绝经后激素受体阳性、her2阴性早期乳腺癌患者接受来曲唑治疗后(新)辅助化疗后的侵袭性无病和总生存率:来自IV期前言试验的经验

IF 4.7 2区 医学 Q1 ONCOLOGY
Milena Beierlein, Lothar Häberle, Naiba Nabieva, Nicolai Maass, Bahriye Aktas, Sherko Kümmel, Christoph Thomssen, Christopher Wolf, Hans-Christian Kolberg, Cosima Brucker, Wolfgang Janni, Peter Dall, Andreas Schneeweiss, Frederik Marme, Marc W Sütterlin, Matthias Ruebner, Anna-Katharin Theuser, Nadine M Hofmann, Sybille Böhm, Katrin Almstedt, Sara Kellner, Paul Gass, Hans-Joachim Lück, Alexander Hein, Sabine Schmatloch, Matthias Kalder, Christoph Uleer, Ingolf Juhasz-Böss, Volker Hanf, Christian Jackisch, Volkmar Müller, Brigitte Rack, Erik Belleville, Diethelm Wallwiener, Achim Rody, Claudia Rauh, Chistian M Bayer, Sabrina Uhrig, Hanna Huebner, Chloë Goossens, Sara Y Brucker, Carolin C Hack, Tanja N Fehm, Peter A Fasching
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引用次数: 0

摘要

激素受体阳性(HRpos)、her2阴性(HER2neg)乳腺癌(BC)患者从新辅助化疗(NACT)中获益少于三阴性和her2阳性乳腺癌患者。在这项IV期临床试验(NCT01908556)的回顾性分析中,绝经后HRpos BC患者(n = 3297)接受了5年的前期辅助来曲唑治疗,我们评估了HRpos/ her2阴性早期BC患者接受辅助化疗与新辅助化疗的预后。具有(neo)辅助化疗信息的HRpos/ her2阴性患者(n = 2895)从所有参加前言试验的患者中回顾性选择。比较新辅助化疗组和辅助化疗组患者的侵袭性无病生存期(iDFS)和总生存期(OS)。化疗1051例(占全部患者的36.3%),其中辅助化疗874例(83.2%),NACT 177例(16.8%)。NACT组病理完全缓解(pCR)率为6.9%。接受NACT治疗的患者预后比辅助化疗的患者差(5年iDFS为81% vs. 88%;5年生存率89% vs. 93%)。在调整了年龄、BMI、淋巴结状况、分级、肿瘤大小和组织学后,这种效果仍然存在(iDFS的风险比:1.95 (95%CI: 1.28-2.95);OS风险比:2.13 (95%CI: 1.24-3.66)。进一步调整紫杉烷为基础的制度没有改变结果。总之,在这项对早期HRpos/ her2阴性BC患者的回顾性分析中,与患者和肿瘤特征无关,NACT患者的预后比辅助治疗的患者更不利。新辅助治疗患者的预后可能受耐药机制的影响,值得进一步研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Invasive disease-free and overall survival after (neo)adjuvant chemotherapy in postmenopausal patients with hormone receptor-positive, HER2-negative early breast cancer treated with upfront letrozole: Experiences from the phase IV PreFace trial.

Patients with hormone receptor-positive (HRpos), HER2-negative (HER2neg) breast cancer (BC) benefit less from neoadjuvant chemotherapy (NACT) than patients with triple-negative and HER2-positive BC. In this retrospective analysis of the phase IV PreFace clinical trial (NCT01908556), where postmenopausal HRpos BC patients (n = 3297) were treated with 5-year upfront adjuvant letrozole therapy, we evaluated the prognosis of patients treated with adjuvant versus neoadjuvant chemotherapy in HRpos/HER2neg early-stage BC. HRpos/HER2neg patients with information on (neo)adjuvant chemotherapy (n = 2895) were retrospectively selected from all patients enrolled in the PreFace trial. Invasive disease-free survival (iDFS) and overall survival (OS) were compared between patient groups that were treated with neoadjuvant or adjuvant chemotherapy. Chemotherapy was given to 1051 patients (36.3% of all patients), of which 874 (83.2%) received adjuvant chemotherapy and 177 (16.8%) NACT. Pathologic complete response (pCR) rate in the NACT group was 6.9%. Patients treated with NACT had a worse outcome than those treated with adjuvant chemotherapy (5-year iDFS rate 81% vs. 88%; 5-year OS rate 89% vs. 93%). This effect was maintained after adjusting for age, BMI, lymph node status, grading, tumor size, and histology (hazard ratio for iDFS: 1.95 (95%CI: 1.28-2.95); hazard ratio for OS: 2.13 (95%CI: 1.24-3.66)). Further adjustment for taxane-based regimes did not alter results. In conclusion, in this retrospective analysis of patients with early-stage HRpos/HER2neg BC, patients with NACT had a more unfavorable prognosis than patients treated adjuvantly, independent of patient and tumor characteristics. Prognosis of neoadjuvant patients might be affected by resistance mechanisms, warranting further investigation.

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来源期刊
CiteScore
13.40
自引率
3.10%
发文量
460
审稿时长
2 months
期刊介绍: The International Journal of Cancer (IJC) is the official journal of the Union for International Cancer Control—UICC; it appears twice a month. IJC invites submission of manuscripts under a broad scope of topics relevant to experimental and clinical cancer research and publishes original Research Articles and Short Reports under the following categories: -Cancer Epidemiology- Cancer Genetics and Epigenetics- Infectious Causes of Cancer- Innovative Tools and Methods- Molecular Cancer Biology- Tumor Immunology and Microenvironment- Tumor Markers and Signatures- Cancer Therapy and Prevention
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