End of induction positron emission tomography complete response (PET‐CR) as a surrogate for progression‐free survival in previously untreated follicular lymphoma

Summary Progression‐free survival (PFS) has been the regulatory primary end‐point for recent phase III trials in first‐line follicular lymphoma (FL), but requires prolonged follow‐up. Complete response (CR) at 30 months after initiation of induction treatment was validated as surrogate end‐point for...

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Veröffentlicht in:British journal of haematology 2022-07, Vol.198 (2), p.333-337
Hauptverfasser: Dixon, Jesse G., Dimier, Natalie, Nielsen, Tina, Zheng, Jamie, Marcus, Robert, Morschhauser, Franck, Evens, Andrew M., Federico, Massimo, Blum, Kristie A., Shi, Qian
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container_end_page 337
container_issue 2
container_start_page 333
container_title British journal of haematology
container_volume 198
creator Dixon, Jesse G.
Dimier, Natalie
Nielsen, Tina
Zheng, Jamie
Marcus, Robert
Morschhauser, Franck
Evens, Andrew M.
Federico, Massimo
Blum, Kristie A.
Shi, Qian
description Summary Progression‐free survival (PFS) has been the regulatory primary end‐point for recent phase III trials in first‐line follicular lymphoma (FL), but requires prolonged follow‐up. Complete response (CR) at 30 months after initiation of induction treatment was validated as surrogate end‐point for PFS. Our objective was to further evaluate surrogacy of CR measured by [18F] fluorodeoxyglucose (FDG) positron emission tomography (PET) imaging at the end of induction (EoI). Individual patient data were analysed from 1505 patients from five randomized trials. Trial‐level surrogacy examining the association between treatment effects on EoI‐PET‐CR and PFS was evaluated using linear regression (RWLS2) and bivariate Copula (RCopula2) models. Although EoI‐PET‐CR strongly predicted PFS at a prognostic level, the trial‐level assessment did not show strong correlation (RWLS2=0.56, confidence interval [CI]: 0.20–0.88; RCopula2=0.35, CI: 0.0–0.82). The high uncertainty in estimation was possibly due to the small number of trials and the population of patients with available PET data. Maintenance therapy affecting PFS beyond induction treatment, but not EoI‐PET‐CR end‐point, may have distorted the association between treatment effects. However, there will probably be a number of additional trials approaching completion with available PET response data. Refined evaluation of PET‐CR based surrogate end‐points is still warranted.
doi_str_mv 10.1111/bjh.18217
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Complete response (CR) at 30 months after initiation of induction treatment was validated as surrogate end‐point for PFS. Our objective was to further evaluate surrogacy of CR measured by [18F] fluorodeoxyglucose (FDG) positron emission tomography (PET) imaging at the end of induction (EoI). Individual patient data were analysed from 1505 patients from five randomized trials. Trial‐level surrogacy examining the association between treatment effects on EoI‐PET‐CR and PFS was evaluated using linear regression (RWLS2) and bivariate Copula (RCopula2) models. Although EoI‐PET‐CR strongly predicted PFS at a prognostic level, the trial‐level assessment did not show strong correlation (RWLS2=0.56, confidence interval [CI]: 0.20–0.88; RCopula2=0.35, CI: 0.0–0.82). The high uncertainty in estimation was possibly due to the small number of trials and the population of patients with available PET data. Maintenance therapy affecting PFS beyond induction treatment, but not EoI‐PET‐CR end‐point, may have distorted the association between treatment effects. However, there will probably be a number of additional trials approaching completion with available PET response data. Refined evaluation of PET‐CR based surrogate end‐points is still warranted.</description><identifier>ISSN: 0007-1048</identifier><identifier>EISSN: 1365-2141</identifier><identifier>DOI: 10.1111/bjh.18217</identifier><identifier>PMID: 35491747</identifier><language>eng</language><publisher>England: Blackwell Publishing Ltd</publisher><subject>Clinical trials ; follicular lymphoma ; Hematology ; Life Sciences ; Lymphoma ; Patients ; PET‐CR ; Positron emission tomography ; previously untreated ; progression‐free survival ; Regression analysis ; surrogate end‐point ; Survival ; Tomography</subject><ispartof>British journal of haematology, 2022-07, Vol.198 (2), p.333-337</ispartof><rights>2022 British Society for Haematology and John Wiley &amp; Sons Ltd.</rights><rights>2022 British Society for Haematology and John Wiley &amp; Sons Ltd</rights><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3877-df0dd9f23efa71a25234d45c65b54c923b8a25828408fb4bff4daf6ad95bbe093</citedby><cites>FETCH-LOGICAL-c3877-df0dd9f23efa71a25234d45c65b54c923b8a25828408fb4bff4daf6ad95bbe093</cites><orcidid>0000-0003-4229-2569 ; 0000-0002-6612-1564</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%2Fbjh.18217$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fbjh.18217$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>230,314,776,780,881,1411,1427,27903,27904,45553,45554,46388,46812</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/35491747$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://hal.univ-lille.fr/hal-04159853$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Dixon, Jesse G.</creatorcontrib><creatorcontrib>Dimier, Natalie</creatorcontrib><creatorcontrib>Nielsen, Tina</creatorcontrib><creatorcontrib>Zheng, Jamie</creatorcontrib><creatorcontrib>Marcus, Robert</creatorcontrib><creatorcontrib>Morschhauser, Franck</creatorcontrib><creatorcontrib>Evens, Andrew M.</creatorcontrib><creatorcontrib>Federico, Massimo</creatorcontrib><creatorcontrib>Blum, Kristie A.</creatorcontrib><creatorcontrib>Shi, Qian</creatorcontrib><title>End of induction positron emission tomography complete response (PET‐CR) as a surrogate for progression‐free survival in previously untreated follicular lymphoma</title><title>British journal of haematology</title><addtitle>Br J Haematol</addtitle><description>Summary Progression‐free survival (PFS) has been the regulatory primary end‐point for recent phase III trials in first‐line follicular lymphoma (FL), but requires prolonged follow‐up. Complete response (CR) at 30 months after initiation of induction treatment was validated as surrogate end‐point for PFS. Our objective was to further evaluate surrogacy of CR measured by [18F] fluorodeoxyglucose (FDG) positron emission tomography (PET) imaging at the end of induction (EoI). Individual patient data were analysed from 1505 patients from five randomized trials. Trial‐level surrogacy examining the association between treatment effects on EoI‐PET‐CR and PFS was evaluated using linear regression (RWLS2) and bivariate Copula (RCopula2) models. Although EoI‐PET‐CR strongly predicted PFS at a prognostic level, the trial‐level assessment did not show strong correlation (RWLS2=0.56, confidence interval [CI]: 0.20–0.88; RCopula2=0.35, CI: 0.0–0.82). The high uncertainty in estimation was possibly due to the small number of trials and the population of patients with available PET data. Maintenance therapy affecting PFS beyond induction treatment, but not EoI‐PET‐CR end‐point, may have distorted the association between treatment effects. However, there will probably be a number of additional trials approaching completion with available PET response data. Refined evaluation of PET‐CR based surrogate end‐points is still warranted.</description><subject>Clinical trials</subject><subject>follicular lymphoma</subject><subject>Hematology</subject><subject>Life Sciences</subject><subject>Lymphoma</subject><subject>Patients</subject><subject>PET‐CR</subject><subject>Positron emission tomography</subject><subject>previously untreated</subject><subject>progression‐free survival</subject><subject>Regression analysis</subject><subject>surrogate end‐point</subject><subject>Survival</subject><subject>Tomography</subject><issn>0007-1048</issn><issn>1365-2141</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><recordid>eNp1kcFu1DAQhi0EosvCgRdAlri0h7R2bG-cY7taWNBKIFTOlhPb3aycONjJotx4BF6CF-NJmLClSEj44tH4m39m_CP0kpJLCueqOuwvqcxp8QgtKFuJLKecPkYLQkiRUcLlGXqW0oEQyoigT9EZE7ykBS8W6MemMzg43HRmrIcmdLgPqRkiBLZtUpozQ2jDXdT9fsJ1aHtvB4ujTX3oksXnHze3P799X3-6wDphjdMYY7jTgLgQcQ8xoLMMQC5aOwPH5qg9tIRne2zCmPyEx26IFsoM1Hnf1KPXEfup7feh1c_RE6d9si_u7yX6_GZzu95muw9v362vd1nNZFFkxhFjSpcz63RBdS5yxg0X9UpUgtdlzioJSZlLTqSreOUcN9qttClFVVlSsiW6OOnutVd9bFodJxV0o7bXOzXnCKeilIIdKbDnJxZ2_DLaNCj4r9p6rzsLK6l8JeRKkJleotf_oIcwxg42AUqWlMiCsL_N6xhSitY9TECJmn1W4LP67TOwr-4Vx6q15oH8YywAVyfga-Pt9H8ldfN-e5L8BTo2trE</recordid><startdate>202207</startdate><enddate>202207</enddate><creator>Dixon, Jesse G.</creator><creator>Dimier, Natalie</creator><creator>Nielsen, Tina</creator><creator>Zheng, Jamie</creator><creator>Marcus, Robert</creator><creator>Morschhauser, Franck</creator><creator>Evens, Andrew M.</creator><creator>Federico, Massimo</creator><creator>Blum, Kristie A.</creator><creator>Shi, Qian</creator><general>Blackwell Publishing Ltd</general><general>Wiley</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7T5</scope><scope>H94</scope><scope>7X8</scope><scope>1XC</scope><orcidid>https://orcid.org/0000-0003-4229-2569</orcidid><orcidid>https://orcid.org/0000-0002-6612-1564</orcidid></search><sort><creationdate>202207</creationdate><title>End of induction positron emission tomography complete response (PET‐CR) as a surrogate for progression‐free survival in previously untreated follicular lymphoma</title><author>Dixon, Jesse G. ; 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Complete response (CR) at 30 months after initiation of induction treatment was validated as surrogate end‐point for PFS. Our objective was to further evaluate surrogacy of CR measured by [18F] fluorodeoxyglucose (FDG) positron emission tomography (PET) imaging at the end of induction (EoI). Individual patient data were analysed from 1505 patients from five randomized trials. Trial‐level surrogacy examining the association between treatment effects on EoI‐PET‐CR and PFS was evaluated using linear regression (RWLS2) and bivariate Copula (RCopula2) models. Although EoI‐PET‐CR strongly predicted PFS at a prognostic level, the trial‐level assessment did not show strong correlation (RWLS2=0.56, confidence interval [CI]: 0.20–0.88; RCopula2=0.35, CI: 0.0–0.82). The high uncertainty in estimation was possibly due to the small number of trials and the population of patients with available PET data. Maintenance therapy affecting PFS beyond induction treatment, but not EoI‐PET‐CR end‐point, may have distorted the association between treatment effects. However, there will probably be a number of additional trials approaching completion with available PET response data. Refined evaluation of PET‐CR based surrogate end‐points is still warranted.</abstract><cop>England</cop><pub>Blackwell Publishing Ltd</pub><pmid>35491747</pmid><doi>10.1111/bjh.18217</doi><tpages>5</tpages><orcidid>https://orcid.org/0000-0003-4229-2569</orcidid><orcidid>https://orcid.org/0000-0002-6612-1564</orcidid></addata></record>
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source Wiley Online Library Journals Frontfile Complete; Wiley Free Content
subjects Clinical trials
follicular lymphoma
Hematology
Life Sciences
Lymphoma
Patients
PET‐CR
Positron emission tomography
previously untreated
progression‐free survival
Regression analysis
surrogate end‐point
Survival
Tomography
title End of induction positron emission tomography complete response (PET‐CR) as a surrogate for progression‐free survival in previously untreated follicular lymphoma
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