Literature DB >> 11208823

Response to cyclophosphamide, methotrexate, and fluorouracil in lymph node-positive breast cancer according to HER2 overexpression and other tumor biologic variables.

S Ménard1, P Valagussa, S Pilotti, L Gianni, E Biganzoli, P Boracchi, G Tomasic, P Casalini, E Marubini, M I Colnaghi, N Cascinelli, G Bonadonna.   

Abstract

PURPOSE: There is considerable interest in biologic markers able to predict the response of cancer patients to therapy. HER2 overexpression is a potential indicator of responsiveness to doxorubicin and paclitaxel and of unresponsiveness to tamoxifen in breast carcinoma patients. However, the significance of HER2 overexpression in responsiveness to cyclophosphamide, methotrexate, and fluorouracil (CMF) has remained unclear. In this study, we investigated this issue in the 386 breast cancer patients in the first CMF controlled clinical trial with a 20-year follow-up. PATIENTS AND METHODS: Node-positive breast carcinoma patients were randomly assigned to receive either no further treatment after radical mastectomy (179 women) or 12 monthly cycles of adjuvant CMF chemotherapy (207 women). Overexpression of HER2 and the status of other tumor variables was assessed by immunohistochemistry in at least 324 (84%) of the 386 patients. Statistical analyses were performed to assess the efficacy of CMF treatment for the subgroups defined by HER2 and the status of other variables using a Bayesian approach. The end points considered were relapse-free survival (RFS) and cause-specific survival (CSS).
RESULTS: Bayesian analysis of the treatment effect for HER2 and other variables indicated a clinical benefit from CMF treatment in all subgroups defined according to variables status. In particular regarding HER2 status, Bayesian estimates of RFS hazard ratios were equal to 0.484 and 0.641 and estimates of CSS hazard ratios were equal to 0.495 and 0.730 for HER2-positive and -negative tumors, respectively.
CONCLUSION: CMF treatment showed a clinical benefit in the considered subgroups, defined according to HER2 and other tumor variables status. Patients with HER2-positive or HER2-negative tumors benefit from CMF treatment, and the poor prognosis associated with the HER2 overexpression in the untreated group could be completely overcome by the chemotherapy treatment.

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Year:  2001        PMID: 11208823     DOI: 10.1200/JCO.2001.19.2.329

Source DB:  PubMed          Journal:  J Clin Oncol        ISSN: 0732-183X            Impact factor:   44.544


  25 in total

1.  30 years' follow up of randomised studies of adjuvant CMF in operable breast cancer: cohort study.

Authors:  Gianni Bonadonna; Angela Moliterni; Milvia Zambetti; Maria Grazia Daidone; Silvana Pilotti; Luca Gianni; Pinuccia Valagussa
Journal:  BMJ       Date:  2005-01-13

Review 2.  Adjuvant chemotherapy for primary breast cancer.

Authors:  Monica Fornier; Clifford Hudis
Journal:  Curr Oncol Rep       Date:  2005-01       Impact factor: 5.075

3.  Clinical and pathological predictors of the response to neoadjuvant anthracycline chemotherapy in locally advanced breast cancer.

Authors:  Mónica Fernández-Sánchez; Armando Gamboa-Dominguez; Norma Uribe; Ana Cristina García-Ulloa; Diana Flores-Estrada; Myrna Candelaria; Oscar Arrieta
Journal:  Med Oncol       Date:  2006       Impact factor: 3.064

Review 4.  Utilizing prognostic and predictive factors in breast cancer.

Authors:  Deepa S Subramaniam; Claudine Isaacs
Journal:  Curr Treat Options Oncol       Date:  2005-03

Review 5.  Prognostic factors in node-negative breast cancer: a review of studies with sample size more than 200 and follow-up more than 5 years.

Authors:  Attiqa N Mirza; Nadeem Q Mirza; Georges Vlastos; S Eva Singletary
Journal:  Ann Surg       Date:  2002-01       Impact factor: 12.969

6.  Spironolactone ameliorates the cardiovascular toxicity induced by concomitant trastuzumab and thoracic radiotherapy.

Authors:  Guler Yavas; Esin Celik; Cagdas Yavas; Cagdas Elsurer; Rengin Elsurer Afsar
Journal:  Rep Pract Oncol Radiother       Date:  2017-05-05

7.  Prospective multi-centre study to validate chromogenic in situ hybridisation for the assessment of HER2 gene amplification in specimens from adjuvant and metastatic breast cancer patients.

Authors:  Sabine Riethdorf; Bernhard Hoegel; Birgit John; German Ott; Peter Fritz; Susanne Thon; Thomas Loening; Klaus Pantel
Journal:  J Cancer Res Clin Oncol       Date:  2010-04-16       Impact factor: 4.553

8.  Side-population cells in luminal-type breast cancer have tumour-initiating cell properties, and are regulated by HER2 expression and signalling.

Authors:  T Nakanishi; S Chumsri; N Khakpour; A H Brodie; B Leyland-Jones; A W Hamburger; D D Ross; A M Burger
Journal:  Br J Cancer       Date:  2010-02-09       Impact factor: 7.640

9.  Assessment of dual-probe Her-2 fluorescent in situ hybridization in breast cancer by the 2013 ASCO/CAP guidelines produces more equivocal results than that by the 2007 ASCO/CAP guidelines.

Authors:  Xiao-Long Qian; Hannah Y Wen; Yi-Ling Yang; Feng Gu; Xiao-Jing Guo; Fang-Fang Liu; Lanjing Zhang; Xin-Min Zhang; Li Fu
Journal:  Breast Cancer Res Treat       Date:  2016-07-25       Impact factor: 4.872

10.  Impact of polysomy 17 on HER-2/neu immunohistochemistry in breast carcinomas without HER-2/neu gene amplification.

Authors:  Priti Lal; Paulo A Salazar; Marc Ladanyi; Beiyun Chen
Journal:  J Mol Diagn       Date:  2003-08       Impact factor: 5.568

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