Titolo | Ten years of experience with weekly chemotherapy in metastatic breast cancer patients: Multivariate analysis of prognostic factors |
---|---|
Tipo di pubblicazione | Articolo su Rivista peer-reviewed |
Anno di Pubblicazione | 2006 |
Autori | Nisticò, C., Cuppone F., Bria E., Fornier M., Giannarelli D., Mottolese M., Novelli Flavia, Natoli G., Cognetti F., and Terzoli E. |
Rivista | Anti-Cancer Drugs |
Volume | 17 |
Paginazione | 1193-1200 |
ISSN | 09594973 |
Parole chiave | adolescent, adult, aged, anthracycline, Antineoplastic Agents, article, Biological, Breast cancer, Breast Neoplasms, cancer adjuvant therapy, cancer chemotherapy, cancer survival, Carcinoma, clinical article, Clinical Trials, controlled study, Disease Progression, drug activity, Drug Administration Schedule, drug tolerability, epirubicin, Female, histopathology, human, human tissue, Humans, lonidamine, metastasis, Middle Aged, Multivariate analysis, navelbine, Neoplasm Metastasis, paclitaxel, Phase II, priority journal, prognosis, proportional hazards model, Retrospective Studies, Survival Analysis, Tumor Markers |
Abstract | {Weekly chemotherapy administration represents an emerging option for the treatment of metastatic breast cancer. In order to identify clinical and biological prognostic factors for outcome, we performed a multivariate analysis in a 10-year experience of weekly chemotherapy for metastatic breast cancer patients. The original databases of phase II trials of metastatic breast cancer patients who had undergone first-line weekly chemotherapy were collected. Clinical and biological covariables were screened for a possible relationship with time to progression and overall survival in a Cox model. From 1990 to 2003, 184 patients were enrolled in three consecutive phase II studies, to evaluate activity and tolerability of weekly epirubicin with lonidamine or vinorelbine or paclitaxel. All patients were evaluable for clinical variables; histological samples were available in 40 patients. At a median follow-up of 24 months, median time to progression was 9 months (95% confidence interval 8-10) and median overall survival was 34 months (95% confidence interval 24-42). Independent variables were response (hazard ratio 2.34, P<0.0001), receptor status (hazard ratio 1.62 |
Note | cited By 5 |
URL | https://www.scopus.com/inward/record.uri?eid=2-s2.0-33750552338&doi=10.1097%2f01.cad.0000231485.17063.d3&partnerID=40&md5=c2777d9b55e342e829f60781756fddb5 |
DOI | 10.1097/01.cad.0000231485.17063.d3 |
Citation Key | Nisticò20061193 |