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Ten years of experience with weekly chemotherapy in metastatic breast cancer patients: Multivariate analysis of prognostic factors

TitoloTen years of experience with weekly chemotherapy in metastatic breast cancer patients: Multivariate analysis of prognostic factors
Tipo di pubblicazioneArticolo su Rivista peer-reviewed
Anno di Pubblicazione2006
AutoriNisticò, C., Cuppone F., Bria E., Fornier M., Giannarelli D., Mottolese M., Novelli Flavia, Natoli G., Cognetti F., and Terzoli E.
RivistaAnti-Cancer Drugs
Volume17
Paginazione1193-1200
ISSN09594973
Parole chiaveadolescent, 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

URLhttps://www.scopus.com/inward/record.uri?eid=2-s2.0-33750552338&doi=10.1097%2f01.cad.0000231485.17063.d3&partnerID=40&md5=c2777d9b55e342e829f60781756fddb5
DOI10.1097/01.cad.0000231485.17063.d3
Citation KeyNisticò20061193