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13-顺式维甲酸与干扰素α-2a联合治疗实体瘤。

Combination 13-cis-retinoic acid and interferon alpha-2a in the therapy of solid tumors.

作者信息

Eisenhauer E A, Lippman S M, Kavanagh J J, Parades-Espinoza M, Arnold A, Hong W K, Massimini G, Schleuniger U, Bollag W, Holdener E E

机构信息

NCIC Clinical Trials Group, Queen's University, Kingston, Canada.

出版信息

Leukemia. 1994 Oct;8(10):1622-5.

PMID:7934156
Abstract

Preclinical data indicate that the combination of retinoids and interferons have synergistic antiproliferative and differentiating effects in some hematologic and solid tumor models. These observations have led to clinical trials in which 13-cis-retinoic acid (13cRA) 1 mg/kg/day was combined with interferon alpha-2a (IFN alpha) 3 or 6 x 10(6) U/day. The first two such trials produced exciting results: 50% response rate in patients with previously untreated stages IB-IVA cervix cancer and 68% in patients with advanced squamous cell skin cancer. These data led to a number of additional trials of the combination, but the high response rates seen in the initial cervix and skin trials have not been duplicated in the other squamous tumors tested (head and neck, lung, pretreated cervix). In addition, trials in two non-squamous histologies were negative (lung and melanoma). However, the regimen was not always studied in an optimal population of previously untreated patients and the negative results in pretreated cervix patients point to the relevance of this consideration. Nevertheless, the observation that the combination of 13cRA and IFN alpha (both of which bind to specific receptors and change gene expression) is able to induce regression in advanced tumors, must be regarded as highly important. Key questions to be addressed include an understanding of the biologic mechanism of specific tumor sensitivity (why some squamous tumors and not others?), and mechanisms of resistance in sensitive tumor types (e.g. cervix). Such data may lead to trials targeted to tumor types with defined biologic features having a high likelihood of clinical benefit. In the meantime, studies integrating this combination with other active treatment modalities such as radiation is warranted in cervix and skin carcinomas.

摘要

临床前数据表明,在一些血液学和实体瘤模型中,类视黄醇与干扰素联合使用具有协同的抗增殖和分化作用。这些观察结果促使开展了临床试验,将13-顺式维甲酸(13cRA)1毫克/千克/天与干扰素α-2a(IFNα)3或6×10⁶单位/天联合使用。最初的两项此类试验产生了令人振奋的结果:在先前未经治疗的IB-IVA期宫颈癌患者中缓解率为50%,在晚期皮肤鳞状细胞癌患者中为68%。这些数据引发了一系列关于该联合用药的额外试验,但在最初的宫颈癌和皮肤癌试验中所见的高缓解率在其他测试的鳞状肿瘤(头颈癌、肺癌、先前治疗过的宫颈癌)中并未重现。此外,两项非鳞状组织学类型的试验结果为阴性(肺癌和黑色素瘤)。然而,该方案并非总是在先前未经治疗的最佳患者群体中进行研究,而先前治疗过的宫颈癌患者的阴性结果表明了这一考虑因素的相关性。尽管如此,13cRA与IFNα联合使用(两者均与特定受体结合并改变基因表达)能够使晚期肿瘤消退这一观察结果,必须被视为非常重要。需要解决的关键问题包括了解特定肿瘤敏感性的生物学机制(为什么某些鳞状肿瘤有反应而其他肿瘤没有?)以及敏感肿瘤类型(如宫颈癌)的耐药机制。此类数据可能会促使针对具有明确生物学特征且临床获益可能性高的肿瘤类型开展试验。与此同时,有必要在宫颈癌和皮肤癌中开展将该联合用药与其他有效治疗方式(如放疗)相结合的研究。

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