Negulescu Miruna, Deilhes Florian, Sibaud Vincent, Tournier Emilie, Lamant Laurence, Boulinguez Serge, Meyer Nicolas
aDepartment of Dermatology, Université Paul Sabatier-Toulouse III et Institut Universitaire du Cancer de Toulouse, Toulouse, France.
bDepartment of Pathology, Université Paul Sabatier-Toulouse III et Institut Universitaire du Cancer de Toulouse, Toulouse, France.
Case Rep Dermatol. 2017 Mar 21;9(1):80-85. doi: 10.1159/000461571. eCollection 2017 Jan-Apr.
The combination of MEK inhibitor (cobimetinib, trametinib) and BRAF inhibitor (vemurafenib, dabrafenib) is now the first-line treatment in patients with BRAF V600-mutated metastatic melanoma. This association reduces cutaneous adverse events induced by BRAF inhibitors alone, including photosensitivity, hand-foot syndrome, hyperkeratosis, alopecia, skin papillomas, keratoacanthomas, and squamous-cell carcinomas. While panniculitis has exceptionally been reported with BRAF inhibitors, this rare side effect has never been described with the use of MEK inhibitors. We present here the first observation of panniculitis strictly induced by MEK inhibitors. Indeed, 10 days after the initiation of combined treatment with cobimetinib and vemurafenib for metastatic melanoma, our patient developed panniculitis predominantly on the upper and lower extremities. These cutaneous nodules disappeared during cobimetinib intermissions and recurred while the molecule was resumed. Recurrence of cutaneous nodules was observed after initiation of trametinib combined with dabrafenib, and resolved once again with trametinib discontinuation. We believe that clinicians should be aware of this cutaneous adverse event in patients treated with combined therapy, which can lead to unfounded BRAF inhibitor treatment discontinuation and compromise the antitumor response. Our case suggests a class effect linked with the MEK inhibition pharmacodynamic activity. Finally, laboratory investigation and histopathological examination are mandatory to exclude other panniculitis etiologies and subcutaneous metastasis of melanoma.
MEK抑制剂(考比替尼、曲美替尼)与BRAF抑制剂(维莫非尼、达拉非尼)联合使用,现已成为BRAF V600突变转移性黑色素瘤患者的一线治疗方案。这种联合用药可减少单独使用BRAF抑制剂引起的皮肤不良事件,包括光敏反应、手足综合征、角化过度、脱发、皮肤乳头状瘤、角化棘皮瘤和鳞状细胞癌。虽然BRAF抑制剂曾罕见报道过脂膜炎,但使用MEK抑制剂从未描述过这种罕见的副作用。我们在此首次报告了由MEK抑制剂严格诱发的脂膜炎。事实上,在使用考比替尼和维莫非尼联合治疗转移性黑色素瘤开始10天后,我们的患者主要在上下肢出现了脂膜炎。这些皮肤结节在考比替尼间歇期消失,在重新使用该药物时复发。在开始使用曲美替尼联合达拉非尼后观察到皮肤结节复发,在停用曲美替尼后再次消退。我们认为临床医生应该意识到联合治疗患者中这种皮肤不良事件,这可能导致毫无根据的BRAF抑制剂治疗中断并影响抗肿瘤反应。我们的病例提示了与MEK抑制药效学活性相关的类效应。最后,必须进行实验室检查和组织病理学检查以排除其他脂膜炎病因和黑色素瘤皮下转移。