Peripheral blasts are associated with responses to ruxolitinib and outcomes in patients with chronic-phase myelofibrosis.


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: 01 03 2022
received: 08 02 2022
accepted: 11 03 2022
pubmed: 2 4 2022
medline: 11 6 2022
entrez: 1 4 2022
Statut: ppublish

Résumé

The presence of peripheral blasts (PB) is a negative prognostic factor in patients with primary and secondary myelofibrosis (MF) and PB ≥4% was associated with a particularly unfavorable prognosis. Ruxolitinib (RUX) is the JAK1/2 inhibitor most used for treatment of MF-related splenomegaly and symptoms. Its role has not been assessed in correlation with PB. In 794 chronic-phase MF patients treated with RUX, we evaluated the impact of baseline percentage of PB on response (spleen and symptoms responses) and outcome (RUX discontinuation-free, leukemia-free, and overall survival). Three subgroups were compared: PB-0 (no PB, 61.3%), PB-4 (PB 1%-4%, 33.5%), and PB-9 (PB 5%-9%, 5.2%). At 3 and 6 months, spleen responses were less frequently achieved by PB-4 (P = .001) and PB-9 (P = .004) compared to PB-0 patients. RUX discontinuation-free, leukemia-free, and overall survival were also worse for PB-4 and PB-9 patients (P = .001, P = .002, and P < .001, respectively). Personalized approaches beyond RUX monotherapy may be useful in PB-4 and particularly in PB-9 patients.

Sections du résumé

BACKGROUND
The presence of peripheral blasts (PB) is a negative prognostic factor in patients with primary and secondary myelofibrosis (MF) and PB ≥4% was associated with a particularly unfavorable prognosis. Ruxolitinib (RUX) is the JAK1/2 inhibitor most used for treatment of MF-related splenomegaly and symptoms. Its role has not been assessed in correlation with PB.
METHODS
In 794 chronic-phase MF patients treated with RUX, we evaluated the impact of baseline percentage of PB on response (spleen and symptoms responses) and outcome (RUX discontinuation-free, leukemia-free, and overall survival). Three subgroups were compared: PB-0 (no PB, 61.3%), PB-4 (PB 1%-4%, 33.5%), and PB-9 (PB 5%-9%, 5.2%).
RESULTS
At 3 and 6 months, spleen responses were less frequently achieved by PB-4 (P = .001) and PB-9 (P = .004) compared to PB-0 patients. RUX discontinuation-free, leukemia-free, and overall survival were also worse for PB-4 and PB-9 patients (P = .001, P = .002, and P < .001, respectively).
CONCLUSIONS
Personalized approaches beyond RUX monotherapy may be useful in PB-4 and particularly in PB-9 patients.

Identifiants

pubmed: 35363892
doi: 10.1002/cncr.34216
pmc: PMC9325504
doi:

Substances chimiques

Nitriles 0
Pyrazoles 0
Pyrimidines 0
ruxolitinib 82S8X8XX8H

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

2449-2454

Informations de copyright

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

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Auteurs

Francesca Palandri (F)

IRCCS Azienda Ospedaliero-Universitaria di Bologna, Istituto di Ematologia "Seràgnoli", Bologna, Italy.

Daniela Bartoletti (D)

IRCCS Azienda Ospedaliero-Universitaria di Bologna, Istituto di Ematologia "Seràgnoli", Bologna, Italy.
Dipartimento di Medicina Specialistica, Diagnostica e Sperimentale, Università di Bologna, Bologna, Italy.

Alessandra Iurlo (A)

Foundation IRCCS Ca' Granda, Ospedale Maggiore Policlinico, Milano, Italy.

Massimiliano Bonifacio (M)

Azienda Ospedaliera Universitaria Integrata Verona, Verona, Italy.

Elisabetta Abruzzese (E)

Ospedale S. Eugenio, Università Tor Vergata, Rome, Italy.

Giovanni Caocci (G)

Polo oncologico "A. Businco", Università degli studi di Cagliari, Cagliari, Italy.

Elena M Elli (EM)

Ospedale San Gerardo, Azienda Socio Sanitaria Territoriale Monza, Monza, Italy.

Giuseppe Auteri (G)

IRCCS Azienda Ospedaliero-Universitaria di Bologna, Istituto di Ematologia "Seràgnoli", Bologna, Italy.
Dipartimento di Medicina Specialistica, Diagnostica e Sperimentale, Università di Bologna, Bologna, Italy.

Mario Tiribelli (M)

Azienda Ospedaliera Universitaria Integrata di Udine, Udine, Italy.

Nicola Polverelli (N)

Azienda Socio Sanitaria Territoriale Spedali Civili di Brescia, Brescia, Italy.

Maurizio Miglino (M)

IRCCS Policlinico San Martino, Genova, Italy.
Dipartimento di Medicina interna e Specialità mediche, Università di Genova, Genova, Italy.

Florian H Heidel (FH)

Innere Medicine C, Universitätsmedizin Greifswald, Greifswald, Germany.
Leibniz Institute on Aging, Fritz Lipmann-Institute, Jena, Germany.

Alessia Tieghi (A)

Azienda USL - IRCCS di Reggio Emilia, Reggio Emilia, Italy.

Giulia Benevolo (G)

Azienda Ospedaliera Universitaria Città della Salute e della Scienza, Torino, Italy.

Eloise Beggiato (E)

Dipartimento di Oncologia, Università di Torino, Torino, Italy.

Carmen Fava (C)

Azienda Ospedaliera Ordine Mauriziano di Torino, Torino, Italy.

Francesco Cavazzini (F)

Azienda Ospedaliera Universitaria Arcispedale S. Anna, Ferrara, Italy.

Novella Pugliese (N)

Dipartimento di Medicina clinica e Chirurgia, Università degli Studi di Napoli Federico II, Napoli, Italy.

Gianni Binotto (G)

Azienda Ospedaliera Universitaria di Padova, Padova, Italy.

Costanza Bosi (C)

AUSL di Piacenza, Piacenza, Italy.

Bruno Martino (B)

Azienda Ospedaliera "Bianchi Melacrino Morelli", Reggio Calabria, Italy.

Monica Crugnola (M)

Azienda Ospedaliero-Universitaria di Parma, Parma, Italy.

Emanuela Ottaviani (E)

IRCCS Azienda Ospedaliero-Universitaria di Bologna, Istituto di Ematologia "Seràgnoli", Bologna, Italy.

Giorgia Micucci (G)

Azienda Ospedaliera Ospedali Riuniti Marche Nord, Azienda Ospedaliera San Salvatore, Pesaro, Italy.

Malgorzata M Trawinska (MM)

Ospedale S. Eugenio, Università Tor Vergata, Rome, Italy.

Antonio Cuneo (A)

Azienda Ospedaliera Universitaria Arcispedale S. Anna, Ferrara, Italy.

Monica Bocchia (M)

Policlinico S. Maria alle Scotte, Azienda Ospedaliera Universitaria Senese, Siena, Italy.

Mauro Krampera (M)

Azienda Ospedaliera Universitaria Integrata Verona, Verona, Italy.

Fabrizio Pane (F)

Dipartimento di Medicina clinica e Chirurgia, Università degli Studi di Napoli Federico II, Napoli, Italy.

Roberto M Lemoli (RM)

IRCCS Policlinico San Martino, Genova, Italy.
Dipartimento di Medicina interna e Specialità mediche, Università di Genova, Genova, Italy.

Daniela Cilloni (D)

Azienda Ospedaliera Ordine Mauriziano di Torino, Torino, Italy.
Azienda Ospedaliera Universitaria San Luigi Gonzaga, Torino, Italy.

Nicola Vianelli (N)

IRCCS Azienda Ospedaliero-Universitaria di Bologna, Istituto di Ematologia "Seràgnoli", Bologna, Italy.

Michele Cavo (M)

IRCCS Azienda Ospedaliero-Universitaria di Bologna, Istituto di Ematologia "Seràgnoli", Bologna, Italy.
Dipartimento di Medicina Specialistica, Diagnostica e Sperimentale, Università di Bologna, Bologna, Italy.

Giuseppe A Palumbo (GA)

Dipartimento di Scienze Mediche, Chirurgiche e Tecnologie Avanzate "G.F. Ingrassia", Università di Catania, Catania, Italy.

Massimo Breccia (M)

Azienda Ospedaliera Universitaria Policlinico Umberto I, Università degli Studi di Roma "La Sapienza", Rome, Italy.

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