Alectinib-Induced Severe Hemolytic Anemia in a Patient with ALK-Positive Non-Small Cell Lung Cancer: A Case Report
Alectinib is a selective anaplastic lymphoma kinase (ALK) tyrosine kinase inhibitor as standard therapy for ALK-rearranged non-small cell lung cancer (NSCLC). Hemolytic anemia is considered as a rare but significant adverse event with alectinib. Here, we report a case of a 73-year-old female with lu...
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Veröffentlicht in: | OncoTargets and therapy 2023-01, Vol.16, p.65-69 |
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creator | Misawa, Kazuhito Nakamichi, Shinji Iida, Hiroki Nagano, Atsuhiro Mikami, Erika Tozuka, Takehiro Matsumoto, Masaru Miyanaga, Akihiko Noro, Rintaro Kubota, Kaoru Yamaguchi, Hiroki Seike, Masahiro |
description | Alectinib is a selective anaplastic lymphoma kinase (ALK) tyrosine kinase inhibitor as standard therapy for ALK-rearranged non-small cell lung cancer (NSCLC). Hemolytic anemia is considered as a rare but significant adverse event with alectinib. Here, we report a case of a 73-year-old female with lung adenocarcinoma, harbouring an ALK fusion gene, who received alectinib as second-line therapy and developed gradually progressive grade 4 (6.4 g/dL) drug-induced hemolytic anemia (DIHA) after complete response. We discontinued alectinib and performed a blood transfusion for the severe anemia. The anemia improved with no recurrence of lung adenocarcinoma over 10 months. Regular hematologic monitoring and the possibility of DIHA should be considered in case of progressive hemolytic anemia during alectinib treatment. |
doi_str_mv | 10.2147/OTT.S398375 |
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Hemolytic anemia is considered as a rare but significant adverse event with alectinib. Here, we report a case of a 73-year-old female with lung adenocarcinoma, harbouring an ALK fusion gene, who received alectinib as second-line therapy and developed gradually progressive grade 4 (6.4 g/dL) drug-induced hemolytic anemia (DIHA) after complete response. We discontinued alectinib and performed a blood transfusion for the severe anemia. The anemia improved with no recurrence of lung adenocarcinoma over 10 months. Regular hematologic monitoring and the possibility of DIHA should be considered in case of progressive hemolytic anemia during alectinib treatment.</description><identifier>ISSN: 1178-6930</identifier><identifier>EISSN: 1178-6930</identifier><identifier>DOI: 10.2147/OTT.S398375</identifier><identifier>PMID: 36718244</identifier><language>eng</language><publisher>New Zealand: Dove Medical Press Limited</publisher><subject>Adenocarcinoma ; Anemia ; Antimitotic agents ; Antineoplastic agents ; Blood transfusion ; Blood transfusions ; Cancer therapies ; Care and treatment ; Case Report ; Case reports ; Drug dosages ; Fusion protein ; Hemoglobin ; Hemolytic anemia ; Laboratories ; Lung cancer ; Lung cancer, Non-small cell ; Lung cancer, Small cell ; Lymphatic system ; Lymphomas ; Metastasis ; Morphology ; Non-small cell lung carcinoma ; Patients ; Protein-tyrosine kinase ; Small cell lung carcinoma ; Tomography</subject><ispartof>OncoTargets and therapy, 2023-01, Vol.16, p.65-69</ispartof><rights>2023 Misawa et al.</rights><rights>COPYRIGHT 2023 Dove Medical Press Limited</rights><rights>2023. This work is licensed under https://creativecommons.org/licenses/by-nc/3.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2023 Misawa et al. 2023 Misawa et al.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c474t-7e9a51d07b4c587aafd902f7852dde23fb513328c94c78e69e5e63d8a238a5213</citedby><cites>FETCH-LOGICAL-c474t-7e9a51d07b4c587aafd902f7852dde23fb513328c94c78e69e5e63d8a238a5213</cites><orcidid>0000-0002-4948-2245 ; 0000-0002-3774-8915 ; 0000-0003-2026-9181</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC9884059/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC9884059/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,3848,27903,27904,53770,53772</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/36718244$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Misawa, Kazuhito</creatorcontrib><creatorcontrib>Nakamichi, Shinji</creatorcontrib><creatorcontrib>Iida, Hiroki</creatorcontrib><creatorcontrib>Nagano, Atsuhiro</creatorcontrib><creatorcontrib>Mikami, Erika</creatorcontrib><creatorcontrib>Tozuka, Takehiro</creatorcontrib><creatorcontrib>Matsumoto, Masaru</creatorcontrib><creatorcontrib>Miyanaga, Akihiko</creatorcontrib><creatorcontrib>Noro, Rintaro</creatorcontrib><creatorcontrib>Kubota, Kaoru</creatorcontrib><creatorcontrib>Yamaguchi, Hiroki</creatorcontrib><creatorcontrib>Seike, Masahiro</creatorcontrib><title>Alectinib-Induced Severe Hemolytic Anemia in a Patient with ALK-Positive Non-Small Cell Lung Cancer: A Case Report</title><title>OncoTargets and therapy</title><addtitle>Onco Targets Ther</addtitle><description>Alectinib is a selective anaplastic lymphoma kinase (ALK) tyrosine kinase inhibitor as standard therapy for ALK-rearranged non-small cell lung cancer (NSCLC). Hemolytic anemia is considered as a rare but significant adverse event with alectinib. Here, we report a case of a 73-year-old female with lung adenocarcinoma, harbouring an ALK fusion gene, who received alectinib as second-line therapy and developed gradually progressive grade 4 (6.4 g/dL) drug-induced hemolytic anemia (DIHA) after complete response. We discontinued alectinib and performed a blood transfusion for the severe anemia. The anemia improved with no recurrence of lung adenocarcinoma over 10 months. Regular hematologic monitoring and the possibility of DIHA should be considered in case of progressive hemolytic anemia during alectinib treatment.</description><subject>Adenocarcinoma</subject><subject>Anemia</subject><subject>Antimitotic agents</subject><subject>Antineoplastic agents</subject><subject>Blood transfusion</subject><subject>Blood transfusions</subject><subject>Cancer therapies</subject><subject>Care and treatment</subject><subject>Case Report</subject><subject>Case reports</subject><subject>Drug dosages</subject><subject>Fusion protein</subject><subject>Hemoglobin</subject><subject>Hemolytic anemia</subject><subject>Laboratories</subject><subject>Lung cancer</subject><subject>Lung cancer, Non-small cell</subject><subject>Lung cancer, Small cell</subject><subject>Lymphatic system</subject><subject>Lymphomas</subject><subject>Metastasis</subject><subject>Morphology</subject><subject>Non-small cell lung carcinoma</subject><subject>Patients</subject><subject>Protein-tyrosine 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Hemolytic anemia is considered as a rare but significant adverse event with alectinib. Here, we report a case of a 73-year-old female with lung adenocarcinoma, harbouring an ALK fusion gene, who received alectinib as second-line therapy and developed gradually progressive grade 4 (6.4 g/dL) drug-induced hemolytic anemia (DIHA) after complete response. We discontinued alectinib and performed a blood transfusion for the severe anemia. The anemia improved with no recurrence of lung adenocarcinoma over 10 months. 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subjects | Adenocarcinoma Anemia Antimitotic agents Antineoplastic agents Blood transfusion Blood transfusions Cancer therapies Care and treatment Case Report Case reports Drug dosages Fusion protein Hemoglobin Hemolytic anemia Laboratories Lung cancer Lung cancer, Non-small cell Lung cancer, Small cell Lymphatic system Lymphomas Metastasis Morphology Non-small cell lung carcinoma Patients Protein-tyrosine kinase Small cell lung carcinoma Tomography |
title | Alectinib-Induced Severe Hemolytic Anemia in a Patient with ALK-Positive Non-Small Cell Lung Cancer: A Case Report |
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