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Hydrocortisone with or without mitoxantrone in men with hormone-refractory prostate cancer: results of the cancer and leukemia group B 9182 study.

Publication ,  Journal Article
Kantoff, PW; Halabi, S; Conaway, M; Picus, J; Kirshner, J; Hars, V; Trump, D; Winer, EP; Vogelzang, NJ
Published in: J Clin Oncol
August 1999

PURPOSE: Approximately 40,000 men die each year of hormone-refractory prostate cancer (HRPC). The results of treatment with chemotherapy have been disappointing to date, with no trials demonstrating a benefit with respect to survival duration. Corticosteroids and mitoxantrone each have been shown to be active agents in this disease. The purpose of this study was to demonstrate an advantage of mitoxantrone and hydrocortisone (M+H) over hydrocortisone alone with respect to survival duration. PATIENTS AND METHODS: Two hundred forty-two patients with HRPC were randomized to receive either M+H or hydrocortisone alone. Patients were monitored for survival, time to disease progression, time to treatment failure, response, and quality-of-life (QOL) parameters. RESULTS: Treatment in both arms was well tolerated. Although there was a delay in time to treatment failure and disease progression in favor of M+H over hydrocortisone alone, there was no difference in overall survival (12.3 months for M+H v 12.6 months for hydrocortisone alone). There was an indication that QOL was better with M+H, in particular with respect to pain control. CONCLUSION: M+H generated more frequent responses and a delay in both time to treatment failure and disease progression compared with hydrocortisone alone. In addition, there was a possible benefit of M+H with respect to pain control over hydrocortisone alone. No improvement in survival was observed. Although M+H could be viewed as a palliative option for patients with HRPC, new drugs and novel strategies are needed to improve survival for this disease.

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Published In

J Clin Oncol

DOI

ISSN

0732-183X

Publication Date

August 1999

Volume

17

Issue

8

Start / End Page

2506 / 2513

Location

United States

Related Subject Headings

  • Treatment Failure
  • Quality of Life
  • Prostatic Neoplasms
  • Proportional Hazards Models
  • Prognosis
  • Pain
  • Oncology & Carcinogenesis
  • Neoplasm Metastasis
  • Mitoxantrone
  • Male
 

Citation

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Kantoff, P. W., Halabi, S., Conaway, M., Picus, J., Kirshner, J., Hars, V., … Vogelzang, N. J. (1999). Hydrocortisone with or without mitoxantrone in men with hormone-refractory prostate cancer: results of the cancer and leukemia group B 9182 study. J Clin Oncol, 17(8), 2506–2513. https://doi.org/10.1200/JCO.1999.17.8.2506
Kantoff, P. W., S. Halabi, M. Conaway, J. Picus, J. Kirshner, V. Hars, D. Trump, E. P. Winer, and N. J. Vogelzang. “Hydrocortisone with or without mitoxantrone in men with hormone-refractory prostate cancer: results of the cancer and leukemia group B 9182 study.J Clin Oncol 17, no. 8 (August 1999): 2506–13. https://doi.org/10.1200/JCO.1999.17.8.2506.
Kantoff PW, Halabi S, Conaway M, Picus J, Kirshner J, Hars V, et al. Hydrocortisone with or without mitoxantrone in men with hormone-refractory prostate cancer: results of the cancer and leukemia group B 9182 study. J Clin Oncol. 1999 Aug;17(8):2506–13.
Kantoff, P. W., et al. “Hydrocortisone with or without mitoxantrone in men with hormone-refractory prostate cancer: results of the cancer and leukemia group B 9182 study.J Clin Oncol, vol. 17, no. 8, Aug. 1999, pp. 2506–13. Pubmed, doi:10.1200/JCO.1999.17.8.2506.
Kantoff PW, Halabi S, Conaway M, Picus J, Kirshner J, Hars V, Trump D, Winer EP, Vogelzang NJ. Hydrocortisone with or without mitoxantrone in men with hormone-refractory prostate cancer: results of the cancer and leukemia group B 9182 study. J Clin Oncol. 1999 Aug;17(8):2506–2513.

Published In

J Clin Oncol

DOI

ISSN

0732-183X

Publication Date

August 1999

Volume

17

Issue

8

Start / End Page

2506 / 2513

Location

United States

Related Subject Headings

  • Treatment Failure
  • Quality of Life
  • Prostatic Neoplasms
  • Proportional Hazards Models
  • Prognosis
  • Pain
  • Oncology & Carcinogenesis
  • Neoplasm Metastasis
  • Mitoxantrone
  • Male