Quaresmini Davide, Di Lauro Alessandra, Fucci Livia, Strippoli Sabino, De Risi Ivana, Sciacovelli Angela Monica, Albano Anna, Achille Gaetano, Montepara Massimo, Russo Sabino, Tassone Gabriella, Guida Michele
Rare Tumors and Melanoma Unit, IRCCS Istituto Tumori Giovanni Paolo II, Bari, Italy.
Otolaryngology Unit, IRCCS Istituto Tumori Giovanni Paolo II, Bari, Italy.
Front Oncol. 2021 Sep 16;11:742666. doi: 10.3389/fonc.2021.742666. eCollection 2021.
Immunotherapy with immune checkpoint inhibitors is one of the main therapies for advanced melanoma. Nevertheless, albeit remarkable, immunotherapy results are still unsatisfactory as more than half of patients progress, and resistance to treatment still has a dramatic impact on clinical outcomes. Local treatments such as radiotherapy or electrochemotherapy (ECT), in addition to local control with palliative intent, have been shown to release tumoral neoantigens that can stimulate a robust systemic antitumor immune response.
We report the case of a patient with multiple nodular melanoma lesions of the scalp initially treated with local ECT. Soon after the procedure, multiple new lesions appeared close to the treated ones, therefore the patient started a systemic treatment with the anti-PD-1 nivolumab. The lesions of the scalp did not respond to immunotherapy, presenting a loco-regional spreading. To control the bleeding and painful lesions, we performed a second ECT, while continuing systemic immunotherapy. The treated lesions responded to the second procedure, while the other lesions continued progressing in number and dimension. Unexpectedly, after 2 months from the second ECT, the patient presented a progressive shrinkage of both treated and untreated lesions until complete remission. Concomitantly, he developed immune-related adverse events including grade 4 thyroid toxicity, grade 2 vitiligo-like depigmentation and grade 2 pemphigoid. At present, after 18 months from the first ECT and 14 months from the starting of anti-PD-1 immunotherapy, the patient is in good clinical condition and complete remission of disease still persists.
This case highlights the potential role of ECT in increasing tumor immunogenicity and consequently in inducing a powerful immune response overcoming primary resistance to checkpoint inhibitor immunotherapy.
免疫检查点抑制剂免疫疗法是晚期黑色素瘤的主要治疗方法之一。然而,尽管免疫疗法效果显著,但仍不尽人意,因为超过一半的患者病情进展,治疗耐药性仍对临床结果产生重大影响。除了以姑息治疗为目的的局部控制外,放疗或电化学疗法(ECT)等局部治疗已被证明可释放肿瘤新抗原,从而刺激强大的全身抗肿瘤免疫反应。
我们报告了一例头皮多发结节性黑色素瘤患者,最初接受局部ECT治疗。治疗后不久,在治疗部位附近出现了多个新病灶,因此患者开始使用抗PD-1纳武单抗进行全身治疗。头皮病灶对免疫疗法无反应,出现局部区域扩散。为了控制出血和疼痛性病灶,我们在继续全身免疫治疗的同时进行了第二次ECT。治疗后的病灶对第二次治疗有反应,而其他病灶在数量和大小上继续进展。出乎意料的是,在第二次ECT治疗2个月后,患者的治疗和未治疗病灶均逐渐缩小,直至完全缓解。与此同时,他出现了免疫相关不良事件,包括4级甲状腺毒性、2级白癜风样色素脱失和2级类天疱疮。目前,在首次ECT治疗18个月和开始抗PD-1免疫治疗14个月后,患者临床状况良好,疾病仍处于完全缓解状态。
本病例突出了ECT在增加肿瘤免疫原性方面的潜在作用,从而诱导强大的免疫反应,克服对检查点抑制剂免疫疗法的原发性耐药。