3-year results of docetaxel-based sequential and combination regimens in the adjuvant therapy of node-positive breast cancer: a pilot study.


Autoria(s): Ferreira Filho, Antonio Fabiano; Crown, John; Cardoso, Fatima; Nogaret, Jean-Marie; Duffy, Karen E.; Dolci, Stella; Rowan, Susan; O'Higgins, Niall J. O.; Batter, V; Paesmans, Marianne; Piccart-Gebhart, Martine; Di Leo, Angelo
Data(s)

2002

Resumo

BACKGROUND: Docetaxel has proven efficacy in metastatic breast cancer. In this pilot study, we explored the efficacy/feasibility of docetaxel-based sequential and combination regimens as adjuvant therapy of node-positive breast cancer. PATIENTS AND METHODS: From March 1996 till March 1998, four consecutive groups of patients with stages II and III breast cancer, aged < or = 70 years, received one of the following regimens: a) sequential Doxorubicin (A) --> Docetaxel (T) --> CMF (Cyclophosphamide+Methotrexate+5-Fluorouracil): A 75 mg/m q 3 wks x 3, followed by T100 mg/m2 q 3 wks x 3, followed by i.v. CMF Days 1+8 q 4 wks x 3; b) sequential accelerated A --> T --> CMF: A and T administered at the same doses q 2 wks with Lenograstin support; c) combination therapy: A 50 mg/m2 + T 75 mg/m2 q 3 wks x 4, followed by CMF x 4; d) sequential T --> A --> CMF: T and A, administered as in group a), with the reverse sequence. When indicated, radiotherapy was administered during or after CMF, and Tamoxifen after CMF. RESULTS: Ninety-three patients were treated. The median age was 48 years (29-66) and the median number of positive axillary nodes was 6 (1-25). Tumors were operable in 94% and locally advanced in 6% of cases. Pathological tumor size was >2 cm in 72% of cases. There were 21 relapses, (18 systemic, 3 locoregional) and 11 patients (12%) have died from disease progression. At median follow-up of 39 months (6-57), overall survival (OS) was 87% (95% CI, 79-94%) and disease-free survival (DFS) was 76% (95% CI, 67%-85%). CONCLUSION: The efficacy of these docetaxel-based regimens, in terms of OS and DFS, appears to be at least as good as standard anthracycline-based adjuvant chemotherapy (CT), in similar high-risk patient populations.

Clinical Trial

Controlled Clinical Trial

Journal Article

Research Support, Non-U.S. Gov't

info:eu-repo/semantics/published

Formato

No full-text files

Identificador

uri/info:pmid/12174946

http://hdl.handle.net/2013/ULB-DIPOT:oai:dipot.ulb.ac.be:2013/55346

Idioma(s)

en

Fonte

Anticancer research, 22 (4

Palavras-Chave #Sciences bio-médicales et agricoles #Adolescent #Aged #Antineoplastic Agents, Phytogenic -- administration & dosage #Antineoplastic Agents, Phytogenic -- therapeutic use #Antineoplastic Combined Chemotherapy Protocols -- administration & dosage #Antineoplastic Combined Chemotherapy Protocols -- therapeutic use #Breast Neoplasms -- drug therapy #Breast Neoplasms -- mortality #Breast Neoplasms -- pathology #Chemotherapy, Adjuvant #Cisplatin -- administration & dosage #Disease-Free Survival #Doxorubicin -- administration & dosage #Female #Fluorouracil -- administration & dosage #Humans #Lymphatic Metastasis #Methotrexate -- administration & dosage #Middle Aged #Paclitaxel -- administration & dosage #Paclitaxel -- analogs & derivatives #Paclitaxel -- therapeutic use #Phytotherapy #Pilot Projects #Survival Rate #Tamoxifen -- administration & dosage #Taxoids #Time Factors #Treatment Outcome
Tipo

info:eu-repo/semantics/article

info:ulb-repo/semantics/articlePeerReview

info:ulb-repo/semantics/openurl/article