Literature DB >> 31316314

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.

Mattea Reinisch1, Oleg Gluz2, Beyhan Ataseven3, Jens-Uwe Blohmer4, Marek Budner5, Christine Dittmer-Grabowski1, Andreas Kohls6, Jutta Krocker7, Aylin Kümmel1, Friederike Hagemann1, Anna Rüland1, Alexander Traut8, Sherko Kümmel1.   

Abstract

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 × epirubicin (E, 90 mg/m<sup>2</sup>) + paclitaxel (P, 175 mg/m<sup>2</sup>) every 2 weeks (q2w) followed by 3 × cyclophosphamide (C)/methotrexate/5-fluorouracil (CMF, 600/40/600 mg/m<sup>2</sup>, q2w), or treatment B, i.e. 4 × E + C (C, 600 mg/m<sup>2</sup>) q3w followed by 3 × 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.

Entities:  

Keywords:  Adjuvant dose-dense chemotherapy; Disease-free survival; Long-term follow-up; Node-positive early breast cancer; Overall survival

Year:  2018        PMID: 31316314      PMCID: PMC6600045          DOI: 10.1159/000491792

Source DB:  PubMed          Journal:  Breast Care (Basel)        ISSN: 1661-3791            Impact factor:   2.860


  26 in total

Review 1.  Dose-dense chemotherapy for primary breast cancer.

Authors:  Sherko Kümmel; Mahdi Rezai; Rainer Kimmig; Peter Schmid
Journal:  Curr Opin Obstet Gynecol       Date:  2007-02       Impact factor: 1.927

2.  Dose-dense adjuvant chemotherapy in early breast cancer patients: results from a randomized trial.

Authors:  Marco Venturini; Lucia Del Mastro; Enrico Aitini; Editta Baldini; Cinzia Caroti; Antonio Contu; Franco Testore; Fulvio Brema; Paolo Pronzato; Giovanna Cavazzini; Mario Roberto Sertoli; Giuseppe Canavese; Riccardo Rosso; Paolo Bruzzi
Journal:  J Natl Cancer Inst       Date:  2005-12-07       Impact factor: 13.506

3.  [Dose intensified adjuvant chemotherapy in high risk breast carcinoma with 4-9 positive lymph nodes].

Authors:  D Elling; J Krocker; S Kümmel; J Blohmer; W Lichtenegger; A Kohls; J Heinrich; J Quass; P Breitbach; U Köhler
Journal:  Zentralbl Gynakol       Date:  2000

4.  Randomized trial comparing cyclophosphamide, epirubicin, and fluorouracil with cyclophosphamide, methotrexate, and fluorouracil in premenopausal women with node-positive breast cancer: update of National Cancer Institute of Canada Clinical Trials Group Trial MA5.

Authors:  Mark N Levine; Kathleen I Pritchard; Vivien H C Bramwell; Lois E Shepherd; Dongsheng Tu; Nancy Paul
Journal:  J Clin Oncol       Date:  2005-08-01       Impact factor: 44.544

5.  Randomized trial of dose-dense versus conventionally scheduled and sequential versus concurrent combination chemotherapy as postoperative adjuvant treatment of node-positive primary breast cancer: first report of Intergroup Trial C9741/Cancer and Leukemia Group B Trial 9741.

Authors:  Marc L Citron; Donald A Berry; Constance Cirrincione; Clifford Hudis; Eric P Winer; William J Gradishar; Nancy E Davidson; Silvana Martino; Robert Livingston; James N Ingle; Edith A Perez; John Carpenter; David Hurd; James F Holland; Barbara L Smith; Carolyn I Sartor; Eleanor H Leung; Jeffrey Abrams; Richard L Schilsky; Hyman B Muss; Larry Norton
Journal:  J Clin Oncol       Date:  2003-02-13       Impact factor: 44.544

6.  Effects of chemotherapy and hormonal therapy for early breast cancer on recurrence and 15-year survival: an overview of the randomised trials.

Authors: 
Journal:  Lancet       Date:  2005 May 14-20       Impact factor: 79.321

7.  Toxicity of older and younger patients treated with adjuvant chemotherapy for node-positive breast cancer: the Cancer and Leukemia Group B Experience.

Authors:  Hyman B Muss; Donald A Berry; Constance Cirrincione; Daniel R Budman; I Craig Henderson; Marc L Citron; Larry Norton; Eric P Winer; Clifford A Hudis
Journal:  J Clin Oncol       Date:  2007-08-20       Impact factor: 44.544

8.  Intensive dose-dense compared with conventionally scheduled preoperative chemotherapy for high-risk primary breast cancer.

Authors:  Michael Untch; Volker Möbus; Walther Kuhn; Bernd Rudolph Muck; Christoph Thomssen; Ingo Bauerfeind; Nadia Harbeck; Christoph Werner; Annette Lebeau; Andreas Schneeweiss; Stephen Kahlert; Franz von Koch; Karl Ulrich Petry; Diethelm Wallwiener; Rolf Kreienberg; Ute-Susann Albert; Hans-Joachim Lück; Axel Hinke; Fritz Jänicke; Gottfried E Konecny
Journal:  J Clin Oncol       Date:  2009-04-13       Impact factor: 44.544

9.  Randomised trial: survival benefit and safety of adjuvant dose-dense chemotherapy for node-positive breast cancer.

Authors:  S Kümmel; J Krocker; A Kohls; G-P Breitbach; G Morack; M Budner; J-U Blohmer; D Elling
Journal:  Br J Cancer       Date:  2006-05-08       Impact factor: 7.640

Review 10.  Adjuvant chemotherapy in oestrogen-receptor-poor breast cancer: patient-level meta-analysis of randomised trials.

Authors:  M Clarke; A S Coates; S C Darby; C Davies; R D Gelber; J Godwin; A Goldhirsch; R Gray; R Peto; K I Pritchard; W C Wood
Journal:  Lancet       Date:  2008-01-05       Impact factor: 79.321

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