Successful treatment of methotrexate-associated classical Hodgkin lymphoma with brentuximab vedotin-combined chemotherapy: a case series

Methotrexate (MTX)-associated classical Hodgkin lymphoma (CHL) is unlikely to regress following discontinuation of MTX, and its treatment usually requires chemotherapy. Standard chemotherapy for CHL is the ABVD regimen, which contains pneumotoxic bleomycin. This can be problematic in MTX–CHL patient...

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Veröffentlicht in:International journal of hematology 2020-05, Vol.111 (5), p.667-672
Hauptverfasser: Ichikawa, Satoshi, Fukuhara, Noriko, Saito, Kei, Onodera, Koichi, Shirai, Tsuyoshi, Onishi, Yasushi, Yokoyama, Hisayuki, Fujii, Hiroshi, Ichinohasama, Ryo, Harigae, Hideo
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container_issue 5
container_start_page 667
container_title International journal of hematology
container_volume 111
creator Ichikawa, Satoshi
Fukuhara, Noriko
Saito, Kei
Onodera, Koichi
Shirai, Tsuyoshi
Onishi, Yasushi
Yokoyama, Hisayuki
Fujii, Hiroshi
Ichinohasama, Ryo
Harigae, Hideo
description Methotrexate (MTX)-associated classical Hodgkin lymphoma (CHL) is unlikely to regress following discontinuation of MTX, and its treatment usually requires chemotherapy. Standard chemotherapy for CHL is the ABVD regimen, which contains pneumotoxic bleomycin. This can be problematic in MTX–CHL patients suffering from an autoimmune disease (AID), such as rheumatoid arthritis (RA), as they frequently have pulmonary complications. However, brentuximab vedotin (BV)-containing chemotherapy without bleomycin (A + AVD regimen) was recently reported to show favorable efficacy for CHL, and could therefore be beneficial in MTX–CHL. We treated three cases of MTX–CHL using the A + AVD regimen. All were female and had received MTX for more than 15 years. Underlying AIDs in these patients were RA in two patients, and overlap syndrome with systemic lupus erythematosus and dermatomyositis in one patient. The A + AVD regimen resulted in a complete response in all patients. Peripheral neuropathy developed in two patients, necessitating reduction of the BV dose. All three patients experienced hematological toxicity necessitating dose reduction; however, no severe adverse effects, including infection or pulmonary complication, were documented. RA was well-controlled without additional immunosuppressants. The A + AVD regimen is a promising chemotherapy for MTX–CHL with favorable efficacy and tolerable toxicity profiles.
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Standard chemotherapy for CHL is the ABVD regimen, which contains pneumotoxic bleomycin. This can be problematic in MTX–CHL patients suffering from an autoimmune disease (AID), such as rheumatoid arthritis (RA), as they frequently have pulmonary complications. However, brentuximab vedotin (BV)-containing chemotherapy without bleomycin (A + AVD regimen) was recently reported to show favorable efficacy for CHL, and could therefore be beneficial in MTX–CHL. We treated three cases of MTX–CHL using the A + AVD regimen. All were female and had received MTX for more than 15 years. Underlying AIDs in these patients were RA in two patients, and overlap syndrome with systemic lupus erythematosus and dermatomyositis in one patient. The A + AVD regimen resulted in a complete response in all patients. Peripheral neuropathy developed in two patients, necessitating reduction of the BV dose. 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All three patients experienced hematological toxicity necessitating dose reduction; however, no severe adverse effects, including infection or pulmonary complication, were documented. RA was well-controlled without additional immunosuppressants. 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Standard chemotherapy for CHL is the ABVD regimen, which contains pneumotoxic bleomycin. This can be problematic in MTX–CHL patients suffering from an autoimmune disease (AID), such as rheumatoid arthritis (RA), as they frequently have pulmonary complications. However, brentuximab vedotin (BV)-containing chemotherapy without bleomycin (A + AVD regimen) was recently reported to show favorable efficacy for CHL, and could therefore be beneficial in MTX–CHL. We treated three cases of MTX–CHL using the A + AVD regimen. All were female and had received MTX for more than 15 years. Underlying AIDs in these patients were RA in two patients, and overlap syndrome with systemic lupus erythematosus and dermatomyositis in one patient. The A + AVD regimen resulted in a complete response in all patients. Peripheral neuropathy developed in two patients, necessitating reduction of the BV dose. All three patients experienced hematological toxicity necessitating dose reduction; however, no severe adverse effects, including infection or pulmonary complication, were documented. RA was well-controlled without additional immunosuppressants. The A + AVD regimen is a promising chemotherapy for MTX–CHL with favorable efficacy and tolerable toxicity profiles.</abstract><cop>Singapore</cop><pub>Springer Singapore</pub><pmid>31955346</pmid><doi>10.1007/s12185-020-02822-z</doi><tpages>6</tpages><orcidid>https://orcid.org/0000-0003-3163-7197</orcidid></addata></record>
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subjects Antineoplastic Combined Chemotherapy Protocols - therapeutic use
Arthritis
Autoimmune diseases
Bleomycin
Bleomycin - administration & dosage
Brentuximab Vedotin - administration & dosage
Chemotherapy
Chronic conditions
Complications
Dermatomyositis
Female
Health services
Hematology
Hodgkin Disease - chemically induced
Hodgkin Disease - drug therapy
Hodgkin's lymphoma
Humans
Immunosuppressive agents
Immunotherapy
Lymphoma
Medicine
Medicine & Public Health
Methotrexate
Methotrexate - adverse effects
Monoclonal antibodies
Oncology
Original Article
Peripheral neuropathy
Reduction
Rheumatoid arthritis
Systemic lupus erythematosus
Targeted cancer therapy
Toxicity
Treatment Outcome
title Successful treatment of methotrexate-associated classical Hodgkin lymphoma with brentuximab vedotin-combined chemotherapy: a case series
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