Evidence map›Paper›PMID 37307169›Full record

ArticleBlood advances2023

Time to progression of disease and outcomes with second-line BTK inhibitors in relapsed/refractory mantle cell lymphoma.

Diego Villa, Aixiang Jiang, Carlo Visco, Nicola Crosbie, Rory McCulloch, Michael J Buege, Anita Kumar, David A Bond, Jonas Paludo, Matthew J Maurer and 9 more

Open access · goldAbstract read
In one paragraph

Article in Blood advances, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
5.9field-weighted citation impact, top 4% 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

12 citing papers in PubMed, 23 citations in OpenAlex.

  1. Article
  2. Advances in targeted and cellular therapies for relapsed/refractory mantle cell lymphoma: immunotherapeutic strategies and challenges.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2026
    Review
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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

19 authors at 9 institutions in 6 countries.

Diego VillaBritish Columbia Cancer Centre for Lymphoid Cancer and University of British Columbia, Vancouver, BC, Canada.ORCID 0000-0002-4625-3009
Aixiang JiangBritish Columbia Cancer Centre for Lymphoid Cancer and University of British Columbia, Vancouver, BC, Canada.
Carlo ViscoDepartment of Medicine, Section of Hematology, University of Verona, Verona, Italy.ORCID 0000-0003-2863-0883
Nicola CrosbieHaematology, University Hospitals Plymouth NHS Trust, Plymouth, United Kingdom.
Rory McCullochDepartment of Haematology, Gloucestershire Hospitals NHS Foundation Trust, Gloucester, United Kingdom.ORCID 0000-0003-0090-7174
Michael J BuegeDepartment of Pharmacy, Memorial Sloan Kettering Cancer Center, New York, NY.ORCID 0000-0001-9063-1495
Anita KumarLymphoma Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY.ORCID 0000-0002-1381-5810
David A BondDivision of Hematology, Department of Internal Medicine, The Ohio State University, Columbus, OH.ORCID 0000-0003-0773-1829
Jonas PaludoDivision of Hematology, Mayo Clinic, Rochester, MN.ORCID 0000-0002-7350-5531
Matthew J MaurerDivision of Clinical Trials and Biostatistics, Mayo Clinic, Rochester, MN.ORCID 0000-0002-1867-0526
Gita ThanarajasingamDivision of Hematology, Mayo Clinic, Rochester, MN.
Katharine L LewisDepartment of Haematology, Sir Charles Gairdner Hospital, Perth, WA, Australia.ORCID 0000-0003-0549-5877
Chan Y CheahDepartment of Haematology, Sir Charles Gairdner Hospital, Perth, WA, Australia.ORCID 0000-0001-7988-1565
Joachim BaechDepartment of Hematology, Clinical Cancer Research Center, Aalborg University Hospital, Haematology, Aalborg, Denmark.ORCID 0000-0001-8848-4879
Tarec C El-GalalyDepartment of Hematology, Clinical Cancer Research Center, Aalborg University Hospital, Haematology, Aalborg, Denmark.ORCID 0000-0002-4406-380X
Laveniya KugathasanFaculty of Medicine, University of British Columbia, Vancouver, BC, Canada.
David W ScottBritish Columbia Cancer Centre for Lymphoid Cancer and University of British Columbia, Vancouver, BC, Canada.ORCID 0000-0002-0435-5947
Alina S GerrieBritish Columbia Cancer Centre for Lymphoid Cancer and University of British Columbia, Vancouver, BC, Canada.ORCID 0000-0003-4727-1425
David LewisHaematology, University Hospitals Plymouth NHS Trust, Plymouth, United Kingdom.
University of British Columbia · CAMayo Clinic · USAalborg University Hospital · DKMemorial Sloan Kettering Cancer Center · USThe University of Western Australia · AUUniversity Hospitals Plymouth NHS Trust · GBGloucestershire Hospitals NHS Foundation Trust · GBThe Ohio State University · USUniversity of Verona · IT

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Nicholas D Socci · 1985 to 2026
$347.4M
The Role of Monocytes in non-Hodgkin LymphomaP50CA097274 · NCI · UNIVERSITY OF IOWA · PI WEINER, GEORGE J. · 2002 to 2021
$45.7M
The OSU Center for Clinical and Translational Science: Advancing Today's Discoveries to Improve HealthUL1TR002733 · NCATS · OHIO STATE UNIVERSITY · PI RINGEL, MATTHEW D · 2018 to 2022
$28.9M
NCATS NIH HHS UL1 TR002733NCI NIH HHS P30 CA008748NCI NIH HHS P50 CA097274
6 · The paper itself

Abstract

Time to progression of disease (POD) after first-line (1L) therapy is prognostic in mantle cell lymphoma (MCL), although studies have included a broad range of 1L, second-line (2L), and subsequent lines of therapy. The purpose of this study was to evaluate the factors predicting outcomes in patients with relapsed/refractory (R/R) MCL exclusively initiating 2L Bruton's tyrosine kinase inhibitors (BTKis) after 1L rituximab-containing therapy. Patients were accrued from 8 international centers (7 main, 1 validation cohort). Multivariable models evaluating the association between time to POD and clinical/pathologic factors were constructed and converted into nomograms and prognostic indexes predicting outcomes in this population. A total of 360 patients were included, including 160 in the main cohort and 200 in the validation cohort. Time to POD, Ki67 ≥ 30%, and MCL International Prognostic Index (MIPI) were associated with progression-free survival (PFS2) and overall survival (OS2) from the start of 2L BTKis. C-indexes were consistently ≥0.68 in both cohorts. Web/application-based calculators based on nomograms and prognostic indexes to estimate PFS2 and OS2 were constructed. The 2L BTKi MIPI identifies 3 groups with distinct 2-year PFS2, including high risk (14%), intermediate risk (50%), and low risk (64%). Time to POD, Ki67, and MIPI are associated with survival outcomes in patients with R/R MCL receiving 2L BTKis. Simple clinical models incorporating these variables may assist in planning for alternative therapies such as chimeric antigen receptor T-cell therapy, allogeneic stem cell transplantation, or novel agents with alternative mechanisms of action.

Indexed as

Hematopoietic Stem Cell TransplantationLymphoma, Mantle-CellAdultAntineoplastic Combined Chemotherapy ProtocolsHumansKi-67 AntigenPrognosisKi-67 Antigen

Identifiers

PMID37307169
PMCPMC10425680
OpenAlexW4380357995

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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Registered trials

None linked

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.