Literature DB >> 20387073

Neoadjuvant sequential epirubicin and docetaxel followed by surgery-radiotherapy and post-operative docetaxel or gemcitabine/vinorelbine combination based on primary response: a multimodality approach for locally advanced breast cancer.

Panteleimon Kountourakis1, Ioannis Missitzis, Dimitrios Doufexis, Vassileios Zobolas, Georgios Pissakas, Niki Arnogiannaki, Savoula Maliou, Anastasia Sotiropoulou, Alexandros Ardavanis.   

Abstract

BACKGROUND: Locally advanced breast cancer (LABC) remains a major clinical issue despite progress achieved in recent years. Herein, we present the mature results of a multimodality treatment program tailoring epirubicin (EPI), docetaxel (DOC) and gemcitabine-vinorelbine (GEV) peri-operatively in LABC. PATIENTS AND METHODS: Stage III, Eastern Cooperative Oncology Group-Performance status ≤2 patients were eligible. A biopsy documentation had to be performed before the start of chemotherapy (CT). Treatment consisted of four EPI (100 mg/m(2), d1q2w) followed by three DOC (100 mg/m(2), d1q3w); surgery 3-4 weeks from CT completion, followed by radiation therapy (RT) and CT according to response; partial or complete (PR/CR):DOC, no change or progressive disease (NC/PD):GEV. Primary endpoints were: (a) response and conversion to operability/conservative surgery and (b) overall survival (OS) and time to recurrence (TTR).
RESULTS: Fifty-six women, aged 32-75 (median 52 years), 24 IIIA and 32 IIIB were enrolled; 53 patients completed the entire program. Toxicity was acceptable and no treatment-related death was observed. EFFICACY: clinical response rate (RR) 71.4% (40 patients); clinical complete response rate 33.9% (19 patients). Pathological response rate (RR) 67.8% (38 patients); pathological complete response rate 21.4% (12 patients). 33 (58.9%) and 19 (33.9%) patients, respectively, had radical and conservative operations without increased morbidity. After a median follow-up of 62 months, median OS has not yet been reached, while median TTR was 42 months. OS was longer in patients with clinical (p = 0.004) and pathological response (p = 0.002), RT (p < 0.0001) and post-operative DOC (p = 0.038). TTR was favorably affected by pR (p < 0.0001), RT (p < 0.0004) and post-operative DOC (p = 0.005). Pre-operative CT seemed to be equally active throughout all subgroups according to histology, ER/PR and HER2 status.
CONCLUSION: The treatment program of the present study allowed for the completion of an effective therapy at the cost of acceptable toxicity. The results of this study suggest a central role of CT for LABC and the value of eventually dose-dense, EPI- and DOC-based CT in a large proportion of LABC patients, regardless of biological tumor profile. Furthermore, tumor response (cR, pR) is an important surrogate for patients survival and further therapy management.

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Year:  2010        PMID: 20387073     DOI: 10.1007/s00432-010-0878-8

Source DB:  PubMed          Journal:  J Cancer Res Clin Oncol        ISSN: 0171-5216            Impact factor:   4.553


  20 in total

1.  New guidelines to evaluate the response to treatment in solid tumors. European Organization for Research and Treatment of Cancer, National Cancer Institute of the United States, National Cancer Institute of Canada.

Authors:  P Therasse; S G Arbuck; E A Eisenhauer; J Wanders; R S Kaplan; L Rubinstein; J Verweij; M Van Glabbeke; A T van Oosterom; M C Christian; S G Gwyther
Journal:  J Natl Cancer Inst       Date:  2000-02-02       Impact factor: 13.506

2.  Multidisciplinary therapy of locally far-advanced or inflammatory breast cancer with fixed perioperative sequence of epirubicin, vinorelbine, and Fluorouracil chemotherapy, surgery, and radiotherapy: long-term results.

Authors:  Alexandros Ardavanis; Andreas Scorilas; Dimitrios Tryfonopoulos; Georgios Orphanos; Ioannis Missitzis; Michael Karamouzis; Minas Chrysochoou; Anastasia Sotiropoulou; Niki Arnogiannaki; Georgios Ioannidis; Georgios Pissakas; Gerassimas Rigatos
Journal:  Oncologist       Date:  2006-06

3.  Doxorubicin with cyclophosphamide followed by docetaxel every 21 days compared with doxorubicin and docetaxel every 14 days as preoperative treatment in operable breast cancer: the GEPARDUO study of the German Breast Group.

Authors:  Gunter von Minckwitz; Günter Raab; Angelika Caputo; Martin Schütte; Jörn Hilfrich; Jens U Blohmer; Bernd Gerber; Serban D Costa; Elisabeth Merkle; Holger Eidtmann; Dieter Lampe; Christian Jackisch; Andreas du Bois; Manfred Kaufmann
Journal:  J Clin Oncol       Date:  2005-04-20       Impact factor: 44.544

4.  Prognostic value of pathologic complete response after primary chemotherapy in relation to hormone receptor status and other factors.

Authors:  Valentina Guarneri; Kristine Broglio; Shu-Wan Kau; Massimo Cristofanilli; Aman U Buzdar; Vicente Valero; Thomas Buchholz; Funda Meric; Lavinia Middleton; Gabriel N Hortobagyi; Ana M Gonzalez-Angulo
Journal:  J Clin Oncol       Date:  2006-03-01       Impact factor: 44.544

5.  Sequential preoperative or postoperative docetaxel added to preoperative doxorubicin plus cyclophosphamide for operable breast cancer:National Surgical Adjuvant Breast and Bowel Project Protocol B-27.

Authors:  Harry D Bear; Stewart Anderson; Roy E Smith; Charles E Geyer; Eleftherios P Mamounas; Bernard Fisher; Ann M Brown; Andre Robidoux; Richard Margolese; Morton S Kahlenberg; Soonmyung Paik; Atilla Soran; D Lawrence Wickerham; Norman Wolmark
Journal:  J Clin Oncol       Date:  2006-04-10       Impact factor: 44.544

6.  Neoadjuvant chemotherapy in breast cancer: significantly enhanced response with docetaxel.

Authors:  Ian C Smith; Steven D Heys; Andrew W Hutcheon; Iain D Miller; Simon Payne; Fiona J Gilbert; Antoinne K Ah-See; Oleg Eremin; Leslie G Walker; Tarun K Sarkar; S Peter Eggleton; Keith N Ogston
Journal:  J Clin Oncol       Date:  2002-03-15       Impact factor: 44.544

7.  Long-term follow-up for locally advanced and inflammatory breast cancer patients treated with multimodality therapy.

Authors:  Jennifer A Low; Arlene W Berman; Seth M Steinberg; David N Danforth; Marc E Lippman; Sandra M Swain
Journal:  J Clin Oncol       Date:  2004-10-15       Impact factor: 44.544

8.  Intravenous vinorelbine as first-line and second-line therapy in advanced breast cancer.

Authors:  B L Weber; C Vogel; S Jones; H Harvey; L Hutchins; J Bigley; J Hohneker
Journal:  J Clin Oncol       Date:  1995-11       Impact factor: 44.544

9.  Neoadjuvant chemotherapy shows similar response in patients with inflammatory or locally advanced breast cancer when compared with operable breast cancer: a secondary analysis of the GeparTrio trial data.

Authors:  Serban Dan Costa; Sibylle Loibl; Manfred Kaufmann; Dirk-Michael Zahm; Jörn Hilfrich; Jens Huober; Holger Eidtmann; Andreas du Bois; Jens-Uwe Blohmer; Beyhan Ataseven; Erich Weiss; Hans Tesch; Bernd Gerber; Klaus H Baumann; Christoph Thomssen; Georg Peter Breitbach; Shaip Ibishi; Christian Jackisch; Keyur Mehta; Gunter von Minckwitz
Journal:  J Clin Oncol       Date:  2009-11-09       Impact factor: 44.544

10.  Effect of preoperative chemotherapy on the outcome of women with operable breast cancer.

Authors:  B Fisher; J Bryant; N Wolmark; E Mamounas; A Brown; E R Fisher; D L Wickerham; M Begovic; A DeCillis; A Robidoux; R G Margolese; A B Cruz; J L Hoehn; A W Lees; N V Dimitrov; H D Bear
Journal:  J Clin Oncol       Date:  1998-08       Impact factor: 44.544

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  2 in total

1.  Neoadjuvant therapy for locally advanced breast cancer: Focus on chemotherapy and biological targeted treatments' armamentarium.

Authors:  Konstantinos Papadimitriou; Konstantinos Papademetriou; Alexandros Ardavanis; Panteleimon Kountourakis
Journal:  J Thorac Dis       Date:  2010-09       Impact factor: 2.895

2.  Pathological complete response rate in hormone receptor-negative breast cancer treated with neoadjuvant FEC, followed by weekly paclitaxel administration: A retrospective study and review of the literature.

Authors:  Takayoshi Kiba; Nao Morii; Hirotoshi Takahashi; Shinji Ozaki; Misao Atsumi; Fumi Masumoto; Hiroyasu Yamashiro
Journal:  Oncol Lett       Date:  2016-03-16       Impact factor: 2.967

  2 in total

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