Concurrent myelodysplastic malignancies and plasma cell neoplasms; a clinicopathological study with prognostic implications.

IF 2.2 4区 医学 Q3 HEMATOLOGY Leukemia & Lymphoma Pub Date : 2024-08-23 DOI:10.1080/10428194.2024.2391905
Folashade Adekunle, Kyungmin Ko, Jeffrey Craig, Elizabeth Courville, Eli Williams, Nadine Aguilera, Ifeyinwa E Obiorah
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Abstract

Plasma cell neoplasms (PCN) have infrequently been reported in patients with myelodysplastic syndrome (MDS) and even more rarely in those with myelodysplastic syndrome/myeloproliferative neoplasm (MDS/MPN). We report the clinicopathologic features of 26 patients with bone marrow myelodysplasia accompanied by PCN, including 21 patients with MDS and 5 with MDS/MPN. The clinicopathologic features of the MDS/MPN-PCN were compared to those of the MDS-PCN group and 68 cases of MDS/MPN without PCN, respectively. The MDS/MPN-PCN group was notable for increased reticulin fibrosis > grade 1 when compared to both the MDS/MPN (p = 0.007) and MDS-PCN (p = 0.02) groups. MDS/MPN-PCN was associated with worse overall survival when compared with MDS-PCN (p = 0.03) and but not with MDS/MPN. Notably, hemoglobin level <8 g/dl (p = 0.008), and IDH2 somatic mutation (p = 0.003) were independent predictors of poor overall survival in all patients with MDS/MPN. Analysis of larger cohorts is required to confirm these associations and provide an insight into the pathogenesis.

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并发骨髓增生异常恶性肿瘤和浆细胞肿瘤;一项具有预后意义的临床病理学研究。
骨髓增生异常综合征(MDS)患者中浆细胞瘤(PCN)的报道并不多见,而骨髓增生异常综合征/骨髓增生性肿瘤(MDS/MPN)患者中浆细胞瘤的报道则更为罕见。我们报告了 26 例骨髓骨髓增生异常伴 PCN 患者的临床病理特征,其中包括 21 例 MDS 患者和 5 例 MDS/MPN 患者。我们分别将MDS/MPN-PCN患者的临床病理特征与MDS-PCN组和68例无PCN的MDS/MPN患者的临床病理特征进行了比较。与 MDS/MPN 组(p = 0.007)和 MDS-PCN 组(p = 0.02)相比,MDS/MPN-PCN 组的网状纤维化程度明显增加,且大于 1 级。与 MDS-PCN 组(p = 0.03)相比,MDS/MPN-PCN 与较差的总生存率相关,但与 MDS/MPN 组无关。值得注意的是,血红蛋白水平(p = 0.008)和 IDH2 体细胞突变(p = 0.003)是所有 MDS/MPN 患者总生存期较差的独立预测因素。要证实这些关联并深入了解发病机制,还需要对更大规模的队列进行分析。
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来源期刊
Leukemia & Lymphoma
Leukemia & Lymphoma 医学-血液学
CiteScore
4.10
自引率
3.80%
发文量
384
审稿时长
1.8 months
期刊介绍: Leukemia & Lymphoma in its fourth decade continues to provide an international forum for publication of high quality clinical, translational, and basic science research, and original observations relating to all aspects of hematological malignancies. The scope ranges from clinical and clinico-pathological investigations to fundamental research in disease biology, mechanisms of action of novel agents, development of combination chemotherapy, pharmacology and pharmacogenomics as well as ethics and epidemiology. Submissions of unique clinical observations or confirmatory studies are considered and published as Letters to the Editor
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