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PMID: 8656243 Published · ppublish English Clinical Trial Journal Article Randomized Controlled Trial Research Support, Non-U.S. Gov't

Chemotherapy with mitoxantrone plus prednisone or prednisone alone for symptomatic hormone-resistant prostate cancer: a Canadian randomized trial with palliative end points.

Tannock IF, Osoba D, Stockler MR, Ernst DS, Neville AJ, Moore MJ, Armitage GR, Wilson JJ, Venner PM, Coppin CM, Murphy KC

Abstract

To investigate the benefit of chemotherapy in patients with symptomatic hormone-resistant prostate cancer using relevant end points of palliation in a randomized controlled trial. We randomized 161 hormone-refractory patients with pain to receive mitoxantrone plus prednisone or prednisone alone (10 mg daily). Nonresponding patients on prednisone could receive mitoxantrone subsequently. The primary end point was a palliative response defined as a 2-point decrease in pain as assessed by a 6-point pain scale completed by patients (or complete loss of pain if initially 1 +) without an increase in analgesic medication and maintained for two consecutive evaluations at least 3 weeks apart. Secondary end points were a decrease of > or = 50% in use of analgesic medication without an increase in pain, duration of response, and survival. Health-related quality of life was evaluated with a series of linear analog self-assessment scales (LASA and the Prostate Cancer-Specific Quality-of-Life Instrument [PROSQOLI]), the core questionnaire of the European Organization for Research and Treatment of Cancer (EORTC), and a disease-specific module. Palliative response was observed in 23 of 80 patients (29%; 95% confidence interval, 19% to 40%) who received mitoxantrone plus prednisone, and in 10 of 81 patients (12%; 95% confidence interval, 6% to 22%) who received prednisone alone (P = .01). An additional seven patients in each group reduced analgesic medication > or = 50% without an increase in pain. The duration of palliation was longer in patients who received chemotherapy (median, 43 and 18 weeks; P < .0001, log-rank). Eleven of 50 patients randomized to prednisone treatment responded after addition of mitoxantrone. There was no difference in overall survival. Treatment was well tolerated, except for five episodes of possible cardiac toxicity in 130 patients who received mitoxantrone. Most responding patients had an improvement in quality-of-life scales and a decrease in serum prostate-specific antigen (PSA) level. Chemotherapy with mitoxantrone and prednisone provides palliation for some patients with symptomatic hormone-resistant prostate cancer.

MeSH Terms
Adenocarcinoma/drug therapy,mortality,pathology,secondary Aged Analgesics/therapeutic use Androgen Antagonists/therapeutic use Antineoplastic Combined Chemotherapy Protocols/adverse effects,therapeutic use Cross-Over Studies Drug Resistance, Neoplasm Humans Male Middle Aged Mitoxantrone/administration & dosage,adverse effects Orchiectomy Pain/etiology Palliative Care Prednisone/administration & dosage,adverse effects Prostate-Specific Antigen/analysis Prostatic Neoplasms/drug therapy,mortality,pathology Quality of Life Survival Rate
Chemicals
Analgesics Androgen Antagonists Mitoxantrone Prostate-Specific Antigen Prednisone
Authors & Affiliations
11 authors, click to expand affiliations / ORCID
Tannock I F
Department of Medicine, Princess Margaret Hospital, Toronto, Canada. ian-tannock@pmh.toronto.on.ca
Osoba D
Stockler M R
Ernst D S
Neville A J
Moore M J
Armitage G R
Wilson J J
Venner P M
Coppin C M
Murphy K C
Article Info
Journal
Journal of clinical oncology : official journal of the American Society of Clinical Oncology
Abbr.
J Clin Oncol
ISSN
0732-183X
Published
1996-06-00
Pages
1756-64
Language
English
Region
United States
NLM ID
8309333
Subset
IM
Corrections
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