Efficacy of adjuvant chemotherapy with carboplatin for early triple negative breast cancer: a single center experience

被引:17
作者
Vetter, Marcus [1 ]
Fokas, Spyridon [2 ]
Biskup, Ewelina [3 ,7 ]
Schmid, Thomas [4 ]
Schwab, Fabienne [2 ]
Schoetzau, Andreas [2 ]
Guth, Uwe [5 ]
Rochlitz, Christoph [1 ]
Zanetti-Dallenbach, Rosanna [6 ]
机构
[1] Univ Hosp Basel, Dept Med Oncol, Basel, Switzerland
[2] Univ Hosp Basel, Womens Hosp, Basel, Switzerland
[3] Univ Hosp Basel, Dept Internal Med, Basel, Switzerland
[4] Royal Marsden Hosp, London, England
[5] Brust Zentrum Zurich, Zurich, Switzerland
[6] Sankt Claraspital, Basel, Switzerland
[7] Shanghai Univ Med & Hlth Sci, Dept Basic Med Coll, Shanghai, Peoples R China
关键词
early breast cancer; triple negative breast cancer; chemotherapy; carboplatin; platinum-based chemotherapy; PATHOLOGICAL COMPLETE RESPONSE; PLATINUM-BASED CHEMOTHERAPY; HIGH-RISK; NEOADJUVANT CISPLATIN; WEEKLY PACLITAXEL; STAGE-II; SUBTYPES; WOMEN; THERAPY; CYCLOPHOSPHAMIDE;
D O I
10.18632/oncotarget.18118
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Anthracycline-and taxane-based adjuvant chemotherapies are the most frequently used systemic treatments for women with triple negative breast cancer (TNBC). Adding platinum derivatives in the neo-adjuvant setting has been shown to not only improve the pCR rates, but also the 3 year DFS for TNBC patients; however, data on platinum derivatives in the adjuvant setting are limited. Methods: We conducted a retrospective, single-center study in a Swiss breast cancer cohort to evaluate the role of carboplatin in addition to standard adjuvant therapy (anthracyclines and/or taxanes) in early TNBC patients. All patients with stage I-III TNBC who underwent primary breast surgery between 2004 and 2014 were included. Results: Eighty-three patients were included in the analysis. Stage and grade were well balanced between patients treated with standard chemotherapy (N=54; cohort A) or standard chemotherapy plus carboplatin (N=29; cohort B). The median time to local relapse (LRFS) was 15.0 months in cohort A versus 16.0 months in cohort B (p=0.655). The median time to distant relapse (DRFS) was 29.5 months in cohort A versus 25.0 months in cohort B (p=0.606) There was also no difference in overall survival between the two cohorts (mean overall survival 98 and 91 months, respectively; p=0.208). Discussion: Our data suggest that in an unselected cohort of early TNBC patients, the addition of carboplatin in the adjuvant setting may not be beneficial with respect to relapse-free and overall survival. Further prospective trials to evaluate the addition of platinum in the adjuvant setting are warranted, especially to define subgroups of TNBC patients, which might benefit from carboplatin therapy.
引用
收藏
页码:75617 / 75626
页数:10
相关论文
共 57 条
  • [1] A randomized phase II trial of platinum salts in basal-like breast cancer patients in the neoadjuvant setting. Results from the GEICAM/2006-03, multicenter study
    Alba, E.
    Chacon, J. I.
    Lluch, A.
    Anton, A.
    Estevez, L.
    Cirauqui, B.
    Carrasco, E.
    Calvo, L.
    Segui, M. A.
    Ribelles, N.
    Alvarez, R.
    Sanchez-Munoz, A.
    Sanchez, R.
    Lopez Garcia-Asenjo, J. A.
    Rodriguez-Martin, C.
    Escudero, M. J.
    Albanell, J.
    [J]. BREAST CANCER RESEARCH AND TREATMENT, 2012, 136 (02) : 487 - 493
  • [2] Anders C, 2008, ONCOLOGY-NY, V22, P1233
  • [3] Anders CK, 2016, ASCO ED B
  • [4] [Anonymous], 2009, TNM CLASSIFICATION M
  • [5] SWOG S0221: A Phase III Trial Comparing Chemotherapy Schedules in High-Risk Early-Stage Breast Cancer
    Budd, George T.
    Barlow, William E.
    Moore, Halle C. F.
    Hobday, Timothy J.
    Stewart, James A.
    Isaacs, Claudine
    Salim, Muhammad
    Cho, Jonathan K.
    Rinn, Kristine J.
    Albain, Kathy S.
    Chew, Helen K.
    Burton, Gary V.
    Moore, Timothy D.
    Srkalovic, Gordan
    McGregor, Bradley A.
    Flaherty, Lawrence E.
    Livingston, Robert B.
    Lew, Danika L.
    Gralow, Julie R.
    Hortobagyi, Gabriel N.
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 2015, 33 (01) : 58 - U95
  • [6] Pathologic complete response to neoadjuvant cisplatin in BRCA1-positive breast cancer patients
    Byrski, T.
    Huzarski, T.
    Dent, R.
    Marczyk, E.
    Jasiowka, M.
    Gronwald, J.
    Jakubowicz, J.
    Cybulski, C.
    Wisniowski, R.
    Godlewski, D.
    Lubinski, J.
    Narod, S. A.
    [J]. BREAST CANCER RESEARCH AND TREATMENT, 2014, 147 (02) : 401 - 405
  • [7] Response to neoadjuvant therapy with cisplatin in BRCA1-positive breast cancer patients
    Byrski, T.
    Huzarski, T.
    Dent, R.
    Gronwald, J.
    Zuziak, D.
    Cybulski, C.
    Kladny, J.
    Gorski, B.
    Lubinski, J.
    Narod, S. A.
    [J]. BREAST CANCER RESEARCH AND TREATMENT, 2009, 115 (02) : 359 - 363
  • [8] Pathologic Complete Response Rates in Young Women With BRCA1-Positive Breast Cancers After Neoadjuvant Chemotherapy
    Byrski, Tomasz
    Gronwald, Jacek
    Huzarski, Tomasz
    Grzybowska, Ewa
    Budryk, Magdalena
    Stawicka, Malgorzata
    Mierzwa, Tomasz
    Szwiec, Marek
    Wisniowski, Rafal
    Siolek, Monika
    Dent, Rebecca
    Lubinski, Jan
    Narod, Steven
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 2010, 28 (03) : 375 - 379
  • [9] Adjuvant bevacizumab-containing therapy in triple-negative breast cancer (BEATRICE): primary results of a randomised, phase 3 trial
    Cameron, David
    Brown, Julia
    Dent, Rebecca
    Jackisch, Christian
    Mackey, John
    Pivot, Xavier
    Steger, Guenther G.
    Suter, Thomas M.
    Toi, Masakazu
    Parmar, Mahesh
    Laeufle, Rita
    Im, Young-Hyuck
    Romieu, Gilles
    Harvey, Vernon
    Lipatov, Oleg
    Pienkowski, Tadeusz
    Cottu, Paul
    Chan, Arlene
    Im, Seock-Ah
    Hall, Peter S.
    Bubuteishvili-Pacaud, Lida
    Henschel, Volkmar
    Deurloo, Regula J.
    Pallaud, Celine
    Bell, Richard
    [J]. LANCET ONCOLOGY, 2013, 14 (10) : 933 - 942
  • [10] Triple-negative breast cancer: disease entity or title of convenience?
    Carey, Lisa
    Winer, Eric
    Viale, Giuseppe
    Cameron, David
    Gianni, Luca
    [J]. NATURE REVIEWS CLINICAL ONCOLOGY, 2010, 7 (12) : 683 - 692