Next-Generation Sequencing—Optimal Sequencing of Therapies in Relapsed/Refractory Chronic Lymphocytic Leukemia (CLL)
Purpose of Review This research paper aims to provide an overview of evidence-based sequencing of therapies in relapsed/refractory chronic lymphocytic leukemia (CLL) in the era of targeted drugs. Recent Findings In the absence of data from randomized clinical trials comparing novel agents head-to-he...
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Veröffentlicht in: | Current oncology reports 2023-10, Vol.25 (10), p.1181-1189 |
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description | Purpose of Review
This research paper aims to provide an overview of evidence-based sequencing of therapies in relapsed/refractory chronic lymphocytic leukemia (CLL) in the era of targeted drugs.
Recent Findings
In the absence of data from randomized clinical trials comparing novel agents head-to-head, growing evidence suggests that patients with late relapse (> 2 years) after fixed-duration therapies benefit from identical retreatment, whereas a class switch is favorable in those with short-lived remissions or progressive disease on continuous drug intake. Treatment of patients previously exposed to both covalent inhibitors of BTK and BCL2 remains an unmet medical need. Novel drugs, in particular noncovalent BTKI, show promising efficacy in this difficult-to-treat subgroup in early clinical trials.
Summary
The optimal sequencing of therapies in CLL requires consideration of individual patient factors and disease characteristics. Double-refractory disease continuous to pose a clinical challenge with a focus on participation in clinical trials whenever possible. |
doi_str_mv | 10.1007/s11912-023-01454-w |
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This research paper aims to provide an overview of evidence-based sequencing of therapies in relapsed/refractory chronic lymphocytic leukemia (CLL) in the era of targeted drugs.
Recent Findings
In the absence of data from randomized clinical trials comparing novel agents head-to-head, growing evidence suggests that patients with late relapse (> 2 years) after fixed-duration therapies benefit from identical retreatment, whereas a class switch is favorable in those with short-lived remissions or progressive disease on continuous drug intake. Treatment of patients previously exposed to both covalent inhibitors of BTK and BCL2 remains an unmet medical need. Novel drugs, in particular noncovalent BTKI, show promising efficacy in this difficult-to-treat subgroup in early clinical trials.
Summary
The optimal sequencing of therapies in CLL requires consideration of individual patient factors and disease characteristics. Double-refractory disease continuous to pose a clinical challenge with a focus on participation in clinical trials whenever possible.</description><identifier>ISSN: 1523-3790</identifier><identifier>EISSN: 1534-6269</identifier><identifier>DOI: 10.1007/s11912-023-01454-w</identifier><identifier>PMID: 37682487</identifier><language>eng</language><publisher>New York: Springer US</publisher><subject>Bcl-2 protein ; Cardiac arrhythmia ; Chronic lymphocytic leukemia ; Class switching ; Clinical trials ; Drugs ; Hypertension ; Infections ; Internal medicine ; Kinases ; Leukemia ; Licenses ; Medicine ; Medicine & Public Health ; Next-generation sequencing ; Oncology ; Patients ; Topical Collection on Lymphomas ; Toxicity</subject><ispartof>Current oncology reports, 2023-10, Vol.25 (10), p.1181-1189</ispartof><rights>The Author(s) 2023</rights><rights>The Author(s) 2023. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c403t-e5376ef230c6c7566fff3270fe27cbc2c0ac3acae9c24657182d2597b63c431a3</cites><orcidid>0000-0002-2066-7377</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/s11912-023-01454-w$$EPDF$$P50$$Gspringer$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s11912-023-01454-w$$EHTML$$P50$$Gspringer$$Hfree_for_read</linktohtml><link.rule.ids>230,314,780,784,885,27924,27925,41488,42557,51319</link.rule.ids></links><search><creatorcontrib>Simon, Florian</creatorcontrib><creatorcontrib>Bohn, Jan-Paul</creatorcontrib><title>Next-Generation Sequencing—Optimal Sequencing of Therapies in Relapsed/Refractory Chronic Lymphocytic Leukemia (CLL)</title><title>Current oncology reports</title><addtitle>Curr Oncol Rep</addtitle><description>Purpose of Review
This research paper aims to provide an overview of evidence-based sequencing of therapies in relapsed/refractory chronic lymphocytic leukemia (CLL) in the era of targeted drugs.
Recent Findings
In the absence of data from randomized clinical trials comparing novel agents head-to-head, growing evidence suggests that patients with late relapse (> 2 years) after fixed-duration therapies benefit from identical retreatment, whereas a class switch is favorable in those with short-lived remissions or progressive disease on continuous drug intake. Treatment of patients previously exposed to both covalent inhibitors of BTK and BCL2 remains an unmet medical need. Novel drugs, in particular noncovalent BTKI, show promising efficacy in this difficult-to-treat subgroup in early clinical trials.
Summary
The optimal sequencing of therapies in CLL requires consideration of individual patient factors and disease characteristics. Double-refractory disease continuous to pose a clinical challenge with a focus on participation in clinical trials whenever possible.</description><subject>Bcl-2 protein</subject><subject>Cardiac arrhythmia</subject><subject>Chronic lymphocytic leukemia</subject><subject>Class switching</subject><subject>Clinical trials</subject><subject>Drugs</subject><subject>Hypertension</subject><subject>Infections</subject><subject>Internal medicine</subject><subject>Kinases</subject><subject>Leukemia</subject><subject>Licenses</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Next-generation sequencing</subject><subject>Oncology</subject><subject>Patients</subject><subject>Topical Collection on Lymphomas</subject><subject>Toxicity</subject><issn>1523-3790</issn><issn>1534-6269</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>C6C</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNp9kcFu1DAQhiNERUvhBThF4lIOacd2bCcnhFZQKkVUKuVseb3jXZfEDnbSsjcegifkSfCyFQUOnDzyfP-vmfmL4gWBUwIgzxIhLaEVUFYBqXld3T0qjghndSWoaB_v6txisoXD4mlKNwAUoIEnxSGToqF1I4-K2w_4darO0WPUkwu-_IhfZvTG-fWPb98vx8kNuv_jswy2vN5keHSYSufLK-z1mHB1doU2ajOFuC0Xmxi8M2W3HcZNMNtpV-P8GQeny5NF1716VhxY3Sd8fv8eF5_evb1evK-6y_OLxZuuMjWwqUKeJ0VLGRhhJBfCWsuoBItUmqWhBrRh2mhsDa0Fl6ShK8pbuRTM1Ixodly83vuO83LAlUE_Rd2rMea14lYF7dTfHe82ah1uFQHOBeEiO5zcO8SQj5AmNbhksO-1xzAnRRvBGDAQNKMv_0Fvwhx93i9TkkHTElJniu4pE0NKEe3vaQioXa5qn6vKuapfuaq7LGJ7UcqwX2N8sP6P6if5XKdg</recordid><startdate>20231001</startdate><enddate>20231001</enddate><creator>Simon, Florian</creator><creator>Bohn, Jan-Paul</creator><general>Springer US</general><general>Springer Nature B.V</general><scope>C6C</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-2066-7377</orcidid></search><sort><creationdate>20231001</creationdate><title>Next-Generation Sequencing—Optimal Sequencing of Therapies in Relapsed/Refractory Chronic Lymphocytic Leukemia (CLL)</title><author>Simon, Florian ; Bohn, Jan-Paul</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c403t-e5376ef230c6c7566fff3270fe27cbc2c0ac3acae9c24657182d2597b63c431a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Bcl-2 protein</topic><topic>Cardiac arrhythmia</topic><topic>Chronic lymphocytic leukemia</topic><topic>Class switching</topic><topic>Clinical trials</topic><topic>Drugs</topic><topic>Hypertension</topic><topic>Infections</topic><topic>Internal medicine</topic><topic>Kinases</topic><topic>Leukemia</topic><topic>Licenses</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Next-generation sequencing</topic><topic>Oncology</topic><topic>Patients</topic><topic>Topical Collection on Lymphomas</topic><topic>Toxicity</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Simon, Florian</creatorcontrib><creatorcontrib>Bohn, Jan-Paul</creatorcontrib><collection>Springer Nature OA Free Journals</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science 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 Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Biological Science 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>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Current oncology reports</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Simon, Florian</au><au>Bohn, Jan-Paul</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Next-Generation Sequencing—Optimal Sequencing of Therapies in Relapsed/Refractory Chronic Lymphocytic Leukemia (CLL)</atitle><jtitle>Current oncology reports</jtitle><stitle>Curr Oncol Rep</stitle><date>2023-10-01</date><risdate>2023</risdate><volume>25</volume><issue>10</issue><spage>1181</spage><epage>1189</epage><pages>1181-1189</pages><issn>1523-3790</issn><eissn>1534-6269</eissn><abstract>Purpose of Review
This research paper aims to provide an overview of evidence-based sequencing of therapies in relapsed/refractory chronic lymphocytic leukemia (CLL) in the era of targeted drugs.
Recent Findings
In the absence of data from randomized clinical trials comparing novel agents head-to-head, growing evidence suggests that patients with late relapse (> 2 years) after fixed-duration therapies benefit from identical retreatment, whereas a class switch is favorable in those with short-lived remissions or progressive disease on continuous drug intake. Treatment of patients previously exposed to both covalent inhibitors of BTK and BCL2 remains an unmet medical need. Novel drugs, in particular noncovalent BTKI, show promising efficacy in this difficult-to-treat subgroup in early clinical trials.
Summary
The optimal sequencing of therapies in CLL requires consideration of individual patient factors and disease characteristics. Double-refractory disease continuous to pose a clinical challenge with a focus on participation in clinical trials whenever possible.</abstract><cop>New York</cop><pub>Springer US</pub><pmid>37682487</pmid><doi>10.1007/s11912-023-01454-w</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0002-2066-7377</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Bcl-2 protein Cardiac arrhythmia Chronic lymphocytic leukemia Class switching Clinical trials Drugs Hypertension Infections Internal medicine Kinases Leukemia Licenses Medicine Medicine & Public Health Next-generation sequencing Oncology Patients Topical Collection on Lymphomas Toxicity |
title | Next-Generation Sequencing—Optimal Sequencing of Therapies in Relapsed/Refractory Chronic Lymphocytic Leukemia (CLL) |
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