Evidence map›Paper›PMID 34516611›Full record

ArticleBlood advances2021

Early relapse identifies MCL patients with inferior survival after intensive or less intensive frontline therapy.

David A Bond, Jeffrey M Switchenko, Diego Villa, Kami Maddocks, Michael Churnetski, Alina S Gerrie, Subir Goyal, Krithika Shanmugasundaram, Oscar Calzada, Bhaskar Kolla and 25 more

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Blood advances, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
4.6field-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

23 citing papers in PubMed, 39 citations in OpenAlex.

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  18. Brexucabtagene Autoleucel for Relapsed or Refractory Mantle Cell Lymphoma in Standard-of-Care Practice: Results From the US Lymphoma CAR T Consortium.Journal of clinical oncology : official journal of the American Society of Clinical Oncology · 2023
    Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

35 authors at 14 institutions in 2 countries.

David A BondDivision of Hematology, The Ohio State University, Columbus, OH.ORCID 0000-0003-0773-1829
Jeffrey M SwitchenkoWinship Cancer Institute, Biostatistics and Bioinformatics, Emory University, Atlanta, GA.ORCID 0000-0002-5563-9325
Diego VillaCentre for Lymphoid Cancer, British Columbia Cancer, Vancouver, BC, Canada.ORCID 0000-0002-4625-3009
Kami MaddocksDivision of Hematology, The Ohio State University, Columbus, OH.
Michael ChurnetskiDepartment of Hematology and Medical Oncology, Winship Cancer Institute, Emory University, Atlanta, GA.
Alina S GerrieCentre for Lymphoid Cancer, British Columbia Cancer, Vancouver, BC, Canada.ORCID 0000-0003-4727-1425
Subir GoyalWinship Cancer Institute, Biostatistics and Bioinformatics, Emory University, Atlanta, GA.
Krithika ShanmugasundaramDepartment of Hematology and Medical Oncology, Winship Cancer Institute, Emory University, Atlanta, GA.
Oscar CalzadaDepartment of Hematology and Medical Oncology, Winship Cancer Institute, Emory University, Atlanta, GA.
Bhaskar KollaDivision of Hematology Oncology and Transplantation, University of Minnesota, Minneapolis, MN.ORCID 0000-0002-4584-9855
Veronika BachanovaDivision of Hematology Oncology and Transplantation, University of Minnesota, Minneapolis, MN.
James N GersonDivision of Hematology/Oncology, Fox Chase Cancer Center, Philadelphia, PA.
Stefan K BartaDivision of Hematology/Oncology, Fox Chase Cancer Center, Philadelphia, PA.
Brian T HillDepartment of Hematology and Medical Oncology, Taussig Cancer Institute,Cleveland Clinic, Cleveland, OH.
Yazeed SawalhaDivision of Hematology, The Ohio State University, Columbus, OH.
Peter MartinDivision of Hematology and Oncology, Weill Cornell Medical Center/New York Presbyterian Hospital, New York, NY.
Edward MaldonadoKnight Cancer Institute, Oregon Health Sciences University, Portland, OR.ORCID 0000-0002-7018-8462
Max GordonKnight Cancer Institute, Oregon Health Sciences University, Portland, OR.ORCID 0000-0003-3940-4451
Alexey V DanilovKnight Cancer Institute, Oregon Health Sciences University, Portland, OR.
Natalie S GroverDivision of Hematology, University of North Carolina, Chapel Hill, NC.ORCID 0000-0002-1346-3157
Stephanie MathewsDivision of Hematology, University of North Carolina, Chapel Hill, NC.
Madelyn BurkartRobert H. Lurie Comprehensive Cancer Center, Feinberg School of Medicine, Division of Hematology, Northwestern University, Chicago, IL.ORCID 0000-0002-5105-0564
Reem KarmaliRobert H. Lurie Comprehensive Cancer Center, Feinberg School of Medicine, Division of Hematology, Northwestern University, Chicago, IL.ORCID 0000-0003-0984-4376
Nilanjan GhoshLevine Cancer Institute, Atrium Health, Charlotte, NC.
Steven I ParkLevine Cancer Institute, Atrium Health, Charlotte, NC.
Narendranath EpperlaDivision of Hematology, The Ohio State University, Columbus, OH.ORCID 0000-0002-8216-3457
Talha BadarBMT Cellular Therapy Program, Division of Hematology and Oncology, Medical College of Wisconsin, Milwaukee, WI; and.ORCID 0000-0003-1548-918X
Jin GuoDivision of Hematology and Oncology, Weill Cornell Medical Center/New York Presbyterian Hospital, New York, NY.
Mehdi HamadaniBMT Cellular Therapy Program, Division of Hematology and Oncology, Medical College of Wisconsin, Milwaukee, WI; and.ORCID 0000-0001-5372-510X
Timothy S FenskeBMT Cellular Therapy Program, Division of Hematology and Oncology, Medical College of Wisconsin, Milwaukee, WI; and.
Mary-Kate MalecekDepartment of Medicine, Washington University, St Louis, MO.ORCID 0000-0001-8352-4675
Brad S KahlDepartment of Medicine, Washington University, St Louis, MO.ORCID 0000-0003-0459-6609
Christopher R FlowersDepartment of Hematology and Medical Oncology, Winship Cancer Institute, Emory University, Atlanta, GA.
Kristie A BlumDepartment of Hematology and Medical Oncology, Winship Cancer Institute, Emory University, Atlanta, GA.
Jonathon B CohenDepartment of Hematology and Medical Oncology, Winship Cancer Institute, Emory University, Atlanta, GA.ORCID 0000-0002-2723-6481
Emory University · USMedical College of Wisconsin · USThe Ohio State University · USCleveland Clinic · USFox Chase Cancer Center · USLevine Cancer Institute · USNewYork–Presbyterian Hospital · USNorthwestern University · USOregon Health & Science University · USThe University of Texas MD Anderson Cancer Center · USUniversity of British Columbia · CAUniversity of Minnesota · USUniversity of North Carolina at Chapel Hill · USWashington University in St. Louis · US

Funding

Winship Cancer Institute Cancer Center Support GrantP30CA138292 · NCI · EMORY UNIVERSITY · PI Suresh S Ramalingam · 2009 to 2026
$47.5M
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 CA138292
6 · The paper itself

Abstract

Although an expanding array of effective treatments has resulted in recent improvement in survival of patients with mantle cell lymphoma (MCL), outcomes remain heterogeneous, and identification of prognostic factors remains a priority. We assessed the prognostic impact of time to progression of disease (POD) after first-line therapy among 455 patients with relapsed MCL. Patients were categorized by duration of first remission as PRF/POD6, defined as progressive disease during induction or POD within 6 months of diagnosis (n = 65; 14%); POD6-24, defined as POD between 6 and 24 months after diagnosis (n = 153; 34%); and POD>24, defined as POD >24 months after diagnosis (n = 237; 53%). The median overall survival from POD (OS2) was 1.3 years (95% confidence interval [CI], 0.9-2.4) for patients with PRF/POD6, 3 years (95% CI, 2-6.8) for those with POD6-24, and 8 years (95% CI, 6.2-NR) for those with POD>24. Median OS2 was inferior in patients with early POD (defined as PRF/POD6 or POD6-24) after both intensive and less intensive frontline treatment. The prognostic performance of time until POD was replicated in an independent cohort of 245 patients with relapsed MCL, with median OS2 of 0.3 years (95% CI, 0.1-0.5) for PRF/POD6, 0.8 years (95% CI, 0.6-0.9) for POD6-24, and 2.4 years (95% CI 2.1-2.7) for POD>24. Early POD is associated with inferior OS2 in patients with relapsed MCL, identifying a high-risk population for future prospective studies.

Indexed as

Lymphoma, Mantle-CellAdultHumansPrognosisProspective StudiesRecurrenceTreatment Outcome

Identifiers

PMID34516611
PMCPMC9153047
OpenAlexW3200845029

What OpenQuestion holds

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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.