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肿瘤性黑变病模拟替莫唑胺治疗后残留黑色素瘤。

Tumoral melanosis mimicking residual melanoma in the setting of talimogene laherparepvec treatment.

机构信息

Division of Dermatology, Department of Medicine, University of Washington, Seattle, Washington, USA.

Department of Laboratory Medicine and Pathology, University of Washington, Seattle, Washington, USA.

出版信息

J Immunother Cancer. 2022 Oct;10(10). doi: 10.1136/jitc-2022-005257.

Abstract

Talimogene laherparepvec (T-VEC) has become an increasingly popular treatment option for surgically non-resectable, recurrent melanoma, usually of cutaneous metastases. The complete response (CR) rate has been reported to be ~20% with a median of ~9 months to achieve it. In real-world practice, decrease of tumor size often occurs rapidly within the first 2-3 months, while improvement of the pigmentation takes several more months. Such clinical observation of lasting pigmentation could be explained by tumorous melanosis-a histopathological term referring to the presence of a melanophage-rich inflammatory infiltrate without remaining viable tumor cells. Herein, we report six patients with metastatic cutaneous melanoma who were treated with T-VEC. Biopsies were performed after observing clinical responses in the injected tumors. Pathological evaluation demonstrated non-viable or absent tumor tissue with tumorous melanosis in all cases. To accurately assess response to therapy and potentially decrease unnecessary additional T-VEC treatments, serial biopsy of 'stable' lesions should be considered to assess the presence or absence of viable tumor.

摘要

替莫唑胺(T-VEC)已成为手术不可切除、复发性黑色素瘤的一种越来越受欢迎的治疗选择,通常为皮肤转移。据报道,完全缓解(CR)率约为 20%,中位时间约为 9 个月。在实际实践中,肿瘤大小的缩小通常在最初的 2-3 个月内迅速发生,而色素沉着的改善则需要更多的几个月。这种持久色素沉着的临床观察可以用瘤性黑色素沉着来解释,这是一个组织病理学术语,指的是存在富含噬黑素细胞的炎症浸润,而没有存活的肿瘤细胞。在此,我们报告了 6 例接受 T-VEC 治疗的转移性皮肤黑色素瘤患者。在观察到注射肿瘤的临床反应后进行了活检。所有病例的病理评估均显示无存活或不存在肿瘤组织,伴有瘤性黑色素沉着。为了准确评估治疗反应并可能减少不必要的额外 T-VEC 治疗,应考虑对“稳定”病变进行连续活检,以评估是否存在存活肿瘤。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5a72/9621191/d2750ae6d439/jitc-2022-005257f01.jpg

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