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Neutrophil to lymphocyte ratio (NLR) improves the risk assessment of ISS staging in newly diagnosed MM patients treated upfront with novel agents

Annals of Hematology volume 94, pages 1875–1883 (2015)Cite this article

Abstract

Recent reports identify the ratio between absolute neutrophil count (ANC) and absolute lymphocyte count (ALC), called neutrophil to lymphocyte ratio (NLR), as a predictor of progression-free survival (PFS) and overall survival (OS) in various malignancies. We retrospectively examined the NLR in a cohort of 309 newly diagnosed multiple myeloma (MM) patients treated upfront with novel agents. NLR was calculated using data obtained from the complete blood count (CBC) at diagnosis and subsequently correlated with PFS and OS. The median NLR was 1.9 (range 0.4–15.9). Higher NLR was independent of international staging system (ISS) stage, plasma cell infiltration or cytogenetics. The 5-year PFS and OS estimates were, respectively, 18.2 and 36.4 % for patients with NLR ≥ 2 versus 25.5 and 66.6 % in patients with NLR < 2. Among younger patients (age <65 years, N = 179), NLR ≥ 2 had a negative prognostic impact on both PFS and OS, in all ISS stages. By combining ISS stage and NLR in a model limited to young patients, we found that 19 % of the patients were classified as very low risk, 70 % standard risk and 11 % very high risk. The 5-year estimates were 39.3, 19.4 and 10.9 % for PFS and 95.8, 50.9 and 23.6 % for OS for very low, standard-risk and very high-risk groups. We found NLR to be a predictor of PFS and OS in MM patients treated upfront with novel agents. NLR can be combined with ISS staging system to identify patients with dismal outcome. However, larger cohorts and prospective studies are needed to use NLR as additional parameter to personalise MM therapy in the era of novel agents.

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Acknowledgments

This work was supported in part by a grant from Ministero della Salute (Ricerca Finalizzata), by Associazione Italiana contro le Leucemie (AIL) of Catania and Fondazione Catanese per lo Studio e la Cura delle Malattie Neoplastiche del Sangue (FON.CA.NE.SA).

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The authors declare that they have conflict of interest.

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Affiliations

  1. Division of Hematology, Azienda Policlinico-Vittorio Emanuele-Catania, Catania, Italy

    A. Romano, N. L. Parrinello, M. L. Consoli, C. Conticello, G. Milone & F. Di Raimondo

  2. Department of Oncology, Johns Hopkins University, Baltimore, MD, USA

    A. Romano, L. Marchionni & I. Borrello

  3. IOM Ricerca, Viagrande, Italy

    S. Forte

  4. Divisione di Ematologia, IRCCS, Fondazione San Matteo, Pavia, Italy

    A. Pompa & A. Corso

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  1. A. Romano
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Correspondence to A. Romano.

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Supplementary Table 1

Characteristics at baseline of 309 newly diagnosed MM patients based on up-front treatment. Group 1, based on proteasome inhibitors alone; Group 2, based on IMiDs alone; Group 3, based on the combo proteasome inhibitor + IMiDs. (DOC 48 kb)

Supplementary Table 2

Characteristics at baseline of 309 newly diagnosed MM patients split randomly 50:50 into a training and a validation set. (DOC 51 kb)

Supplementary Table 3

Distribution in the training and validation set based on NLR-ISS stratification risk in the whole cohort and in patients younger than 65 years. (DOC 42 kb)

Supplementary Figure 1

Progression free survival analysis based on up-front treatment. Group 1, based on proteasome inhibitors alone; Group 2, based on IMiDs alone; Group 3, based on the combo proteasome inhibitor + IMiDs. (DOC 81 kb)

Supplementary Figure 2

Progression free survival and overall survival analysis based on NLR-ISS stratification risk in the training (left panels) and validation set (right panels) in the whole cohort (1-2) and in the cohort of young patients, age < 65 years (3-4). (DOC 167 kb)

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Romano, A., Parrinello, N.L., Consoli, M.L. et al. Neutrophil to lymphocyte ratio (NLR) improves the risk assessment of ISS staging in newly diagnosed MM patients treated upfront with novel agents. Ann Hematol 94, 1875–1883 (2015). https://doi.org/10.1007/s00277-015-2462-4

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Keywords

  • Multiple myeloma
  • Granulocyte
  • Lymphocyte
  • ISS