边缘区淋巴瘤的 CD5 表达不能预测较差的预后,与不太活跃的淋巴瘤有相似之处

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

摘要CD5表达在边缘区淋巴瘤(MZL)中的预后相关性仍不十分明确。我们旨在比较CD5+ MZL患者和CD5-历史匹配对照的基线特征和预后。我们假设 CD5+ MZL 患者可能与其他 CD5 表达的 B 细胞淋巴瘤有相似之处,这在考虑针对这一 MZL 亚群的替代治疗方法时可能具有参考价值。我们对 64 例 CD5+ MZL 患者和 137 例 CD5- MZL 对照组进行了回顾性分析。CD5+和CD5-病例在粘膜相关淋巴组织(MALT)-淋巴瘤国际预后指数或结节受累发生率方面没有差异。CD5+患者骨髓受累的发生率明显高于CD5-患者(67.5% vs 47.2%; P = .048)。免疫球蛋白重链可变区基因突变在CD5+患者(80.0%)中比CD5-患者(64.0%)更常见,但这种关联并不显著(P = .327)。总生存期计算至任何原因死亡为止,疾病特异性生存期计算至淋巴瘤相关死亡为止,从诊断到首次治疗的时间计算考虑了所有干预措施或仅考虑了系统治疗。这些结果均与 CD5 表达无关。
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CD5 expression in marginal zone lymphoma does not predict inferior outcome and has similarities to indolent lymphomas

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%; P = .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 (P = .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.
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