» Articles » PMID: 39424808

Evaluation of Ki-67 Expression and Large Cell Content As Prognostic Markers in MZL: a Multicenter Cohort Study

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.

Citing Articles

A comparative analysis of transformed indolent lymphomas and de novo diffuse large B-cell lymphoma: a population-based cohort study.

Vaughn J, Ramdhanny A, Munir M, Rimmalapudi S, Epperla N Blood Cancer J. 2024; 14(1):212.

PMID: 39609401 PMC: 11604794. DOI: 10.1038/s41408-024-01194-5.

References
1.
Thieblemont C, Cascione L, Conconi A, Kiesewetter B, Raderer M, Gaidano G . A MALT lymphoma prognostic index. Blood. 2017; 130(12):1409-1417. DOI: 10.1182/blood-2017-03-771915. View

2.
Epperla N, Welkie R, Torka P, Shouse G, Karmali R, Shea L . Impact of early relapse within 24 months after first-line systemic therapy (POD24) on outcomes in patients with marginal zone lymphoma: A US multisite study. J Hematol Oncol. 2023; 16(1):49. PMC: 10165748. DOI: 10.1186/s13045-023-01448-y. View

3.
Epperla N, Zhao Q, Karmali R, Torka P, Shea L, Oh T . Impact of detectable monoclonal protein at diagnosis on outcomes in marginal zone lymphoma: a multicenter cohort study. Blood Adv. 2023; 7(17):5038-5046. PMC: 10471932. DOI: 10.1182/bloodadvances.2023010133. View

4.
Petit B, Chaury M, Le Clorennec C, Jaccard A, Gachard N, Moalic-Judge S . Indolent lymphoplasmacytic and marginal zone B-cell lymphomas: absence of both IRF4 and Ki67 expression identifies a better prognosis subgroup. Haematologica. 2005; 90(2):200-6. View

5.
Thieblemont C, Molina T, Davi F . Optimizing therapy for nodal marginal zone lymphoma. Blood. 2016; 127(17):2064-71. DOI: 10.1182/blood-2015-12-624296. View