Treatment outcomes with purine nucleoside analog alone or with rituximab for hairy cell leukemia at first relapse

Introduction Frontline treatment of hairy cell leukemia (HCL) with a single course of the purine nucleoside analog (PNA) produces a high rate of complete remission (CR) with prolonged durations. At the time of relapse, although treatment guidelines recommend re‐treatment with a PNA alone or in combi...

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Veröffentlicht in:European journal of haematology 2022-05, Vol.108 (5), p.379-382
Hauptverfasser: Hu, Rachel, Wei, Wei, Mian, Agrima, Gonter‐Aubin, Kristen, Kabel, Charlene, Mato, Anthony, Stephens, Deborah M., Hanlon, Ashley, Khajavian, Sirin, Shadman, Mazyar, Brander, Danielle, Madanat, Yazan, Park, Jae H., Tallman, Martin, Pinilla‐Ibarz, Javier, Hill, Brian T.
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container_end_page 382
container_issue 5
container_start_page 379
container_title European journal of haematology
container_volume 108
creator Hu, Rachel
Wei, Wei
Mian, Agrima
Gonter‐Aubin, Kristen
Kabel, Charlene
Mato, Anthony
Stephens, Deborah M.
Hanlon, Ashley
Khajavian, Sirin
Shadman, Mazyar
Brander, Danielle
Madanat, Yazan
Park, Jae H.
Tallman, Martin
Pinilla‐Ibarz, Javier
Hill, Brian T.
description Introduction Frontline treatment of hairy cell leukemia (HCL) with a single course of the purine nucleoside analog (PNA) produces a high rate of complete remission (CR) with prolonged durations. At the time of relapse, although treatment guidelines recommend re‐treatment with a PNA alone or in combination with rituximab (R), practice patterns vary and data supporting each approach are limited. Methods We conducted a multisite outcomes analysis of patients treated for HCL between 1995 and 2018 at six US medical centers. All patients were treated with frontline PNA and subsequently required treatment with a PNA alone (PNA) or with R (+R). Results Of the 88 patients analyzed, 56 (63.6%) received second‐line PNA and 22 (36.4%) received a PNA + R. Baseline characteristics of both groups were similar. There was no difference in median PFS [67 months (95% CI 43.8 non‐reached (NR)) vs. 65 months (95% CI 60‐NR)] or 5‐year OS [98% (95% CI 0.94–1) vs. 94% (95% CI 0.83–1), p = .104] in the PNA versus PNA + R cohorts, respectively. Conclusion To our knowledge, this is the largest study evaluating the role of R in treatment of relapsed HCL and suggests that there is no advantage to the addition of R to PNA therapy at the time of first re‐treatment.
doi_str_mv 10.1111/ejh.13744
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At the time of relapse, although treatment guidelines recommend re‐treatment with a PNA alone or in combination with rituximab (R), practice patterns vary and data supporting each approach are limited. Methods We conducted a multisite outcomes analysis of patients treated for HCL between 1995 and 2018 at six US medical centers. All patients were treated with frontline PNA and subsequently required treatment with a PNA alone (PNA) or with R (+R). Results Of the 88 patients analyzed, 56 (63.6%) received second‐line PNA and 22 (36.4%) received a PNA + R. Baseline characteristics of both groups were similar. There was no difference in median PFS [67 months (95% CI 43.8 non‐reached (NR)) vs. 65 months (95% CI 60‐NR)] or 5‐year OS [98% (95% CI 0.94–1) vs. 94% (95% CI 0.83–1), p = .104] in the PNA versus PNA + R cohorts, respectively. Conclusion To our knowledge, this is the largest study evaluating the role of R in treatment of relapsed HCL and suggests that there is no advantage to the addition of R to PNA therapy at the time of first re‐treatment.</description><identifier>ISSN: 0902-4441</identifier><identifier>EISSN: 1600-0609</identifier><identifier>DOI: 10.1111/ejh.13744</identifier><identifier>PMID: 35043475</identifier><language>eng</language><publisher>England: Wiley Subscription Services, Inc</publisher><subject>Hairy cell leukemia ; Humans ; Leukemia ; Leukemia, Hairy Cell - drug therapy ; Nucleoside analogs ; Nucleosides ; Patients ; purine nucleoside analog ; Purine Nucleosides ; Purines ; Recurrence ; Remission ; Rituximab ; Rituximab - therapeutic use ; Treatment Outcome</subject><ispartof>European journal of haematology, 2022-05, Vol.108 (5), p.379-382</ispartof><rights>2022 John Wiley &amp; Sons A/S. Published by John Wiley &amp; Sons Ltd.</rights><rights>Copyright © 2022 John Wiley &amp; Sons A/S. Published by John Wiley &amp; Sons Ltd</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c3134-82c3b7cc0f311044f2b62691e7ea94a036e41a75bc40bdaa653e93827ff39a563</cites><orcidid>0000-0002-4467-1856 ; 0000-0002-3365-6562</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fejh.13744$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fejh.13744$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,27924,27925,45574,45575</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/35043475$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Hu, Rachel</creatorcontrib><creatorcontrib>Wei, Wei</creatorcontrib><creatorcontrib>Mian, Agrima</creatorcontrib><creatorcontrib>Gonter‐Aubin, Kristen</creatorcontrib><creatorcontrib>Kabel, Charlene</creatorcontrib><creatorcontrib>Mato, Anthony</creatorcontrib><creatorcontrib>Stephens, Deborah M.</creatorcontrib><creatorcontrib>Hanlon, Ashley</creatorcontrib><creatorcontrib>Khajavian, Sirin</creatorcontrib><creatorcontrib>Shadman, Mazyar</creatorcontrib><creatorcontrib>Brander, Danielle</creatorcontrib><creatorcontrib>Madanat, Yazan</creatorcontrib><creatorcontrib>Park, Jae H.</creatorcontrib><creatorcontrib>Tallman, Martin</creatorcontrib><creatorcontrib>Pinilla‐Ibarz, Javier</creatorcontrib><creatorcontrib>Hill, Brian T.</creatorcontrib><title>Treatment outcomes with purine nucleoside analog alone or with rituximab for hairy cell leukemia at first relapse</title><title>European journal of haematology</title><addtitle>Eur J Haematol</addtitle><description>Introduction Frontline treatment of hairy cell leukemia (HCL) with a single course of the purine nucleoside analog (PNA) produces a high rate of complete remission (CR) with prolonged durations. At the time of relapse, although treatment guidelines recommend re‐treatment with a PNA alone or in combination with rituximab (R), practice patterns vary and data supporting each approach are limited. Methods We conducted a multisite outcomes analysis of patients treated for HCL between 1995 and 2018 at six US medical centers. All patients were treated with frontline PNA and subsequently required treatment with a PNA alone (PNA) or with R (+R). Results Of the 88 patients analyzed, 56 (63.6%) received second‐line PNA and 22 (36.4%) received a PNA + R. Baseline characteristics of both groups were similar. There was no difference in median PFS [67 months (95% CI 43.8 non‐reached (NR)) vs. 65 months (95% CI 60‐NR)] or 5‐year OS [98% (95% CI 0.94–1) vs. 94% (95% CI 0.83–1), p = .104] in the PNA versus PNA + R cohorts, respectively. 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Wei, Wei ; Mian, Agrima ; Gonter‐Aubin, Kristen ; Kabel, Charlene ; Mato, Anthony ; Stephens, Deborah M. ; Hanlon, Ashley ; Khajavian, Sirin ; Shadman, Mazyar ; Brander, Danielle ; Madanat, Yazan ; Park, Jae H. ; Tallman, Martin ; Pinilla‐Ibarz, Javier ; Hill, Brian T.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3134-82c3b7cc0f311044f2b62691e7ea94a036e41a75bc40bdaa653e93827ff39a563</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Hairy cell leukemia</topic><topic>Humans</topic><topic>Leukemia</topic><topic>Leukemia, Hairy Cell - drug therapy</topic><topic>Nucleoside analogs</topic><topic>Nucleosides</topic><topic>Patients</topic><topic>purine nucleoside analog</topic><topic>Purine Nucleosides</topic><topic>Purines</topic><topic>Recurrence</topic><topic>Remission</topic><topic>Rituximab</topic><topic>Rituximab - therapeutic use</topic><topic>Treatment Outcome</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hu, Rachel</creatorcontrib><creatorcontrib>Wei, Wei</creatorcontrib><creatorcontrib>Mian, Agrima</creatorcontrib><creatorcontrib>Gonter‐Aubin, Kristen</creatorcontrib><creatorcontrib>Kabel, Charlene</creatorcontrib><creatorcontrib>Mato, Anthony</creatorcontrib><creatorcontrib>Stephens, Deborah M.</creatorcontrib><creatorcontrib>Hanlon, Ashley</creatorcontrib><creatorcontrib>Khajavian, Sirin</creatorcontrib><creatorcontrib>Shadman, Mazyar</creatorcontrib><creatorcontrib>Brander, Danielle</creatorcontrib><creatorcontrib>Madanat, Yazan</creatorcontrib><creatorcontrib>Park, Jae H.</creatorcontrib><creatorcontrib>Tallman, Martin</creatorcontrib><creatorcontrib>Pinilla‐Ibarz, Javier</creatorcontrib><creatorcontrib>Hill, Brian T.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Animal Behavior Abstracts</collection><collection>Immunology Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>European journal of haematology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hu, Rachel</au><au>Wei, Wei</au><au>Mian, Agrima</au><au>Gonter‐Aubin, Kristen</au><au>Kabel, Charlene</au><au>Mato, Anthony</au><au>Stephens, Deborah M.</au><au>Hanlon, Ashley</au><au>Khajavian, Sirin</au><au>Shadman, Mazyar</au><au>Brander, Danielle</au><au>Madanat, Yazan</au><au>Park, Jae H.</au><au>Tallman, Martin</au><au>Pinilla‐Ibarz, Javier</au><au>Hill, Brian T.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Treatment outcomes with purine nucleoside analog alone or with rituximab for hairy cell leukemia at first relapse</atitle><jtitle>European journal of haematology</jtitle><addtitle>Eur J Haematol</addtitle><date>2022-05</date><risdate>2022</risdate><volume>108</volume><issue>5</issue><spage>379</spage><epage>382</epage><pages>379-382</pages><issn>0902-4441</issn><eissn>1600-0609</eissn><abstract>Introduction Frontline treatment of hairy cell leukemia (HCL) with a single course of the purine nucleoside analog (PNA) produces a high rate of complete remission (CR) with prolonged durations. At the time of relapse, although treatment guidelines recommend re‐treatment with a PNA alone or in combination with rituximab (R), practice patterns vary and data supporting each approach are limited. Methods We conducted a multisite outcomes analysis of patients treated for HCL between 1995 and 2018 at six US medical centers. All patients were treated with frontline PNA and subsequently required treatment with a PNA alone (PNA) or with R (+R). Results Of the 88 patients analyzed, 56 (63.6%) received second‐line PNA and 22 (36.4%) received a PNA + R. Baseline characteristics of both groups were similar. There was no difference in median PFS [67 months (95% CI 43.8 non‐reached (NR)) vs. 65 months (95% CI 60‐NR)] or 5‐year OS [98% (95% CI 0.94–1) vs. 94% (95% CI 0.83–1), p = .104] in the PNA versus PNA + R cohorts, respectively. 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subjects Hairy cell leukemia
Humans
Leukemia
Leukemia, Hairy Cell - drug therapy
Nucleoside analogs
Nucleosides
Patients
purine nucleoside analog
Purine Nucleosides
Purines
Recurrence
Remission
Rituximab
Rituximab - therapeutic use
Treatment Outcome
title Treatment outcomes with purine nucleoside analog alone or with rituximab for hairy cell leukemia at first relapse
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