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dc.contributor.authorGarcía-Sáenz, José A.
dc.contributor.authorMartín, Miguel
dc.contributor.authorPuente, Javier
dc.contributor.authorLópez-Tarruella, Sara
dc.contributor.authorCasado, Antonio
dc.contributor.authorMoreno, Fernando
dc.contributor.authorGrande-Pulido, E.
dc.contributor.authorDíaz-Rubio, E.
dc.date.accessioned2024-01-23T12:32:06Z
dc.date.available2024-01-23T12:32:06Z
dc.date.issued2005
dc.identifier.issn1938-0666spa
dc.identifier.urihttps://hdl.handle.net/10641/3804
dc.description.abstractPurpose To determine the activity of successive trastuzumab-containing regimens in HER2-overexpressing metastatic breast cancer (MBC) as well as the response rate (RR), time to progression (TTP), and predictive factors for response. Patients and Methods We performed a descriptive retrospective study of trastuzumab activity in patients with HER2-overexpressing MBC treated at our hospital from October 1999 to October 2003. Results Fifty-eight patients were evaluated, in whom an overall RR (complete response plus partial response) of 39.7% was obtained for first-time administration of trastuzumab; stable disease (SD) was seen in 29.3%, and the clinical benefit rate was 69%. Median TTP was 6 months (range, 1 months to > 39 months). A total of 31 patients (53.4%) received a second trastuzumab-containing regimen, with an RR of 25.8%; SD was seen in 12.9%, and the clinical benefit rate was 38.7%. Median TTP was 3 months (range, 1 months to > 22 months). A total of 8 patients (14.3%) received a third trastuzumab-containing regimen. The RR for the third trastuzumab regimen was 12.5%; SD was seen in 12.5%, and the clinical benefit rate was 25%. Median TTP was 2 months (range, 1 months to > 12 months). A total of 4 patients (7.1%) received a fourth trastuzumab-containing regimen, with an RR of zero and SD in 25%. Predictive factors for response were disease in soft tissue or bone (P = 0.03; odds ratio [OR], 3.25; 95% confidence interval [CI], 1.08–9.8) and metastases at > 2 sites (P = 0.03; OR, 6.2; 95% CI, 1.25–30.9). We observed a better RR in the second trastuzumab-containing regimen when the patient responded to the first regimen (P = 0.03; OR, 13.2; 95% CI, 1.36–126). Conclusion Trastuzumab-containing regimens beyond disease progression in MBC show activity even in heavily pretreated patients. The activity noted does not allow us to ascertain the independent contribution of trastuzumab in this setting. There were more responses in patients with few metastases in the soft tissues or bone. Patients who have shown a previous response to trastuzumab can show a response to a second trastuzumab-containing regimen.spa
dc.language.isoengspa
dc.publisherClinical breast cancerspa
dc.rightsAtribución-NoComercial-SinDerivadas 3.0 España*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/es/*
dc.subjectChemotherapyspa
dc.subjectHER2spa
dc.subjectFluorescence in situ hybridizationspa
dc.subjectImmunohistochemistryspa
dc.subjectPredictive factorsspa
dc.titleTrastuzumab Associated with Successive Cytotoxic Therapies Beyond Disease Progression in Metastatic Breast Cancer.spa
dc.typejournal articlespa
dc.type.hasVersionSMURspa
dc.rights.accessRightsmetadata only accessspa
dc.description.extent237 KBspa
dc.identifier.doi10.3816/CBC.2005.n.035spa
dc.relation.publisherversionhttps://www.clinical-breast-cancer.com/article/S1526-8209(11)70851-5/pdfspa


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