Evidence map›Paper›PMID 37158890›Full record

ArticleJournal of hematology & oncology2023

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.

Narendranath Epperla, Rina Li Welkie, Pallawi Torka, Geoffrey Shouse, Reem Karmali, Lauren Shea, Andrea Anampa-Guzmán, Timothy S Oh, Heather Reaves, Montreh Tavakkoli and 13 more

Open access · goldAbstract readLetter
In one paragraph

Article in Journal of hematology & oncology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
4.8field-weighted citation impact, top 5% of its field
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

17 citing papers in PubMed, 19 citations in OpenAlex.

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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

23 authors at 13 institutions in 1 country.

Narendranath EpperlaDivision of Hematology, Department of Medicine, Ohio State University Comprehensive Cancer Center, Columbus, OH, 43210, USA. Narendranath.Epperla@osumc.edu.
Rina Li WelkieDivision of Hematology, Department of Medicine, Ohio State University Comprehensive Cancer Center, Columbus, OH, 43210, USA.
Pallawi TorkaRoswell Park Cancer Institute, Buffalo, NY, USA.
Geoffrey ShouseCity of Hope, Duarte, CA, USA.
Reem KarmaliNorthwestern University, Chicago, IL, USA.
Lauren SheaSiteman Cancer Center, Washington University School of Medicine, St. Louis, MO, USA.
Andrea Anampa-GuzmánRoswell Park Cancer Institute, Buffalo, NY, USA.
Timothy S OhNorthwestern University, Chicago, IL, USA.
Heather ReavesHarold C. Simmons Comprehensive Cancer Center, UT Southwestern Medical Center, Dallas, TX, USA.
Montreh TavakkoliUniversity of Pennsylvania, Philadelphia, PA, USA.
Kathryn LindseyHollings Cancer Center, Medical University of South Carolina, Charleston, SC, USA.
Irl Brian GreenwellHollings Cancer Center, Medical University of South Carolina, Charleston, SC, USA.
Emily HansingerThomas Jefferson University, Philadelphia, PA, USA.
Colin ThomasThomas Jefferson University, Philadelphia, PA, USA.
Sayan Mullick ChowdhuryDivision of Hematology, Department of Medicine, Ohio State University Comprehensive Cancer Center, Columbus, OH, 43210, USA.
Kaitlin AnnunzioDivision of Hematology, Department of Medicine, Ohio State University Comprehensive Cancer Center, Columbus, OH, 43210, USA.
Beth ChristianDivision of Hematology, Department of Medicine, Ohio State University Comprehensive Cancer Center, Columbus, OH, 43210, USA.
Stefan K BartaUniversity of Pennsylvania, Philadelphia, PA, USA.
Praveen Ramakrishnan GeethakumariHarold C. Simmons Comprehensive Cancer Center, UT Southwestern Medical Center, Dallas, TX, USA.
Nancy L BartlettSiteman Cancer Center, Washington University School of Medicine, St. Louis, MO, USA.
Alex F HerreraCity of Hope, Duarte, CA, USA.
Natalie S GroverLineberger Comprehensive Cancer Center, University of North Carolina, Chapel Hill, NC, USA.
Adam J OlszewskiBrown University, Providence, RI, USA.
The Ohio State University · USCity of Hope · USNorthwestern University · USRoswell Park Comprehensive Cancer Center · USThomas Jefferson University · USUniversity of Pennsylvania · USWashington University in St. Louis · USBrown University · USMedical University of South Carolina · USMUSC Hollings Cancer Center · USSouthwestern Medical CenterThe University of Texas Southwestern Medical Center · USUniversity of North Carolina at Chapel Hill · US

Funding

Translational Therapeutics Research Program (TT)P30CA016058 · NCI · OHIO STATE UNIVERSITY · PI Tasleem J Padamsee · 1985 to 2026
$132.3M
NCI NIH HHS P30 CA016058
6 · The paper itself

Abstract

Progression of disease within 24 months (POD24) from diagnosis in marginal zone lymphoma (MZL) was shown to portend poor outcomes in prior studies. However, many patients with MZL do not require immediate therapy, and the time from diagnosis-to-treatment interval can be highly variable with no universal criteria to initiate systemic therapy. Hence, we sought to evaluate the prognostic relevance of early relapse or progression within 24 months from systemic therapy initiation in a large US cohort. The primary objective was to evaluate the overall survival (OS) in the two groups. The secondary objective included the evaluation of factors predictive of POD24 and the assessment of cumulative incidence of histologic transformation (HT) in POD24 versus non-POD24 groups. The study included 524 patients with 143 (27%) in POD24 and 381 (73%) in non-POD24 groups. Patients with POD24 had inferior OS compared to those without POD24, regardless of the type of systemic therapy received (rituximab monotherapy or immunochemotherapy) at diagnosis. After adjusting for factors associated with inferior OS in the univariate Cox model, POD24 remained associated with significantly inferior OS (HR = 2.50, 95% CI = 1.53-4.09, p = 0.0003) in multivariable analysis. The presence of monoclonal protein at diagnosis and those who received first-line rituximab monotherapy had higher odds of POD24 on logistic regression analysis. Patients with POD24 had a significantly higher risk for HT compared to those without POD24. POD24 in MZL might be associated with adverse biology and could be used as an additional information point in clinical trials and investigated as a marker for worse prognosis.

Indexed as

ImmunotherapyLymphomaAntibodies, MonoclonalHumansRecurrenceRituximabAntibodies, MonoclonalRituximabMarginal zone lymphomaNon-POD24Overall survivalPOD24

Identifiers

PMID37158890
PMCPMC10165748
OpenAlexW4375863990

What OpenQuestion holds

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LicenceCC BY
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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.