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黑色素瘤的靶向治疗

Targeted therapies in melanoma.

作者信息

Queirolo Paola, Acquati Mirko

机构信息

Department of Medical Oncology A, National Institute for Cancer Research, Largo Rosanna Benzi 10, Genoa 16132, Italy.

出版信息

Cancer Treat Rev. 2006 Nov;32(7):524-31. doi: 10.1016/j.ctrv.2006.07.009. Epub 2006 Sep 27.

DOI:10.1016/j.ctrv.2006.07.009
PMID:17008014
Abstract

In the last decade the incidence of melanoma has been rising. Despite this, survival remains substantially constant because early diagnosis of thin lesions has increased. By contrast, metastatic melanoma continues to have a poor prognosis and it still represents a challenge for oncologists. Response rates with single agent dacarbazine range from 10% to 25% with median survival of 8 months. The advent of new drugs with specific mechanisms of action could help to improve the poor results of traditional therapies. In this review, we focused on the novel agents that entered clinical trials in melanoma patients. We show the results of some clinical trials with target-oriented drugs in melanoma patients. Moreover pre-clinical data and rationale for use in melanoma was explained. Trials with protein-kinase inhibitors, anti-CTLA-4 agents, pro-apoptotic oligonucleotides and anti-angiogenic agents were reviewed. Combinations with chemotherapeutic agents, immunotherapy and vaccine therapy were also analyzed.

摘要

在过去十年中,黑色素瘤的发病率一直在上升。尽管如此,由于对薄病变的早期诊断有所增加,生存率基本保持稳定。相比之下,转移性黑色素瘤的预后仍然很差,对肿瘤学家来说仍是一个挑战。单药达卡巴嗪的缓解率为10%至25%,中位生存期为8个月。具有特定作用机制的新药的出现可能有助于改善传统疗法的不佳效果。在本综述中,我们重点关注了进入黑色素瘤患者临床试验的新型药物。我们展示了一些针对黑色素瘤患者的靶向药物的临床试验结果。此外,还解释了临床前数据以及在黑色素瘤中使用的基本原理。对蛋白激酶抑制剂、抗CTLA-4药物、促凋亡寡核苷酸和抗血管生成药物的试验进行了综述。还分析了与化疗药物、免疫疗法和疫苗疗法的联合应用。

相似文献

1
Targeted therapies in melanoma.黑色素瘤的靶向治疗
Cancer Treat Rev. 2006 Nov;32(7):524-31. doi: 10.1016/j.ctrv.2006.07.009. Epub 2006 Sep 27.
2
Emerging therapies for melanoma.黑色素瘤的新兴疗法
Expert Rev Anticancer Ther. 2008 Apr;8(4):553-60. doi: 10.1586/14737140.8.4.553.
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Angiogenesis in cutaneous malignant melanoma and potential therapeutic strategies.皮肤恶性黑色素瘤中的血管生成及潜在治疗策略。
Expert Rev Anticancer Ther. 2009 Nov;9(11):1583-98. doi: 10.1586/era.09.135.
4
Prospects for non-immunological molecular therapeutics in melanoma.黑色素瘤非免疫分子疗法的前景
J BUON. 2010 Jan-Mar;15(1):9-18.
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Novel treatment strategies for malignant melanoma: a new beginning?恶性黑色素瘤的新型治疗策略:新的开端?
Crit Rev Oncol Hematol. 2007 Apr;62(1):16-22. doi: 10.1016/j.critrevonc.2006.11.007. Epub 2007 Jan 5.
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Chemotherapy and targeted therapy combinations in advanced melanoma.晚期黑色素瘤的化疗与靶向治疗联合方案
Clin Cancer Res. 2006 Apr 1;12(7 Pt 2):2366s-2370s. doi: 10.1158/1078-0432.CCR-05-2505.
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Metastatic melanoma: scientific rationale for sorafenib treatment and clinical results.
Onkologie. 2008 Jul;31(7):398-403. doi: 10.1159/000137714. Epub 2008 Jun 23.
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Advances in targeted therapy for unresectable melanoma: new drugs and combinations.不可切除黑色素瘤靶向治疗的进展:新药与联合治疗
Cancer Lett. 2015 Apr 1;359(1):1-8. doi: 10.1016/j.canlet.2014.12.050. Epub 2015 Jan 8.
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Management of metastatic melanoma 2005.转移性黑色素瘤的管理 2005年
Surg Oncol Clin N Am. 2006 Apr;15(2):419-37. doi: 10.1016/j.soc.2005.12.002.
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Overcoming apoptosis deficiency of melanoma-hope for new therapeutic approaches.克服黑色素瘤的凋亡缺陷——新治疗方法的希望
Drug Resist Updat. 2007 Dec;10(6):218-34. doi: 10.1016/j.drup.2007.09.001. Epub 2007 Dec 3.

引用本文的文献

1
Immunotoxins: a promising treatment modality for metastatic melanoma?免疫毒素:转移性黑色素瘤的一种有前景的治疗方式?
Ochsner J. 2010 Fall;10(3):193-9.
2
Cytotoxicity of the matrix metalloproteinase-activated anthrax lethal toxin is dependent on gelatinase expression and B-RAF status in human melanoma cells.基质金属蛋白酶激活的炭疽致死毒素的细胞毒性取决于人黑色素瘤细胞中明胶酶的表达和B-RAF状态。
Mol Cancer Ther. 2008 May;7(5):1218-26. doi: 10.1158/1535-7163.MCT-08-0024.
3
Gamma-IFN-inducible-lysosomal thiol reductase modulates acidic proteases and HLA class II antigen processing in melanoma.
γ-干扰素诱导的溶酶体硫醇还原酶调节黑色素瘤中的酸性蛋白酶和HLA II类抗原加工。
Cancer Immunol Immunother. 2008 Oct;57(10):1461-70. doi: 10.1007/s00262-008-0483-8. Epub 2008 Mar 15.
4
The Italian Network for Tumor Biotherapy (NIBIT): getting together to push the field forward.意大利肿瘤生物治疗网络(NIBIT):携手共进推动该领域发展。
J Transl Med. 2008 Feb 12;6:8. doi: 10.1186/1479-5876-6-8.