Department of Dermatology, Hôpital Cochin, AP-HP.
Paris Descartes University.
Melanoma Res. 2020 Jun;30(3):317-320. doi: 10.1097/CMR.0000000000000649.
Combined BRAF and MEK inhibition is one of the first-line treatment strategies for patients with advanced BRAF-mutant melanoma. Sarcoid-like reactions (SLRs) have occasionally been described with melanoma systemic treatments such as immunotherapy or the BRAF inhibitor vemurafenib, but very few cases have been reported with dabrafenib and trametinib. Our aim was to better characterize SLR induced by this combination. We conducted a monocentric retrospective observational study among patients treated with dabrafenib and trametinib for BRAF-mutant advanced melanoma from January 2015 to March 2019. Patients presenting with histologically proven SLR were included. We also searched Medline database for all reported cases of SLR induced by targeted therapy. Of 63 patients on dabrafenib/trametinib combination, seven were diagnosed with a SLR. They all had specific cutaneous involvement, and one also displayed mediastinal and salivary glands involvement. None required systemic corticosteroids or dabrafenib/trametinib discontinuation. Three of them (43%) reached melanoma complete remission and are still on targeted therapy; and four patients progressed and died. A literature review yielded 22 additional cases of SLR induced by targeted therapy: the main affected organ was the skin, 11 patients (50%) had systemic involvement, five patients (23%) required systemic corticosteroids to reach partial or complete remission of SLR, 12 (55%) reached partial or complete response of melanoma while six (27%) progressed. BRAF and MEK inhibitors are potential triggers of SLR, although pathological mechanisms remain unclear. The mainstay of treatment is systemic or topical corticotherapy; targeted therapy discontinuation is usually not necessary.
联合 BRAF 和 MEK 抑制是治疗晚期 BRAF 突变型黑色素瘤患者的一线治疗策略之一。肉瘤样反应 (SLR) 偶尔在黑色素瘤全身治疗中描述,如免疫治疗或 BRAF 抑制剂 vemurafenib,但很少有报道涉及 dabrafenib 和 trametinib。我们的目的是更好地描述这种联合用药引起的 SLR。我们对 2015 年 1 月至 2019 年 3 月期间接受 dabrafenib 和 trametinib 治疗的 BRAF 突变型晚期黑色素瘤患者进行了一项单中心回顾性观察性研究。纳入了组织学证实为 SLR 的患者。我们还在 Medline 数据库中搜索了所有报道的靶向治疗引起的 SLR 病例。在接受 dabrafenib/trametinib 联合治疗的 63 例患者中,有 7 例被诊断为 SLR。他们都有特定的皮肤受累,1 例还显示纵隔和唾液腺受累。无一例需要全身皮质类固醇或 dabrafenib/trametinib 停药。其中 3 例(43%)达到黑色素瘤完全缓解,仍在接受靶向治疗;4 例患者进展并死亡。文献复习还获得了 22 例由靶向治疗引起的 SLR 额外病例:主要受累器官为皮肤,11 例(50%)有全身受累,5 例(23%)需要全身皮质类固醇治疗以达到 SLR 的部分或完全缓解,12 例(55%)达到黑色素瘤的部分或完全缓解,6 例(27%)进展。BRAF 和 MEK 抑制剂是 SLR 的潜在触发因素,尽管病理机制尚不清楚。治疗的主要方法是全身或局部皮质激素治疗;通常不需要停止靶向治疗。