Evidence map›Paper›PMID 32702097›Full record

ArticleBlood advances2020

High metabolic tumor volume is associated with decreased efficacy of axicabtagene ciloleucel in large B-cell lymphoma.

Erin A Dean, Rahul S Mhaskar, Hong Lu, Mina S Mousa, Gabriel S Krivenko, Aleksandr Lazaryan, Christina A Bachmeier, Julio C Chavez, Taiga Nishihori, Marco L Davila and 7 more

2 registry-linked trialsAbstract read
In one paragraph

Article in Blood advances, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 168 papers, 5 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
168citing papers in PubMed, 5 pooled it
–field-weighted citation impact
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.

NCT06339255 recruitingnot on this map

A Multicenter Prospective Observational Study on Chimeric Antigen Receptor (CAR) T-cell Therapy for Lymphoma: Monitoring Feasibility, Efficacy, Toxicity and Biomarkers in a Real Life Setting

TypeobservationalSponsorPaolo CorradiniRan2019 to 2029Enrolled5,300ConditionsDiffuse Low Grade B-Cell Lymphoma, Primary Mediastinal Large B-cell Lymphoma (PMBCL), Mantle Cell Lymphoma, Follicular Lymphoma
NCT07638982 phase1not yet recruitingnot on this mapstarted 2026, after this paper: background citation

An Open-label, Phase I Trial, With an Expansion Cohort: Macrophage Conditioning to Synergize With CAR-T in High-risk Lymphoma (MAC-SHIFT)

TypeinterventionalSponsorNorthside Hospital, Inc.Ran2026 to 2029Enrolled29ConditionsDiffuse Large B Cell Lymphoma (DLBCL), Transformed Indolent B-Cell Non-Hodgkin Lymphoma to Diffuse Large B-Cell Lymphoma, High-grade B-cell Lymphoma (HGBCL), High-Grade B-Cell Lymphoma, NosArmsAxatilimab
3 · Its place in the literature

Who cites it

168 citing papers in PubMed, 5 syntheses or guidelines pooled it.

  1. Pooled it
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  4. The prognostic utility ofFrontiers in immunology · 2024
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  12. Standardized FDG-PET interpretation during CAR T-cell therapy in R/R DLBCL: a DESCAR-T study.European journal of nuclear medicine and molecular imaging · 2026
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  15. Observational
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  19. Naïve CD4Nature communications · 2026
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108 more citing papers are in PubMed but not listed here.

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

17 authors.

Erin A DeanDepartment of Malignant Hematology, H. Lee Moffitt Cancer and Research Institute, Tampa, FL.
Rahul S MhaskarDepartment of Internal Medicine, University of South Florida Morsani College of Medicine, Tampa, FL.
Hong LuTianjin Medical University Cancer Institute and Hospital, Tianjin, China.
Mina S MousaDepartment of Diagnostic Imaging and Interventional Radiology.
Gabriel S KrivenkoDepartment of Blood and Marrow Transplant and Cellular Immunotherapy, and.
Aleksandr LazaryanDepartment of Blood and Marrow Transplant and Cellular Immunotherapy, and.
Christina A BachmeierDepartment of Blood and Marrow Transplant and Cellular Immunotherapy, and.
Julio C ChavezDepartment of Malignant Hematology, H. Lee Moffitt Cancer and Research Institute, Tampa, FL.
Taiga NishihoriDepartment of Blood and Marrow Transplant and Cellular Immunotherapy, and.
Marco L DavilaDepartment of Blood and Marrow Transplant and Cellular Immunotherapy, and.
Farhad KhimaniDepartment of Blood and Marrow Transplant and Cellular Immunotherapy, and.
Hien D LiuDepartment of Blood and Marrow Transplant and Cellular Immunotherapy, and.
Javier Pinilla-IbarzDepartment of Malignant Hematology, H. Lee Moffitt Cancer and Research Institute, Tampa, FL.
Bijal D ShahDepartment of Malignant Hematology, H. Lee Moffitt Cancer and Research Institute, Tampa, FL.
Michael D JainDepartment of Blood and Marrow Transplant and Cellular Immunotherapy, and.
Yoganand BalagurunathanDepartment of Biostatistics and Bioinformatics, and.
Frederick L LockeDepartment of Blood and Marrow Transplant and Cellular Immunotherapy, and.

Funding

TRANSLATIONAL RESEARCHP30CA076292 · NCI · UNIVERSITY OF SOUTH FLORIDA · PI KENNETH Lynn WRIGHT · 1998 to 2026
$93.5M
Breaking immune tolerance to Survivin in Multiple MyelomaK23CA201594 · NCI · H. LEE MOFFITT CANCER CTR & RES INST · PI LOCKE, FREDERICK · 2015 to 2019
$821k
NCI NIH HHS K23 CA201594NCI NIH HHS P30 CA076292
6 · The paper itself

Abstract

High metabolic tumor volume (MTV) predicts worse outcomes in lymphoma treated with chemotherapy. However, it is unknown if this holds for patients treated with axicabtagene ciloleucel (axi-cel), an anti-CD19 targeted chimeric antigen receptor T-cell therapy. The primary objective of this retrospective study was to investigate the relationship between MTV and survival (overall survival [OS] and progression-free survival [PFS]) in patients with relapsed/refractory large B-cell lymphoma (LBCL) treated with axi-cel. Secondary objectives included finding the association of MTV with response rates and toxicity. The MTV values on baseline positron emission tomography of 96 patients were calculated via manual methodology using commercial software. Based on a median MTV cutoff value of 147.5 mL in the first cohort (n = 48), patients were divided into high and low MTV groups. Median follow-up for survivors was 24.98 months (range, 10.59-51.02 months). Patients with low MTV had significantly superior OS (hazard ratio [HR], 0.25; 95% confidence interval [CI], 0.10-0.66) and PFS (HR, 0.40; 95% CI, 0.18-0.89). Results were successfully validated in a second cohort of 48 patients with a median follow-up for survivors of 12.03 months (range, 0.89-25.74 months). Patients with low MTV were found to have superior OS (HR, 0.14; 95% CI, 0.05-0.42) and PFS (HR, 0.29; 95% CI, 0.12-0.69). In conclusion, baseline MTV is associated with OS and PFS in axi-cel recipients with LBCL.

Indexed as

Antigens, CD19Immunotherapy, AdoptiveBiological ProductsHumansRetrospective StudiesTumor BurdenAntigens, CD19axicabtagene ciloleucelBiological Products

Identifiers

PMID32702097
PMCPMC7391155

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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.