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Long-term response to avelumab and management of oligoprogression in Merkel cell carcinoma: A case report

BACKGROUND: Merkel cell carcinoma (MCC) is a rare and aggressive cutaneous neuroendocrine neoplasia, with high risk of recurrence and metastasis and poor survival. Immune checkpoint inhibitors, like the anti-programmed death-ligand 1 agent avelumab, were recently approved for the treatment of advanc...

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Autores principales: Leão, Inês, Marinho, Joana, Costa, Telma
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Baishideng Publishing Group Inc 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8223835/
https://www.ncbi.nlm.nih.gov/pubmed/34222455
http://dx.doi.org/10.12998/wjcc.v9.i18.4829
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author Leão, Inês
Marinho, Joana
Costa, Telma
author_facet Leão, Inês
Marinho, Joana
Costa, Telma
author_sort Leão, Inês
collection PubMed
description BACKGROUND: Merkel cell carcinoma (MCC) is a rare and aggressive cutaneous neuroendocrine neoplasia, with high risk of recurrence and metastasis and poor survival. Immune checkpoint inhibitors, like the anti-programmed death-ligand 1 agent avelumab, were recently approved for the treatment of advanced MCC. We, herein, report the first case of advanced MCC with oligoprogression managed with avelumab and local radical treatment. CASE SUMMARY: A 61-year-old man was presented to the hospital with sporadic fever and an exudative malodorous mass (10 cm of diameter), located on the right gluteal region. The final diagnosis was MCC, cT4N3M1c (AJCC, TNM staging 8(th) edition, 2017), with invasion of adjacent muscle, in-transit metastasis, and bone lesions. Patient started chemotherapy (cisplatin and etoposide), and after six cycles, the main tumor increased, evidencing disease progression. Two months later, the patient started second line treatment with avelumab (under an early access program). After two cycles of treatment, the lesion started to decrease, achieving a major response. Local progression was documented after 16 cycles. However, as the tumor became resectable, salvage surgery was performed, while keeping the systemic treatment with avelumab. Since the patient developed bilateral pneumonia, immunotherapy was suspended. More than 2.5 years after surgery (last 19 mo without systemic therapy), the patient maintains complete local response and stable bone lesions. CONCLUSION: This report highlights the efficacy and long-term response of avelumab on the management of a chemotherapy resistant advanced MCC, with evidence of oligoprogression, in combination with local radical treatment.
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spelling pubmed-82238352021-07-02 Long-term response to avelumab and management of oligoprogression in Merkel cell carcinoma: A case report Leão, Inês Marinho, Joana Costa, Telma World J Clin Cases Case Report BACKGROUND: Merkel cell carcinoma (MCC) is a rare and aggressive cutaneous neuroendocrine neoplasia, with high risk of recurrence and metastasis and poor survival. Immune checkpoint inhibitors, like the anti-programmed death-ligand 1 agent avelumab, were recently approved for the treatment of advanced MCC. We, herein, report the first case of advanced MCC with oligoprogression managed with avelumab and local radical treatment. CASE SUMMARY: A 61-year-old man was presented to the hospital with sporadic fever and an exudative malodorous mass (10 cm of diameter), located on the right gluteal region. The final diagnosis was MCC, cT4N3M1c (AJCC, TNM staging 8(th) edition, 2017), with invasion of adjacent muscle, in-transit metastasis, and bone lesions. Patient started chemotherapy (cisplatin and etoposide), and after six cycles, the main tumor increased, evidencing disease progression. Two months later, the patient started second line treatment with avelumab (under an early access program). After two cycles of treatment, the lesion started to decrease, achieving a major response. Local progression was documented after 16 cycles. However, as the tumor became resectable, salvage surgery was performed, while keeping the systemic treatment with avelumab. Since the patient developed bilateral pneumonia, immunotherapy was suspended. More than 2.5 years after surgery (last 19 mo without systemic therapy), the patient maintains complete local response and stable bone lesions. CONCLUSION: This report highlights the efficacy and long-term response of avelumab on the management of a chemotherapy resistant advanced MCC, with evidence of oligoprogression, in combination with local radical treatment. Baishideng Publishing Group Inc 2021-06-26 2021-06-26 /pmc/articles/PMC8223835/ /pubmed/34222455 http://dx.doi.org/10.12998/wjcc.v9.i18.4829 Text en ©The Author(s) 2021. Published by Baishideng Publishing Group Inc. All rights reserved. https://creativecommons.org/licenses/by-nc/4.0/This article is an open-access article which was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial.
spellingShingle Case Report
Leão, Inês
Marinho, Joana
Costa, Telma
Long-term response to avelumab and management of oligoprogression in Merkel cell carcinoma: A case report
title Long-term response to avelumab and management of oligoprogression in Merkel cell carcinoma: A case report
title_full Long-term response to avelumab and management of oligoprogression in Merkel cell carcinoma: A case report
title_fullStr Long-term response to avelumab and management of oligoprogression in Merkel cell carcinoma: A case report
title_full_unstemmed Long-term response to avelumab and management of oligoprogression in Merkel cell carcinoma: A case report
title_short Long-term response to avelumab and management of oligoprogression in Merkel cell carcinoma: A case report
title_sort long-term response to avelumab and management of oligoprogression in merkel cell carcinoma: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8223835/
https://www.ncbi.nlm.nih.gov/pubmed/34222455
http://dx.doi.org/10.12998/wjcc.v9.i18.4829
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