Identificador persistente para citar o vincular este elemento: http://hdl.handle.net/10553/47961
Campo DC Valoridioma
dc.contributor.authorIsorna Martínez de la Riva, Santiagoen_US
dc.contributor.authorBelón-López Tomasetti, José Antonioen_US
dc.contributor.authorMarrero Domínguez, Reinaldoen_US
dc.contributor.authorÁlvarez Cruz, Enriqueen_US
dc.contributor.authorSantamaría Blanco, Palomaen_US
dc.date.accessioned2018-11-23T17:50:46Z-
dc.date.available2018-11-23T17:50:46Z-
dc.date.issued2004en_US
dc.identifier.issn0004-0614en_US
dc.identifier.urihttp://hdl.handle.net/10553/47961-
dc.description.abstractOBJECTIVES: To evaluate the oncological and functional resulte of radical prostatectomy as monotherapy for stage T3a prostete cancer. METHODS: We include our initial and consecutive series of 83 patiente with prostete cancer (studied by digital rectal examination and transrectal ultrasound) who had not received neoadjuvant treatment under-going radical prostatectomy from July 1988 to December 2003. No patient received adjuvant treatment, and deferred intermittent androgen blockade was used when patients with biochemical progression exceeded a FSA of 4 ng/ ml. Up RESULTS: After a mean follow-up of 68.7 (1-139) months overall and specific survival 97.6% and 100% respectively; biochemical progression 36.1 % (22 pT2 (0%),41 p 73a (36.6%),13 pT3b (61.5%) and 7 pT4a (100%)). Positive margins 61.4% (41.2% unifocal with a progression rate of 23.8% 96.4% achieved continence and 39.6% recovered potency. Among 30 patients with biochemical progression, 19 required treatment witih deferred intermittent androgen blockade (one cycle in 10 patients, two cycles in six, and three cycles in the remaining three). CONCLUSIONS: Our results support the indication of radical prostatectomy as angle therapy without neoadjuvant treatment as a curative indication for locally advanced prostate cancer (73 a) whenever complete excision is expected: Gleason 7 T3 tumors without diffuse extension on ultrasound. 26.5% of these T3a patients were overstaged and resulted to be organconfined (p72). Ten-year probability of biochemical progression-free survival was 100% for pT2 and 81.9% for the lower risk pT3a (well or moderately-differentiated with negative surgical margins or unifocal). Functional results for T3a were similar to the ones of the clinically-localized (T2) series for both retropubic and perineal approaches. 30 patients had developed biochemical progression at the time of study closure and were free of hormonal treatment during 81.6% of the total follow-up time with our deferred intermittent androgen blockade treatment line, so that we consider we can offer it as the first treatment option for progression providing a maximal quality of life and allowing ulterior second line therapies. Futiente who mainly benefited were those on progression who have recovered sexual function: 41.7% of potent patients after radical prostatectomy recovered potency again over the second phase (no treatment) of the deferred intermittent androgen blockade.
dc.languagespaen_US
dc.publisher0004-0614-
dc.relation.ispartofArchivos españoles de urologíaen_US
dc.sourceArchivos Espanoles de Urologia[ISSN 0004-0614],v. 57 (7), p. 679-692en_US
dc.subject321316 Urologíaen_US
dc.titleRadical prostatectomy as monotherapy for locally advanced (T3a) prostate cancer: 12 years of follow-upen_US
dc.title.alternativeProstatectomía radical como monoterapia en el cáncer de próstata localmente avanzado T3a: 12 años de seguimientoen_US
dc.typeinfo:eu-repo/semantics/Articleen_US
dc.typeArticleen_US
dc.identifier.scopus16544376379-
dc.contributor.authorscopusid26422187000-
dc.contributor.authorscopusid6504542663-
dc.contributor.authorscopusid26422049600-
dc.contributor.authorscopusid26422027800-
dc.contributor.authorscopusid57206237260
dc.contributor.authorscopusid26421914500-
dc.description.lastpage692-
dc.description.firstpage679-
dc.relation.volume57-
dc.investigacionCiencias de la Saluden_US
dc.type2Artículoen_US
dc.utils.revisionen_US
dc.date.coverdateSeptiembre 2004
dc.identifier.ulpgces
dc.description.scieSCIE
item.grantfulltextnone-
item.fulltextSin texto completo-
crisitem.author.deptGIR IUIBS: Patología y Tecnología médica-
crisitem.author.deptIU de Investigaciones Biomédicas y Sanitarias-
crisitem.author.deptGIR IUIBS: Patología y Tecnología médica-
crisitem.author.deptIU de Investigaciones Biomédicas y Sanitarias-
crisitem.author.parentorgIU de Investigaciones Biomédicas y Sanitarias-
crisitem.author.parentorgIU de Investigaciones Biomédicas y Sanitarias-
crisitem.author.fullNameIsorna Martínez De La Riva,Santiago-
crisitem.author.fullNameBelon Lopez-Tomasety,Jose-
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