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Please use this identifier to cite or link to this item: http://acervodigital.unesp.br/handle/11449/128346
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dc.contributor.authorMaesta, Izildinha-
dc.contributor.authorHorowitz, Neil S.-
dc.contributor.authorGoldstein, Donald P.-
dc.contributor.authorBernstein, Marilyn R.-
dc.contributor.authorRamirez, Luz Angela C.-
dc.contributor.authorMoulder, Janelle-
dc.contributor.authorBerkowitz, Ross S.-
dc.date.accessioned2015-10-21T13:09:10Z-
dc.date.accessioned2016-10-25T20:59:23Z-
dc.date.available2015-10-21T13:09:10Z-
dc.date.available2016-10-25T20:59:23Z-
dc.date.issued2015-05-01-
dc.identifierhttp://ovidsp.tx.ovid.com/sp-3.17.0a/ovidweb.cgi?QS2=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-
dc.identifier.citationInternational Journal Of Gynecological Cancer, v. 25, n. 4, p. 734-740, 2015.-
dc.identifier.issn1048-891X-
dc.identifier.urihttp://hdl.handle.net/11449/128346-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/128346-
dc.description.abstractObjective Despite rising global obesity rates, the impact of obesity on gestational trophoblastic neoplasia (GTN) remains uninvestigated. This study aimed at investigating whether overweight/obesity relates to response to chemotherapy in low-risk GTN patients.Methods This nonconcurrent cohort study included 300 patients with International Federation of Gynecology and Obstetrics-defined postmolar low-risk GTN treated with a single-agent chemotherapymethotrexate or actinomycin-D (actD)between 1973 and 2012 at the New England Trophoblastic Disease Center. Chemotherapy dosing was based on actual body weight regardless of obesity status, except for 5-day courses or pulse regimens of actD. Patients were classified as overweight/obese (body mass index [BMI] 25 kg/m(2)) or non-overweight/obese (BMI <25 kg/m(2)). Information on patient characteristics and response to chemotherapy (need for second-line chemotherapy, reason for changing to an alternative chemotherapy, number of cycles, need for combination chemotherapy, and time to human chorionic gonadotropin remission) was obtained.Results Of 300 low-risk GTN patients, 81 (27%) were overweight/obese. Overweight/obese patients were older than the non-overweight/obese patients (median age: 30 vs 28 years, P = 0.004). First-line therapy using actD was more frequent in overweight/obese patients (6.2% vs 1.4%, P = 0.036). Resistance and toxicity were similar between groups. No significant difference in the number of chemotherapy cycles needed for remission or time required to achieve remission was found between groups.Conclusions No association between overweight/obesity and low-risk GTN outcomes was found. Current chemotherapy dosing using BMI seems to be appropriate for overweight/obese patients with low-risk GTN.en
dc.format.extent734-740-
dc.language.isoeng-
dc.publisherLippincott Williams &wilkins-
dc.sourceWeb of Science-
dc.subjectLow-risk gestational trophoblastic neoplasiaen
dc.subjectOverweighten
dc.subjectobesityen
dc.subjectChemotherapyen
dc.subjectOutcomesen
dc.titleResponse to Chemotherapy in Overweight/Obese Patients With Low-Risk Gestational Trophoblastic Neoplasiaen
dc.typeoutro-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.contributor.institutionBrigham &Womens Hosp-
dc.contributor.institutionDonald P Goldstein MD Tumor Registry-
dc.contributor.institutionDana Farber Canc Inst-
dc.contributor.institutionHarvard Univ-
dc.contributor.institutionCaldas Univ-
dc.contributor.institutionMassachusetts Gen Hosp-
dc.description.affiliationUNESP Sao Paulo State Univ, Dept Gynecol &Obstet, BR-18618970 Sao Paulo, Brazil-
dc.description.affiliationUNESP Sao Paulo State Univ, Botucatu Med Sch, Trophoblast Dis Ctr, BR-18618970 Sao Paulo, Brazil-
dc.description.affiliationBrigham &Womens Hosp, Dept Obstet &Gynecol, Div Gynecol Oncol, Boston, MA 02115 USA-
dc.description.affiliationDonald P Goldstein MD Tumor Registry, New England Trophoblast Dis Ctr, Boston, MA USA-
dc.description.affiliationDana Farber Canc Inst, Harvard Canc Ctr, Boston, MA 02115 USA-
dc.description.affiliationHarvard Univ, Sch Med, Boston, MA USA-
dc.description.affiliationCaldas Univ, Clin Dept, Manizales, Caldas, Colombia-
dc.description.affiliationMassachusetts Gen Hosp, Dept Obstet &Gynecol, Boston, MA 02114 USA-
dc.description.affiliationUnespUNESP Sao Paulo State Univ, Dept Gynecol &Obstet, BR-18618970 Sao Paulo, Brazil-
dc.description.affiliationUnespUNESP Sao Paulo State Univ, Botucatu Med Sch, Trophoblast Dis Ctr, BR-18618970 Sao Paulo, Brazil-
dc.identifier.doihttp://dx.doi.org/10.1097/IGC.0000000000000398-
dc.identifier.wosWOS:000354103000030-
dc.rights.accessRightsAcesso restrito-
dc.relation.ispartofInternational Journal Of Gynecological Cancer-
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

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