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 |
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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 >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.</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 >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.</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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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><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.
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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.</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> |
fulltext | fulltext |
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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