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米托蒽醌联合泼尼松或单用泼尼松治疗有症状的激素抵抗性前列腺癌的化疗:一项以姑息治疗为终点的加拿大随机试验

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

作者信息

Tannock I F, 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

机构信息

Department of Medicine, Princess Margaret Hospital, Toronto, Canada.

出版信息

J Clin Oncol. 1996 Jun;14(6):1756-64. doi: 10.1200/JCO.1996.14.6.1756.

Abstract

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 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.

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 > 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.

CONCLUSION

Chemotherapy with mitoxantrone and prednisone provides palliation for some patients with symptomatic hormone-resistant prostate cancer.

摘要

目的

在一项随机对照试验中,使用相关的姑息治疗终点来研究化疗对有症状的激素抵抗性前列腺癌患者的益处。

患者与方法

我们将161例有疼痛症状的激素难治性患者随机分组,分别接受米托蒽醌加泼尼松或单独使用泼尼松(每日10毫克)治疗。对泼尼松无反应的患者随后可接受米托蒽醌治疗。主要终点是姑息治疗反应,定义为患者通过6分疼痛量表评估疼痛减轻2分(如果初始疼痛评分为1分则疼痛完全消失),且镇痛药物用量未增加,并在至少间隔3周的连续两次评估中保持这一状态。次要终点包括镇痛药物用量减少≥50%且疼痛未加重、反应持续时间和生存期。使用一系列线性模拟自我评估量表(LASA和前列腺癌特异性生活质量工具[PROSQOLI])、欧洲癌症研究与治疗组织(EORTC)的核心问卷以及一个疾病特异性模块对健康相关生活质量进行评估。

结果

接受米托蒽醌加泼尼松治疗的80例患者中有23例(29%;95%置信区间,19%至40%)出现姑息治疗反应,而单独接受泼尼松治疗的81例患者中有10例(12%;95%置信区间,6%至22%)出现姑息治疗反应(P = 0.01)。每组另有7例患者镇痛药物用量减少≥50%且疼痛未加重。接受化疗的患者姑息治疗持续时间更长(中位数分别为43周和18周;P < 0.0001,对数秩检验)。随机接受泼尼松治疗的50例患者中有11例在加用米托蒽醌后有反应。总生存期无差异。治疗耐受性良好,接受米托蒽醌治疗的130例患者中有5例出现可能的心脏毒性事件。大多数有反应的患者生活质量量表得分改善,血清前列腺特异性抗原(PSA)水平下降。

结论

米托蒽醌和泼尼松化疗可为一些有症状的激素抵抗性前列腺癌患者提供姑息治疗。

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