Long-term outcome of the REMAGUS 02 trial, a multicenter randomised phase II trial in locally advanced breast cancer patients treated with neoadjuvant chemotherapy with or without celecoxib or trastuzumab according to HER2 status

被引:23
作者
Giacchetti, Sylvie [1 ]
Hamy, Anne-Sophie [2 ]
Delaloge, Suzette [3 ]
Brain, Etienne [4 ]
Berger, Frederique [5 ]
Sigal-Zafrani, Brigitte [6 ]
Mathieu, Marie-Christine [7 ]
Bertheau, Philippe [8 ]
Guinebretiere, Jean Marc [6 ]
Saghatchian, Mahasti [3 ]
Lerebours, Florence [4 ]
mazouni, chafouny [9 ]
Tembo, Olivier [11 ]
Espie, Marc [1 ]
Reyal, Fabien [2 ,10 ]
Marty, Michel [1 ,11 ]
Asselain, Bernard [12 ]
Pierga, Jean-Yves [4 ,13 ]
机构
[1] Univ Paris Diderot, Hop St Louis, AP HP, Breast Dis Unit, F-75475 Paris, France
[2] PSL Res Univ, Inst Curie, Translat Res Dept,INSERM,U932 Immunity & Canc, Residual Tumor & Response Treatment Lab RT2Lab, Paris, France
[3] Gustave Roussy, Dept Med Oncol, Canc Ctr Villejuif, Villejuif, France
[4] Inst Curie, Dept Med Oncol, Paris, France
[5] Inst Curie, Biostat Dept, Paris, France
[6] Inst Curie, Dept Tumor Biol, Paris, France
[7] Gustave Roussy, Canc Ctr Villejuif, Dept Pathol, Villejuif, France
[8] Univ Paris Diderot, Hop St Louis, AP HP, Dept Pathol, Paris, France
[9] Gustave Roussy, Canc Ctr Villejuif, Dept Surg, Villejuif, France
[10] Inst Curie, Dept Surg, Paris, France
[11] Hop St Louis, APHP, Ctr Therapeut Innovat Oncol & Haematol CITOH, Paris, France
[12] Univ Paris Sud, UMR 8081, IR4M, F-91400 Orsay, France
[13] Univ Paris 05, Sorbonne Paris Cite, Paris, France
关键词
Neoadjuvant chemotherapy; Celecoxib; Trastuzumab; Breast cancer; Long-term outcome; PATHOLOGICAL COMPLETE RESPONSE; OPEN-LABEL; PROGNOSTIC VALUE; SURVIVAL; THERAPY; ASSOCIATION; PERTUZUMAB; LAPATINIB; NEOSPHERE; RELAPSE;
D O I
10.1016/j.ejca.2017.01.008
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: The REMAGUS-02 multicenter randomised phase II trial showed that the addition to neoadjuvant chemotherapy (NAC) of trastuzumab in patients with localised HER2-positive breast cancer (BC) increased the pathological complete response (pCR) rate and that the addition of celecoxib in HER2-negative cases did not increase the pCR rate. We report here the long-term follow-up results for disease-free survival (DFS) and overall survival (OS). Patients and methods: From 2004 to 2007, 340 stage II III BC patients were randomly assigned to receive neoadjuvant EC-T (four cycles of epirubicin cyclophosphamide followed by four cycles of docetaxel) +/- celecoxib in HER2-negative cases (n = 220) and trastuzumab in HER2-positive cases (n = 120). From September 2005, all patients with HER2-positive BC received adjuvant T (n = 106). Results: Median follow-up was nearly 8 years (94.4 months, 20-127 m). In the HER2-negative subgroup, addition of celecoxib was not associated with a DFS benefit. Favourable factors were smaller tumour size, expression of progesterone receptor status (PgR) and pCR. In the HER2-positive population, neoadjuvant trastuzumab was not associated with a DFS benefit. Axillary pCR was the only prognostic factor associated with DFS in this group [HR = 0.44, 95% CI = 0.2-0.97], p = 0.035]. To note, DFS and OS were significantly higher in the HER2-positive than in HER2-negative BC patients (HR = 0.58 [0.36-0.92], p = 0.021). Conclusion: Celecoxib combined with NAC provided neither pCR nor survival benefit in patients with HER2-negative BC. Absence of PgR is a major prognostic factor. Neoadjuvant trastuzumab increased pCR rates without translation into a DFS or OS benefit compared with adjuvant trastuzumab only. Axillary pCR could be a more relevant surrogate of survival than in the breast in HER2-positive population. A retrospective comparison shows that patients with HER2-positive tumours have a better outcome than HER2-negative BC patients showing the impact of trastuzumab on the natural history of BC. (C) 2017 Elsevier Ltd. All rights reserved.
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收藏
页码:323 / 332
页数:10
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