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边缘区淋巴瘤中CD5的表达并不能预测不良预后,且与惰性淋巴瘤有相似之处。

CD5 expression in marginal zone lymphoma does not predict inferior outcome and has similarities to indolent lymphomas.

作者信息

Ghione Paola, Bantilan Kurt S, Joffe Erel, Palomba M Lia, Noy Ariela, Caron Philip, Hamlin Paul, Kumar Anita, Matasar Matthew, Owens Colette, Moskowitz Alison, Falchi Lorenzo, Straus David, Horwitz Steven, Salles Gilles, Dogan Ahmet, Zelenetz Andrew D

机构信息

Lymphoma Service, Memorial Sloan Kettering Cancer Center, New York, NY.

Hematopathology, Memorial Sloan Kettering Cancer Center, New York, NY.

出版信息

Blood Neoplasia. 2024 Jul 31;1(4):100031. doi: 10.1016/j.bneo.2024.100031. eCollection 2024 Dec.

DOI:10.1016/j.bneo.2024.100031
PMID:40552129
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12182842/
Abstract

The prognostic relevance of CD5 expression in marginal zone lymphoma (MZL) remains poorly characterized. We aimed to compare baseline characteristics and outcomes of patients with CD5 MZL and CD5 historical matched controls. We hypothesized that patients with CD5 MZL may have similarities to other CD5 expressing B-cell lymphomas, which may be informative when considering alternative therapeutic approaches for this MZL subgroup. We retrospectively analyzed 64 patients with CD5 MZL and 137 CD5 MZL controls matched on age at diagnosis and sex. The CD5 and CD5 cases did not differ in terms of mucosa assiociated lymphoid tissue (MALT)-lymphoma International Prognostic Index or incidence of nodal involvement. Bone marrow involvement was significantly more frequent in CD5 patients than in CD5 patients (67.5% vs 47.2%;  = .048). Mutated immunoglobulin heavy chain variable region gene was more common in CD5 patients (80.0%) than CD5 patients (64.0%), but this association was not significant ( = .327). Overall survival was calculated until death from any cause, disease-specific survival until lymphoma-related death, and time from diagnosis to first treatment was calculated either considering all interventions or only systemic treatments. None of these outcomes were associated with CD5 expression.

摘要

边缘区淋巴瘤(MZL)中CD5表达的预后相关性仍未得到充分描述。我们旨在比较CD5阳性MZL患者与CD5阴性历史匹配对照的基线特征和预后。我们假设CD5阳性MZL患者可能与其他表达CD5的B细胞淋巴瘤有相似之处,这在考虑该MZL亚组的替代治疗方法时可能具有参考价值。我们回顾性分析了64例CD5阳性MZL患者和137例在诊断时年龄和性别相匹配的CD5阴性MZL对照。CD5阳性和CD5阴性病例在黏膜相关淋巴组织(MALT)淋巴瘤国际预后指数或淋巴结受累发生率方面没有差异。CD5阳性患者的骨髓受累明显比CD5阴性患者更频繁(67.5%对47.2%;P = .048)。免疫球蛋白重链可变区基因突变在CD5阳性患者(80.0%)中比CD5阴性患者(64.0%)更常见,但这种关联不显著(P = .327)。计算总生存期直至因任何原因死亡,疾病特异性生存期直至淋巴瘤相关死亡,从诊断到首次治疗的时间计算时考虑所有干预措施或仅考虑全身治疗。这些预后指标均与CD5表达无关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a590/12182842/79085147a43d/BNEO_NEO-2024-000207-gr6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a590/12182842/14d186da50b6/BNEO_NEO-2024-000207-ga1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a590/12182842/1150d4535215/BNEO_NEO-2024-000207-gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a590/12182842/50032c20d351/BNEO_NEO-2024-000207-gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a590/12182842/b24b916a7fe2/BNEO_NEO-2024-000207-gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a590/12182842/355c865f5828/BNEO_NEO-2024-000207-gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a590/12182842/7bba2df41ca8/BNEO_NEO-2024-000207-gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a590/12182842/79085147a43d/BNEO_NEO-2024-000207-gr6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a590/12182842/14d186da50b6/BNEO_NEO-2024-000207-ga1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a590/12182842/1150d4535215/BNEO_NEO-2024-000207-gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a590/12182842/50032c20d351/BNEO_NEO-2024-000207-gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a590/12182842/b24b916a7fe2/BNEO_NEO-2024-000207-gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a590/12182842/355c865f5828/BNEO_NEO-2024-000207-gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a590/12182842/7bba2df41ca8/BNEO_NEO-2024-000207-gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a590/12182842/79085147a43d/BNEO_NEO-2024-000207-gr6.jpg

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本文引用的文献

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CD5 Gene Signature Identifies Diffuse Large B-Cell Lymphomas Sensitive to Bruton's Tyrosine Kinase Inhibition.CD5 基因标志物可识别对布鲁顿酪氨酸激酶抑制敏感的弥漫性大 B 细胞淋巴瘤。
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