Single administration of avelumab induced a complete response in thyroid transcription factor 1‐positive combined Merkel cell carcinoma
Merkel cell carcinoma (MCC) is an aggressive neoplasm and patients with metastasis have poor survival outcomes. Recently, avelumab, an anti‐programmed death ligand 1 (PD‐L1) immune checkpoint inhibitor, was approved for first‐line treatment in patients with metastatic MCC. While the administration i...
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Veröffentlicht in: | Journal of dermatology 2020-11, Vol.47 (11), p.1317-1321 |
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creator | Kanemaru, Hisashi Fukushima, Satoshi Mizukami, Yukari Sawamura, Soichiro Nakamura, Kayo Honda, Noritoshi Makino, Katsunari Kajihara, Ikko Aoi, Jun Makino, Takamitsu Kawasaki, Takeshi Kudou, Erina Jhono, Masayoshi Ito, Takaaki Arima, Nobuyuki Ihn, Hironobu |
description | Merkel cell carcinoma (MCC) is an aggressive neoplasm and patients with metastasis have poor survival outcomes. Recently, avelumab, an anti‐programmed death ligand 1 (PD‐L1) immune checkpoint inhibitor, was approved for first‐line treatment in patients with metastatic MCC. While the administration interval of avelumab is every 2 weeks, the durable effect of a single administration of avelumab is unknown. Additionally, the effect of avelumab in pure MCC or combined MCC concurrent with non‐MCC histology has not been fully elucidated. Herein, we report a case of combined MCC concurrent with squamous cell carcinoma; the patient had a complete response after a single administration of avelumab. Although the levels of avelumab were outside the detection limit within 12 weeks, a remarkable efficacy remained for more than 28 weeks after administration. Immunohistochemical analyses revealed that the expression of PD‐L1 and Merkel cell polyomavirus large T antigen was almost negative or only partial in the primary tumor lesion of this patient. Conversely, thyroid transcription factor 1 (TTF‐1) expression was positive in the primary MCC lesion, which is consistent with a previous report that combined MCC is positive for TTF‐1 expression. In conclusion, this case study presents a rare case of TTF‐1‐positive combined MCC showing complete response after a single administration of avelumab. |
doi_str_mv | 10.1111/1346-8138.15543 |
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Recently, avelumab, an anti‐programmed death ligand 1 (PD‐L1) immune checkpoint inhibitor, was approved for first‐line treatment in patients with metastatic MCC. While the administration interval of avelumab is every 2 weeks, the durable effect of a single administration of avelumab is unknown. Additionally, the effect of avelumab in pure MCC or combined MCC concurrent with non‐MCC histology has not been fully elucidated. Herein, we report a case of combined MCC concurrent with squamous cell carcinoma; the patient had a complete response after a single administration of avelumab. Although the levels of avelumab were outside the detection limit within 12 weeks, a remarkable efficacy remained for more than 28 weeks after administration. Immunohistochemical analyses revealed that the expression of PD‐L1 and Merkel cell polyomavirus large T antigen was almost negative or only partial in the primary tumor lesion of this patient. Conversely, thyroid transcription factor 1 (TTF‐1) expression was positive in the primary MCC lesion, which is consistent with a previous report that combined MCC is positive for TTF‐1 expression. In conclusion, this case study presents a rare case of TTF‐1‐positive combined MCC showing complete response after a single administration of avelumab.</description><identifier>ISSN: 0385-2407</identifier><identifier>EISSN: 1346-8138</identifier><identifier>DOI: 10.1111/1346-8138.15543</identifier><identifier>PMID: 32794263</identifier><language>eng</language><publisher>England: Wiley Subscription Services, Inc</publisher><subject>Antibodies, Monoclonal ; Antibodies, Monoclonal, Humanized ; anti‐programmed death ligand 1 inhibitor ; Apoptosis ; avelumab ; Carcinoma, Merkel Cell - drug therapy ; Case reports ; Humans ; immune checkpoint inhibitor ; Immune checkpoint inhibitors ; Immunotherapy ; Merkel cell carcinoma ; Metastases ; Monoclonal antibodies ; PD-L1 protein ; Skin cancer ; Skin Neoplasms - drug therapy ; Squamous cell carcinoma ; Targeted cancer therapy ; Thyroid gland ; Thyroid Nuclear Factor 1 ; Thyroid transcription factor 1 ; Transcription factors</subject><ispartof>Journal of dermatology, 2020-11, Vol.47 (11), p.1317-1321</ispartof><rights>2020 Japanese Dermatological Association</rights><rights>2020 Japanese Dermatological Association.</rights><rights>Copyright © 2020 Japanese Dermatological Association</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c4153-1cc229dfefc6f33dbc80782379f3e7044355c89f17935f763aabde1ace31429b3</cites><orcidid>0000-0002-0988-2471 ; 0000-0003-1697-9316 ; 0000-0002-0622-7682 ; 0000-0002-3080-1621 ; 0000-0002-4422-2049 ; 0000-0003-3725-6213</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2F1346-8138.15543$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2F1346-8138.15543$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32794263$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kanemaru, Hisashi</creatorcontrib><creatorcontrib>Fukushima, Satoshi</creatorcontrib><creatorcontrib>Mizukami, Yukari</creatorcontrib><creatorcontrib>Sawamura, Soichiro</creatorcontrib><creatorcontrib>Nakamura, Kayo</creatorcontrib><creatorcontrib>Honda, Noritoshi</creatorcontrib><creatorcontrib>Makino, Katsunari</creatorcontrib><creatorcontrib>Kajihara, Ikko</creatorcontrib><creatorcontrib>Aoi, Jun</creatorcontrib><creatorcontrib>Makino, Takamitsu</creatorcontrib><creatorcontrib>Kawasaki, Takeshi</creatorcontrib><creatorcontrib>Kudou, Erina</creatorcontrib><creatorcontrib>Jhono, Masayoshi</creatorcontrib><creatorcontrib>Ito, Takaaki</creatorcontrib><creatorcontrib>Arima, Nobuyuki</creatorcontrib><creatorcontrib>Ihn, Hironobu</creatorcontrib><title>Single administration of avelumab induced a complete response in thyroid transcription factor 1‐positive combined Merkel cell carcinoma</title><title>Journal of dermatology</title><addtitle>J Dermatol</addtitle><description>Merkel cell carcinoma (MCC) is an aggressive neoplasm and patients with metastasis have poor survival outcomes. Recently, avelumab, an anti‐programmed death ligand 1 (PD‐L1) immune checkpoint inhibitor, was approved for first‐line treatment in patients with metastatic MCC. While the administration interval of avelumab is every 2 weeks, the durable effect of a single administration of avelumab is unknown. Additionally, the effect of avelumab in pure MCC or combined MCC concurrent with non‐MCC histology has not been fully elucidated. Herein, we report a case of combined MCC concurrent with squamous cell carcinoma; the patient had a complete response after a single administration of avelumab. Although the levels of avelumab were outside the detection limit within 12 weeks, a remarkable efficacy remained for more than 28 weeks after administration. Immunohistochemical analyses revealed that the expression of PD‐L1 and Merkel cell polyomavirus large T antigen was almost negative or only partial in the primary tumor lesion of this patient. Conversely, thyroid transcription factor 1 (TTF‐1) expression was positive in the primary MCC lesion, which is consistent with a previous report that combined MCC is positive for TTF‐1 expression. In conclusion, this case study presents a rare case of TTF‐1‐positive combined MCC showing complete response after a single administration of avelumab.</description><subject>Antibodies, Monoclonal</subject><subject>Antibodies, Monoclonal, Humanized</subject><subject>anti‐programmed death ligand 1 inhibitor</subject><subject>Apoptosis</subject><subject>avelumab</subject><subject>Carcinoma, Merkel Cell - drug therapy</subject><subject>Case reports</subject><subject>Humans</subject><subject>immune checkpoint inhibitor</subject><subject>Immune checkpoint inhibitors</subject><subject>Immunotherapy</subject><subject>Merkel cell carcinoma</subject><subject>Metastases</subject><subject>Monoclonal antibodies</subject><subject>PD-L1 protein</subject><subject>Skin cancer</subject><subject>Skin Neoplasms - drug therapy</subject><subject>Squamous cell carcinoma</subject><subject>Targeted cancer therapy</subject><subject>Thyroid gland</subject><subject>Thyroid Nuclear Factor 1</subject><subject>Thyroid transcription factor 1</subject><subject>Transcription factors</subject><issn>0385-2407</issn><issn>1346-8138</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkT1v1TAUhi0EopfCzIYssbCkjX3sG2dEpXypVQdgthznGFwSO9hJ0d1Y2fiN_SU4vaUDSz3Y0vHzPjrSS8hzVh-xco4ZiG2lGKgjJqWAB2RzN3lINjUoWXFRNwfkSc6Xdc1byerH5AB40wq-hQ35_cmHrwNS048--DwnM_sYaHTUXOGwjKajPvSLxZ4aauM4DTgjTZinGDKWPzp_26Xoe1qiIdvkpxuBM3aOibLrX3-mmP3sr3CNdz4U0zmm7zhQi0O5TLI-xNE8JY-cGTI-u30PyZe3p59P3ldnF-8-nLw-q6xgEipmLedt79DZrQPoO6vqRnFoWgfY1EKAlFa1jjUtSNdswZiuR2YsAhO87eCQvNp7pxR_LJhnPfq8rmICxiVrLkAIJTi0BX35H3oZlxTKdoWSjWIcVFOo4z1lU8w5odNT8qNJO81qvbak10702om-aakkXtx6l27E_o7_V0sB5B746Qfc3efTH9-c7sV_AYAvnwI</recordid><startdate>202011</startdate><enddate>202011</enddate><creator>Kanemaru, Hisashi</creator><creator>Fukushima, Satoshi</creator><creator>Mizukami, Yukari</creator><creator>Sawamura, Soichiro</creator><creator>Nakamura, Kayo</creator><creator>Honda, Noritoshi</creator><creator>Makino, Katsunari</creator><creator>Kajihara, Ikko</creator><creator>Aoi, Jun</creator><creator>Makino, Takamitsu</creator><creator>Kawasaki, Takeshi</creator><creator>Kudou, Erina</creator><creator>Jhono, Masayoshi</creator><creator>Ito, Takaaki</creator><creator>Arima, Nobuyuki</creator><creator>Ihn, Hironobu</creator><general>Wiley Subscription Services, Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7T5</scope><scope>H94</scope><scope>K9.</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-0988-2471</orcidid><orcidid>https://orcid.org/0000-0003-1697-9316</orcidid><orcidid>https://orcid.org/0000-0002-0622-7682</orcidid><orcidid>https://orcid.org/0000-0002-3080-1621</orcidid><orcidid>https://orcid.org/0000-0002-4422-2049</orcidid><orcidid>https://orcid.org/0000-0003-3725-6213</orcidid></search><sort><creationdate>202011</creationdate><title>Single administration of avelumab induced a complete response in thyroid transcription factor 1‐positive combined Merkel cell carcinoma</title><author>Kanemaru, Hisashi ; 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Recently, avelumab, an anti‐programmed death ligand 1 (PD‐L1) immune checkpoint inhibitor, was approved for first‐line treatment in patients with metastatic MCC. While the administration interval of avelumab is every 2 weeks, the durable effect of a single administration of avelumab is unknown. Additionally, the effect of avelumab in pure MCC or combined MCC concurrent with non‐MCC histology has not been fully elucidated. Herein, we report a case of combined MCC concurrent with squamous cell carcinoma; the patient had a complete response after a single administration of avelumab. Although the levels of avelumab were outside the detection limit within 12 weeks, a remarkable efficacy remained for more than 28 weeks after administration. Immunohistochemical analyses revealed that the expression of PD‐L1 and Merkel cell polyomavirus large T antigen was almost negative or only partial in the primary tumor lesion of this patient. Conversely, thyroid transcription factor 1 (TTF‐1) expression was positive in the primary MCC lesion, which is consistent with a previous report that combined MCC is positive for TTF‐1 expression. In conclusion, this case study presents a rare case of TTF‐1‐positive combined MCC showing complete response after a single administration of avelumab.</abstract><cop>England</cop><pub>Wiley Subscription Services, Inc</pub><pmid>32794263</pmid><doi>10.1111/1346-8138.15543</doi><tpages>5</tpages><orcidid>https://orcid.org/0000-0002-0988-2471</orcidid><orcidid>https://orcid.org/0000-0003-1697-9316</orcidid><orcidid>https://orcid.org/0000-0002-0622-7682</orcidid><orcidid>https://orcid.org/0000-0002-3080-1621</orcidid><orcidid>https://orcid.org/0000-0002-4422-2049</orcidid><orcidid>https://orcid.org/0000-0003-3725-6213</orcidid></addata></record> |
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subjects | Antibodies, Monoclonal Antibodies, Monoclonal, Humanized anti‐programmed death ligand 1 inhibitor Apoptosis avelumab Carcinoma, Merkel Cell - drug therapy Case reports Humans immune checkpoint inhibitor Immune checkpoint inhibitors Immunotherapy Merkel cell carcinoma Metastases Monoclonal antibodies PD-L1 protein Skin cancer Skin Neoplasms - drug therapy Squamous cell carcinoma Targeted cancer therapy Thyroid gland Thyroid Nuclear Factor 1 Thyroid transcription factor 1 Transcription factors |
title | Single administration of avelumab induced a complete response in thyroid transcription factor 1‐positive combined Merkel cell carcinoma |
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