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dc.contributor.authorMiller, M.
dc.contributor.authorKim, N.H.
dc.contributor.authorThosani, M.K.
dc.contributor.authorMoser, J.C.
dc.date.accessioned2024-03-22T17:35:25Z
dc.date.available2024-03-22T17:35:25Z
dc.date.issued2023-06-13
dc.identifier.citationMax 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/10.1159/000530851
dc.identifier.issn1662-6567
dc.identifier.doi10.1159/000530851
dc.identifier.urihttp://hdl.handle.net/10150/671741
dc.description.abstractA 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).
dc.language.isoen
dc.publisherS. Karger AG
dc.rights© 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).
dc.rights.urihttps://creativecommons.org/licenses/by-nc/4.0/
dc.subjectCase report
dc.subjectImmunotherapy
dc.subjectOrgan transplant recipient
dc.subjectTalimogene laherparepvec
dc.subjectTransplant associated squamous cell carcinoma
dc.titleUse of Talimogene Laherparepvec to Treat Cutaneous Squamous Cell Carcinoma in a Renal Transplant Patient
dc.typeArticle
dc.typetext
dc.contributor.departmentUniversity of Arizona, College of Medicine - Phoenix
dc.identifier.journalCase Reports in Dermatology
dc.description.noteOpen access journal
dc.description.collectioninformationThis 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.
dc.eprint.versionFinal Published Version
dc.source.journaltitleCase Reports in Dermatology
refterms.dateFOA2024-03-22T17:35:25Z


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© 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).
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).