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The Derived Neutrophil-to-Lymphocyte Ratio Is an Independent Prognostic Factor in Transplantation Ineligible Patients with Multiple Myeloma.

Authors :
Lee, Gyeong-Won
Park, Sung Woo
Go, Se-Il
Kim, Hoon-Gu
Kim, Min Kyoung
Min, Chang-Ki
Kwak, Jae-Yong
Bae, Sang-Byung
Yoon, Sung-Soo
Lee, Je-Jung
Kim, Ki Hwan
Nam, Seung-Hyun
Mun, Yeung-Chul
Kim, Hyo Jung
Bae, Sung Hwa
Shin, Ho-Jin
Lee, Jung-Hee
Park, Joon Seong
Jeong, Seong Hyun
Lee, Mark Hong
Source :
Acta Haematologica; Nov2018, Vol. 140 Issue 3, p146-156, 11p, 5 Charts, 2 Graphs
Publication Year :
2018

Abstract

Background: The neutrophil-to-lymphocyte ratio (NLR) is an independent prognostic marker in solid and hematological cancers. While the derived NLR (dNLR) was shown to be non-inferior to the NLR in large cohorts of patients with different cancer types, it has not been validated as a prognostic marker for multiple myeloma (MM) to date. Methods: Between May 22, 2011 and May 29, 2014, 176 patients with MM from 38 centers who were ineligible for autologous stem cell transplantation were analyzed. The dNLR was calculated using complete blood count differential data. The optimal dNLR cut-off value according to receiver operating characteristic analysis of overall survival (OS) was 1.51. All patients were treated with melphalan and prednisone combined with bortezomib. Results: The complete response rate was lower in the high dNLR group compared to the low dNLR group (7 vs. 26.1%, respectively; p = 0.0148); the corresponding 2-year OS rates were 72.2 and 84.7%, respectively (p = 0.0354). A high dNLR was an independent poor prognostic factor for OS (hazard ratio 2.217, 95% CI 1.015–4.842; p = 0.0458). Conclusion: The dNLR is a readily available and cheaply obtained parameter in clinical studies, and shows considerable potential as a new prognostic marker for transplantation-ineligible patients with MM. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00015792
Volume :
140
Issue :
3
Database :
Complementary Index
Journal :
Acta Haematologica
Publication Type :
Academic Journal
Accession number :
132806887
Full Text :
https://doi.org/10.1159/000490488