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Neoadjuvant Chemotherapy Using Reduced-Dose Docetaxel Followed by Radical Prostatectomy for Patients With Intermediate and High-Risk Prostate Cancer: A Single-Center Study.
Nosov, Alexander; Reva, Sergey; Petrov, Sergey; Mamijev, Eldar; Novikov, Roman; Veliev, Evgeniy; Imkamp, Florian; Tolkach, Yuri; Moiseenko, Vladimir.
Afiliação
  • Nosov A; Department of Oncological Urology, Petrov N.N. Research Institute of Oncology, Saint-Petersburg, Russia.
  • Reva S; Department of Oncological Urology, Petrov N.N. Research Institute of Oncology, Saint-Petersburg, Russia. sgreva79@mail.ru.
  • Petrov S; Department of Oncological Urology, Petrov N.N. Research Institute of Oncology, Saint-Petersburg, Russia.
  • Mamijev E; Department of Oncological Urology, Petrov N.N. Research Institute of Oncology, Saint-Petersburg, Russia.
  • Novikov R; Department of Oncological Urology, Petrov N.N. Research Institute of Oncology, Saint-Petersburg, Russia.
  • Veliev E; Urology Clinic of the S.P. Botkin City Clinical Hospital, Moscow, Russia.
  • Imkamp F; Clinic for Urology and Urologic Oncology, Hannover Medical School, Hannover, Germany.
  • Tolkach Y; Clinic for Urology and Urologic Oncology, Hannover Medical School, Hannover, Germany.
  • Moiseenko V; Institute of Pathology, University Hospital of Bonn, Bonn, Germany.
Prostate ; 76(15): 1345-52, 2016 11.
Article em En | MEDLINE | ID: mdl-26864707
ABSTRACT

BACKGROUND:

To assess safety, pathologic response rate, and long-term oncologic outcomes of radical prostatectomy (RP) after neoadjuvant chemotherapy using reduced-dose docetaxel without androgen-deprivation therapy in prostate cancer (PCa) patients of intermediate- and high-risk groups.

METHODS:

Forty-four patients with PCa (PSA > 10 ng/ml, Gleason score 7 or more, or clinical stage cT2c or more) were included with a median follow-up of 11.4 years after RP. One group (NCT/RP) received neoadjuvant treatment 3-weekly with docetaxel (36 mg/m(2) for up to six cycles, 21 patients), the other (control) group (RP, 23 patients) received RP only.

RESULTS:

Toxicities were mild with grade 3 events not exceeding 10%. A statistically significant reduction of PSA > 50% post-chemotherapy was observed in 52.4% cases. Cancer-specific survival (CSS) was 90% in the NCT/RP group and 60.9% in the RP group (P = 0.042). The biochemical recurrence-free survival was 68.5% in the NCT/RP and 37.7% in the RP groups; overall survival was 75.5% and 54.6%, respectively (both P > 0.05).

CONCLUSIONS:

The use of neoadjuvant chemotherapy before RP in a selected regimen and dose represents a safe strategy and results in benefits in CSS. Given the limitations of the study, this concept should be evaluated in large, prospective, controlled studies. Prostate 76 1345-1352, 2016. © 2016 Wiley Periodicals, Inc.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Prostatectomia / Neoplasias da Próstata / Taxoides / Antineoplásicos Tipo de estudo: Etiology_studies / Risk_factors_studies Limite: Aged / Humans / Male / Middle aged Idioma: En Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Prostatectomia / Neoplasias da Próstata / Taxoides / Antineoplásicos Tipo de estudo: Etiology_studies / Risk_factors_studies Limite: Aged / Humans / Male / Middle aged Idioma: En Ano de publicação: 2016 Tipo de documento: Article