Phase II trial of neoadjuvant gemcitabine and cisplatin in patients with resectable bladder carcinoma

Detalhes bibliográficos
Autor(a) principal: Herchenhorn,Daniel
Data de Publicação: 2007
Outros Autores: Dienstmann,Rodrigo, Peixoto,Fabio A., Campos,Franz S. de, Santos,Valdelice O., Moreira,Denise M., Cardoso,Hedilene, Small,Isabele A., Ferreira,Carlos G.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: International Braz J Urol (Online)
Texto Completo: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1677-55382007000500004
Resumo: OBJECTIVES: Gemcitabine and cisplatin (GC) is an active combination in the treatment of metastatic bladder cancer. We have prospectively analyzed the efficacy and tolerability of GC as neoadjuvant treatment of invasive bladder cancer MATERIALS AND METHODS: In this single-institution phase II trial, patients with muscle-invasive transitional cell carcinoma received three cycles of gemcitabine 1200 mg/m² on days 1 and 8 with cisplatin 75 mg/m² on day 1 prior to surgery. Radiologic response was evaluated by computed tomography and magnetic resonance imaging. All patients were referred to surgery after chemotherapy completion RESULTS: Between June 2002 and March 2005, 22 patients (19 males) were enrolled. Median age was 63 years. Initial stage was II (T2) in 11 and III (T3-4) in 11 patients. Median follow-up is 26 months (4-43). Partial or complete radiologic response rate was documented in 13 out of 20 assessable patients (70%). One patient was excluded due to sarcomatoid carcinoma at definitive pathologic examination. Cystectomy was performed in 15 patients and pelvic radiotherapy in four patients. Nine out of 21 patients (43%) relapsed and four (19%) died due to disease progression. Complete pathologic response was observed in four patients (26.7% of 15). Median progression-free survival was 27 months (CI 95% not reached) with median overall survival of 36 months (CI 95%: 28.7 - 43.3). Grade III/IV toxicity was infrequent, with no deaths due to chemotherapy CONCLUSIONS: The combination of GC is effective and well-tolerated when used as neoadjuvant therapy in muscle-invasive bladder cancer. Longer follow-up is necessary to evaluate its impact on the overall survival of these patients.
id SBU-1_ac4bd7641c7e1d79887a8938512ae771
oai_identifier_str oai:scielo:S1677-55382007000500004
network_acronym_str SBU-1
network_name_str International Braz J Urol (Online)
repository_id_str
spelling Phase II trial of neoadjuvant gemcitabine and cisplatin in patients with resectable bladder carcinomabladder neoplasmsneoadjuvant therapycisplatingemcitabineOBJECTIVES: Gemcitabine and cisplatin (GC) is an active combination in the treatment of metastatic bladder cancer. We have prospectively analyzed the efficacy and tolerability of GC as neoadjuvant treatment of invasive bladder cancer MATERIALS AND METHODS: In this single-institution phase II trial, patients with muscle-invasive transitional cell carcinoma received three cycles of gemcitabine 1200 mg/m² on days 1 and 8 with cisplatin 75 mg/m² on day 1 prior to surgery. Radiologic response was evaluated by computed tomography and magnetic resonance imaging. All patients were referred to surgery after chemotherapy completion RESULTS: Between June 2002 and March 2005, 22 patients (19 males) were enrolled. Median age was 63 years. Initial stage was II (T2) in 11 and III (T3-4) in 11 patients. Median follow-up is 26 months (4-43). Partial or complete radiologic response rate was documented in 13 out of 20 assessable patients (70%). One patient was excluded due to sarcomatoid carcinoma at definitive pathologic examination. Cystectomy was performed in 15 patients and pelvic radiotherapy in four patients. Nine out of 21 patients (43%) relapsed and four (19%) died due to disease progression. Complete pathologic response was observed in four patients (26.7% of 15). Median progression-free survival was 27 months (CI 95% not reached) with median overall survival of 36 months (CI 95%: 28.7 - 43.3). Grade III/IV toxicity was infrequent, with no deaths due to chemotherapy CONCLUSIONS: The combination of GC is effective and well-tolerated when used as neoadjuvant therapy in muscle-invasive bladder cancer. Longer follow-up is necessary to evaluate its impact on the overall survival of these patients.Sociedade Brasileira de Urologia2007-10-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S1677-55382007000500004International braz j urol v.33 n.5 2007reponame:International Braz J Urol (Online)instname:Sociedade Brasileira de Urologia (SBU)instacron:SBU10.1590/S1677-55382007000500004info:eu-repo/semantics/openAccessHerchenhorn,DanielDienstmann,RodrigoPeixoto,Fabio A.Campos,Franz S. deSantos,Valdelice O.Moreira,Denise M.Cardoso,HedileneSmall,Isabele A.Ferreira,Carlos G.eng2008-02-29T00:00:00Zoai:scielo:S1677-55382007000500004Revistahttp://www.brazjurol.com.br/ONGhttps://old.scielo.br/oai/scielo-oai.php||brazjurol@brazjurol.com.br1677-61191677-5538opendoar:2008-02-29T00:00International Braz J Urol (Online) - Sociedade Brasileira de Urologia (SBU)false
dc.title.none.fl_str_mv Phase II trial of neoadjuvant gemcitabine and cisplatin in patients with resectable bladder carcinoma
title Phase II trial of neoadjuvant gemcitabine and cisplatin in patients with resectable bladder carcinoma
spellingShingle Phase II trial of neoadjuvant gemcitabine and cisplatin in patients with resectable bladder carcinoma
Herchenhorn,Daniel
bladder neoplasms
neoadjuvant therapy
cisplatin
gemcitabine
title_short Phase II trial of neoadjuvant gemcitabine and cisplatin in patients with resectable bladder carcinoma
title_full Phase II trial of neoadjuvant gemcitabine and cisplatin in patients with resectable bladder carcinoma
title_fullStr Phase II trial of neoadjuvant gemcitabine and cisplatin in patients with resectable bladder carcinoma
title_full_unstemmed Phase II trial of neoadjuvant gemcitabine and cisplatin in patients with resectable bladder carcinoma
title_sort Phase II trial of neoadjuvant gemcitabine and cisplatin in patients with resectable bladder carcinoma
author Herchenhorn,Daniel
author_facet Herchenhorn,Daniel
Dienstmann,Rodrigo
Peixoto,Fabio A.
Campos,Franz S. de
Santos,Valdelice O.
Moreira,Denise M.
Cardoso,Hedilene
Small,Isabele A.
Ferreira,Carlos G.
author_role author
author2 Dienstmann,Rodrigo
Peixoto,Fabio A.
Campos,Franz S. de
Santos,Valdelice O.
Moreira,Denise M.
Cardoso,Hedilene
Small,Isabele A.
Ferreira,Carlos G.
author2_role author
author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Herchenhorn,Daniel
Dienstmann,Rodrigo
Peixoto,Fabio A.
Campos,Franz S. de
Santos,Valdelice O.
Moreira,Denise M.
Cardoso,Hedilene
Small,Isabele A.
Ferreira,Carlos G.
dc.subject.por.fl_str_mv bladder neoplasms
neoadjuvant therapy
cisplatin
gemcitabine
topic bladder neoplasms
neoadjuvant therapy
cisplatin
gemcitabine
description OBJECTIVES: Gemcitabine and cisplatin (GC) is an active combination in the treatment of metastatic bladder cancer. We have prospectively analyzed the efficacy and tolerability of GC as neoadjuvant treatment of invasive bladder cancer MATERIALS AND METHODS: In this single-institution phase II trial, patients with muscle-invasive transitional cell carcinoma received three cycles of gemcitabine 1200 mg/m² on days 1 and 8 with cisplatin 75 mg/m² on day 1 prior to surgery. Radiologic response was evaluated by computed tomography and magnetic resonance imaging. All patients were referred to surgery after chemotherapy completion RESULTS: Between June 2002 and March 2005, 22 patients (19 males) were enrolled. Median age was 63 years. Initial stage was II (T2) in 11 and III (T3-4) in 11 patients. Median follow-up is 26 months (4-43). Partial or complete radiologic response rate was documented in 13 out of 20 assessable patients (70%). One patient was excluded due to sarcomatoid carcinoma at definitive pathologic examination. Cystectomy was performed in 15 patients and pelvic radiotherapy in four patients. Nine out of 21 patients (43%) relapsed and four (19%) died due to disease progression. Complete pathologic response was observed in four patients (26.7% of 15). Median progression-free survival was 27 months (CI 95% not reached) with median overall survival of 36 months (CI 95%: 28.7 - 43.3). Grade III/IV toxicity was infrequent, with no deaths due to chemotherapy CONCLUSIONS: The combination of GC is effective and well-tolerated when used as neoadjuvant therapy in muscle-invasive bladder cancer. Longer follow-up is necessary to evaluate its impact on the overall survival of these patients.
publishDate 2007
dc.date.none.fl_str_mv 2007-10-01
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1677-55382007000500004
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1677-55382007000500004
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.1590/S1677-55382007000500004
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv text/html
dc.publisher.none.fl_str_mv Sociedade Brasileira de Urologia
publisher.none.fl_str_mv Sociedade Brasileira de Urologia
dc.source.none.fl_str_mv International braz j urol v.33 n.5 2007
reponame:International Braz J Urol (Online)
instname:Sociedade Brasileira de Urologia (SBU)
instacron:SBU
instname_str Sociedade Brasileira de Urologia (SBU)
instacron_str SBU
institution SBU
reponame_str International Braz J Urol (Online)
collection International Braz J Urol (Online)
repository.name.fl_str_mv International Braz J Urol (Online) - Sociedade Brasileira de Urologia (SBU)
repository.mail.fl_str_mv ||brazjurol@brazjurol.com.br
_version_ 1750318070503571456