Neutrophil to lymphocyte ratio in myelofibrosis patients treated with ruxolitinib may predict prognosis and rate of discontinuation

Author:

Laganà Alessandro1ORCID,Passucci Mauro1ORCID,Pepe Sara1ORCID,Scalzulli Emilia1,Carmosino Ida1,Costa Alessandro2ORCID,Bisegna Maria Laura1,Ielo Claudia1ORCID,Martelli Maurizio1,Breccia Massimo1ORCID

Affiliation:

1. Hematology, Department of Translational and Precision Medicine Policlinico Umberto I‐Sapienza University Rome Italy

2. Hematology Unit, Businco Hospital, Department of Medical Sciences and Public Health University of Cagliari Cagliari Italy

Abstract

AbstractBackgroundMyelofibrosis (MF) is a clonal Philadelphia chromosome negative myeloproliferative neoplasm (Ph‐MPN). MF is featured by an inflammatory condition that can also drive the progression of disease. Ruxolitinib (ruxo) is the‐first‐in‐class Jak1/2 inhibitor approved for treatment of MF, proved to reduce spleen volume and decrease symptom burden. In various malignancies neutrophil‐to‐lymphocyte ratio (NLR) has been indicated as predictor of progression free survival (PFS) and overall survival (OS). NLR might reflect the balance between systemic inflammation and immunity and is emerging as a prognostic biomarker in several neoplasms, including the hematological ones.MethodsWe analyzed a cohort of 140 MF patients treated with ruxo to validate baseline NLR (as a continuous variable and as a cut‐off 2) as predictor of OS and of ruxo treatment discontinuation.ResultsWe found that both baseline NLR as a continuous variable [HR 0.8 (95% CI: 0.7–0.9) (p = .006)] and NLR (<2 vs. ≥2) [HR 3.4 (95% CI: 1.6–7.0) (p = .001)] were significantly associated with OS. Censoring for patients undergone allotransplant, baseline NLR <2 was predictive of an earlier ruxo any‐other‐cause discontinuation [HR 3.7 (95%CI 1.7–8.3) (p < .001)].ConclusionsNLR before starting ruxo treatment may be used as a simple and early predictor of OS and earlier ruxo discontinuation in clinical practice.

Publisher

Wiley

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