Department of Dermatology and Allergy, University of Bonn, Sigmund-Freud-Str. 25, Venusberg-Campus 1, 53127, Bonn, Germany.
Department of Gynecology, University of Bonn, Sigmund-Freud-Str. 25, 53127, Bonn, Germany.
Cancer Immunol Immunother. 2020 May;69(5):759-769. doi: 10.1007/s00262-020-02487-x. Epub 2020 Feb 12.
Resistance to immune checkpoint blockade and targeted therapy in melanoma patients is currently one of the major clinical challenges. With the approval of talimogene laherparepvec (T-VEC), oncolytic viruses are now in clinical practice for locally advanced or non-resectable melanoma. Here, we describe the usage of T-VEC in stage IVM1b-M1c melanoma patients, who achieved complete remission or stable disease upon systemic treatment but suffered from a loco-regional recurrence. To our knowledge, there are no case reports so far describing T-VEC as a means to overcome acquired resistance to immune checkpoint blockade or targeted therapy.
All melanoma patients in our department treated with T-VEC in the period of 2016-2018 were evaluated retrospectively. Data on clinicopathological characteristics, treatment response, and toxicity were analyzed.
Fourteen melanoma patients were treated with T-VEC in our center. Six patients (43%) received T-VEC first-line. In eight patients (57%), T-VEC followed a prior systemic therapy. Three patients with M1b stage and one patient with M1c stage melanoma were treated with T-VEC. These patients suffered from loco-regional progress, whilst distant metastases had regressed during prior systemic treatment. 64% of patients showed a benefit from therapy with T-VEC. The durable response rate was 36%.
T-VEC represents an effective and tolerable treatment option. This is true not only for loco-regionally advanced melanoma patients, but also for patients with stable or regressive systemic metastases who develop loco-regionally acquired resistance upon treatment with immune checkpoint blockade or targeted therapy. A sensible selection of suitable patients seems to be crucial.
黑色素瘤患者对免疫检查点抑制剂和靶向治疗的耐药性是目前面临的主要临床挑战之一。随着溶瘤病毒替莫唑胺拉帕替尼(T-VEC)的批准,目前已将其用于局部晚期或不可切除的黑色素瘤的临床治疗。在此,我们描述了 T-VEC 在 IVM1b-M1c 期黑色素瘤患者中的应用,这些患者在全身治疗后达到完全缓解或疾病稳定,但出现局部区域复发。据我们所知,目前尚无病例报告描述 T-VEC 可克服免疫检查点抑制剂或靶向治疗获得性耐药。
回顾性分析了 2016 年至 2018 年期间在我院接受 T-VEC 治疗的所有黑色素瘤患者。分析了临床病理特征、治疗反应和毒性。
在我院中心,有 14 名黑色素瘤患者接受了 T-VEC 治疗。6 名患者(43%)接受 T-VEC 一线治疗。8 名患者(57%)在先前的全身治疗后接受 T-VEC 治疗。3 名 M1b 期和 1 名 M1c 期黑色素瘤患者接受了 T-VEC 治疗。这些患者出现局部区域进展,而远处转移在先前的全身治疗中已经消退。64%的患者接受 T-VEC 治疗后获益。持久缓解率为 36%。
T-VEC 是一种有效且耐受良好的治疗选择。不仅对局部晚期黑色素瘤患者如此,而且对那些在接受免疫检查点抑制剂或靶向治疗后出现局部区域获得性耐药、但远处转移稳定或消退的患者也如此。对合适患者的合理选择似乎至关重要。