The simplified follicular lymphoma PRIMA‐prognostic index is useful in patients with first‐line chemo‐free rituximab‐based therapy

Summary Follicular lymphoma (FL) is a heterogeneous disease; therefore, reliable prognostic tools are needed to plan treatment strategies. The FL International Prognostic Index (FLIPI) was developed before the rituximab era, while the PRIMA‐PI was built on rituximab chemotherapy. Our objective was t...

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Veröffentlicht in:British journal of haematology 2020-12, Vol.191 (5), p.738-747
Hauptverfasser: Kimby, Eva, Lockmer, Sandra, Holte, Harald, Hagberg, Hans, Wahlin, Björn E., Brown, Peter, Østenstad, Bjørn
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container_issue 5
container_start_page 738
container_title British journal of haematology
container_volume 191
creator Kimby, Eva
Lockmer, Sandra
Holte, Harald
Hagberg, Hans
Wahlin, Björn E.
Brown, Peter
Østenstad, Bjørn
description Summary Follicular lymphoma (FL) is a heterogeneous disease; therefore, reliable prognostic tools are needed to plan treatment strategies. The FL International Prognostic Index (FLIPI) was developed before the rituximab era, while the PRIMA‐PI was built on rituximab chemotherapy. Our objective was to evaluate these two prognostic tools in a cohort of 291 patients with FL treated in two prospective randomised Nordic Lymphoma Group trials with rituximab ± interferon. All patients had symptomatic/progressive disease and were previously untreated. The PRIMA‐PI was prognostic for both time to treatment failure (TTF) and overall survival (OS) (log‐rank P = 0·003 and P 
doi_str_mv 10.1111/bjh.16692
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The FL International Prognostic Index (FLIPI) was developed before the rituximab era, while the PRIMA‐PI was built on rituximab chemotherapy. Our objective was to evaluate these two prognostic tools in a cohort of 291 patients with FL treated in two prospective randomised Nordic Lymphoma Group trials with rituximab ± interferon. All patients had symptomatic/progressive disease and were previously untreated. The PRIMA‐PI was prognostic for both time to treatment failure (TTF) and overall survival (OS) (log‐rank P = 0·003 and P &lt; 0·001, respectively). The PRIMA‐PI high‐risk identified a small group of patients with a very short TTF and OS compared to the low‐risk group, with a hazard ratio (HR) of 1·90 (95% confidence interval [CI] 1·30–2·78, P = 0·001) and HR of 3·19 (95% CI 1·75–5·83, P &lt; 0·001), respectively. The FLIPI risk groups were prognostic only for OS (log‐rank P = 0·018). The simplified PRIMA‐PI was valid in our FL cohort with first‐line rituximab‐containing chemo‐free therapy and shows an improved risk stratification compared to the FLIPI, especially in patients aged &gt;60 years. Patients in the PRIMA‐PI high‐risk group should be considered for alternative therapies.</description><identifier>ISSN: 0007-1048</identifier><identifier>ISSN: 1365-2141</identifier><identifier>EISSN: 1365-2141</identifier><identifier>DOI: 10.1111/bjh.16692</identifier><identifier>PMID: 32410260</identifier><language>eng</language><publisher>England: Blackwell Publishing Ltd</publisher><subject>Adult ; Age Factors ; Aged ; Aged, 80 and over ; chemo-free regimen ; Chemotherapy ; Clinical trials ; Disease-Free Survival ; Female ; follicular lymphoma ; Hematology ; Humans ; Immunotherapy ; Interferon ; Lymphoma ; Lymphoma, Follicular - drug therapy ; Lymphoma, Follicular - mortality ; Male ; Middle Aged ; Monoclonal antibodies ; prognosis ; Risk Factors ; Risk groups ; Rituximab ; Rituximab - administration &amp; dosage ; Rituximab - adverse effects ; Survival Rate ; Targeted cancer therapy</subject><ispartof>British journal of haematology, 2020-12, Vol.191 (5), p.738-747</ispartof><rights>2020 The Authors. published by British Society for Haematology and John Wiley &amp; Sons Ltd.</rights><rights>2020 The Authors. 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The FL International Prognostic Index (FLIPI) was developed before the rituximab era, while the PRIMA‐PI was built on rituximab chemotherapy. Our objective was to evaluate these two prognostic tools in a cohort of 291 patients with FL treated in two prospective randomised Nordic Lymphoma Group trials with rituximab ± interferon. All patients had symptomatic/progressive disease and were previously untreated. The PRIMA‐PI was prognostic for both time to treatment failure (TTF) and overall survival (OS) (log‐rank P = 0·003 and P &lt; 0·001, respectively). The PRIMA‐PI high‐risk identified a small group of patients with a very short TTF and OS compared to the low‐risk group, with a hazard ratio (HR) of 1·90 (95% confidence interval [CI] 1·30–2·78, P = 0·001) and HR of 3·19 (95% CI 1·75–5·83, P &lt; 0·001), respectively. The FLIPI risk groups were prognostic only for OS (log‐rank P = 0·018). The simplified PRIMA‐PI was valid in our FL cohort with first‐line rituximab‐containing chemo‐free therapy and shows an improved risk stratification compared to the FLIPI, especially in patients aged &gt;60 years. 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dosage</topic><topic>Rituximab - adverse effects</topic><topic>Survival Rate</topic><topic>Targeted cancer therapy</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kimby, Eva</creatorcontrib><creatorcontrib>Lockmer, Sandra</creatorcontrib><creatorcontrib>Holte, Harald</creatorcontrib><creatorcontrib>Hagberg, Hans</creatorcontrib><creatorcontrib>Wahlin, Björn E.</creatorcontrib><creatorcontrib>Brown, Peter</creatorcontrib><creatorcontrib>Østenstad, Bjørn</creatorcontrib><collection>Wiley Online Library Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Immunology Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>NORA - Norwegian Open Research Archives</collection><collection>SWEPUB Uppsala universitet full text</collection><collection>SwePub</collection><collection>SwePub Articles</collection><collection>SWEPUB Freely available online</collection><collection>SWEPUB Uppsala universitet</collection><collection>SwePub Articles full text</collection><jtitle>British journal of haematology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kimby, Eva</au><au>Lockmer, Sandra</au><au>Holte, Harald</au><au>Hagberg, Hans</au><au>Wahlin, Björn E.</au><au>Brown, Peter</au><au>Østenstad, Bjørn</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The simplified follicular lymphoma PRIMA‐prognostic index is useful in patients with first‐line chemo‐free rituximab‐based therapy</atitle><jtitle>British journal of haematology</jtitle><addtitle>Br J Haematol</addtitle><date>2020-12</date><risdate>2020</risdate><volume>191</volume><issue>5</issue><spage>738</spage><epage>747</epage><pages>738-747</pages><issn>0007-1048</issn><issn>1365-2141</issn><eissn>1365-2141</eissn><abstract>Summary Follicular lymphoma (FL) is a heterogeneous disease; therefore, reliable prognostic tools are needed to plan treatment strategies. The FL International Prognostic Index (FLIPI) was developed before the rituximab era, while the PRIMA‐PI was built on rituximab chemotherapy. Our objective was to evaluate these two prognostic tools in a cohort of 291 patients with FL treated in two prospective randomised Nordic Lymphoma Group trials with rituximab ± interferon. All patients had symptomatic/progressive disease and were previously untreated. The PRIMA‐PI was prognostic for both time to treatment failure (TTF) and overall survival (OS) (log‐rank P = 0·003 and P &lt; 0·001, respectively). The PRIMA‐PI high‐risk identified a small group of patients with a very short TTF and OS compared to the low‐risk group, with a hazard ratio (HR) of 1·90 (95% confidence interval [CI] 1·30–2·78, P = 0·001) and HR of 3·19 (95% CI 1·75–5·83, P &lt; 0·001), respectively. The FLIPI risk groups were prognostic only for OS (log‐rank P = 0·018). The simplified PRIMA‐PI was valid in our FL cohort with first‐line rituximab‐containing chemo‐free therapy and shows an improved risk stratification compared to the FLIPI, especially in patients aged &gt;60 years. Patients in the PRIMA‐PI high‐risk group should be considered for alternative therapies.</abstract><cop>England</cop><pub>Blackwell Publishing Ltd</pub><pmid>32410260</pmid><doi>10.1111/bjh.16692</doi><tpages>10</tpages><orcidid>https://orcid.org/0000-0001-9799-9428</orcidid><orcidid>https://orcid.org/0000-0003-3078-6131</orcidid><oa>free_for_read</oa></addata></record>
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source Wiley Free Content; MEDLINE; NORA - Norwegian Open Research Archives; Wiley Online Library Journals Frontfile Complete; SWEPUB Freely available online
subjects Adult
Age Factors
Aged
Aged, 80 and over
chemo-free regimen
Chemotherapy
Clinical trials
Disease-Free Survival
Female
follicular lymphoma
Hematology
Humans
Immunotherapy
Interferon
Lymphoma
Lymphoma, Follicular - drug therapy
Lymphoma, Follicular - mortality
Male
Middle Aged
Monoclonal antibodies
prognosis
Risk Factors
Risk groups
Rituximab
Rituximab - administration & dosage
Rituximab - adverse effects
Survival Rate
Targeted cancer therapy
title The simplified follicular lymphoma PRIMA‐prognostic index is useful in patients with first‐line chemo‐free rituximab‐based therapy
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