Evidence map›Paper›PMID 36735393›Full record

ArticleBlood advances2023

A validated composite comorbidity index predicts outcomes of CAR T-cell therapy in patients with diffuse large B-cell lymphoma.

Geoffrey Shouse, Andy Kaempf, Max J Gordon, Andy Artz, David Yashar, Audrey M Sigmund, Gordon Smilnak, Steven M Bair, Agrima Mian, Lindsey A Fitzgerald and 13 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 26 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed, 1 pooled it
10.6field-weighted citation impact, top 1% 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

26 citing papers in PubMed, 1 synthesis or guideline pooled it, 46 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

23 authors at 9 institutions in 1 country.

Geoffrey ShouseDivision of Lymphoma, Department of Hematology and Hematopoietic Cell Transplantation, City of Hope National Medical Center, Duarte, CA.ORCID 0000-0002-7917-5713
Andy KaempfBiostatistics Shared Resource, Knight Cancer Institute, Oregon Health & Science University, Portland, OR.
Max J GordonDepartment of Lymphoma, MD Anderson Cancer Center, Houston, TX.
Andy ArtzDivision of Lymphoma, Department of Hematology and Hematopoietic Cell Transplantation, City of Hope National Medical Center, Duarte, CA.ORCID 0000-0003-0803-9607
David YasharDivision of Lymphoma, Department of Hematology and Hematopoietic Cell Transplantation, City of Hope National Medical Center, Duarte, CA.
Audrey M SigmundDivision of Hematology, Department of Internal Medicine, The Ohio State University, Columbus, OH.ORCID 0000-0003-0706-4843
Gordon SmilnakDivision of Hematology/Oncology, Northwestern University, Chicago, IL.
Steven M BairUniversity of Colorado Cancer Center, University of Colorado, Aurora, CO.
Agrima MianDepartment of Hematology and Medical Oncology, Taussig Cancer Institute, Cleveland Clinic, Cleveland, OH.ORCID 0000-0001-6992-4883
Lindsey A FitzgeraldHuntsman Cancer Institute, The University of Utah, Salt Lake City, UT.
Amneet BajwaDivision of Hematology, Department of Internal Medicine, The Ohio State University, Columbus, OH.
Samantha JaglowskiDivision of Hematology, Department of Internal Medicine, The Ohio State University, Columbus, OH.ORCID 0000-0002-4335-2554
Neil BaileyCenter for Blood Disorders and Cellular Therapy, Swedish Cancer Institute, Seattle, WA.ORCID 0000-0002-3809-3236
Mazyar ShadmanClinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, WA.ORCID 0000-0002-3365-6562
Krish PatelCenter for Blood Disorders and Cellular Therapy, Swedish Cancer Institute, Seattle, WA.ORCID 0000-0002-2446-098X
Deborah M StephensHuntsman Cancer Institute, The University of Utah, Salt Lake City, UT.ORCID 0000-0001-9188-5008
Manali KamdarUniversity of Colorado Cancer Center, University of Colorado, Aurora, CO.
Brian T HillDepartment of Hematology and Medical Oncology, Taussig Cancer Institute, Cleveland Clinic, Cleveland, OH.
Jordan GauthierClinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, WA.
Reem KarmaliDivision of Hematology/Oncology, Northwestern University, Chicago, IL.ORCID 0000-0003-0984-4376
Loretta J NastoupilDepartment of Lymphoma, MD Anderson Cancer Center, Houston, TX.ORCID 0000-0001-6071-8610
Adam S KittaiDivision of Hematology, Department of Internal Medicine, The Ohio State University, Columbus, OH.
Alexey V DanilovDivision of Lymphoma, Department of Hematology and Hematopoietic Cell Transplantation, City of Hope National Medical Center, Duarte, CA.
City Of Hope National Medical Center · USThe Ohio State University · USCleveland Clinic · USFred Hutch Cancer Center · USNorthwestern University · USThe University of Texas MD Anderson Cancer Center · USUniversity of Colorado Cancer Center · USUniversity of Utah · USOregon Health & Science University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chimeric antigen receptor T-cell therapy (CART) has extended survival of patients with relapsed/refractory diffuse large B-cell lymphoma (DLBCL). However, limited durability of response and prevalent toxicities remain problematic. Identifying patients who are at high risk of disease progression, toxicity, and death would inform treatment decisions. Although the cumulative illness rating scale (CIRS) has been shown to correlate with survival in B-cell malignancies, no prognostic score has been independently validated in CART recipients. We retrospectively identified 577 patients with relapsed/refractory DLBCL indicated for CART at 9 academic centers to form a learning cohort (LC). Random survival forest modeling of overall survival (OS) and progression-free survival (PFS) was performed to determine the most influential CIRS organ systems and severity grades. The presence of a severe comorbidity (CIRS score ≥ 3) in the respiratory, upper gastrointestinal, hepatic, or renal system, herein termed "Severe4," had the greatest impact on post-CART survival. Controlling for other prognostic factors (number of prior therapies, Eastern Cooperative Oncology Group performance status, BCL6 translocation, and molecular subtype), Severe4 was strongly associated with shorter PFS and OS in the LC and in an independent single-center validation cohort (VC). Severe4 was also a significant predictor of grade ≥3 cytokine release syndrome in the LC, while maintaining this trend in the VC. Thus, our results indicate that adverse outcomes for patients with DLBCL meant to receive CART can be predicted using a simplified CIRS-derived comorbidity index.

Indexed as

Immunotherapy, AdoptiveLymphoma, Large B-Cell, DiffuseAntineoplastic Combined Chemotherapy ProtocolsComorbidityHumansPrognosisRetrospective Studies

Identifiers

PMID36735393
PMCPMC10362276
OpenAlexW4319061751

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.