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首页> 外文期刊>Melanoma research >Severe skin toxicity with organ damage under the combination of targeted therapy following immunotherapy in metastatic melanoma
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Severe skin toxicity with organ damage under the combination of targeted therapy following immunotherapy in metastatic melanoma

机译:在转移性黑色素瘤中的靶向治疗组合下对器官损伤的严重皮肤毒性

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Targeted therapy combination (TTC: antiRAF+antiMEK) is known to improve metastatic melanoma survival. Few severe skin toxicities (grade 3) are described with first-line TTC (17% for vemurafenib+cobimetinib and none for dabrafenib+trametinib) in a phase III trial. Among our 42 patients treated by TTC between January 2014 and March 2017, 4.8% (2/42) of those treated in the first line presented severe skin rash versus 19% (8/42) of patients treated in the second line after previous immunotherapy. In particular, we observed one case of Stevens-Johnson syndrome and four cases of severe drug reaction with eosinophilia and systemic symptoms syndrome under TTC in patients who had received immunotherapy previously. Thus, previous immunotherapy appears to play an important role in the skin rash onset and severity induced by TTC.
机译:已知有针对性的治疗组合(TTC:抗替氏+ antimek)改善转移性黑色素瘤生存率。 在III期试验中,用一线TTC(vemurafenib + cobimetinib和DabrafeNib + Trametinib的17%,描述了很少的严重皮肤毒性(3级)。 在2014年1月至2017年1月至2017年3月间的TTC治疗的42名患者中,第一行待遇的4.8%(2/42)患者呈现严重的皮疹,并且在先前的免疫疗法后在第二行患者治疗的患者的19%(8/42) 。 特别是,我们观察了史蒂文森综合征的一个例子和与先前接受免疫疗法的TTC下的TTC下与嗜酸性粒细胞症和全身症状综合征的四种情况。 因此,先前的免疫疗法似乎在TTC诱导的皮疹发作和严重程度中起重要作用。

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