Tronconi Maria Chiara, Marinello Arianna, Solferino Alessandra, Grimaudo Susanna, Ciccarelli Michele, Manara Sofia, Cozzaglio Luca, Mancini Luca, Borroni Riccardo, Santoro Armando
Department of Biomedical Sciences, Humanitas University, Milan, Italy.
IRCCS Humanitas Research Hospital, Humanitas Cancer Center, Milan, Italy.
Case Rep Oncol. 2022 May 30;15(2):560-565. doi: 10.1159/000524185. eCollection 2022 May-Aug.
BRAF inhibitors (BRAFi) and MEK inhibitors (MEKi) exert a cytotoxic and immune-mediated effect on metastatic melanoma. The immune-mediated mechanism can lead to some adverse events, including panniculitis, erythema, keratitis, vitiligo-like lesions, or, more rarely, sarcoid-like skin reactions. In particular, sarcoidosis-related manifestations during melanoma treatment are characterized mainly by skin involvement and are seldom associated with chest or lymph node lesions. Overall, managing these adverse events can be very challenging from the diagnostic and therapeutic points of view. We present a case of pulmonary sarcoidosis; it is the first without skin involvement and initially only with lung presentation, diagnosed during treatment with BRAFi and MEKi for metastatic cutaneous melanoma. After about 2 years of treatment, with an oncological complete response, a histologically confirmed form of pulmonary sarcoidosis was diagnosed and initially interpreted as tumor progression. Sarcoidosis has always remained asymptomatic. After progression in the thorax and supraclavicular lymph nodes, steroid therapy with prednisone was instituted with total remission of the signs of disease. The targeted therapy has never been interrupted, and the patient still shows a complete response. This clinical case suggests that rare immune-mediated events, such as pulmonary sarcoidosis, should be considered during targeted therapy for metastatic melanoma and not only during treatment with immune checkpoint inhibitors. It also suggests that the interruption of targeted treatment should be accurately considered based on the expected risks or benefits since such immune-mediated events may have low clinical impact.
BRAF抑制剂(BRAFi)和MEK抑制剂(MEKi)对转移性黑色素瘤具有细胞毒性和免疫介导作用。免疫介导机制可导致一些不良事件,包括脂膜炎、红斑、角膜炎、白癜风样病变,或更罕见的结节病样皮肤反应。特别是,黑色素瘤治疗期间与结节病相关的表现主要以皮肤受累为特征,很少与胸部或淋巴结病变相关。总体而言,从诊断和治疗角度来看,管理这些不良事件可能非常具有挑战性。我们报告一例肺结节病病例;这是首例无皮肤受累且最初仅表现为肺部症状的病例,在使用BRAFi和MEKi治疗转移性皮肤黑色素瘤期间被诊断出来。经过约2年的治疗,达到肿瘤学完全缓解,随后诊断出组织学确诊的肺结节病形式,最初被解释为肿瘤进展。结节病一直无症状。在胸部和锁骨上淋巴结出现病变进展后,开始使用泼尼松进行类固醇治疗,疾病症状完全缓解。靶向治疗从未中断,患者仍显示完全缓解。该临床病例表明,在转移性黑色素瘤的靶向治疗期间,应考虑罕见的免疫介导事件,如肺结节病,而不仅仅是在免疫检查点抑制剂治疗期间。这也表明,应根据预期风险或益处准确考虑中断靶向治疗,因为此类免疫介导事件可能临床影响较小。