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

被引:1244
作者
Tannock, IF
Osoba, D
Stockler, MR
Ernst, DS
Neville, AJ
Moore, MJ
Armitage, GR
Wilson, JJ
Venner, PM
Coppin, CML
Murphy, KC
机构
[1] UNIV TORONTO,DEPT MED,TORONTO,ON M5S 1A1,CANADA
[2] HUMBER MEM HOSP,TORONTO,ON,CANADA
[3] UNIV BRITISH COLUMBIA,VANCOUVER,BC V5Z 1M9,CANADA
[4] BRITISH COLUMBIA CANC AGCY,VANCOUVER,BC V5Z 4E6,CANADA
[5] UNIV CALGARY,CALGARY,AB,CANADA
[6] HAMILTON REG CANC CTR,HAMILTON,ON L8V 1C3,CANADA
[7] SASKATOON CANC CTR,SASKATOON,SK,CANADA
[8] CROSS CANC INST,EDMONTON,AB T6G 1Z2,CANADA
[9] TOM BAKER CANC CLIN,CALGARY,AB,CANADA
关键词
D O I
10.1200/JCO.1996.14.6.1756
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose; 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. Patients and Methods: We randomized 161 hormone-refractory patients with pain to receive mitoxantrone plus prednisone or prednisone alone (10 mg daily). Nonresponding patients an 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 greater than or equal to 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. Results: 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 greater than or equal to 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. Conclusion: Chemotherapy with mitoxantrone and prednisone provides palliation far some patients with symptomatic hormone-resistant prostate cancer. (C) 1996 by American Society of Clinical Oncology.
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收藏
页码:1756 / 1764
页数:9
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