This Is a Title: Single-Center Data Report of Clhag Regimen for R/R-AML Patients

Objectives:To explore the synergistic effect of CLAG combination with HHT in cell experiments and to evaluate the effectiveness and safety of the CLHAG regimen for patients with relapsed/refractory acute myeloid leukemia(R/R-AML). Methods:In thecell experiments, the Kasumi-1 cell line was treated wi...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Blood 2020-11, Vol.136 (Supplement 1), p.3-3
Hauptverfasser: Jiang, Chuanyan, Wang, Yu, Zou, Mengying, Wang, Yijing, Wang, Jun, Wu, Jiafei, Yang, Xi, LI, Hui
Format: Artikel
Sprache:eng
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 3
container_issue Supplement 1
container_start_page 3
container_title Blood
container_volume 136
creator Jiang, Chuanyan
Wang, Yu
Zou, Mengying
Wang, Yijing
Wang, Jun
Wu, Jiafei
Yang, Xi
LI, Hui
description Objectives:To explore the synergistic effect of CLAG combination with HHT in cell experiments and to evaluate the effectiveness and safety of the CLHAG regimen for patients with relapsed/refractory acute myeloid leukemia(R/R-AML). Methods:In thecell experiments, the Kasumi-1 cell line was treated with a single drug or CLAG combined with HHT. MTT colorimetric method was used to determine the cell growth inhibition rate(GIR). CompuSyn drug cooperation software was used to assess the synergistic effect.In the clinical study,eligible R/ R-AML patients (n=24) were included and CLHAG regimen (cladribine 5mg/m2, d1-5, arabinoside cytosine 2g/m2 q12h, d1-5, homoharringtonine 2mg/m2, d1-d5, GCSF 300μg, d0-d5, WBC>20×109/L disuse) was performed.The efficacy was evaluated by CR, PR, ORR, PFS, OS, and ED. The safety were evaluated by hematological toxicity and non-hematological toxicity. Results:The GIR value with a combined treatmentregimenwas higher than the sum that with the single drug treatment, showing thata synergistic effect. Twenty-four patients with R/R-AML were included in the clinical study, including 2 cases of sAML (MDS transformation), 8 cases of primary refractory, and 14 cases of relapse.The total ORR was 70.8%; among them,14 cases achieved complete remission, and 3 cases achieved partial remission. Besides, seven patients underwentallo-HSCTsuccessfully. In this study, all patients were well tolerated, and early death was not observed. The IV grade hematological toxicity was the major adverse reaction, and no IV grade non-hematological toxicity occurred. Conclusions:TheCLHAG regimen is well tolerated and has a high remission rate in R/R-AML patients, and it can be used as a choice of salvage treatment for R/R-AML patients. No relevant conflicts of interest to declare.
doi_str_mv 10.1182/blood-2020-139708
format Article
fullrecord <record><control><sourceid>elsevier_cross</sourceid><recordid>TN_cdi_crossref_primary_10_1182_blood_2020_139708</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0006497118728607</els_id><sourcerecordid>S0006497118728607</sourcerecordid><originalsourceid>FETCH-LOGICAL-c1378-a76092b683b6d92c8f1dd052458afd8ac60d215ef1e59ac7973f51a8998a3d4b3</originalsourceid><addsrcrecordid>eNp9kM1KAzEUhYMoWKsP4C4vEJuf-Ul0VUarhYql1nXIJDdtZNqUZBB8e6fWtavDPfBdDh9Ct4zeMSb5pO1idIRTTgkTqqbyDI1YySWhQ3WORpTSihSqZpfoKudPSlkheDlCy_U2ZDzP2OB16Du4x-9hv-mANLDvIeFH0xu8gkNMPY4eN93WbIZ7E3awxz4mvJqsyPR1gZemDwOSr9GFN12Gm78co4_Z07p5IYu353kzXRDLRC2JqSuqeFtJ0VZOcSs9c46WvCil8U4aW1HHWQmeQamMrVUtfMmMVEoa4YpWjBE7_bUp5pzA60MKO5O-NaP6qET_KtFHJfqkZGAeTgwMw74CJJ3tMNqCCwlsr10M_9A_9I5nRg</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>This Is a Title: Single-Center Data Report of Clhag Regimen for R/R-AML Patients</title><source>EZB-FREE-00999 freely available EZB journals</source><source>Alma/SFX Local Collection</source><creator>Jiang, Chuanyan ; Wang, Yu ; Zou, Mengying ; Wang, Yijing ; Wang, Jun ; Wu, Jiafei ; Yang, Xi ; LI, Hui</creator><creatorcontrib>Jiang, Chuanyan ; Wang, Yu ; Zou, Mengying ; Wang, Yijing ; Wang, Jun ; Wu, Jiafei ; Yang, Xi ; LI, Hui</creatorcontrib><description>Objectives:To explore the synergistic effect of CLAG combination with HHT in cell experiments and to evaluate the effectiveness and safety of the CLHAG regimen for patients with relapsed/refractory acute myeloid leukemia(R/R-AML). Methods:In thecell experiments, the Kasumi-1 cell line was treated with a single drug or CLAG combined with HHT. MTT colorimetric method was used to determine the cell growth inhibition rate(GIR). CompuSyn drug cooperation software was used to assess the synergistic effect.In the clinical study,eligible R/ R-AML patients (n=24) were included and CLHAG regimen (cladribine 5mg/m2, d1-5, arabinoside cytosine 2g/m2 q12h, d1-5, homoharringtonine 2mg/m2, d1-d5, GCSF 300μg, d0-d5, WBC&gt;20×109/L disuse) was performed.The efficacy was evaluated by CR, PR, ORR, PFS, OS, and ED. The safety were evaluated by hematological toxicity and non-hematological toxicity. Results:The GIR value with a combined treatmentregimenwas higher than the sum that with the single drug treatment, showing thata synergistic effect. Twenty-four patients with R/R-AML were included in the clinical study, including 2 cases of sAML (MDS transformation), 8 cases of primary refractory, and 14 cases of relapse.The total ORR was 70.8%; among them,14 cases achieved complete remission, and 3 cases achieved partial remission. Besides, seven patients underwentallo-HSCTsuccessfully. In this study, all patients were well tolerated, and early death was not observed. The IV grade hematological toxicity was the major adverse reaction, and no IV grade non-hematological toxicity occurred. Conclusions:TheCLHAG regimen is well tolerated and has a high remission rate in R/R-AML patients, and it can be used as a choice of salvage treatment for R/R-AML patients. No relevant conflicts of interest to declare.</description><identifier>ISSN: 0006-4971</identifier><identifier>EISSN: 1528-0020</identifier><identifier>DOI: 10.1182/blood-2020-139708</identifier><language>eng</language><publisher>Elsevier Inc</publisher><ispartof>Blood, 2020-11, Vol.136 (Supplement 1), p.3-3</ispartof><rights>2020 American Society of Hematology</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids></links><search><creatorcontrib>Jiang, Chuanyan</creatorcontrib><creatorcontrib>Wang, Yu</creatorcontrib><creatorcontrib>Zou, Mengying</creatorcontrib><creatorcontrib>Wang, Yijing</creatorcontrib><creatorcontrib>Wang, Jun</creatorcontrib><creatorcontrib>Wu, Jiafei</creatorcontrib><creatorcontrib>Yang, Xi</creatorcontrib><creatorcontrib>LI, Hui</creatorcontrib><title>This Is a Title: Single-Center Data Report of Clhag Regimen for R/R-AML Patients</title><title>Blood</title><description>Objectives:To explore the synergistic effect of CLAG combination with HHT in cell experiments and to evaluate the effectiveness and safety of the CLHAG regimen for patients with relapsed/refractory acute myeloid leukemia(R/R-AML). Methods:In thecell experiments, the Kasumi-1 cell line was treated with a single drug or CLAG combined with HHT. MTT colorimetric method was used to determine the cell growth inhibition rate(GIR). CompuSyn drug cooperation software was used to assess the synergistic effect.In the clinical study,eligible R/ R-AML patients (n=24) were included and CLHAG regimen (cladribine 5mg/m2, d1-5, arabinoside cytosine 2g/m2 q12h, d1-5, homoharringtonine 2mg/m2, d1-d5, GCSF 300μg, d0-d5, WBC&gt;20×109/L disuse) was performed.The efficacy was evaluated by CR, PR, ORR, PFS, OS, and ED. The safety were evaluated by hematological toxicity and non-hematological toxicity. Results:The GIR value with a combined treatmentregimenwas higher than the sum that with the single drug treatment, showing thata synergistic effect. Twenty-four patients with R/R-AML were included in the clinical study, including 2 cases of sAML (MDS transformation), 8 cases of primary refractory, and 14 cases of relapse.The total ORR was 70.8%; among them,14 cases achieved complete remission, and 3 cases achieved partial remission. Besides, seven patients underwentallo-HSCTsuccessfully. In this study, all patients were well tolerated, and early death was not observed. The IV grade hematological toxicity was the major adverse reaction, and no IV grade non-hematological toxicity occurred. Conclusions:TheCLHAG regimen is well tolerated and has a high remission rate in R/R-AML patients, and it can be used as a choice of salvage treatment for R/R-AML patients. No relevant conflicts of interest to declare.</description><issn>0006-4971</issn><issn>1528-0020</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><recordid>eNp9kM1KAzEUhYMoWKsP4C4vEJuf-Ul0VUarhYql1nXIJDdtZNqUZBB8e6fWtavDPfBdDh9Ct4zeMSb5pO1idIRTTgkTqqbyDI1YySWhQ3WORpTSihSqZpfoKudPSlkheDlCy_U2ZDzP2OB16Du4x-9hv-mANLDvIeFH0xu8gkNMPY4eN93WbIZ7E3awxz4mvJqsyPR1gZemDwOSr9GFN12Gm78co4_Z07p5IYu353kzXRDLRC2JqSuqeFtJ0VZOcSs9c46WvCil8U4aW1HHWQmeQamMrVUtfMmMVEoa4YpWjBE7_bUp5pzA60MKO5O-NaP6qET_KtFHJfqkZGAeTgwMw74CJJ3tMNqCCwlsr10M_9A_9I5nRg</recordid><startdate>20201105</startdate><enddate>20201105</enddate><creator>Jiang, Chuanyan</creator><creator>Wang, Yu</creator><creator>Zou, Mengying</creator><creator>Wang, Yijing</creator><creator>Wang, Jun</creator><creator>Wu, Jiafei</creator><creator>Yang, Xi</creator><creator>LI, Hui</creator><general>Elsevier Inc</general><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>20201105</creationdate><title>This Is a Title: Single-Center Data Report of Clhag Regimen for R/R-AML Patients</title><author>Jiang, Chuanyan ; Wang, Yu ; Zou, Mengying ; Wang, Yijing ; Wang, Jun ; Wu, Jiafei ; Yang, Xi ; LI, Hui</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c1378-a76092b683b6d92c8f1dd052458afd8ac60d215ef1e59ac7973f51a8998a3d4b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Jiang, Chuanyan</creatorcontrib><creatorcontrib>Wang, Yu</creatorcontrib><creatorcontrib>Zou, Mengying</creatorcontrib><creatorcontrib>Wang, Yijing</creatorcontrib><creatorcontrib>Wang, Jun</creatorcontrib><creatorcontrib>Wu, Jiafei</creatorcontrib><creatorcontrib>Yang, Xi</creatorcontrib><creatorcontrib>LI, Hui</creatorcontrib><collection>CrossRef</collection><jtitle>Blood</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Jiang, Chuanyan</au><au>Wang, Yu</au><au>Zou, Mengying</au><au>Wang, Yijing</au><au>Wang, Jun</au><au>Wu, Jiafei</au><au>Yang, Xi</au><au>LI, Hui</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>This Is a Title: Single-Center Data Report of Clhag Regimen for R/R-AML Patients</atitle><jtitle>Blood</jtitle><date>2020-11-05</date><risdate>2020</risdate><volume>136</volume><issue>Supplement 1</issue><spage>3</spage><epage>3</epage><pages>3-3</pages><issn>0006-4971</issn><eissn>1528-0020</eissn><abstract>Objectives:To explore the synergistic effect of CLAG combination with HHT in cell experiments and to evaluate the effectiveness and safety of the CLHAG regimen for patients with relapsed/refractory acute myeloid leukemia(R/R-AML). Methods:In thecell experiments, the Kasumi-1 cell line was treated with a single drug or CLAG combined with HHT. MTT colorimetric method was used to determine the cell growth inhibition rate(GIR). CompuSyn drug cooperation software was used to assess the synergistic effect.In the clinical study,eligible R/ R-AML patients (n=24) were included and CLHAG regimen (cladribine 5mg/m2, d1-5, arabinoside cytosine 2g/m2 q12h, d1-5, homoharringtonine 2mg/m2, d1-d5, GCSF 300μg, d0-d5, WBC&gt;20×109/L disuse) was performed.The efficacy was evaluated by CR, PR, ORR, PFS, OS, and ED. The safety were evaluated by hematological toxicity and non-hematological toxicity. Results:The GIR value with a combined treatmentregimenwas higher than the sum that with the single drug treatment, showing thata synergistic effect. Twenty-four patients with R/R-AML were included in the clinical study, including 2 cases of sAML (MDS transformation), 8 cases of primary refractory, and 14 cases of relapse.The total ORR was 70.8%; among them,14 cases achieved complete remission, and 3 cases achieved partial remission. Besides, seven patients underwentallo-HSCTsuccessfully. In this study, all patients were well tolerated, and early death was not observed. The IV grade hematological toxicity was the major adverse reaction, and no IV grade non-hematological toxicity occurred. Conclusions:TheCLHAG regimen is well tolerated and has a high remission rate in R/R-AML patients, and it can be used as a choice of salvage treatment for R/R-AML patients. No relevant conflicts of interest to declare.</abstract><pub>Elsevier Inc</pub><doi>10.1182/blood-2020-139708</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 0006-4971
ispartof Blood, 2020-11, Vol.136 (Supplement 1), p.3-3
issn 0006-4971
1528-0020
language eng
recordid cdi_crossref_primary_10_1182_blood_2020_139708
source EZB-FREE-00999 freely available EZB journals; Alma/SFX Local Collection
title This Is a Title: Single-Center Data Report of Clhag Regimen for R/R-AML Patients
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-20T06%3A28%3A20IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-elsevier_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=This%20Is%20a%20Title:%20Single-Center%20Data%20Report%20of%20Clhag%20Regimen%20for%20R/R-AML%20Patients&rft.jtitle=Blood&rft.au=Jiang,%20Chuanyan&rft.date=2020-11-05&rft.volume=136&rft.issue=Supplement%201&rft.spage=3&rft.epage=3&rft.pages=3-3&rft.issn=0006-4971&rft.eissn=1528-0020&rft_id=info:doi/10.1182/blood-2020-139708&rft_dat=%3Celsevier_cross%3ES0006497118728607%3C/elsevier_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_id=info:pmid/&rft_els_id=S0006497118728607&rfr_iscdi=true