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Phase II study of nab-paclitaxel and bevacizumab as first-line therapy for patients with unresectable stage III and IV melanoma.nab-紫杉醇联合贝伐珠单抗一线治疗不可切除 III 期和 IV 期黑色素瘤的 II 期研究。
Am J Clin Oncol. 2015 Feb;38(1):61-7. doi: 10.1097/COC.0b013e318287bbae.
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A dose-escalation and signal-generating study of the immunocytokine L19-IL2 in combination with dacarbazine for the therapy of patients with metastatic melanoma.一种免疫细胞因子 L19-IL2 与达卡巴嗪联合用于治疗转移性黑色素瘤患者的剂量递增和信号产生研究。
Clin Cancer Res. 2011 Dec 15;17(24):7732-42. doi: 10.1158/1078-0432.CCR-11-1203. Epub 2011 Oct 25.
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The novel gamma secretase inhibitor RO4929097 reduces the tumor initiating potential of melanoma.新型γ-分泌酶抑制剂 RO4929097 降低了黑色素瘤的肿瘤起始能力。
PLoS One. 2011;6(9):e25264. doi: 10.1371/journal.pone.0025264. Epub 2011 Sep 29.
4
Overexpression of Notch ligand Dll1 in B16 melanoma cells leads to reduced tumor growth due to attenuated vascularization.Notch 配体 Dll1 在 B16 黑色素瘤细胞中的过表达导致肿瘤生长减少,这是由于血管生成减弱所致。
Cancer Lett. 2011 Oct 28;309(2):220-7. doi: 10.1016/j.canlet.2011.06.008. Epub 2011 Jun 24.
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A randomised, phase II study of intetumumab, an anti-αv-integrin mAb, alone and with dacarbazine in stage IV melanoma.一项关于 intetumumab(一种抗 αv-整联蛋白 mAb)单药及联合达卡巴嗪治疗 IV 期黑色素瘤的随机、II 期研究。
Br J Cancer. 2011 Jul 26;105(3):346-52. doi: 10.1038/bjc.2011.183. Epub 2011 Jul 12.
6
Ipilimumab plus dacarbazine for previously untreated metastatic melanoma.依匹单抗联合达卡巴嗪治疗未经治疗的转移性黑色素瘤。
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7
Improved survival with vemurafenib in melanoma with BRAF V600E mutation.BRAF V600E 突变型黑色素瘤患者采用威罗菲尼治疗后生存改善。
N Engl J Med. 2011 Jun 30;364(26):2507-16. doi: 10.1056/NEJMoa1103782. Epub 2011 Jun 5.
8
Extended schedule, escalated dose temozolomide versus dacarbazine in stage IV melanoma: final results of a randomised phase III study (EORTC 18032).扩展方案、递增剂量替莫唑胺与达卡巴嗪治疗 IV 期黑色素瘤:一项随机 III 期研究(EORTC 18032)的最终结果。
Eur J Cancer. 2011 Jul;47(10):1476-83. doi: 10.1016/j.ejca.2011.04.030. Epub 2011 May 18.
9
A phase II trial of nab-paclitaxel (ABI-007) and carboplatin in patients with unresectable stage IV melanoma : a North Central Cancer Treatment Group Study, N057E(1).一项nab-紫杉醇(ABI-007)联合卡铂治疗不可切除的 IV 期黑色素瘤的 II 期临床试验:一项美国北部肿瘤协作组研究,N057E(1)。
Cancer. 2011 Apr 15;117(8):1704-10. doi: 10.1002/cncr.25659. Epub 2010 Nov 8.
10
Temozolomide chemoresistance heterogeneity in melanoma with different treatment regimens: DNA damage accumulation contribution.不同治疗方案下黑色素瘤中替莫唑胺化疗耐药异质性:DNA 损伤积累的贡献。
Melanoma Res. 2011 Jun;21(3):206-16. doi: 10.1097/CMR.0b013e328345af95.

晚期皮肤恶性黑色素瘤的化学治疗。

Chemotherapy in the management of advanced cutaneous malignant melanoma.

机构信息

Department of Medicine, Melanoma and Sarcoma Service, Memorial Sloan-Kettering Cancer Center, New York, NY 10065, USA.

出版信息

Clin Dermatol. 2013 May-Jun;31(3):290-7. doi: 10.1016/j.clindermatol.2012.08.016.

DOI:10.1016/j.clindermatol.2012.08.016
PMID:23608448
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3709980/
Abstract

The recent past has witnessed unprecedented clinical progress in the treatment of advanced malignant melanoma through targeting of mutant BRAF in approximately 50% of patients and immune check point blockade in all patients. As has been well documented, responses to targeted therapy are of limited duration, and rates of clinical benefit to immunotherapy are modest. Given these factors, palliation of patients with chemotherapy remains an essential aspect of melanoma oncology. Many chemotherapeutics (and combinations with other agents, such as immunotherapy) have been evaluated in melanoma, although no chemotherapy regimen has been documented to provide an overall survival benefit in a prospective, randomized, well-controlled phase III study. We provide an overview of the development of the most common chemotherapy regimens for melanoma, discuss the clinical trial evidence supporting and contrasting them, and highlight appropriate clinical situations in which they might be used. We also discuss the future of chemotherapy for melanoma, noting the potential for combinations of chemotherapy with either targeted or immunotherapeutic agents.

摘要

近年来,通过针对大约 50%的患者的突变 BRAF 和所有患者的免疫检查点阻断,在治疗晚期恶性黑色素瘤方面取得了前所未有的临床进展。正如已有充分记录的那样,靶向治疗的反应持续时间有限,免疫治疗的临床获益率也较低。鉴于这些因素,化疗缓解患者的病情仍然是黑色素瘤肿瘤学的一个重要方面。已经评估了许多化疗药物(以及与其他药物的联合治疗,如免疫治疗)在黑色素瘤中的应用,尽管没有一种化疗方案在前瞻性、随机、对照的 III 期研究中被证明能提供总体生存获益。我们提供了黑色素瘤最常见化疗方案的发展概述,讨论了支持和对比它们的临床试验证据,并强调了在适当的临床情况下使用它们的情况。我们还讨论了化疗治疗黑色素瘤的未来,指出化疗与靶向或免疫治疗药物联合应用的潜力。