Evidence map›Paper›PMID 38302846›Full record

ArticleAdvances in therapy2024

Treatment Outcomes with Standard of Care in Relapsed/Refractory Diffuse Large B-Cell Lymphoma: Real-World Data Analysis.

Andrew Ip, Alex Mutebi, Tongsheng Wang, Monika Jun, Anupama Kalsekar, Fernando Rivas Navarro, Anthony Wang, Rajesh Kamalakar, Mariana Sacchi, Brian Elliott

Open access · hybridAbstract read
In one paragraph

Article in Advances in therapy, 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
3.1field-weighted citation impact, top 7% 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

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

  1. Pooled it
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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

10 authors at 3 institutions in 1 country.

Andrew IpHackensack Meridian Health, Hackensack University Medical Center, Hackensack, NJ, USA.
Alex MutebiGenmab US, Inc., 777 Scudders Mill Road, Plainsboro, NJ, 08536, USA. almu@genmab.com.
Tongsheng WangGenmab US, Inc., 777 Scudders Mill Road, Plainsboro, NJ, 08536, USA.
Monika JunGenmab US, Inc., 777 Scudders Mill Road, Plainsboro, NJ, 08536, USA.
Anupama KalsekarGenmab US, Inc., 777 Scudders Mill Road, Plainsboro, NJ, 08536, USA.
Fernando Rivas NavarroGenmab US, Inc., 777 Scudders Mill Road, Plainsboro, NJ, 08536, USA.
Anthony WangAbbVie, Inc., North Chicago, IL, USA.
Rajesh KamalakarAbbVie, Inc., North Chicago, IL, USA.
Mariana SacchiGenmab US, Inc., 777 Scudders Mill Road, Plainsboro, NJ, 08536, USA.
Brian ElliottGenmab US, Inc., 777 Scudders Mill Road, Plainsboro, NJ, 08536, USA.
Genmab (United States) · USAbbVie (United States) · USHackensack University Medical Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionDespite new therapies for relapsed or refractory (R/R) diffuse large B-cell lymphoma (DLBCL), treatments with chemotherapy, single-agent rituximab/obinutuzumab, single-agent lenalidomide, or combinations of these agents continue to be commonly used.

methodsThis retrospective study utilized longitudinal data from 4226 real-world electronic health records to characterize outcomes in patients with R/R DLBCL. Eligible patients were diagnosed with DLBCL between January 2010 and March 2022 and had R/R disease treated with ≥ 1 prior systemic line of therapy (LOT), including ≥ 1 anti-CD20-containing regimen.

resultsA total of 573 patients treated with ≥ 1 prior LOT were included (31.2% and 13.4% with ≥ 2 and ≥ 3 prior LOTs, respectively). Median duration of follow-up was 7.7 months. Most patients (57.1%) were male; mean standard deviation (SD) age was 63 (14.7) years. Overall and complete response rates (95% confidence interval (CI) were 52% (48-56) and 23% (19-27). Median duration of response and duration of complete response were 3.5 and 18.4 months. Median progression-free and overall survival (95% CI) was 3.0 (2.8-3.3) and 12.9 (10.1-16.9) months, respectively. Patients with a higher number of prior LOTs, primary refractoriness, refractoriness to last LOT, refractoriness to last anti-CD20-containing regimen, and prior CAR T exposure had worse outcomes (i.e., challenging-to-treat R/R DLBCL) compared with those without these characteristics.

conclusionsOutcomes in patients with R/R DLBCL treated with chemotherapy, single-agent rituximab/obinutuzumab, single-agent lenalidomide, or combinations of these agents remain poor, especially for those with challenging-to-treat R/R DLBCL. These findings underscore the unmet need for new, safe, and effective therapies, especially for challenging-to-treat R/R DLBCL populations.

Indexed as

Lymphoma, Large B-Cell, DiffuseLymphoma, Non-HodgkinAntineoplastic Combined Chemotherapy ProtocolsData AnalysisFemaleHumansLenalidomideMaleMiddle AgedRetrospective StudiesRituximabStandard of CareTreatment OutcomeLenalidomideRituximabBispecific antibodyChimeric antigen receptorImmunotherapyObservationalReal-world evidenceRetrospectiveSalvage therapyStandard of care

Identifiers

PMID38302846
PMCPMC10879405
OpenAlexW4391481737

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

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.