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凡德他尼治疗引起的光敏反应后的皮肤色素沉着。

Cutaneous pigmentation after photosensitivity induced by vandetanib therapy.

作者信息

Kong Heidi H, Fine Howard A, Stern Jere B, Turner Maria L Chanco

机构信息

Dermatology Branch, Center for Cancer Research, National Cancer Institute, Bldg 10, Room 12N238, 10 Center Dr, Bethesda, MD 20892, USA.

出版信息

Arch Dermatol. 2009 Aug;145(8):923-5. doi: 10.1001/archdermatol.2009.177.

DOI:10.1001/archdermatol.2009.177
PMID:19687425
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3521518/
Abstract

BACKGROUND

Photosensitivity has been reported in patients who were treated with vandetanib (ZD6474), an inhibitor of epidermal growth factor receptor, vascular endothelial growth factor receptor, and the RET (rearranged during transfection) kinases.

OBSERVATIONS

We describe the occurrence of cutaneous hyperpigmentation after photosensitivity in 2 patients who were treated with vandetanib. The pigmentation patterns were variable within and between patients. Biopsy specimens from different sites revealed variability in Perls and Fontana staining patterns.

CONCLUSIONS

These 2 cases highlight the unusual occurrence of cutaneous hyperpigmentation after vandetanib-associated photosensitivity, a reaction that demonstrates that medications are important causes of acquired photosensitivity and hyperpigmentation. Aggressive photoprotection may facilitate the resolution of diffuse hyperpigmentation. Dermatologists should endeavor to identify and report novel cutaneous adverse effects as new targeted therapies are developed.

摘要

背景

有报道称,接受凡德他尼(ZD6474)治疗的患者出现了光敏反应。凡德他尼是一种表皮生长因子受体、血管内皮生长因子受体和RET(转染期间重排)激酶的抑制剂。

观察结果

我们描述了2例接受凡德他尼治疗的患者在出现光敏反应后发生皮肤色素沉着过度的情况。患者内部和患者之间的色素沉着模式各不相同。不同部位的活检标本显示普鲁士蓝染色和Fontana染色模式存在差异。

结论

这2例病例突出了凡德他尼相关光敏反应后出现皮肤色素沉着过度这一不寻常情况,这种反应表明药物是获得性光敏反应和色素沉着过度的重要原因。积极的光防护可能有助于弥漫性色素沉着过度的消退。随着新的靶向治疗方法的开发,皮肤科医生应努力识别和报告新的皮肤不良反应。

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本文引用的文献

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A randomized, double-blind, phase IIa dose-finding study of Vandetanib (ZD6474) in Japanese patients with non-small cell lung cancer.凡德他尼(ZD6474)在日本非小细胞肺癌患者中进行的一项随机、双盲、IIa期剂量探索研究。
J Thorac Oncol. 2008 Apr;3(4):386-93. doi: 10.1097/JTO.0b013e318168d228.
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Randomized, placebo-controlled phase II study of vandetanib plus docetaxel in previously treated non small-cell lung cancer.凡德他尼联合多西他赛用于既往治疗过的非小细胞肺癌的随机、安慰剂对照II期研究。
J Clin Oncol. 2007 Sep 20;25(27):4270-7. doi: 10.1200/JCO.2006.10.5122.
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A phase I dose-escalation study of ZD6474 in Japanese patients with solid, malignant tumors.ZD6474在日本实体恶性肿瘤患者中的I期剂量递增研究。
J Thorac Oncol. 2006 Nov;1(9):1002-9.
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The effects of ZD6474, an inhibitor of VEGF signaling, on cutaneous wound healing in mice.VEGF信号通路抑制剂ZD6474对小鼠皮肤伤口愈合的影响。
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Cutaneous side-effects of kinase inhibitors and blocking antibodies.激酶抑制剂和阻断抗体的皮肤副作用。
Lancet Oncol. 2005 Jul;6(7):491-500. doi: 10.1016/S1470-2045(05)70243-6.
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Drug-induced skin pigmentation. Epidemiology, diagnosis and treatment.药物性皮肤色素沉着。流行病学、诊断与治疗。
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