Loading…
An analysis of 97 previously diagnosed de novo adult acute erythroid leukemia patients following the 2016 revision to World Health Organization classification
The incidence of acute erythroid leukemia subtype (AEL) is rare, accounting for 5% of cases of acute myeloid leukemia (AML), and the outcome is dismal. However, in 2016 revision to the WHO classification, the subcategory of AEL has been removed. Myeloblasts are redefined as the percentage of total m...
Saved in:
Published in: | BMC cancer 2017-08, Vol.17 (1), p.534-534, Article 534 |
---|---|
Main Authors: | , , , , , , , , , , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | cdi_FETCH-LOGICAL-c691t-70b127baa711e29203cac1273ef2221588f5885e57b5fce3d3d142986834190c3 |
---|---|
cites | cdi_FETCH-LOGICAL-c691t-70b127baa711e29203cac1273ef2221588f5885e57b5fce3d3d142986834190c3 |
container_end_page | 534 |
container_issue | 1 |
container_start_page | 534 |
container_title | BMC cancer |
container_volume | 17 |
creator | Qiu, Shaowei Jiang, Erlie Wei, Hui Lin, Dong Zhang, Guangji Wei, Shuning Zhou, Chunlin Liu, Kaiqi Wang, Ying Liu, Bingcheng Liu, Yuntao Gong, Benfa Gong, Xiaoyuan Feng, Sizhou Mi, Yingchang Han, Mingzhe Wang, Jianxiang |
description | The incidence of acute erythroid leukemia subtype (AEL) is rare, accounting for 5% of cases of acute myeloid leukemia (AML), and the outcome is dismal. However, in 2016 revision to the WHO classification, the subcategory of AEL has been removed. Myeloblasts are redefined as the percentage of total marrow cells, not non-erythroid cells. Therefore, the previously diagnosed AEL cases are currently diagnosed as AML or myelodyspalstic syndrome (MDS) according to new criteria.
We respectively reviewed cases of 97 de novo previously diagnosed AEL and all the patients were diagnosed as AML or MDS according to the new classification scheme, and then the clinical characteristics of these two subtypes were compared. Statistical analyses were performed by SPSS software version 18.0.
The median age was 37 years-old, the two-thirds of previous AEL cases were diagnosed as MDS, and there was no obvious difference between two subtypes except for male/female ratio and age. Cytogenetic, rather than MDS/AML subtypes, can better represent the prognostic factor of previously diagnosed AEL patients. When the cytogenetic risk of patients belonged to MRC intermediate category and age were below 40 years-old in previous AEL cases, the patients who received induction chemotherapy without transplantation had a similar survival compared with the patients who underwent transplantation (3-year OS: 67.2% vs 68.5%).
Cytogenetic, rather than MDS/AML subtypes, can better represent the prognostic factor of previously diagnosed AEL patients. Transplantation was a better choice for those whose cytogenetic category was unfavorable. |
doi_str_mv | 10.1186/s12885-017-3528-6 |
format | article |
fullrecord | <record><control><sourceid>gale_doaj_</sourceid><recordid>TN_cdi_doaj_primary_oai_doaj_org_article_e77db0d0b8114d19aa8410ff4b39ac10</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><galeid>A511262645</galeid><doaj_id>oai_doaj_org_article_e77db0d0b8114d19aa8410ff4b39ac10</doaj_id><sourcerecordid>A511262645</sourcerecordid><originalsourceid>FETCH-LOGICAL-c691t-70b127baa711e29203cac1273ef2221588f5885e57b5fce3d3d142986834190c3</originalsourceid><addsrcrecordid>eNptkt-K1DAUxoso7rr6AN5IQBC96JqkTZPeCMOi7sDCgn_wMqRJ2smaScYkHR0fxmc1nVnXqUgJbU9-3xdyzlcUTxE8R4g1ryPCjJESIlpWBLOyuVecopqiEteQ3j_6PikexXgDM8gge1icYEbbilFyWvxaOCCcsLtoIvA9aCnYBL01fox2B5QRg_NRK6A0cH7rgVCjTUDIMWmgwy6tgjcKWD1-1WsjwEYko12KoPfW-u_GDSCtNMAQNWCyjcY7kDz44oNV4FILm1bgOgzCmZ9ZmjelFTGa3sj97-PiQS9s1E9u32fF53dvP11cllfX75cXi6tSNi1KJYUdwrQTgiKkcYthJYXMlUr3GGNEGOvzIprQjvRSV6pSqMYta1hVoxbK6qxYHnyVFzd8E8xahB33wvB9wYeBi5CMtJprSlUHFewYQrVCrRCsRrDv665q86Ewe705eG3Gbq2VzP0Iws5M5zvOrPjgt5wQAlvWZoOXtwbBfxt1THxtotTWCqfzXDhqMWUVxIRl9Pk_6I0fQ57nRFV1kwNSk7_UIPIFjOt9PldOpnxBEMINbvbU-X-o_Kg8Wumd7k2uzwSvZoLMJP0jDWKMkS8_fpizL47Y1X7w0dtxGnKcg-gAyuBjDLq_axyCfEo9P6Se5zDzKfW8yZpnxx2_U_yJefUbzcz7_Q</addsrcrecordid><sourcetype>Open Website</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1934612845</pqid></control><display><type>article</type><title>An analysis of 97 previously diagnosed de novo adult acute erythroid leukemia patients following the 2016 revision to World Health Organization classification</title><source>Publicly Available Content Database</source><source>PubMed Central</source><creator>Qiu, Shaowei ; Jiang, Erlie ; Wei, Hui ; Lin, Dong ; Zhang, Guangji ; Wei, Shuning ; Zhou, Chunlin ; Liu, Kaiqi ; Wang, Ying ; Liu, Bingcheng ; Liu, Yuntao ; Gong, Benfa ; Gong, Xiaoyuan ; Feng, Sizhou ; Mi, Yingchang ; Han, Mingzhe ; Wang, Jianxiang</creator><creatorcontrib>Qiu, Shaowei ; Jiang, Erlie ; Wei, Hui ; Lin, Dong ; Zhang, Guangji ; Wei, Shuning ; Zhou, Chunlin ; Liu, Kaiqi ; Wang, Ying ; Liu, Bingcheng ; Liu, Yuntao ; Gong, Benfa ; Gong, Xiaoyuan ; Feng, Sizhou ; Mi, Yingchang ; Han, Mingzhe ; Wang, Jianxiang</creatorcontrib><description>The incidence of acute erythroid leukemia subtype (AEL) is rare, accounting for 5% of cases of acute myeloid leukemia (AML), and the outcome is dismal. However, in 2016 revision to the WHO classification, the subcategory of AEL has been removed. Myeloblasts are redefined as the percentage of total marrow cells, not non-erythroid cells. Therefore, the previously diagnosed AEL cases are currently diagnosed as AML or myelodyspalstic syndrome (MDS) according to new criteria.
We respectively reviewed cases of 97 de novo previously diagnosed AEL and all the patients were diagnosed as AML or MDS according to the new classification scheme, and then the clinical characteristics of these two subtypes were compared. Statistical analyses were performed by SPSS software version 18.0.
The median age was 37 years-old, the two-thirds of previous AEL cases were diagnosed as MDS, and there was no obvious difference between two subtypes except for male/female ratio and age. Cytogenetic, rather than MDS/AML subtypes, can better represent the prognostic factor of previously diagnosed AEL patients. When the cytogenetic risk of patients belonged to MRC intermediate category and age were below 40 years-old in previous AEL cases, the patients who received induction chemotherapy without transplantation had a similar survival compared with the patients who underwent transplantation (3-year OS: 67.2% vs 68.5%).
Cytogenetic, rather than MDS/AML subtypes, can better represent the prognostic factor of previously diagnosed AEL patients. Transplantation was a better choice for those whose cytogenetic category was unfavorable.</description><identifier>ISSN: 1471-2407</identifier><identifier>EISSN: 1471-2407</identifier><identifier>DOI: 10.1186/s12885-017-3528-6</identifier><identifier>PMID: 28793875</identifier><language>eng</language><publisher>England: BioMed Central Ltd</publisher><subject>Acute erythroid leukemia ; Acute myelocytic leukemia ; Acute myeloid leukemia ; Adolescent ; Adult ; Aged ; Biomarkers ; Blood ; Bone marrow ; Bone Marrow - pathology ; Care and treatment ; Chemotherapy ; Child ; Classification ; Combined Modality Therapy ; Cytogenetic Analysis ; Cytogenetics ; Diagnosis ; Diagnosis, Differential ; DNA Mutational Analysis ; Erythroid cells ; Female ; Humans ; Leukemia ; Leukemia, Erythroblastic, Acute - diagnosis ; Leukemia, Erythroblastic, Acute - mortality ; Leukemia, Erythroblastic, Acute - therapy ; Leukemia, Myeloid, Acute - diagnosis ; Male ; Medical prognosis ; Middle Aged ; Multivariate analysis ; Mutation ; Myelodyspalstic syndrome ; Myelodysplastic syndrome ; Myelodysplastic Syndromes - diagnosis ; Myeloid leukemia ; Practice Guidelines as Topic ; Prognosis ; Retrospective Studies ; Stem cells ; Survival Analysis ; Transplantation ; World Health Organization ; Young Adult</subject><ispartof>BMC cancer, 2017-08, Vol.17 (1), p.534-534, Article 534</ispartof><rights>COPYRIGHT 2017 BioMed Central Ltd.</rights><rights>Copyright BioMed Central 2017</rights><rights>The Author(s). 2017</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c691t-70b127baa711e29203cac1273ef2221588f5885e57b5fce3d3d142986834190c3</citedby><cites>FETCH-LOGICAL-c691t-70b127baa711e29203cac1273ef2221588f5885e57b5fce3d3d142986834190c3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5550989/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/1934612845?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25753,27924,27925,37012,37013,44590,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28793875$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Qiu, Shaowei</creatorcontrib><creatorcontrib>Jiang, Erlie</creatorcontrib><creatorcontrib>Wei, Hui</creatorcontrib><creatorcontrib>Lin, Dong</creatorcontrib><creatorcontrib>Zhang, Guangji</creatorcontrib><creatorcontrib>Wei, Shuning</creatorcontrib><creatorcontrib>Zhou, Chunlin</creatorcontrib><creatorcontrib>Liu, Kaiqi</creatorcontrib><creatorcontrib>Wang, Ying</creatorcontrib><creatorcontrib>Liu, Bingcheng</creatorcontrib><creatorcontrib>Liu, Yuntao</creatorcontrib><creatorcontrib>Gong, Benfa</creatorcontrib><creatorcontrib>Gong, Xiaoyuan</creatorcontrib><creatorcontrib>Feng, Sizhou</creatorcontrib><creatorcontrib>Mi, Yingchang</creatorcontrib><creatorcontrib>Han, Mingzhe</creatorcontrib><creatorcontrib>Wang, Jianxiang</creatorcontrib><title>An analysis of 97 previously diagnosed de novo adult acute erythroid leukemia patients following the 2016 revision to World Health Organization classification</title><title>BMC cancer</title><addtitle>BMC Cancer</addtitle><description>The incidence of acute erythroid leukemia subtype (AEL) is rare, accounting for 5% of cases of acute myeloid leukemia (AML), and the outcome is dismal. However, in 2016 revision to the WHO classification, the subcategory of AEL has been removed. Myeloblasts are redefined as the percentage of total marrow cells, not non-erythroid cells. Therefore, the previously diagnosed AEL cases are currently diagnosed as AML or myelodyspalstic syndrome (MDS) according to new criteria.
We respectively reviewed cases of 97 de novo previously diagnosed AEL and all the patients were diagnosed as AML or MDS according to the new classification scheme, and then the clinical characteristics of these two subtypes were compared. Statistical analyses were performed by SPSS software version 18.0.
The median age was 37 years-old, the two-thirds of previous AEL cases were diagnosed as MDS, and there was no obvious difference between two subtypes except for male/female ratio and age. Cytogenetic, rather than MDS/AML subtypes, can better represent the prognostic factor of previously diagnosed AEL patients. When the cytogenetic risk of patients belonged to MRC intermediate category and age were below 40 years-old in previous AEL cases, the patients who received induction chemotherapy without transplantation had a similar survival compared with the patients who underwent transplantation (3-year OS: 67.2% vs 68.5%).
Cytogenetic, rather than MDS/AML subtypes, can better represent the prognostic factor of previously diagnosed AEL patients. Transplantation was a better choice for those whose cytogenetic category was unfavorable.</description><subject>Acute erythroid leukemia</subject><subject>Acute myelocytic leukemia</subject><subject>Acute myeloid leukemia</subject><subject>Adolescent</subject><subject>Adult</subject><subject>Aged</subject><subject>Biomarkers</subject><subject>Blood</subject><subject>Bone marrow</subject><subject>Bone Marrow - pathology</subject><subject>Care and treatment</subject><subject>Chemotherapy</subject><subject>Child</subject><subject>Classification</subject><subject>Combined Modality Therapy</subject><subject>Cytogenetic Analysis</subject><subject>Cytogenetics</subject><subject>Diagnosis</subject><subject>Diagnosis, Differential</subject><subject>DNA Mutational Analysis</subject><subject>Erythroid cells</subject><subject>Female</subject><subject>Humans</subject><subject>Leukemia</subject><subject>Leukemia, Erythroblastic, Acute - diagnosis</subject><subject>Leukemia, Erythroblastic, Acute - mortality</subject><subject>Leukemia, Erythroblastic, Acute - therapy</subject><subject>Leukemia, Myeloid, Acute - diagnosis</subject><subject>Male</subject><subject>Medical prognosis</subject><subject>Middle Aged</subject><subject>Multivariate analysis</subject><subject>Mutation</subject><subject>Myelodyspalstic syndrome</subject><subject>Myelodysplastic syndrome</subject><subject>Myelodysplastic Syndromes - diagnosis</subject><subject>Myeloid leukemia</subject><subject>Practice Guidelines as Topic</subject><subject>Prognosis</subject><subject>Retrospective Studies</subject><subject>Stem cells</subject><subject>Survival Analysis</subject><subject>Transplantation</subject><subject>World Health Organization</subject><subject>Young Adult</subject><issn>1471-2407</issn><issn>1471-2407</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNptkt-K1DAUxoso7rr6AN5IQBC96JqkTZPeCMOi7sDCgn_wMqRJ2smaScYkHR0fxmc1nVnXqUgJbU9-3xdyzlcUTxE8R4g1ryPCjJESIlpWBLOyuVecopqiEteQ3j_6PikexXgDM8gge1icYEbbilFyWvxaOCCcsLtoIvA9aCnYBL01fox2B5QRg_NRK6A0cH7rgVCjTUDIMWmgwy6tgjcKWD1-1WsjwEYko12KoPfW-u_GDSCtNMAQNWCyjcY7kDz44oNV4FILm1bgOgzCmZ9ZmjelFTGa3sj97-PiQS9s1E9u32fF53dvP11cllfX75cXi6tSNi1KJYUdwrQTgiKkcYthJYXMlUr3GGNEGOvzIprQjvRSV6pSqMYta1hVoxbK6qxYHnyVFzd8E8xahB33wvB9wYeBi5CMtJprSlUHFewYQrVCrRCsRrDv665q86Ewe705eG3Gbq2VzP0Iws5M5zvOrPjgt5wQAlvWZoOXtwbBfxt1THxtotTWCqfzXDhqMWUVxIRl9Pk_6I0fQ57nRFV1kwNSk7_UIPIFjOt9PldOpnxBEMINbvbU-X-o_Kg8Wumd7k2uzwSvZoLMJP0jDWKMkS8_fpizL47Y1X7w0dtxGnKcg-gAyuBjDLq_axyCfEo9P6Se5zDzKfW8yZpnxx2_U_yJefUbzcz7_Q</recordid><startdate>20170809</startdate><enddate>20170809</enddate><creator>Qiu, Shaowei</creator><creator>Jiang, Erlie</creator><creator>Wei, Hui</creator><creator>Lin, Dong</creator><creator>Zhang, Guangji</creator><creator>Wei, Shuning</creator><creator>Zhou, Chunlin</creator><creator>Liu, Kaiqi</creator><creator>Wang, Ying</creator><creator>Liu, Bingcheng</creator><creator>Liu, Yuntao</creator><creator>Gong, Benfa</creator><creator>Gong, Xiaoyuan</creator><creator>Feng, Sizhou</creator><creator>Mi, Yingchang</creator><creator>Han, Mingzhe</creator><creator>Wang, Jianxiang</creator><general>BioMed Central Ltd</general><general>BioMed Central</general><general>BMC</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>ISR</scope><scope>3V.</scope><scope>7TO</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>H94</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20170809</creationdate><title>An analysis of 97 previously diagnosed de novo adult acute erythroid leukemia patients following the 2016 revision to World Health Organization classification</title><author>Qiu, Shaowei ; Jiang, Erlie ; Wei, Hui ; Lin, Dong ; Zhang, Guangji ; Wei, Shuning ; Zhou, Chunlin ; Liu, Kaiqi ; Wang, Ying ; Liu, Bingcheng ; Liu, Yuntao ; Gong, Benfa ; Gong, Xiaoyuan ; Feng, Sizhou ; Mi, Yingchang ; Han, Mingzhe ; Wang, Jianxiang</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c691t-70b127baa711e29203cac1273ef2221588f5885e57b5fce3d3d142986834190c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Acute erythroid leukemia</topic><topic>Acute myelocytic leukemia</topic><topic>Acute myeloid leukemia</topic><topic>Adolescent</topic><topic>Adult</topic><topic>Aged</topic><topic>Biomarkers</topic><topic>Blood</topic><topic>Bone marrow</topic><topic>Bone Marrow - pathology</topic><topic>Care and treatment</topic><topic>Chemotherapy</topic><topic>Child</topic><topic>Classification</topic><topic>Combined Modality Therapy</topic><topic>Cytogenetic Analysis</topic><topic>Cytogenetics</topic><topic>Diagnosis</topic><topic>Diagnosis, Differential</topic><topic>DNA Mutational Analysis</topic><topic>Erythroid cells</topic><topic>Female</topic><topic>Humans</topic><topic>Leukemia</topic><topic>Leukemia, Erythroblastic, Acute - diagnosis</topic><topic>Leukemia, Erythroblastic, Acute - mortality</topic><topic>Leukemia, Erythroblastic, Acute - therapy</topic><topic>Leukemia, Myeloid, Acute - diagnosis</topic><topic>Male</topic><topic>Medical prognosis</topic><topic>Middle Aged</topic><topic>Multivariate analysis</topic><topic>Mutation</topic><topic>Myelodyspalstic syndrome</topic><topic>Myelodysplastic syndrome</topic><topic>Myelodysplastic Syndromes - diagnosis</topic><topic>Myeloid leukemia</topic><topic>Practice Guidelines as Topic</topic><topic>Prognosis</topic><topic>Retrospective Studies</topic><topic>Stem cells</topic><topic>Survival Analysis</topic><topic>Transplantation</topic><topic>World Health Organization</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Qiu, Shaowei</creatorcontrib><creatorcontrib>Jiang, Erlie</creatorcontrib><creatorcontrib>Wei, Hui</creatorcontrib><creatorcontrib>Lin, Dong</creatorcontrib><creatorcontrib>Zhang, Guangji</creatorcontrib><creatorcontrib>Wei, Shuning</creatorcontrib><creatorcontrib>Zhou, Chunlin</creatorcontrib><creatorcontrib>Liu, Kaiqi</creatorcontrib><creatorcontrib>Wang, Ying</creatorcontrib><creatorcontrib>Liu, Bingcheng</creatorcontrib><creatorcontrib>Liu, Yuntao</creatorcontrib><creatorcontrib>Gong, Benfa</creatorcontrib><creatorcontrib>Gong, Xiaoyuan</creatorcontrib><creatorcontrib>Feng, Sizhou</creatorcontrib><creatorcontrib>Mi, Yingchang</creatorcontrib><creatorcontrib>Han, Mingzhe</creatorcontrib><creatorcontrib>Wang, Jianxiang</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Gale In Context: Science</collection><collection>ProQuest Central (Corporate)</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>ProQuest Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</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)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>PML(ProQuest Medical Library)</collection><collection>Publicly Available Content Database</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><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>BMC cancer</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Qiu, Shaowei</au><au>Jiang, Erlie</au><au>Wei, Hui</au><au>Lin, Dong</au><au>Zhang, Guangji</au><au>Wei, Shuning</au><au>Zhou, Chunlin</au><au>Liu, Kaiqi</au><au>Wang, Ying</au><au>Liu, Bingcheng</au><au>Liu, Yuntao</au><au>Gong, Benfa</au><au>Gong, Xiaoyuan</au><au>Feng, Sizhou</au><au>Mi, Yingchang</au><au>Han, Mingzhe</au><au>Wang, Jianxiang</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>An analysis of 97 previously diagnosed de novo adult acute erythroid leukemia patients following the 2016 revision to World Health Organization classification</atitle><jtitle>BMC cancer</jtitle><addtitle>BMC Cancer</addtitle><date>2017-08-09</date><risdate>2017</risdate><volume>17</volume><issue>1</issue><spage>534</spage><epage>534</epage><pages>534-534</pages><artnum>534</artnum><issn>1471-2407</issn><eissn>1471-2407</eissn><abstract>The incidence of acute erythroid leukemia subtype (AEL) is rare, accounting for 5% of cases of acute myeloid leukemia (AML), and the outcome is dismal. However, in 2016 revision to the WHO classification, the subcategory of AEL has been removed. Myeloblasts are redefined as the percentage of total marrow cells, not non-erythroid cells. Therefore, the previously diagnosed AEL cases are currently diagnosed as AML or myelodyspalstic syndrome (MDS) according to new criteria.
We respectively reviewed cases of 97 de novo previously diagnosed AEL and all the patients were diagnosed as AML or MDS according to the new classification scheme, and then the clinical characteristics of these two subtypes were compared. Statistical analyses were performed by SPSS software version 18.0.
The median age was 37 years-old, the two-thirds of previous AEL cases were diagnosed as MDS, and there was no obvious difference between two subtypes except for male/female ratio and age. Cytogenetic, rather than MDS/AML subtypes, can better represent the prognostic factor of previously diagnosed AEL patients. When the cytogenetic risk of patients belonged to MRC intermediate category and age were below 40 years-old in previous AEL cases, the patients who received induction chemotherapy without transplantation had a similar survival compared with the patients who underwent transplantation (3-year OS: 67.2% vs 68.5%).
Cytogenetic, rather than MDS/AML subtypes, can better represent the prognostic factor of previously diagnosed AEL patients. Transplantation was a better choice for those whose cytogenetic category was unfavorable.</abstract><cop>England</cop><pub>BioMed Central Ltd</pub><pmid>28793875</pmid><doi>10.1186/s12885-017-3528-6</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1471-2407 |
ispartof | BMC cancer, 2017-08, Vol.17 (1), p.534-534, Article 534 |
issn | 1471-2407 1471-2407 |
language | eng |
recordid | cdi_doaj_primary_oai_doaj_org_article_e77db0d0b8114d19aa8410ff4b39ac10 |
source | Publicly Available Content Database; PubMed Central |
subjects | Acute erythroid leukemia Acute myelocytic leukemia Acute myeloid leukemia Adolescent Adult Aged Biomarkers Blood Bone marrow Bone Marrow - pathology Care and treatment Chemotherapy Child Classification Combined Modality Therapy Cytogenetic Analysis Cytogenetics Diagnosis Diagnosis, Differential DNA Mutational Analysis Erythroid cells Female Humans Leukemia Leukemia, Erythroblastic, Acute - diagnosis Leukemia, Erythroblastic, Acute - mortality Leukemia, Erythroblastic, Acute - therapy Leukemia, Myeloid, Acute - diagnosis Male Medical prognosis Middle Aged Multivariate analysis Mutation Myelodyspalstic syndrome Myelodysplastic syndrome Myelodysplastic Syndromes - diagnosis Myeloid leukemia Practice Guidelines as Topic Prognosis Retrospective Studies Stem cells Survival Analysis Transplantation World Health Organization Young Adult |
title | An analysis of 97 previously diagnosed de novo adult acute erythroid leukemia patients following the 2016 revision to World Health Organization classification |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-07T12%3A53%3A46IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_doaj_&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=An%20analysis%20of%2097%20previously%20diagnosed%20de%20novo%20adult%20acute%20erythroid%20leukemia%20patients%20following%20the%202016%20revision%20to%20World%20Health%20Organization%20classification&rft.jtitle=BMC%20cancer&rft.au=Qiu,%20Shaowei&rft.date=2017-08-09&rft.volume=17&rft.issue=1&rft.spage=534&rft.epage=534&rft.pages=534-534&rft.artnum=534&rft.issn=1471-2407&rft.eissn=1471-2407&rft_id=info:doi/10.1186/s12885-017-3528-6&rft_dat=%3Cgale_doaj_%3EA511262645%3C/gale_doaj_%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c691t-70b127baa711e29203cac1273ef2221588f5885e57b5fce3d3d142986834190c3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=1934612845&rft_id=info:pmid/28793875&rft_galeid=A511262645&rfr_iscdi=true |