First-line bevacizumab-containing therapy for HER2-negative locally advanced/metastatic breast cancer: Real-world experience from >2000 patients treated in the multicentre AVANTI study

被引:4
|
作者
Mueller, Volkmar [1 ]
Ruhnke, Markus [2 ,11 ]
Hoffmann, Oliver [3 ]
Grafe, Andrea [4 ]
Tome, Oliver [5 ]
Fett, Werner [6 ]
Bruch, Harald-Robert [7 ]
Sommer-Joos, Ann-Katrin [8 ,9 ]
Schneeweiss, Andreas [10 ]
机构
[1] Univ Klinikum Hamburg Eppendorf, Klin & Poliklin Gynakol, Martinistr 52, D-20246 Hamburg, Germany
[2] Paracelsus Klin Osnabruck, Osnabruck, Germany
[3] Univ Klinikum Essen, Comprehens Canc Ctr, Natl Ctr Tumorerkrankungen, Westdeutsch Tumorzentrum Essen WTZ,Klin Frauenhei, Essen, Germany
[4] MVZ Nordhausen gGmbh, Praxis Dr Grafe Brustzentrum Frauenklin, Sudharz Klinikum Nordhausen gGmbh, Nordhausen, Germany
[5] St Vincentius Kliniken gAG, Karlsruhe, Germany
[6] Onkol Praxis, Wuppertal, Germany
[7] Schwerpunktpraxis Bonn, Bonn, Germany
[8] Roche Pharma AG, Grenzach Wyhlen, Germany
[9] Univ Klinikum, Natl Ctr Tumorerkrankungen, Heidelberg, Germany
[10] Deutsch Krebsforschungszentrum, Heidelberg, Germany
[11] Helios Klinikum Aue, Aue, Germany
来源
BREAST | 2021年 / 60卷
关键词
Bevacizumab; Metastatic breast cancer; Non-interventional study; PACLITAXEL PLUS BEVACIZUMAB; PHASE-III TRIAL; OPEN-LABEL; NON-INFERIORITY; CAPECITABINE; EFFICACY;
D O I
10.1016/j.breast.2021.08.014
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Aim: The multicentre non-interventional AVANTI study assessed safety, effectiveness and patientreported outcomes with approved first-line bevacizumab-containing regimens for HER2-negative locally recurrent/metastatic breast cancer (LR/MBC) in German routine oncology practice. Methods: Eligible patients had HER2-negative LR/MBC, no bevacizumab contraindications and no prior chemotherapy for LR/MBC. Chemotherapy schedule, diagnostics and follow-up were at physicians' discretion. Data were collected for 1 year after starting bevacizumab, then every 6 months for 1.5 years (maximum follow-up: 2.5 years). Patients and physicians rated treatment satisfaction. Subgroup analyses were prespecified in clinically relevant populations, including triple-negative breast cancer (TNBC). Results: Between November 1, 2009 and April 30, 2016, 2065 eligible patients at 346 centres received bevacizumab with paclitaxel or capecitabine. Patients receiving bevacizumab-capecitabine were less likely to have de novo disease and more likely to have TNBC, age >60 years and prior anthracycline/ taxane and/or endocrine therapy. Median PFS was 12.6 (95% CI 11.9-13.2) months (12.8 with bevacizumab-paclitaxel, 10.5 with bevacizumab-capecitabine); median OS was 23.9 (95% CI 22.2-25.1) months. Outcomes were worse in patients with TNBC, prior anthracycline/taxane or prior endocrine therapy. Grade >3 adverse events occurred in 27% of patients. Treatment was discontinued for adverse events in 15%. Treatment satisfaction was rated as good or better by 304/394 responding patients (77%) at week 54 and in 1393/2065 patients (67%) by physicians overall. Conclusions: In routine clinical practice, effectiveness and safety of first-line bevacizumab-containing therapy for LR/MBC were consistent with experience from phase III trials. Patient and physician treatment satisfaction showed high concordance. (c) 2021 The Authors. Published by Elsevier Ltd. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
引用
收藏
页码:70 / 77
页数:8
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