Evaluation of Ki-67 expression and large cell content as prognostic markers in MZL: a multicenter cohort study

IF 12.9 1区 医学 Q1 HEMATOLOGY Blood Cancer Journal Pub Date : 2024-10-18 DOI:10.1038/s41408-024-01162-z
Natalie S. Grover, Kaitlin Annunzio, Marcus Watkins, Pallawi Torka, Reem Karmali, Andrea Anampa-Guzmán, Timothy S. Oh, Heather Reves, Montreh Tavakkoli, Emily Hansinger, Beth Christian, Colin Thomas, Stefan K. Barta, Praveen Ramakrishnan Geethakumari, Nancy L. Bartlett, Geoffrey Shouse, Adam J. Olszewski, Narendranath Epperla
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Abstract

Marginal zone lymphoma (MZL) can have varied presentations and pathologic features, including high Ki-67 expression ( > 20%) as well as increased numbers of large B cells (LC). However, there are limited data available demonstrating the prognostic significance of these variables in patients with MZL. In this multi-institutional retrospective cohort study of patients with MZL treated at 10 centers, we evaluated the association between the presence of Ki-67 expression and increased LCs on survival and risk of histologic transformation (HT). A total of 785 patients were included (60% with extranodal MZL, 20% with nodal MZL, and 20% with splenic MZL). Among the 440 patients with Ki-67 staining, 22% had high Ki-67 (Ki-67 >20%). The median progression-free survival (PFS) for patients with high Ki-67 was 5.4 years compared to 7.0 years for patients with low Ki-67 (HR = 1.45, 95%CI = 1.03–2.05). Ki-67 > 20% strongly correlated with high LDH level. The risk of HT was higher in patients with increased Ki-67 than those without (5-year risk, 9.8% vs 3.87%, p = 0.01). Twelve percent of patients had LC reported on biopsy with 6% having >10% LC. The presence of LC was associated with high Ki-67 (p < 0.001), but not associated with shorter PFS or overall survival (OS). The cumulative risk for HT was higher in patients with LC compared to those without LC (5-year risk, 9.4% vs 2.9%, p = 0.04). Receipt of anthracycline-based therapy did not impact PFS or OS in either group. Ki-67 staining >20% was a prognostic factor for worse survival and strongly correlated with elevated LDH. Novel therapies should be investigated for their potential ability to overcome the high-risk features in MZL. Our data reinforce the importance of obtaining biopsies at relapse or progression, particularly in patients with baseline high Ki-67 and increased LCs, given their increased risk for HT.

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评估作为 MZL 预后标志的 Ki-67 表达和大细胞含量:一项多中心队列研究
边缘区淋巴瘤(MZL)的表现和病理特征多种多样,包括高Ki-67表达(20%)和大B细胞(LC)数量增加。然而,目前能证明这些变量对MZL患者预后意义的数据非常有限。在这项针对在 10 个中心接受治疗的 MZL 患者的多机构回顾性队列研究中,我们评估了 Ki-67 表达和 LC 增高与患者生存期和组织学转化(HT)风险之间的关系。研究共纳入了 785 例患者(60% 为结外 MZL,20% 为结节 MZL,20% 为脾 MZL)。在440名有Ki-67染色的患者中,22%为高Ki-67(Ki-67 >20%)。高Ki-67患者的中位无进展生存期(PFS)为5.4年,而低Ki-67患者为7.0年(HR = 1.45,95%CI = 1.03-2.05)。Ki-67>20%与高LDH水平密切相关。Ki-67增高的患者发生高密度脂蛋白血症的风险高于Ki-67未增高的患者(5年风险,9.8% vs 3.87%,P = 0.01)。12%的患者在活检时报告有 LC,6%的患者有>10%的 LC。LC的存在与高Ki-67有关(p = 0.001),但与较短的PFS或总生存期(OS)无关。与无 LC 的患者相比,有 LC 的患者发生 HT 的累积风险更高(5 年风险为 9.4% vs 2.9%,p = 0.04)。接受蒽环类药物治疗对两组患者的预后和生存期均无影响。Ki-67染色>20%是生存率降低的预后因素,与LDH升高密切相关。应研究新型疗法,以确定其克服MZL高危特征的潜在能力。我们的数据强调了在复发或病情进展时进行活检的重要性,尤其是对于基线Ki-67高和LCs增高的患者,因为他们的HT风险更高。
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来源期刊
CiteScore
16.70
自引率
2.30%
发文量
153
审稿时长
>12 weeks
期刊介绍: Blood Cancer Journal is dedicated to publishing high-quality articles related to hematologic malignancies and related disorders. The journal welcomes submissions of original research, reviews, guidelines, and letters that are deemed to have a significant impact in the field. While the journal covers a wide range of topics, it particularly focuses on areas such as: Preclinical studies of new compounds, especially those that provide mechanistic insights Clinical trials and observations Reviews related to new drugs and current management of hematologic malignancies Novel observations related to new mutations, molecular pathways, and tumor genomics Blood Cancer Journal offers a forum for expedited publication of novel observations regarding new mutations or altered pathways.
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