Evidence map›Paper›PMID 39424808›Full record

ArticleBlood cancer journal2024

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

Natalie S Grover, Kaitlin Annunzio, Marcus Watkins, Pallawi Torka, Reem Karmali, Andrea Anampa-Guzmán, Timothy S Oh, Heather Reves, Montreh Tavakkoli, Emily Hansinger and 8 more

Abstract readMulticenter Study
In one paragraph

Article in Blood cancer journal, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 1 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

11 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. [The guideline for the diagnosis and treatment of marginal zone lymphoma in China (2025)].Zhonghua xue ye xue za zhi = Zhonghua xueyexue zazhi · 2025
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

18 authors.

Natalie S GroverDepartment of Medicine, Lineberger Comprehensive Cancer Center, University of North Carolina, Chapel Hill, NC, USA.ORCID 0000-0002-1346-3157
Kaitlin AnnunzioDivsion of Hematology, Department of Medicine, The Ohio State University Comprehensive Cancer Center, Columbus, OH, USA.
Marcus WatkinsDepartment of Medicine, Siteman Cancer Center, Washington University School of Medicine, St. Louis, MO, USA.
Pallawi TorkaDepartment of Medicine, Roswell Park Cancer Institute, Buffalo, NY, USA.ORCID 0000-0002-1681-5883
Reem KarmaliDepartment of Medicine, Robert H. Lurie Comprehensive Cancer Center, Northwestern University, Chicago, IL, USA.ORCID 0000-0003-0984-4376
Andrea Anampa-GuzmánDepartment of Medicine, Roswell Park Cancer Institute, Buffalo, NY, USA.ORCID 0000-0002-4292-1137
Timothy S OhDepartment of Medicine, Robert H. Lurie Comprehensive Cancer Center, Northwestern University, Chicago, IL, USA.
Heather RevesSection of Hematologic Malignancies and Cellular Therapy, Division of Hematology-Oncology, Department of Internal Medicine, Harold C. Simmons Comprehensive Cancer Center, UT Southwestern Medical Center, Dallas, TX, USA.
Montreh TavakkoliDepartment of Medicine, University of Pennsylvania, Philadelphia, PA, USA.
Emily HansingerDepartment of Medicine, Thomas Jefferson University, Philadelphia, PA, USA.
Beth ChristianDivsion of Hematology, Department of Medicine, The Ohio State University Comprehensive Cancer Center, Columbus, OH, USA.
Colin ThomasDepartment of Medicine, University of Pennsylvania, Philadelphia, PA, USA.
Stefan K BartaDepartment of Medicine, University of Pennsylvania, Philadelphia, PA, USA.ORCID 0000-0002-3280-5271
Praveen Ramakrishnan GeethakumariSection of Hematologic Malignancies and Cellular Therapy, Division of Hematology-Oncology, Department of Internal Medicine, Harold C. Simmons Comprehensive Cancer Center, UT Southwestern Medical Center, Dallas, TX, USA.
Nancy L BartlettDepartment of Medicine, Siteman Cancer Center, Washington University School of Medicine, St. Louis, MO, USA.
Geoffrey ShouseDepartment of Medicine, City of Hope National Medical Center, Duarte, CA, USA.
Adam J Olszewski *Department of Medicine, Brown University, Providence, RI, USA.ORCID 0000-0002-6472-6658
Narendranath Epperla *Divsion of Hematology, Department of Medicine, The Ohio State University Comprehensive Cancer Center, Columbus, OH, USA. naren.epperla@hci.utah.edu.ORCID 0000-0002-8216-3457

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Hongbiao Carl Lekaye · 1985 to 2026
$347.4M
NCI NIH HHS P30 CA008748
6 · The paper itself

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.

Indexed as

Ki-67 AntigenLymphoma, B-Cell, Marginal ZoneAdultAgedAged, 80 and overBiomarkers, TumorFemaleHumansMaleMiddle AgedPrognosisRetrospective StudiesYoung AdultBiomarkers, TumorKi-67 Antigen

Identifiers

PMID39424808
PMCPMC11489653

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.