Abstract

Bone marrow fibrosis (BMF) is manually assessed by reticulin and trichrome stain of bone marrow (BM) biopsy and graded on a semi-quantitative scale. Krebs von den Lungen 6 (KL-6) and Mac-2 binding protein glycosylation isomer (M2BPGi) are known to be associated with lung and liver fibrosis, respectively. We explored the usefulness of KL-6 and M2BPGi to assess BMF. A total of 250 patients who underwent BM biopsy with hematologic or non-hematologic diseases were included, and 42 patients with lung and liver diseases were excluded. The patients’ data, including age, sex, diagnosis, white blood cell, hemoglobin (Hb), platelet, and lactate dehydrogenase (LDH) were collected. Measured KL-6 and M2BPGi levels were compared with reticulin grade (RG) (grade 0–3). KL-6 levels were significantly elevated with an increase in RG, but M2BPGi did not show a significant difference. Hb, LDH, or KL-6 were independent predictors for BMF (odds ratio: 1.96, 2.26, 2.91, respectively), but showed poor predictive ability (area under the curve [AUC] 0.62, 0.61, 0.60, respectively). The combination of Hb, LDH, and KL-6 showed a significantly improved predictive ability for BMF (AUC 0.73; integrated discrimination improvement 0.057; category-free net reclassification improvement 0.625). This is the first study to evaluate the usefulness of KL-6 for assessing BMF. The combination of Hb, LDH, and KL-6 would be an objective and relevant biomarker approach and be applied to risk stratification for BMF.

Highlights

  • A wide variety of hematologic and non-hematologic diseases are associated with bone marrow fibrosis (BMF)

  • BMF is associated with the prognosis of hematological malignancies such as primary myelofibrosis (PMF), myelodysplastic syndromes, chronic myeloid leukemia, and myeloproliferative neoplasm (MPN) [3–6]

  • We investigated the association of Krebs von den Lungen 6 (KL-6) and Mac-2 binding protein glycosylation isomer (M2BPGi) with reticulin grade (RG)

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Summary

Introduction

A wide variety of hematologic and non-hematologic diseases are associated with bone marrow fibrosis (BMF). BMF is characterized by increased reticulin and/or collagen fibers deposition in bone marrow (BM) [1]. The etiology and clinical relevance of fiber deposition are not well understood. A pathological increase of BMF contributes to variable degrees of cytopenia, a leukoerythroblastic feature, hepatomegaly/splenomegaly, and an increase in disease-related morbidity [2]. BMF is associated with the prognosis of hematological malignancies such as primary myelofibrosis (PMF), myelodysplastic syndromes, chronic myeloid leukemia, and myeloproliferative neoplasm (MPN) [3–6]. Identification and grading of BMF are relevant in assessing disease stages and predicting diseases prognosis

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