T-VEC和咪喹莫特联合免疫疗法成功治疗了转移性黑色素瘤。

IF 10.3 1区 医学 Q1 IMMUNOLOGY
Marisa Lenga, Esther Choi, Jeffrey Sosman, Sunandana Chandra, Danielle Lam, Kirsten Johnson, Lauren Schiemann, Jennifer Choi
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引用次数: 0

摘要

恶性黑色素瘤的转移是一项重大的临床挑战,尤其是对有全身治疗禁忌症的患者而言。虽然手术切除和全身免疫疗法仍是标准治疗方法,但局部疗法,如能刺激肿瘤特异性T细胞反应的鞘内talimogene laherparepvec(T-VEC)和局部咪喹莫特,因其潜在的疗效和耐受性而日益受到关注。虽然这些疗法的单独疗效已得到充分证实,但它们的联合使用及其协同效应却没有得到充分证实。本病例系列报告了2018年11月至2023年5月期间,西北纪念医院采用T-VEC和咪喹莫特治疗的5例转移中黑色素瘤患者。患者在中位 6 个月(5-9 个月)内接受了 13 次(8-20 次)T-VEC 注射,其中 4 个月同时使用 T-VEC 和咪喹莫特乳膏。五名患者中有四名在疗程结束时获得了完全应答(CR)。一名患者在治疗期间出现全身性进展,导致治疗提前结束。所有获得 CR 的患者都选择在 T-VEC 治疗后继续局部应用咪喹莫特作为维持治疗,中位时间为 6 个月(2-14 个月)。四名获得 CR 的患者中只有一人在最后一次注射 T-VEC 10 个月后出现了转移性结节病。其他三名患者在最后一次注射 T-VEC 2-57 个月后均未出现皮肤和全身疾病。所有患者都能很好地耐受治疗,没有患者因副作用而中断治疗。这些研究结果表明,鞘内注射 T-VEC 和外用咪喹莫特可以有效、安全地治疗恶性黑色素瘤的转移灶。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Successful treatment of in-transit metastatic melanoma with combination intralesional T-VEC and topical imiquimod immunotherapy.

In-transit metastases of malignant melanoma pose a significant clinical challenge, particularly in patients with contraindications to systemic therapies. While surgical excision and systemic immunotherapies remain standard treatments, localized therapies such as intralesional talimogene laherparepvec (T-VEC) and topical imiquimod, which stimulate tumor-specific T-cell responses, have garnered increasing attention for their potential efficacy and tolerability. Although the individual efficacy of these therapies is well-documented, their combined use and their synergistic effects have not been well-documented. This case series reports on five patients with in-transit melanoma metastases treated with T-VEC and imiquimod at Northwestern Memorial Hospital from November 2018 to May 2023. Patients received a median of 13 (range 8-20) T-VEC injections over a median of 6 months (range 5-9), of which 4 of those months were with concurrent T-VEC and imiquimod cream. Four of the five patients achieved complete response (CR) by the end of the treatment course. One patient developed systemic progression during therapy, leading to early cessation of treatment. All patients with CR elected to continue topical imiquimod applications as maintenance following T-VEC for a median of 6 months (range 2-14 months). Only one of the four patients who achieved CR developed metastatic nodal disease 10 months after the last T-VEC injection. The three other patients are free of cutaneous and systemic disease 2-57 months after their last injection. All patients tolerated treatment well with zero patients discontinuing treatment due to side effects. These findings suggest that the combination of intralesional T-VEC and topical imiquimod can be an effective and safe treatment of in-transit metastases of malignant melanoma.

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来源期刊
Journal for Immunotherapy of Cancer
Journal for Immunotherapy of Cancer Biochemistry, Genetics and Molecular Biology-Molecular Medicine
CiteScore
17.70
自引率
4.60%
发文量
522
审稿时长
18 weeks
期刊介绍: The Journal for ImmunoTherapy of Cancer (JITC) is a peer-reviewed publication that promotes scientific exchange and deepens knowledge in the constantly evolving fields of tumor immunology and cancer immunotherapy. With an open access format, JITC encourages widespread access to its findings. The journal covers a wide range of topics, spanning from basic science to translational and clinical research. Key areas of interest include tumor-host interactions, the intricate tumor microenvironment, animal models, the identification of predictive and prognostic immune biomarkers, groundbreaking pharmaceutical and cellular therapies, innovative vaccines, combination immune-based treatments, and the study of immune-related toxicity.
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