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间歇性三联雄激素阻断治疗局限性前列腺癌:110例连续患者的初步结果。

Treatment of localized prostate cancer with intermittent triple androgen blockade: preliminary results in 110 consecutive patients.

作者信息

Leibowitz R L, Tucker S J

机构信息

Compassionate Oncology Medical Group, 2080 Century Park East, #601, Los Angeles, CA 90067, USA.

出版信息

Oncologist. 2001;6(2):177-82. doi: 10.1634/theoncologist.6-2-177.

Abstract

OBJECTIVES

To determine the effectiveness of triple androgen blockade as an alternative to watchful waiting, radical prostatectomy or radiation therapy in the management of patients with clinical stage T1 to T3 prostate cancer.

METHODS

The records of 110 consecutive patients were retrospectively evaluated. Patients were treated with a three-drug androgen blockade regimen, consisting of a luteinizing hormone-releasing hormone agonist (leuprolide or goserelin) plus an antiandrogen (flutamide or bicalutamide) plus finasteride (a 5-alpha-reductase inhibitor), followed by finasteride maintenance therapy, as the sole intervention. All patients refused local therapy and had their prostates intact. Determinants of efficacy included serum prostate-specific antigen (PSA) levels and disease-specific survival.

RESULTS

Patients were treated for a median of 13 months with triple androgen blockade. At baseline, mean PSA level was 13.2 +/- 1.2 ng/ml (range, 0.39-100 ng/ml), and mean Gleason score was 6.6 +/- 0.1 (range, 4-10). During treatment, PSA levels declined to < or =0.1 ng/ml in all patients, with a median time of 3 months. After a median follow-up of 36 months since initiation of treatment, PSA levels have remained stable in 105 of 110 patients (95.5%). At a median follow-up of 55 months (range, 38-125 months), the mean PSA level for the first 57 patients treated in this series is 1.88 +/- 0.1 (range, 0-11.0 ng/ml). Only 9 of 110 (8.1%) patients have a PSA level > or =4.0 ng/ml. To date, no patient has received a second cycle of hormone blockade.

CONCLUSIONS

Although median follow-up is short, triple androgen blockade therapy followed by finasteride maintenance appears to be a promising alternative for the management of patients with clinically localized or locally advanced prostate cancer. Further study of this approach is warranted.

摘要

目的

确定三联雄激素阻断疗法作为临床T1至T3期前列腺癌患者管理中观察等待、根治性前列腺切除术或放射治疗替代方案的有效性。

方法

回顾性评估110例连续患者的记录。患者接受由促性腺激素释放激素激动剂(亮丙瑞林或戈舍瑞林)加抗雄激素药物(氟他胺或比卡鲁胺)加非那雄胺(一种5-α还原酶抑制剂)组成的三联药物雄激素阻断方案治疗,随后进行非那雄胺维持治疗,作为唯一干预措施。所有患者均拒绝局部治疗且前列腺完整。疗效的决定因素包括血清前列腺特异性抗原(PSA)水平和疾病特异性生存率。

结果

患者接受三联雄激素阻断治疗的中位时间为13个月。基线时,平均PSA水平为13.2±1.2 ng/ml(范围0.39 - 100 ng/ml),平均Gleason评分为6.6±0.1(范围4 - 10)。治疗期间,所有患者的PSA水平均降至≤0.1 ng/ml,中位时间为3个月。自开始治疗起中位随访36个月后,110例患者中有105例(95.5%)的PSA水平保持稳定。在中位随访55个月(范围38 - 125个月)时,本系列中最初治疗的57例患者的平均PSA水平为1.88±0.1(范围0 - 11.0 ng/ml)。110例患者中只有9例(8.1%)的PSA水平≥4.0 ng/ml。迄今为止,没有患者接受第二个周期的激素阻断治疗。

结论

尽管中位随访时间较短,但三联雄激素阻断疗法联合非那雄胺维持治疗似乎是临床局限性或局部晚期前列腺癌患者管理的一种有前景的替代方案。对该方法进行进一步研究是必要的。

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