The new diagnostic criteria for myelodysplasia-related acute myeloid leukemia is useful for predicting clinical outcome: comparison of the 4th and 5th World Health Organization classifications
Mutations in myelodysplasia-related (MR) genes, rather than morphological features, have been included in the diagnostic criteria of the new 5th World Health Organization (WHO) classification for myelodysplastic syndrome (MDS)-associated acute myeloid leukemia (AML). This study compares the clinical...
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Veröffentlicht in: | Annals of hematology 2022-12, Vol.101 (12), p.2645-2654 |
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description | Mutations in myelodysplasia-related (MR) genes, rather than morphological features, have been included in the diagnostic criteria of the new 5th World Health Organization (WHO) classification for myelodysplastic syndrome (MDS)-associated acute myeloid leukemia (AML). This study compares the clinical relevance of the new criteria with those of the previous version. In a cohort of 135 patients with newly diagnosed AML, the MDS-related AML patients were classified according to the 5th and 4th edition of the WHO classification (AML, myelodysplasia-related [AML-MR
5th
] and AML with myelodysplasia-related changes [AML-MRC
4th
], respectively). The median age of the patients was 70.4 years. MR gene mutations were found in 48 patients (35.6%). Sixty-one patients (46.6%) were diagnosed with AML-MRC
4th
, while 71 patients (53.0%) were diagnosed with AML-MR
5th
. Patients with AML-MR
5th
were significantly older with significantly lower treatment response rate, higher recurrence rate, and shorter relapse-free survival after chemotherapy, whereas AML-MRC
4th
patients did not show any association with the treatment outcome. Overall, the following prognostic factors for survival were identified: age over 75 years, antecedent MDS or MDS/myeloproliferative neoplasm, chromosome 5 or 7 abnormalities, and
KRAS
and
ZSZR2
mutations. The 5th WHO classification is more useful for predicting the treatment response of patients with AML-MR than the previous version. Among the MR genes,
ZSZR2
mutations were found to be independent prognostic factors affecting survival. |
doi_str_mv | 10.1007/s00277-022-05002-7 |
format | Article |
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5th
] and AML with myelodysplasia-related changes [AML-MRC
4th
], respectively). The median age of the patients was 70.4 years. MR gene mutations were found in 48 patients (35.6%). Sixty-one patients (46.6%) were diagnosed with AML-MRC
4th
, while 71 patients (53.0%) were diagnosed with AML-MR
5th
. Patients with AML-MR
5th
were significantly older with significantly lower treatment response rate, higher recurrence rate, and shorter relapse-free survival after chemotherapy, whereas AML-MRC
4th
patients did not show any association with the treatment outcome. Overall, the following prognostic factors for survival were identified: age over 75 years, antecedent MDS or MDS/myeloproliferative neoplasm, chromosome 5 or 7 abnormalities, and
KRAS
and
ZSZR2
mutations. The 5th WHO classification is more useful for predicting the treatment response of patients with AML-MR than the previous version. Among the MR genes,
ZSZR2
mutations were found to be independent prognostic factors affecting survival.</description><identifier>ISSN: 0939-5555</identifier><identifier>EISSN: 1432-0584</identifier><identifier>DOI: 10.1007/s00277-022-05002-7</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer Berlin Heidelberg</publisher><subject>Hematology ; Leukemia ; Medical diagnosis ; Medical prognosis ; Medicine ; Medicine & Public Health ; Mutation ; Myelodysplastic syndromes ; Oncology ; Original Article</subject><ispartof>Annals of hematology, 2022-12, Vol.101 (12), p.2645-2654</ispartof><rights>The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature 2022. Springer Nature or its licensor holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c352t-661c63eeccdad5bb8e1ab787c3603198f878fa56baacfa1fb17ed164f96a9023</citedby><cites>FETCH-LOGICAL-c352t-661c63eeccdad5bb8e1ab787c3603198f878fa56baacfa1fb17ed164f96a9023</cites><orcidid>0000-0001-8128-3310</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s00277-022-05002-7$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s00277-022-05002-7$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,776,780,27901,27902,41464,42533,51294</link.rule.ids></links><search><creatorcontrib>Park, Hee Sue</creatorcontrib><creatorcontrib>Kim, Hee Kyung</creatorcontrib><creatorcontrib>Kim, Hong-sik</creatorcontrib><creatorcontrib>Yang, Yaewon</creatorcontrib><creatorcontrib>Han, Hye Sook</creatorcontrib><creatorcontrib>Lee, Ki Hyeong</creatorcontrib><creatorcontrib>Son, Bo Ra</creatorcontrib><creatorcontrib>Kwon, Jihyun</creatorcontrib><title>The new diagnostic criteria for myelodysplasia-related acute myeloid leukemia is useful for predicting clinical outcome: comparison of the 4th and 5th World Health Organization classifications</title><title>Annals of hematology</title><addtitle>Ann Hematol</addtitle><description>Mutations in myelodysplasia-related (MR) genes, rather than morphological features, have been included in the diagnostic criteria of the new 5th World Health Organization (WHO) classification for myelodysplastic syndrome (MDS)-associated acute myeloid leukemia (AML). This study compares the clinical relevance of the new criteria with those of the previous version. In a cohort of 135 patients with newly diagnosed AML, the MDS-related AML patients were classified according to the 5th and 4th edition of the WHO classification (AML, myelodysplasia-related [AML-MR
5th
] and AML with myelodysplasia-related changes [AML-MRC
4th
], respectively). The median age of the patients was 70.4 years. MR gene mutations were found in 48 patients (35.6%). Sixty-one patients (46.6%) were diagnosed with AML-MRC
4th
, while 71 patients (53.0%) were diagnosed with AML-MR
5th
. Patients with AML-MR
5th
were significantly older with significantly lower treatment response rate, higher recurrence rate, and shorter relapse-free survival after chemotherapy, whereas AML-MRC
4th
patients did not show any association with the treatment outcome. Overall, the following prognostic factors for survival were identified: age over 75 years, antecedent MDS or MDS/myeloproliferative neoplasm, chromosome 5 or 7 abnormalities, and
KRAS
and
ZSZR2
mutations. The 5th WHO classification is more useful for predicting the treatment response of patients with AML-MR than the previous version. Among the MR genes,
ZSZR2
mutations were found to be independent prognostic factors affecting survival.</description><subject>Hematology</subject><subject>Leukemia</subject><subject>Medical diagnosis</subject><subject>Medical prognosis</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Mutation</subject><subject>Myelodysplastic syndromes</subject><subject>Oncology</subject><subject>Original Article</subject><issn>0939-5555</issn><issn>1432-0584</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>BENPR</sourceid><recordid>eNp9kc1q3DAUhU1pIdOkL5CVoJtu3OjHtuzuSmiaQiCbgS7NtXQ1USpLriRTpk_XR4smLhSyqBa6Oug7lwOnqi4Z_cgolVeJUi5lTTmvaVvetXxV7VgjTrJvXlc7Ooihbss5q96m9Egp433Dd9Wf_QMSj7-ItnDwIWWriIo2Y7RATIhkPqIL-pgWB8lCHdFBRk1ArRm3T6uJw_UHzsVhE1kTmtU9e5eI2qps_YEoZ71V4EhYswozfiLlXiDaFDwJhuQSo8kPBLwmbZnfQ3Sa3CK4Iu7jAbz9DdkWWJUgyZqy7CTTRfXGgEv47u88r_Y3X_bXt_Xd_ddv15_vaiVanuuuY6oTiEpp0O009chgkr1UoqOCDb3pZW-g7SYAZYCZiUnUrGvM0MFAuTivPmxrlxh-rpjyONuk0DnwGNY0cskb3lApREHfv0Afwxp9CVco0TS8lYIVim-UiiGliGZcop0hHkdGx1On49bpWDodnzsdZTGJzZQK7A8Y_63-j-sJkDKptA</recordid><startdate>20221201</startdate><enddate>20221201</enddate><creator>Park, Hee Sue</creator><creator>Kim, Hee Kyung</creator><creator>Kim, Hong-sik</creator><creator>Yang, Yaewon</creator><creator>Han, Hye Sook</creator><creator>Lee, Ki Hyeong</creator><creator>Son, Bo Ra</creator><creator>Kwon, Jihyun</creator><general>Springer Berlin Heidelberg</general><general>Springer Nature B.V</general><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7RV</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>KB0</scope><scope>M0S</scope><scope>M1P</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0001-8128-3310</orcidid></search><sort><creationdate>20221201</creationdate><title>The new diagnostic criteria for myelodysplasia-related acute myeloid leukemia is useful for predicting clinical outcome: comparison of the 4th and 5th World Health Organization classifications</title><author>Park, Hee Sue ; Kim, Hee Kyung ; Kim, Hong-sik ; Yang, Yaewon ; Han, Hye Sook ; Lee, Ki Hyeong ; Son, Bo Ra ; Kwon, Jihyun</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c352t-661c63eeccdad5bb8e1ab787c3603198f878fa56baacfa1fb17ed164f96a9023</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Hematology</topic><topic>Leukemia</topic><topic>Medical diagnosis</topic><topic>Medical prognosis</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Mutation</topic><topic>Myelodysplastic syndromes</topic><topic>Oncology</topic><topic>Original Article</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Park, Hee Sue</creatorcontrib><creatorcontrib>Kim, Hee Kyung</creatorcontrib><creatorcontrib>Kim, Hong-sik</creatorcontrib><creatorcontrib>Yang, Yaewon</creatorcontrib><creatorcontrib>Han, Hye Sook</creatorcontrib><creatorcontrib>Lee, Ki Hyeong</creatorcontrib><creatorcontrib>Son, Bo Ra</creatorcontrib><creatorcontrib>Kwon, Jihyun</creatorcontrib><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Nursing & Allied Health Database</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Nursing & Allied Health Premium</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><jtitle>Annals of hematology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Park, Hee Sue</au><au>Kim, Hee Kyung</au><au>Kim, Hong-sik</au><au>Yang, Yaewon</au><au>Han, Hye Sook</au><au>Lee, Ki Hyeong</au><au>Son, Bo Ra</au><au>Kwon, Jihyun</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The new diagnostic criteria for myelodysplasia-related acute myeloid leukemia is useful for predicting clinical outcome: comparison of the 4th and 5th World Health Organization classifications</atitle><jtitle>Annals of hematology</jtitle><stitle>Ann Hematol</stitle><date>2022-12-01</date><risdate>2022</risdate><volume>101</volume><issue>12</issue><spage>2645</spage><epage>2654</epage><pages>2645-2654</pages><issn>0939-5555</issn><eissn>1432-0584</eissn><abstract>Mutations in myelodysplasia-related (MR) genes, rather than morphological features, have been included in the diagnostic criteria of the new 5th World Health Organization (WHO) classification for myelodysplastic syndrome (MDS)-associated acute myeloid leukemia (AML). This study compares the clinical relevance of the new criteria with those of the previous version. In a cohort of 135 patients with newly diagnosed AML, the MDS-related AML patients were classified according to the 5th and 4th edition of the WHO classification (AML, myelodysplasia-related [AML-MR
5th
] and AML with myelodysplasia-related changes [AML-MRC
4th
], respectively). The median age of the patients was 70.4 years. MR gene mutations were found in 48 patients (35.6%). Sixty-one patients (46.6%) were diagnosed with AML-MRC
4th
, while 71 patients (53.0%) were diagnosed with AML-MR
5th
. Patients with AML-MR
5th
were significantly older with significantly lower treatment response rate, higher recurrence rate, and shorter relapse-free survival after chemotherapy, whereas AML-MRC
4th
patients did not show any association with the treatment outcome. Overall, the following prognostic factors for survival were identified: age over 75 years, antecedent MDS or MDS/myeloproliferative neoplasm, chromosome 5 or 7 abnormalities, and
KRAS
and
ZSZR2
mutations. The 5th WHO classification is more useful for predicting the treatment response of patients with AML-MR than the previous version. Among the MR genes,
ZSZR2
mutations were found to be independent prognostic factors affecting survival.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer Berlin Heidelberg</pub><doi>10.1007/s00277-022-05002-7</doi><tpages>10</tpages><orcidid>https://orcid.org/0000-0001-8128-3310</orcidid></addata></record> |
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subjects | Hematology Leukemia Medical diagnosis Medical prognosis Medicine Medicine & Public Health Mutation Myelodysplastic syndromes Oncology Original Article |
title | The new diagnostic criteria for myelodysplasia-related acute myeloid leukemia is useful for predicting clinical outcome: comparison of the 4th and 5th World Health Organization classifications |
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