Real-world analysis of main clinical outcomes in patients with polycythemia vera treated with ruxolitinib or best available therapy after developing resistance/intolerance to hydroxyurea.


Journal

Cancer
ISSN: 1097-0142
Titre abrégé: Cancer
Pays: United States
ID NLM: 0374236

Informations de publication

Date de publication:
01 07 2022
Historique:
revised: 21 01 2022
received: 29 10 2021
accepted: 14 02 2022
pubmed: 14 4 2022
medline: 11 6 2022
entrez: 13 4 2022
Statut: ppublish

Résumé

Ruxolitinib is approved for patients with polycythemia vera (PV) who are resistant/intolerant to hydroxyurea, but its impact on preventing thrombosis or disease-progression is unknown. A retrospective, real-world analysis was performed on the outcomes of 377 patients with resistance/intolerance to hydroxyurea from the Spanish Registry of Polycythemia Vera according to subsequent treatment with ruxolitinib (n = 105) or the best available therapy (BAT; n = 272). Survival probabilities and rates of thrombosis, hemorrhage, acute myeloid leukemia, myelofibrosis, and second primary cancers were calculated according to treatment. To minimize biases in treatment allocation, all results were adjusted by a propensity score for receiving ruxolitinib or BAT. Patients receiving ruxolitinib had a significantly lower rate of arterial thrombosis than those on BAT (0.4% vs 2.3% per year; P = .03), and this persisted as a trend after adjustment for the propensity to have received the drug (incidence rate ratio, 0.18; 95% confidence interval, 0.02-1.3; P = .09). There were no significant differences in the rates of venous thrombosis (0.8% and 1.1% for ruxolitinib and BAT, respectively; P = .7) and major bleeding (0.8% and 0.9%, respectively; P = .9). Ruxolitinib exposure was not associated with a higher rate of second primary cancers, including all types of neoplasia, noncutaneous cancers, and nonmelanoma skin cancers. After a median follow-up of 3.5 years, there were no differences in survival or progression to acute leukemia or myelofibrosis between the 2 groups. The results suggest that ruxolitinib treatment for PV patients with resistance/intolerance to hydroxyurea may reduce the incidence of arterial thrombosis. Ruxolitinib is better than other available therapies in achieving hematocrit control and symptom relief in patients with polycythemia vera who are resistant/intolerant to hydroxyurea, but we still do not know whether ruxolitinib provides an additional benefit in preventing thrombosis or disease progression. We retrospectively studied the outcomes of 377 patients with resistance/intolerance to hydroxyurea from the Spanish Registry of Polycythemia Vera according to whether they subsequently received ruxolitinib (n = 105) or the best available therapy (n = 272). Our findings suggest that ruxolitinib could reduce the incidence of arterial thrombosis, but a disease-modifying effect could not be demonstrated for ruxolitinib in this patient population.

Sections du résumé

BACKGROUND
Ruxolitinib is approved for patients with polycythemia vera (PV) who are resistant/intolerant to hydroxyurea, but its impact on preventing thrombosis or disease-progression is unknown.
METHODS
A retrospective, real-world analysis was performed on the outcomes of 377 patients with resistance/intolerance to hydroxyurea from the Spanish Registry of Polycythemia Vera according to subsequent treatment with ruxolitinib (n = 105) or the best available therapy (BAT; n = 272). Survival probabilities and rates of thrombosis, hemorrhage, acute myeloid leukemia, myelofibrosis, and second primary cancers were calculated according to treatment. To minimize biases in treatment allocation, all results were adjusted by a propensity score for receiving ruxolitinib or BAT.
RESULTS
Patients receiving ruxolitinib had a significantly lower rate of arterial thrombosis than those on BAT (0.4% vs 2.3% per year; P = .03), and this persisted as a trend after adjustment for the propensity to have received the drug (incidence rate ratio, 0.18; 95% confidence interval, 0.02-1.3; P = .09). There were no significant differences in the rates of venous thrombosis (0.8% and 1.1% for ruxolitinib and BAT, respectively; P = .7) and major bleeding (0.8% and 0.9%, respectively; P = .9). Ruxolitinib exposure was not associated with a higher rate of second primary cancers, including all types of neoplasia, noncutaneous cancers, and nonmelanoma skin cancers. After a median follow-up of 3.5 years, there were no differences in survival or progression to acute leukemia or myelofibrosis between the 2 groups.
CONCLUSIONS
The results suggest that ruxolitinib treatment for PV patients with resistance/intolerance to hydroxyurea may reduce the incidence of arterial thrombosis.
LAY SUMMARY
Ruxolitinib is better than other available therapies in achieving hematocrit control and symptom relief in patients with polycythemia vera who are resistant/intolerant to hydroxyurea, but we still do not know whether ruxolitinib provides an additional benefit in preventing thrombosis or disease progression. We retrospectively studied the outcomes of 377 patients with resistance/intolerance to hydroxyurea from the Spanish Registry of Polycythemia Vera according to whether they subsequently received ruxolitinib (n = 105) or the best available therapy (n = 272). Our findings suggest that ruxolitinib could reduce the incidence of arterial thrombosis, but a disease-modifying effect could not be demonstrated for ruxolitinib in this patient population.

Identifiants

pubmed: 35417564
doi: 10.1002/cncr.34195
pmc: PMC9324831
doi:

Substances chimiques

Nitriles 0
Pyrazoles 0
Pyrimidines 0
ruxolitinib 82S8X8XX8H
Hydroxyurea X6Q56QN5QC

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

2441-2448

Informations de copyright

© 2022 The Authors. Cancer published by Wiley Periodicals LLC on behalf of American Cancer Society.

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Auteurs

Alberto Alvarez-Larrán (A)

Hospital Clínic, Institut d'Investigacions Biomèdiques August Pi i Sunyer, Barcelona, Spain.

Marta Garrote (M)

Hospital Clínic, Institut d'Investigacions Biomèdiques August Pi i Sunyer, Barcelona, Spain.

Francisca Ferrer-Marín (F)

Hospital Morales Messeguer, Universidad Católica San Antonio de Murcia, Murcia, Centro de Investigación Biomédica en Red de Enfermedades Raras, Murcia, Spain.

Manuel Pérez-Encinas (M)

Hospital Clínico Universitario, Santiago de Compostela, Spain.

M Isabel Mata-Vazquez (MI)

Hospital Costa del Sol, Marbella, Spain.

Beatriz Bellosillo (B)

Hospital del Mar, Barcelona, Spain.

Eduardo Arellano-Rodrigo (E)

Hospital Clínic, Institut d'Investigacions Biomèdiques August Pi i Sunyer, Barcelona, Spain.

Montse Gómez (M)

Hospital Clínico, Valencia, Spain.

Regina García (R)

Hospital Virgen de la Victoria, Málaga, Spain.

Valentín García-Gutiérrez (V)

Hospital Ramón y Cajal, Instituto Ramón y Cajal de investigación sanitaria, Madrid, Spain.

Mercedes Gasior (M)

Hospital La Paz, Madrid, Spain.

Beatriz Cuevas (B)

Hospital Universitario de Burgos, Burgos, Spain.

Anna Angona (A)

Hospital Josep Trueta, Institut Català d'Oncologia, Girona, Spain.

María Teresa Gómez-Casares (MT)

Hospital Doctor Negrín, Las Palmas de Gran Canaria, Spain.

Clara M Martínez (CM)

Hospital de la Santa Creu i Sant Pau, Barcelona, Spain.

Elena Magro (E)

Hospital Príncipe de Asturias, Alcalá de Henares, Spain.

Rosa Ayala (R)

Hospital Universitario 12 de Octubre, Madrid, Spain.

Rafael Del Orbe-Barreto (R)

Hospital Universitario de Cruces, Barakaldo, Spain.

Raúl Pérez-López (R)

Hospital Virgen de la Arrixaca, Murcia, Spain.

Maria Laura Fox (ML)

Hospital Vall d'Hebron, Barcelona, Spain.

José-María Raya (JM)

Hospital Universitario de Canarias, Santa Cruz de Tenerife, Spain.

Lucía Guerrero (L)

Hospital Río Carrión, Palencia, Spain.

Carmen García-Hernández (C)

Hospital General, Alicante, Spain.

Gonzalo Caballero (G)

Hospital Miguel Servet, Zaragoza, Spain.

Ilda Murillo (I)

Hospital San Jorge, Huesca, Spain.

Blanca Xicoy (B)

Hospital Germans Trias i Pujol, Institut Català d'Oncologia, Josep Carreras Leukemia Research Institute, Universitat Autònoma de Barcelona, Badalona, Spain.

M José Ramírez (MJ)

Hospital General, Jerez de la Frontera, Spain.

Gonzalo Carreño-Tarragona (G)

Hospital Universitario 12 de Octubre, Madrid, Spain.

Juan Carlos Hernández-Boluda (JC)

Hospital Clínico, Valencia, Spain.

Arturo Pereira (A)

Hospital Clínic, Institut d'Investigacions Biomèdiques August Pi i Sunyer, Barcelona, Spain.

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