Prolonged response after TPO-RA discontinuation in primary ITP: results of a prospective multicenter study

•High rate of sustained response after TPO-RA discontinuation in patients with persistent or chronic ITP achieving initial CR on treatment.•Increased expression of CD69 on CD8+ T cells at the time of tapering TPO-RA could predict relapses. [Display omitted] Sustained response off treatment (SROT) af...

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Veröffentlicht in:Blood 2023-06, Vol.141 (23), p.2867-2877
Hauptverfasser: Guillet, Stéphanie, Crickx, Etienne, Azzaoui, Imane, Chappert, Pascal, Boutin, Emmanuelle, Viallard, Jean-François, Rivière, Etienne, Gobert, Delphine, Galicier, Lionel, Malphettes, Marion, Cheze, Stéphane, Lefrere, François, Audia, Sylvain, Bonnotte, Bernard, Lambotte, Olivier, Noel, Nicolas, Fain, Olivier, Moulis, Guillaume, Hamidou, Mohamed, Gerfaud-Valentin, Mathieu, Marolleau, Jean-Pierre, Terriou, Louis, Martis, Nihal, Morin, Anne-Sophie, Perlat, Antoinette, Le Gallou, Thomas, Roy-Peaud, Frédérique, Robbins, Ailsa, Lega, Jean-Christophe, Puyade, Matthieu, Comont, Thibault, Limal, Nicolas, Languille, Laetitia, Zarrour, Anissa, Luka, Marine, Menager, Mickael, Belmondo, Thibault, Hue, Sophie, Canoui-Poitrine, Florence, Michel, Marc, Godeau, Bertrand, Mahévas, Matthieu
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container_end_page 2877
container_issue 23
container_start_page 2867
container_title Blood
container_volume 141
creator Guillet, Stéphanie
Crickx, Etienne
Azzaoui, Imane
Chappert, Pascal
Boutin, Emmanuelle
Viallard, Jean-François
Rivière, Etienne
Gobert, Delphine
Galicier, Lionel
Malphettes, Marion
Cheze, Stéphane
Lefrere, François
Audia, Sylvain
Bonnotte, Bernard
Lambotte, Olivier
Noel, Nicolas
Fain, Olivier
Moulis, Guillaume
Hamidou, Mohamed
Gerfaud-Valentin, Mathieu
Marolleau, Jean-Pierre
Terriou, Louis
Martis, Nihal
Morin, Anne-Sophie
Perlat, Antoinette
Le Gallou, Thomas
Roy-Peaud, Frédérique
Robbins, Ailsa
Lega, Jean-Christophe
Puyade, Matthieu
Comont, Thibault
Limal, Nicolas
Languille, Laetitia
Zarrour, Anissa
Luka, Marine
Menager, Mickael
Belmondo, Thibault
Hue, Sophie
Canoui-Poitrine, Florence
Michel, Marc
Godeau, Bertrand
Mahévas, Matthieu
description •High rate of sustained response after TPO-RA discontinuation in patients with persistent or chronic ITP achieving initial CR on treatment.•Increased expression of CD69 on CD8+ T cells at the time of tapering TPO-RA could predict relapses. [Display omitted] Sustained response off treatment (SROT) after thrombopoietin receptor agonist (TPO-RA) discontinuation has been reported in immune thrombocytopenia (ITP). This prospective multicenter interventional study enrolled adults with persistent or chronic primary ITP and complete response (CR) on TPO-RAs. The primary end point was the proportion of patients achieving SROT (platelet count >30 × 109/L and no bleeding) at week 24 (W24) with no other ITP-specific medications. Secondary end points included the proportion of sustained CR off-treatment (SCROT, platelet count >100 × 109/L and no bleeding) and SROT at W52, bleeding events, and pattern of response to a new course of TPO-RAs. We included 48 patients with a median age of 58.5 years; 30 of 48 had chronic ITP at TPO-RA initiation. In the intention-to-treat analysis, 27 of 48 achieved SROT, 15 of 48 achieved SCROT at W24; 25 of 48 achieved SROT, and 14 of 48 achieved SCROT at W52. No severe bleeding episode occurred in patients who relapsed. Among patients rechallenged with TPO-RA, 11 of 12 achieved CR. We found no significant clinical predictors of SROT at W24. Single-cell RNA sequencing revealed enrichment of a tumor necrosis factor α signaling via NF-κB signature in CD8+ T cells of patients with no sustained response after TPO-RA discontinuation, which was further confirmed by a significant overexpression of CD69 on CD8+ T cells at baseline in these patients as compared with those achieving SCROT/SROT. Our results strongly support a strategy based on progressive tapering and discontinuation of TPO-RAs for patients with chronic ITP who achieved a stable CR on treatment. This trial was registered at www.clinicaltrials.gov as #NCT03119974. Guillet et al present results of thrombopoietin receptor agonist (TPO-RA) discontinuation in a selected population of patients with persistent or chronic immune thrombocytopenia (ITP). They report that in patients in stable remission with a platelet count of >100 × 109/L for at least 2 months (48 of 388 patients), 56% maintained a platelet count of >30 × 109/L off therapy. This suggests that a subset of patients on chronic treatment with TPO-RA can be successfully tapered off therapy.
doi_str_mv 10.1182/blood.2022018665
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[Display omitted] Sustained response off treatment (SROT) after thrombopoietin receptor agonist (TPO-RA) discontinuation has been reported in immune thrombocytopenia (ITP). This prospective multicenter interventional study enrolled adults with persistent or chronic primary ITP and complete response (CR) on TPO-RAs. The primary end point was the proportion of patients achieving SROT (platelet count &gt;30 × 109/L and no bleeding) at week 24 (W24) with no other ITP-specific medications. Secondary end points included the proportion of sustained CR off-treatment (SCROT, platelet count &gt;100 × 109/L and no bleeding) and SROT at W52, bleeding events, and pattern of response to a new course of TPO-RAs. We included 48 patients with a median age of 58.5 years; 30 of 48 had chronic ITP at TPO-RA initiation. In the intention-to-treat analysis, 27 of 48 achieved SROT, 15 of 48 achieved SCROT at W24; 25 of 48 achieved SROT, and 14 of 48 achieved SCROT at W52. No severe bleeding episode occurred in patients who relapsed. Among patients rechallenged with TPO-RA, 11 of 12 achieved CR. We found no significant clinical predictors of SROT at W24. Single-cell RNA sequencing revealed enrichment of a tumor necrosis factor α signaling via NF-κB signature in CD8+ T cells of patients with no sustained response after TPO-RA discontinuation, which was further confirmed by a significant overexpression of CD69 on CD8+ T cells at baseline in these patients as compared with those achieving SCROT/SROT. Our results strongly support a strategy based on progressive tapering and discontinuation of TPO-RAs for patients with chronic ITP who achieved a stable CR on treatment. This trial was registered at www.clinicaltrials.gov as #NCT03119974. Guillet et al present results of thrombopoietin receptor agonist (TPO-RA) discontinuation in a selected population of patients with persistent or chronic immune thrombocytopenia (ITP). They report that in patients in stable remission with a platelet count of &gt;100 × 109/L for at least 2 months (48 of 388 patients), 56% maintained a platelet count of &gt;30 × 109/L off therapy. This suggests that a subset of patients on chronic treatment with TPO-RA can be successfully tapered off therapy.</description><identifier>ISSN: 0006-4971</identifier><identifier>EISSN: 1528-0020</identifier><identifier>DOI: 10.1182/blood.2022018665</identifier><identifier>PMID: 36893453</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Adult ; Autoimmunity ; Human health and pathology ; Humans ; Hydrazines - therapeutic use ; Life Sciences ; Middle Aged ; Platelet Count ; Prospective Studies ; Purpura, Thrombocytopenic, Idiopathic - drug therapy ; Receptors, Fc - therapeutic use ; Recombinant Fusion Proteins - therapeutic use ; Thrombocytopenia - drug therapy ; Thrombopoietin - therapeutic use</subject><ispartof>Blood, 2023-06, Vol.141 (23), p.2867-2877</ispartof><rights>2023 The American Society of Hematology</rights><rights>2023 by The American Society of Hematology.</rights><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c426t-265692cc472b7d7cc7f4a8b67b902b391c6d4a0b1e6d155212ad32913954a1bc3</citedby><orcidid>0000-0001-9182-1434 ; 0000-0002-8932-3169 ; 0000-0002-6838-2389 ; 0000-0002-2530-7346 ; 0000-0002-9799-4608 ; 0000-0001-7500-9323 ; 0000-0002-9398-2968 ; 0000-0002-3964-4968 ; 0000-0001-9970-6051 ; 0000-0003-4055-617X ; 0000-0002-1098-4598 ; 0000-0002-1974-3870 ; 0000-0001-7229-3808</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,776,780,881,27903,27904</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/36893453$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://u-picardie.hal.science/hal-04032447$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Guillet, Stéphanie</creatorcontrib><creatorcontrib>Crickx, Etienne</creatorcontrib><creatorcontrib>Azzaoui, Imane</creatorcontrib><creatorcontrib>Chappert, Pascal</creatorcontrib><creatorcontrib>Boutin, Emmanuelle</creatorcontrib><creatorcontrib>Viallard, Jean-François</creatorcontrib><creatorcontrib>Rivière, Etienne</creatorcontrib><creatorcontrib>Gobert, Delphine</creatorcontrib><creatorcontrib>Galicier, Lionel</creatorcontrib><creatorcontrib>Malphettes, Marion</creatorcontrib><creatorcontrib>Cheze, Stéphane</creatorcontrib><creatorcontrib>Lefrere, François</creatorcontrib><creatorcontrib>Audia, Sylvain</creatorcontrib><creatorcontrib>Bonnotte, Bernard</creatorcontrib><creatorcontrib>Lambotte, Olivier</creatorcontrib><creatorcontrib>Noel, Nicolas</creatorcontrib><creatorcontrib>Fain, Olivier</creatorcontrib><creatorcontrib>Moulis, Guillaume</creatorcontrib><creatorcontrib>Hamidou, Mohamed</creatorcontrib><creatorcontrib>Gerfaud-Valentin, Mathieu</creatorcontrib><creatorcontrib>Marolleau, Jean-Pierre</creatorcontrib><creatorcontrib>Terriou, Louis</creatorcontrib><creatorcontrib>Martis, Nihal</creatorcontrib><creatorcontrib>Morin, Anne-Sophie</creatorcontrib><creatorcontrib>Perlat, Antoinette</creatorcontrib><creatorcontrib>Le Gallou, Thomas</creatorcontrib><creatorcontrib>Roy-Peaud, Frédérique</creatorcontrib><creatorcontrib>Robbins, Ailsa</creatorcontrib><creatorcontrib>Lega, Jean-Christophe</creatorcontrib><creatorcontrib>Puyade, Matthieu</creatorcontrib><creatorcontrib>Comont, Thibault</creatorcontrib><creatorcontrib>Limal, Nicolas</creatorcontrib><creatorcontrib>Languille, Laetitia</creatorcontrib><creatorcontrib>Zarrour, Anissa</creatorcontrib><creatorcontrib>Luka, Marine</creatorcontrib><creatorcontrib>Menager, Mickael</creatorcontrib><creatorcontrib>Belmondo, Thibault</creatorcontrib><creatorcontrib>Hue, Sophie</creatorcontrib><creatorcontrib>Canoui-Poitrine, Florence</creatorcontrib><creatorcontrib>Michel, Marc</creatorcontrib><creatorcontrib>Godeau, Bertrand</creatorcontrib><creatorcontrib>Mahévas, Matthieu</creatorcontrib><title>Prolonged response after TPO-RA discontinuation in primary ITP: results of a prospective multicenter study</title><title>Blood</title><addtitle>Blood</addtitle><description>•High rate of sustained response after TPO-RA discontinuation in patients with persistent or chronic ITP achieving initial CR on treatment.•Increased expression of CD69 on CD8+ T cells at the time of tapering TPO-RA could predict relapses. [Display omitted] Sustained response off treatment (SROT) after thrombopoietin receptor agonist (TPO-RA) discontinuation has been reported in immune thrombocytopenia (ITP). This prospective multicenter interventional study enrolled adults with persistent or chronic primary ITP and complete response (CR) on TPO-RAs. The primary end point was the proportion of patients achieving SROT (platelet count &gt;30 × 109/L and no bleeding) at week 24 (W24) with no other ITP-specific medications. Secondary end points included the proportion of sustained CR off-treatment (SCROT, platelet count &gt;100 × 109/L and no bleeding) and SROT at W52, bleeding events, and pattern of response to a new course of TPO-RAs. We included 48 patients with a median age of 58.5 years; 30 of 48 had chronic ITP at TPO-RA initiation. In the intention-to-treat analysis, 27 of 48 achieved SROT, 15 of 48 achieved SCROT at W24; 25 of 48 achieved SROT, and 14 of 48 achieved SCROT at W52. No severe bleeding episode occurred in patients who relapsed. Among patients rechallenged with TPO-RA, 11 of 12 achieved CR. We found no significant clinical predictors of SROT at W24. Single-cell RNA sequencing revealed enrichment of a tumor necrosis factor α signaling via NF-κB signature in CD8+ T cells of patients with no sustained response after TPO-RA discontinuation, which was further confirmed by a significant overexpression of CD69 on CD8+ T cells at baseline in these patients as compared with those achieving SCROT/SROT. Our results strongly support a strategy based on progressive tapering and discontinuation of TPO-RAs for patients with chronic ITP who achieved a stable CR on treatment. This trial was registered at www.clinicaltrials.gov as #NCT03119974. Guillet et al present results of thrombopoietin receptor agonist (TPO-RA) discontinuation in a selected population of patients with persistent or chronic immune thrombocytopenia (ITP). They report that in patients in stable remission with a platelet count of &gt;100 × 109/L for at least 2 months (48 of 388 patients), 56% maintained a platelet count of &gt;30 × 109/L off therapy. This suggests that a subset of patients on chronic treatment with TPO-RA can be successfully tapered off therapy.</description><subject>Adult</subject><subject>Autoimmunity</subject><subject>Human health and pathology</subject><subject>Humans</subject><subject>Hydrazines - therapeutic use</subject><subject>Life Sciences</subject><subject>Middle Aged</subject><subject>Platelet Count</subject><subject>Prospective Studies</subject><subject>Purpura, Thrombocytopenic, Idiopathic - drug therapy</subject><subject>Receptors, Fc - therapeutic use</subject><subject>Recombinant Fusion Proteins - therapeutic use</subject><subject>Thrombocytopenia - drug therapy</subject><subject>Thrombopoietin - therapeutic 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Etienne</creatorcontrib><creatorcontrib>Azzaoui, Imane</creatorcontrib><creatorcontrib>Chappert, Pascal</creatorcontrib><creatorcontrib>Boutin, Emmanuelle</creatorcontrib><creatorcontrib>Viallard, Jean-François</creatorcontrib><creatorcontrib>Rivière, Etienne</creatorcontrib><creatorcontrib>Gobert, Delphine</creatorcontrib><creatorcontrib>Galicier, Lionel</creatorcontrib><creatorcontrib>Malphettes, Marion</creatorcontrib><creatorcontrib>Cheze, Stéphane</creatorcontrib><creatorcontrib>Lefrere, François</creatorcontrib><creatorcontrib>Audia, Sylvain</creatorcontrib><creatorcontrib>Bonnotte, Bernard</creatorcontrib><creatorcontrib>Lambotte, Olivier</creatorcontrib><creatorcontrib>Noel, Nicolas</creatorcontrib><creatorcontrib>Fain, Olivier</creatorcontrib><creatorcontrib>Moulis, Guillaume</creatorcontrib><creatorcontrib>Hamidou, Mohamed</creatorcontrib><creatorcontrib>Gerfaud-Valentin, Mathieu</creatorcontrib><creatorcontrib>Marolleau, Jean-Pierre</creatorcontrib><creatorcontrib>Terriou, 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Matthieu</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Hyper Article en Ligne (HAL)</collection><jtitle>Blood</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Guillet, Stéphanie</au><au>Crickx, Etienne</au><au>Azzaoui, Imane</au><au>Chappert, Pascal</au><au>Boutin, Emmanuelle</au><au>Viallard, Jean-François</au><au>Rivière, Etienne</au><au>Gobert, Delphine</au><au>Galicier, Lionel</au><au>Malphettes, Marion</au><au>Cheze, Stéphane</au><au>Lefrere, François</au><au>Audia, Sylvain</au><au>Bonnotte, Bernard</au><au>Lambotte, Olivier</au><au>Noel, Nicolas</au><au>Fain, Olivier</au><au>Moulis, Guillaume</au><au>Hamidou, Mohamed</au><au>Gerfaud-Valentin, Mathieu</au><au>Marolleau, Jean-Pierre</au><au>Terriou, Louis</au><au>Martis, Nihal</au><au>Morin, Anne-Sophie</au><au>Perlat, Antoinette</au><au>Le Gallou, Thomas</au><au>Roy-Peaud, Frédérique</au><au>Robbins, Ailsa</au><au>Lega, Jean-Christophe</au><au>Puyade, Matthieu</au><au>Comont, Thibault</au><au>Limal, Nicolas</au><au>Languille, Laetitia</au><au>Zarrour, Anissa</au><au>Luka, Marine</au><au>Menager, Mickael</au><au>Belmondo, Thibault</au><au>Hue, Sophie</au><au>Canoui-Poitrine, Florence</au><au>Michel, Marc</au><au>Godeau, Bertrand</au><au>Mahévas, Matthieu</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Prolonged response after TPO-RA discontinuation in primary ITP: results of a prospective multicenter study</atitle><jtitle>Blood</jtitle><addtitle>Blood</addtitle><date>2023-06-08</date><risdate>2023</risdate><volume>141</volume><issue>23</issue><spage>2867</spage><epage>2877</epage><pages>2867-2877</pages><issn>0006-4971</issn><eissn>1528-0020</eissn><abstract>•High rate of sustained response after TPO-RA discontinuation in patients with persistent or chronic ITP achieving initial CR on treatment.•Increased expression of CD69 on CD8+ T cells at the time of tapering TPO-RA could predict relapses. [Display omitted] Sustained response off treatment (SROT) after thrombopoietin receptor agonist (TPO-RA) discontinuation has been reported in immune thrombocytopenia (ITP). This prospective multicenter interventional study enrolled adults with persistent or chronic primary ITP and complete response (CR) on TPO-RAs. The primary end point was the proportion of patients achieving SROT (platelet count &gt;30 × 109/L and no bleeding) at week 24 (W24) with no other ITP-specific medications. Secondary end points included the proportion of sustained CR off-treatment (SCROT, platelet count &gt;100 × 109/L and no bleeding) and SROT at W52, bleeding events, and pattern of response to a new course of TPO-RAs. We included 48 patients with a median age of 58.5 years; 30 of 48 had chronic ITP at TPO-RA initiation. In the intention-to-treat analysis, 27 of 48 achieved SROT, 15 of 48 achieved SCROT at W24; 25 of 48 achieved SROT, and 14 of 48 achieved SCROT at W52. No severe bleeding episode occurred in patients who relapsed. Among patients rechallenged with TPO-RA, 11 of 12 achieved CR. We found no significant clinical predictors of SROT at W24. Single-cell RNA sequencing revealed enrichment of a tumor necrosis factor α signaling via NF-κB signature in CD8+ T cells of patients with no sustained response after TPO-RA discontinuation, which was further confirmed by a significant overexpression of CD69 on CD8+ T cells at baseline in these patients as compared with those achieving SCROT/SROT. Our results strongly support a strategy based on progressive tapering and discontinuation of TPO-RAs for patients with chronic ITP who achieved a stable CR on treatment. This trial was registered at www.clinicaltrials.gov as #NCT03119974. Guillet et al present results of thrombopoietin receptor agonist (TPO-RA) discontinuation in a selected population of patients with persistent or chronic immune thrombocytopenia (ITP). They report that in patients in stable remission with a platelet count of &gt;100 × 109/L for at least 2 months (48 of 388 patients), 56% maintained a platelet count of &gt;30 × 109/L off therapy. This suggests that a subset of patients on chronic treatment with TPO-RA can be successfully tapered off therapy.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>36893453</pmid><doi>10.1182/blood.2022018665</doi><tpages>11</tpages><orcidid>https://orcid.org/0000-0001-9182-1434</orcidid><orcidid>https://orcid.org/0000-0002-8932-3169</orcidid><orcidid>https://orcid.org/0000-0002-6838-2389</orcidid><orcidid>https://orcid.org/0000-0002-2530-7346</orcidid><orcidid>https://orcid.org/0000-0002-9799-4608</orcidid><orcidid>https://orcid.org/0000-0001-7500-9323</orcidid><orcidid>https://orcid.org/0000-0002-9398-2968</orcidid><orcidid>https://orcid.org/0000-0002-3964-4968</orcidid><orcidid>https://orcid.org/0000-0001-9970-6051</orcidid><orcidid>https://orcid.org/0000-0003-4055-617X</orcidid><orcidid>https://orcid.org/0000-0002-1098-4598</orcidid><orcidid>https://orcid.org/0000-0002-1974-3870</orcidid><orcidid>https://orcid.org/0000-0001-7229-3808</orcidid><oa>free_for_read</oa></addata></record>
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identifier ISSN: 0006-4971
ispartof Blood, 2023-06, Vol.141 (23), p.2867-2877
issn 0006-4971
1528-0020
language eng
recordid cdi_hal_primary_oai_HAL_hal_04032447v1
source MEDLINE; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Alma/SFX Local Collection
subjects Adult
Autoimmunity
Human health and pathology
Humans
Hydrazines - therapeutic use
Life Sciences
Middle Aged
Platelet Count
Prospective Studies
Purpura, Thrombocytopenic, Idiopathic - drug therapy
Receptors, Fc - therapeutic use
Recombinant Fusion Proteins - therapeutic use
Thrombocytopenia - drug therapy
Thrombopoietin - therapeutic use
title Prolonged response after TPO-RA discontinuation in primary ITP: results of a prospective multicenter study
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