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.

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

Fava C.;Cilloni D.;
2022-01-01

Abstract

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.
2022
1
6
myelofibrosis; outcome; peripheral blasts; response; ruxolitinib
Palandri F.; Bartoletti D.; Iurlo A.; Bonifacio M.; Abruzzese E.; Caocci G.; Elli E.M.; Auteri G.; Tiribelli M.; Polverelli N.; Miglino M.; Heidel F.H.; Tieghi A.; Benevolo G.; Beggiato E.; Fava C.; Cavazzini F.; Pugliese N.; Binotto G.; Bosi C.; Martino B.; Crugnola M.; Ottaviani E.; Micucci G.; Trawinska M.M.; Cuneo A.; Bocchia M.; Krampera M.; Pane F.; Lemoli R.M.; Cilloni D.; Vianelli N.; Cavo M.; Palumbo G.A.; Breccia M.
File in questo prodotto:
File Dimensione Formato  
Palandri et al_ 2022.pdf

Accesso aperto

Tipo di file: PDF EDITORIALE
Dimensione 573.87 kB
Formato Adobe PDF
573.87 kB Adobe PDF Visualizza/Apri

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2318/1861222
Citazioni
  • ???jsp.display-item.citation.pmc??? 0
  • Scopus 5
  • ???jsp.display-item.citation.isi??? 5
social impact