Use of Talimogene Laherparepvec to Treat Cutaneous Squamous Cell Carcinoma in a Renal Transplant Patient
Affiliation
University of Arizona, College of Medicine - PhoenixIssue Date
2023-06-13Keywords
Case reportImmunotherapy
Organ transplant recipient
Talimogene laherparepvec
Transplant associated squamous cell carcinoma
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S. Karger AGCitation
Max Miller, Nancy H Kim, Maya K Thosani, Justin C Moser; Use of Talimogene Laherparepvec to Treat Cutaneous Squamous Cell Carcinoma in a Renal Transplant Patient. Case Rep Dermatol 21 December 2023; 15 (1): 99–104. https://doi.org/10.1159/000530851Journal
Case Reports in DermatologyRights
© 2023 The Author(s). Published by S. Karger AG, Basel. This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License (CC BY-NC).Collection Information
This item from the UA Faculty Publications collection is made available by the University of Arizona with support from the University of Arizona Libraries. If you have questions, please contact us at repository@u.library.arizona.edu.Abstract
A 66-year-old female with a history of two renal transplants due to recurrent thrombotic thrombocytopenic purpura presented to clinic with multiple lesions identified to be non-metastatic cutaneous squamous cell carcinoma (CSCC). The patient previously underwent multiple Mohs procedures and radiation therapy treatment but continued to develop CSCC lesions with increasing frequency. After discussing multiple treatment options, it was elected to pursue treatment with Talimogene laherparepvec (T-VEC) given the systemic immune responses it can cause, with low theoretical risk of graft rejection. After starting intratumoral T-VEC injections, treated lesions began to decrease in size, and a reduction in the rate of new CSCC lesions was observed. Treatment was held due to unrelated renal complications during which time new CSCCs developed. Patient was restarted on T-VEC therapy with no recurrent renal issues. Upon reinitiating treatment, injected and non-injected lesions showed reduction in size, and the development of new lesions again ceased. One injected lesion was resected via Mohs micrographic surgery due to its size and discomfort. On sectioning, this demonstrated an exuberant lymphocytic perivascular infiltrate which was consistent with treatment response to T-VEC, with little active tumor. With high rates of non-melanoma skin cancer in renal transplant patients, their transplant status significantly limits treatment options, specifically with regards to anti-PD-1 therapy. This case suggests T-VEC can generate local and systemic immune responses in the setting of immunosuppression and that T-VEC may be a beneficial therapeutic option for transplant patients with CSCC. © 2023 The Author(s).Note
Open access journalISSN
1662-6567Version
Final Published Versionae974a485f413a2113503eed53cd6c53
10.1159/000530851
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Except where otherwise noted, this item's license is described as © 2023 The Author(s). Published by S. Karger AG, Basel. This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License (CC BY-NC).

