Updated Survival Analysis after a Median Follow-up of 12 Years of an Anthracycline-Containing Adjuvant Prospective Multicentre, Randomised Phase III Trial on Dose-Dense Chemotherapy in Primary Node-Positive, High-Risk Breast Cancer Patients

被引:2
|
作者
Reinisch, Mattea [1 ]
Gluz, Oleg [2 ,3 ]
Ataseven, Beyhan [4 ]
Blohmer, Jens-Uwe [5 ]
Budner, Marek [6 ]
Dittmer-Grabowski, Christine [1 ]
Kohls, Andreas [7 ]
Krocker, Jutta [8 ]
Kuemmel, Aylin [1 ]
Hagemann, Friederike [1 ]
Rueland, Anna [1 ]
Traut, Alexander [9 ]
Kuemmel, Sherko [1 ]
机构
[1] Kliniken Essen Mitte, Evangel Huyssens Stiftung, Breast Unit, Essen, Germany
[2] Bethesda Hosp, Breast Ctr Niederrhein, Monchengladbach, Germany
[3] West German Study Grp, Monchengladbach, Germany
[4] Kliniken Essen Mitte, Evangel Huyssens Stiftung, Dept Gynecol & Gynecol Oncol, Essen, Germany
[5] Charite Hosp Berlin, Breast Ctr, Berlin, Germany
[6] HELIOS Klin, Breast Unit, Bad Saarow Pieskow, Germany
[7] Evangel Krankenhaus Ludwigsfelde Teltow, Breast Unit, Ludwigsfelde Teltow, Germany
[8] Sana Klinikum Berlin Lichtenberg, Breast Unit, Berlin, Germany
[9] Kliniken Essen Mitte, Essen, Germany
关键词
Adjuvant dose-dense chemotherapy; Node-positive early breast cancer; Long-term follow-up; Disease-free survival; Overall survival; EPIRUBICIN; WOMEN; CYCLOPHOSPHAMIDE; FLUOROURACIL; METHOTREXATE; METAANALYSIS; STANDARD; LEUKEMIA; RECURRENCE; THERAPY;
D O I
10.1159/000491792
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: Although dose- dense (dd) chemotherapy plays a fundamental role in the treatment of breast cancer (BC), a variety of trials have presented divergent survival results. Here, we present data of patients with more than 3 positive axillary lymph nodes (+ aLN) receiving dd chemotherapy after a median follow-up period of 12.3 years. Methods: In the years 1996- 2000, 231 patients with invasive BC, >= pN2a and no evidence of distant metastases were recruited to receive treatment A, i. e. dd 3 x epirubicin (E, 90 mg/m(2)) + paclitaxel (P, 175 mg/m(2)) every 2 weeks (q2w) followed by 3 x cyclophosphamide (C)/methotrexate/5-fluorouracil (CMF, 600/40/600 mg/m(2), q2w), or treatment B, i. e. 4 x E + C (C, 600 mg/m(2)) q3w followed by 3 x CMF q3w. Results: 113 patients in arm A and 113 patients in arm B were analysed after an updated median follow- up of 12.3 years. The median age was 55 years, with a median number of 6 + aLN, 50.4% had a T2 and 79.2% hormone receptor-positive BC. The disease-free survival (DFS) rate was 53.1% in arm A and 42.5% in arm B (adjusted p = 0.027). The overall survival (OS) rate was 54.9% in arm A and 48.7% in arm B (adjusted p = 0.058). In the multivariable analysis, the tumour burden was a significant predictor for DFS and OS. Conclusion: The adjuvant use of dd chemotherapy led to a statistically significant improvement of DFS after a follow- up of 12.3 years. (C) 2018 S. Karger AG, Basel
引用
收藏
页码:159 / 164
页数:6
相关论文
共 50 条
  • [21] A randomised phase III trial comparing two dose-dense, dose-intensified approaches (EPC and PM(Cb)) for neoadjuvant treatment of patients with high-risk early breast cancer (GeparOcto)
    Schneeweiss, Andreas
    Moebus, Volker
    Tesch, Hans
    Hanusch, Claus
    Denkert, Carsten
    Luebbe, Kristina
    Huober, Jens Bodo
    Klare, Peter
    Kummel, Sherko
    Untch, Michael
    Kast, Karin
    Jackisch, Christian
    Thomalla, Jorg
    Heppner, Barbara Ingold
    Blohmer, Jens U.
    Rezai, Mandi
    Frank, Matthias
    Nekljudova, Valentina
    Von Minckwitz, Gunter
    Loibl, Sibylle
    JOURNAL OF CLINICAL ONCOLOGY, 2017, 35
  • [22] A randomised phase III trial comparing two dose-dense, dose-intensified approaches (ETC and PM(Cb)) for neoadjuvant treatment of patients with high-risk early breast cancer (GeparOcto)
    Schneeweiss, A.
    Moebus, V.
    Tesch, H.
    Hanusch, C.
    Denkert, C.
    Luebbe, K.
    Huober, J.
    Klare, P.
    Kuemmel, S.
    Untch, M.
    Kast, K.
    Jackisch, C.
    Ingold-Heppner, B.
    Thomalla, J.
    Blohmer, J-U
    Rezai, M.
    Nekljudova, V.
    von Minckwitz, G.
    Loibl, S.
    CANCER RESEARCH, 2017, 77
  • [23] GAIN2: Adjuvant phase III trial comparing an intensified dose-dense adjuvant therapy with EnPC compared to a dose-dense, dose-adapted therapy with dtEC-dtD in patients with primary high risk breast cancer: Results of the second safety interim analysis
    Moebus, V
    Lueck, H. -J
    Forstbauer, H.
    Wachsmann, G.
    Ober, A.
    Schneeweiss, A.
    Christensen, B.
    Ekkehard, E.
    Grischke, E. -M
    Hoeffkes, H. -G
    Klare, P.
    Ko, Y. D.
    Schmatloch, S.
    Burchardi, N.
    Loibl, S.
    von Minckwitz, G.
    Oncology Research and Treatment, 2015, 38 : 125 - 125
  • [24] Ten-year results of intense dose-dense chemotherapy show superior survival compared with a conventional schedule in high-risk primary breast cancer: final results of AGO phase III iddEPC trial
    Moebus, V.
    Jackisch, C.
    Luck, H. J.
    du Bois, A.
    Thomssen, C.
    Kuhn, W.
    Nitz, U.
    Schneeweiss, A.
    Huober, J.
    Harbeck, N.
    von Minckwitz, G.
    Runnebaum, I. B.
    Hinke, A.
    Konecny, G. E.
    Untch, M.
    Kurbacher, C.
    ANNALS OF ONCOLOGY, 2018, 29 (01) : 178 - 185
  • [25] Survival analysis of the randomised phase III GeparOcto trial comparing neoadjuvant chemotherapy of intense dose-dense epirubicin, paclitaxel, cyclophosphamide versus weekly paclitaxel, liposomal doxorubicin (plus carboplatin in triple-negative breast cancer) for patients with high-risk early breast cancer
    Schneeweiss, Andreas
    Michel, Laura L.
    Moebus, Volker
    Tesch, Hans
    Klare, Peter
    Hahnen, Eric
    Denkert, Carsten
    Kast, Karin
    Pohl-Rescigno, Esther
    Hanusch, Claus
    Link, Theresa
    Untch, Michael
    Jackisch, Christian
    Blohmer, Jens-Uwe
    Fasching, Peter A.
    Solbach, Christine
    Schmutzler, Rita K.
    Huober, Jens
    Rhiem, Kerstin
    Nekljudova, Valentina
    Luebbe, Kristina
    Loibl, Sibylle
    EUROPEAN JOURNAL OF CANCER, 2022, 160 : 100 - 111
  • [26] Sixteen months follow-up of health related quality of life in women with high-risk breast cancer after random assignment to adjuvant treatment with tailored dose-dense chemotherapy vs standard three-weekly adjuvant chemotherapy (PANTHER study)
    Brandberg, Y.
    Foukakis, T.
    Johansson, H.
    Hellstrom, M.
    Gnant, M.
    Loibl, S.
    Bergh, J.
    EUROPEAN JOURNAL OF CANCER, 2017, 72 : S3 - S3
  • [27] Benefit of a high-dose epirubicin regimen in adjuvant chemotherapy for node-positive breast cancer patients with poor prognostic factors:: 5-year follow-up results of French adjuvant study group 05 randomized trial
    Adenis, A
    Bonneterre, J
    Bonneterre, ME
    Pion, JM
    Vanlemmens, L
    Gladieff, L
    de Lafontan, B
    Martel, P
    Mihura, J
    Roché, H
    Gédouin, D
    Kerbrat, P
    Lesimple, T
    Brémond, A
    Devaux, Y
    Delecroix, V
    Fumoleau, P
    Maugard-Louboutin, C
    Namer, M
    Goudier, MJ
    Morice, F
    Montcuquet, P
    Schraub, S
    Coudert, B
    Fargeot, P
    de Gislain, C
    Mayer, F
    Bastit, P
    Chevallier, B
    Grandgirard, A
    Monnier, A
    Sun, X
    Clavère, P
    Ollivier, JP
    Rhein, B
    Roullet, B
    Datchary, J
    Audhuy, B
    Barats, JC
    Kohser, F
    Dides, S
    Ramos, R
    Cattan, A
    Eymard, JC
    Pourny, C
    Weber, B
    de Laroche, G
    Pichon, A
    Seffert, P
    Hayat, M
    JOURNAL OF CLINICAL ONCOLOGY, 2001, 19 (03) : 602 - 611
  • [28] GAIN2: Adjuvant phase III trial comparing an intensified dose-dense (idd) adjuvant therapy with EnPC compared to a dose-dense (dd), dose-adapted therapy with dtEC-dtD in patients with primary high risk breast cancer: Results of the second safety interim analysis
    Moebus, V.
    Lueck, H. -J.
    Forstbauer, H.
    Wachsmann, G.
    Ober, A.
    Schneeweiss, A.
    Christensen, B.
    von Abel, E.
    Grischke, E. -M.
    Hoeffkes, H-G
    Klare, P.
    Ko, Y-D
    Schmatloch, S.
    Burchardi, N.
    Loibl, S.
    von Minckwitz, G.
    ONCOLOGY RESEARCH AND TREATMENT, 2016, 39 : 57 - 58
  • [29] PANTHER: Prospective randomized phase III trial of tailored and dose-dense versus standard tri-weekly adjuvant chemotherapy for high-risk breast cancer in the modern era of endocrine and anti-HER2 therapy.
    Bergh, Jonas C. S.
    Foukakis, Theodoros
    von Minckwitz, Gunter
    Bengtsson, Nils-Olof
    Wallberg, Birgitta
    Fornander, Tommy
    Mlineritsch, Brigitte
    Schmatloch, Sabine
    Singer, Christian F.
    Steger, Guenther G.
    Karlsson, Eva
    Carlsson, Lena
    Loibl, Sibylle
    Untch, Michael
    Hellstrom, Mats
    Johansson, Hemming
    Malmstrom, Per
    Gnant, Michael
    Greil, Richard
    Moebus, Volker
    JOURNAL OF CLINICAL ONCOLOGY, 2016, 34 (15)
  • [30] Optimal duration of adjuvant chemotherapy for high-risk node-negative (N-) breast cancer patients: 6-year results of the prospective randomised multicentre phase III UNICANCER-PACS 05 trial (UCBG-0106)
    Kerbrat, Pierre
    Desmoulins, Isabelle
    Roca, Lise
    Levy, Christelle
    Lortholary, Alain
    Marre, Alain
    Delva, Remy
    Rios, Maria
    Viens, Patrice
    Brain, Etienne
    Serin, Daniel
    Edel, Magali
    Debled, Marc
    Campone, Mario
    Mourret-Reynier, Marie-Ange
    Bachelot, Thomas
    Foucher-Goudier, Marie-Josephe
    Asselain, Bernard
    Lemonnier, Jerome
    Martin, Anne-Laure
    Roche, Henri
    EUROPEAN JOURNAL OF CANCER, 2017, 79 : 166 - 175