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黑色素瘤的辅助治疗。

Adjuvant therapy of melanoma.

作者信息

Shah Gaurav D, Chapman Paul B

机构信息

Department of Medicine, Melanoma/Sarcoma Service, Memorial Sloan-Kettering Cancer Center, New York, NY 10021-6007, USA.

出版信息

Cancer J. 2007 May-Jun;13(3):217-22. doi: 10.1097/PPO.0b013e318074dfd4.

Abstract

PURPOSE

The purpose of this article was to review the current state of knowledge regarding the efficacy of adjuvant therapy for melanoma.

PATIENTS AND METHODS

We reviewed the published literature, focusing on randomized clinical trials.

RESULTS

There have been no meaningful trials addressing adjuvant chemotherapy in melanoma because all trials have been underpowered. Adjuvant interferon-alpha has been tested both at high dose and at lower doses. None of the trials have shown a reproducible benefit in survival, although the high-dose trials and some of the low-dose trials have shown improvement in time to relapse. These experiences raise the question of whether chronic administration is more important than dose. An adjuvant pegylated interferon-alpha trial using a 5-year treatment period is currently under investigation. At least 7 randomized adjuvant vaccine trials have been published, but none have shown a beneficial effect on relapse-free or overall survival except in subset analyses.

CONCLUSIONS

To date, no adjuvant therapy has resulted in improved overall survival. To be attractive as an adjuvant therapy, experience from other tumor types indicates that a chemotherapy regimen should have a response rate of at least 20% in metastatic melanoma. Currently, biochemotherapy is being tested as an adjuvant treatment but other, less toxic, regimens should be sought. Once such a regimen with acceptable toxicity is identified, it would be reasonable to test it as an adjuvant therapy in a properly powered randomized trial. High-dose interferon-alpha for 1 year remains the only U.S. Food and Drug Administration-approved adjuvant therapy for melanoma, but long-term chronic dosing of interferon-alpha may prove more effective than short-term dose schedules. Development of melanoma vaccines remains an appealing and important goal. New technologies and understanding of the immune response against melanoma are leading to novel vaccine strategies designed to break immunologic tolerance against melanoma.

摘要

目的

本文旨在综述黑色素瘤辅助治疗疗效的当前知识状态。

患者与方法

我们回顾了已发表的文献,重点关注随机临床试验。

结果

尚无针对黑色素瘤辅助化疗的有意义试验,因为所有试验的样本量均不足。辅助性α干扰素已在高剂量和低剂量下进行了测试。尽管高剂量试验和一些低剂量试验显示复发时间有所改善,但没有一项试验显示出生存方面可重复的益处。这些经验引发了关于长期给药是否比剂量更重要的问题。一项使用5年治疗期的聚乙二醇化α干扰素辅助试验目前正在进行研究。至少已发表了7项随机辅助疫苗试验,但除了亚组分析外,没有一项试验显示对无复发生存或总生存有有益影响。

结论

迄今为止,尚无辅助治疗能提高总生存率。从其他肿瘤类型的经验来看,作为一种辅助治疗要有吸引力,化疗方案在转移性黑色素瘤中的缓解率应至少达到20%。目前,生物化疗正在作为辅助治疗进行测试,但应寻求其他毒性较小的方案。一旦确定了这样一种毒性可接受的方案,在一项样本量充足的随机试验中作为辅助治疗进行测试将是合理的。1年的高剂量α干扰素仍然是美国食品药品监督管理局批准的唯一黑色素瘤辅助治疗方法,但α干扰素的长期慢性给药可能比短期给药方案更有效。黑色素瘤疫苗的研发仍然是一个有吸引力且重要的目标。新技术以及对黑色素瘤免疫反应的理解正导致设计出旨在打破对黑色素瘤免疫耐受的新型疫苗策略。

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