISSN of 0008-5472 and an online ISSN of 1538-7445. Cancer Research is abstracted and/or indexed in various databases and platforms, including BIOSIS Previews (R) Database, MEDLINE, Current Contents/Life Sciences, Current Contents/Clinical Medicine, Science Citation Index, Scopus, and Web of Science.
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