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1127 Discontinuation of Thrombopoietin Receptor Agonists: A 10 Year Real-World Experience from an Academic Hospital in Madrid

Program: Oral and Poster Abstracts
Session: 311. Disorders of Platelet Number or Function: Clinical and Epidemiological: Poster I
Hematology Disease Topics & Pathways:
Research, Bleeding and Clotting, Clinical Research, platelet disorders, Diseases, thrombocytopenias, real-world evidence
Saturday, December 10, 2022, 5:30 PM-7:30 PM

Andres Ramirez Lopez1,2*, María Teresa Alvarez Román, MD, PhD1,3,4*, María Isabel Rivas Pollmar, MD, PhD1,3*, Mónica Martín Salces, MD, PhD1,3*, Mar Gutierrez, MD1,3*, Eduardo Garcia Perez, MD1,3*, Elena G Arias-Salgado, PhD1,3*, Elena Monzón Manzano, PhD1,3*, Paula Acuña, BSc1,3*, Víctor Jiménez Yuste, MD, PhD1,3,4*, Nora V. Butta, PhD3,5* and Cédric Hermans, MD, MRCP, PhD6

1Hospital Universitario La Paz, Madrid, Spain
2Hospital General La Mancha Centro, Alcazar de San Juan, Spain
3IdiPAZ, Madrid, Spain
4Universidad Autónoma de Madrid, Madrid, Spain
5Hospital Universitario La Paz, Madrid, Madrid, Spain
6Division of Hematology, Cliniques Univ. Saint-Luc, Brussels, Belgium

Background: Thrombopoietin receptor agonists (TPO-RAs) have become the second line treatment for patients with immune thrombocytopenia (ITP). Despite TPO-RAs are currently indicated for continuous treatment, some patients can achieve a sustained response that allows tapering and discontinuation. Predictors of responses and relapses after discontinuation are unknown factors that are being under investigation.

Methods: This is a retrospective study approved by Hospital Universitario La Paz Ethical Committee. We describe our experience during 10 years in discontinuation of TPO-RAs and relapses in the ITP patient cohort from Hospital Universitario La Paz in Madrid.We included all ITP patients treated with TPO-RAs between 1st January 2011 and 31st December 2020. We analyzed response, discontinuation, and relapses after TPO-RAs treatments, with a follow-up period until 31st December 2021.

This research was funded by ISCIII-Fondos FEDER PI19/00772 and Platelet Disorder Support Association.

Results:One-hundred-fifty-one ITP patients were treated with TPO-RAs between 1st January 2011 and 31st December 2020. We excluded those without complete information about response, discontinuation, and relapses after TPO-RAs, analyzing a total of 133 patients. Thirteen received Romiplostim, 7 men and 6 women, with a median age of 66y (range 3-98). All of them achieved a clinical response according to standard criteria and in 4 it was possible to discontinue TPO-AR, with no need of retreatment with a median follow-up of 17,4 months (13,6-39,5).

Seventy-five patients were treated with Eltrombopag, 33 men and 42 women, with a median age of 49y (range 1-98). Seventy-one patients get a clinical response, which allows discontinuation of TPO-AR in 43 of them, with 25 sustained responses and a median follow-up of 40,5 months (9,9-60,3).

We also included 45 ITP patients, 21 men and 24 women, median age of 53y (range 2-93), who received both TPO-AR because of lack of response or intolerance with the first (4 Romiplostim and 41 Eltrombopag). Among the 34 patients who achieved a response, 17 were able to discontinue TPO-ARs and 7 needed retreatments. The follow-up period for this cohort was 23,4 months (1,9-75).

Globally, 39 patients discontinue TPO-RAs with no need of further ITP treatment with a median follow-up of 28,4months (1,9-75) since discontinuation until the end of the study.Results are summarized in Table 1.

Conclusion: In conclusion, 29% (39/113) of ITP patients who were treated with TPO-RAs could discontinue this treatment without relapses with a median follow-up of 28,4months (1,9-75) since discontinuation.

Disclosures: Ramirez Lopez: Janssen: Speakers Bureau; Sanofi: Speakers Bureau; Kyowa: Speakers Bureau. Alvarez Román: Octapharma: Consultancy, Membership on an entity's Board of Directors or advisory committees, Other: Sponsored Symposia; CSL-Behring: Consultancy, Membership on an entity's Board of Directors or advisory committees, Other: Sponsored Symposia; Amgen: Consultancy, Membership on an entity's Board of Directors or advisory committees, Other: Sponsored Symposia; Roche: Membership on an entity's Board of Directors or advisory committees, Other: Sponsored Symposia; Sobi: Consultancy, Membership on an entity's Board of Directors or advisory committees, Other: Advisory Board ; Takeda: Consultancy, Membership on an entity's Board of Directors or advisory committees, Other: Sponsored Symposia; Novo Nordisk: Consultancy, Membership on an entity's Board of Directors or advisory committees, Other: Sponsored Symposia; Pfizer: Consultancy, Membership on an entity's Board of Directors or advisory committees, Other: Sponsored Symposia; Biomarin: Consultancy, Honoraria, Research Funding; Grifols: Consultancy, Honoraria, Research Funding; Bayer: Consultancy, Membership on an entity's Board of Directors or advisory committees, Other; Novartis: Consultancy, Membership on an entity's Board of Directors or advisory committees, Other: Sponsored Symposia. Jiménez Yuste: Grifols: Consultancy, Honoraria, Research Funding; CSL Behring: Consultancy, Honoraria, Research Funding; Bayer: Consultancy, Honoraria, Research Funding; Octapharma: Consultancy, Honoraria, Research Funding; NovoNordisk: Consultancy, Honoraria, Research Funding; Sobi: Consultancy, Honoraria, Research Funding; BioMarin: Consultancy; Takeda: Consultancy, Honoraria, Research Funding; Sanofi: Consultancy, Honoraria, Research Funding; F. Hoffmann-La Roche: Consultancy, Honoraria, Research Funding; Pfizer: Consultancy, Honoraria, Research Funding. Butta: Roche: Speakers Bureau; CSL-Bering: Research Funding; Takeda: Research Funding, Speakers Bureau; Novo-Nordisk: Speakers Bureau. Hermans: oche, Novo Nordisk, Sanofi, Sobi, Takeda, Grifols, Bayer, Pfizer, Spark, Octapharma, CSL Behring: Research Funding; oche, Novo Nordisk, Sanofi, Sobi, Takeda, Grifols, Bayer, Pfizer, Spark, Octapharma, CSL Behring: Honoraria; oche, Novo Nordisk, Sanofi, Sobi, Takeda, Grifols, Bayer, Pfizer, Spark, BioMarin, Octapharma, CSL Behring: Consultancy.

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