Evidence map›Paper›PMID 35839452›Full record

Trial reportBlood2022

Patient-reported outcomes in ZUMA-7, a phase 3 study of axicabtagene ciloleucel in second-line large B-cell lymphoma.

Mahmoud Elsawy, Julio C Chavez, Irit Avivi, Jean-François Larouche, Luciano Wannesson, Kate Cwynarski, Keren Osman, Kelly Davison, Jakob D Rudzki, Saurabh Dahiya and 21 more

Registry-linked trialOpen access · hybridAbstract readClinical Trial, Phase III
In one paragraph

Trial report in Blood, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03391466 (A Phase 3, Randomized, Open-Label Study Evaluating the Efficacy of Axicabtagene Ciloleucel Versus Standard of Care Therapy in Subjects With Relapsed/Refractory Diffuse Large B Cell Lymphoma), which is not on this map. Cited by 51 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
51citing papers in PubMed, 4 pooled it
6.5field-weighted citation impact, top 2% 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.

NCT03391466 phase3completednot on this map

A Phase 3, Randomized, Open-Label Study Evaluating the Efficacy of Axicabtagene Ciloleucel Versus Standard of Care Therapy in Subjects With Relapsed/Refractory Diffuse Large B Cell Lymphoma (ZUMA-7)

TypeinterventionalSponsorKite, A Gilead CompanyRan2018 to 2024Enrolled359ConditionsRelapsed/Refractory Diffuse Large B-Cell Lymphoma (DLBCL)ArmsAxicabtagene Ciloleucel, Platinum-containing Salvage Chemotherapy, Cyclophosphamide, Fludarabine
3 · Its place in the literature

Who cites it

51 citing papers in PubMed, 4 syntheses or guidelines pooled it, 71 citations in OpenAlex.

  1. Pooled it
  2. Patient-Reported Outcome Measures (PROMS) in Lymphoma.Current oncology (Toronto, Ont.) · 2025
    Pooled it
  3. Pooled it
  4. Pooled it
  5. Trial
  6. Trial
  7. Trial
  8. Trial
  9. Trial
  10. Review
  11. Review
  12. Article
  13. Article
  14. Quality of Life in CAR-T Cell Therapy.Hematology reports · 2026
    Review
  15. Article
  16. Article
  17. Review
  18. Article
  19. Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

31 authors at 20 institutions in 11 countries.

Mahmoud ElsawyQueen Elizabeth II Health Sciences Centre and Division of Hematology, Department of Medicine, Dalhousie University, Halifax, NS, Canada.
Julio C ChavezMoffitt Cancer Center, Tampa, FL.
Irit AviviHematology Institute, Tel Aviv Sourasky Medical Center and Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
Jean-François LaroucheCentre Hospitalier Universitaire (CHU) de Québec, Hôpital de l'Enfant-Jésus, Québec, QC, Canada.
Luciano WannessonIstituto Oncologico della Svizzera Italiana, Bellinzona, Switzerland.
Kate CwynarskiDepartment of Haematology, University College London Hospitals National Health Services (NHS) Foundation Trust, London, United Kingdom.
Keren OsmanIcahn School of Medicine at Mount Sinai, New York, NY.
Kelly DavisonRoyal Victoria Hospital, McGill University Health Centre, Montreal, QC, Canada.
Jakob D RudzkiDepartment of Hematology & Oncology, The Medical University of Innsbruck, University Clinic for Internal Medicine, Innsbruck, Austria.
Saurabh DahiyaGreenebaum Comprehensive Cancer Center, Transplant and Cellular Therapy Program, University of Maryland Medical Center, Baltimore, MD.
Kathleen DorritieUniversity of Pittsburgh Medical Center (UPMC) Hillman Cancer Center, Pittsburgh, PA.ORCID 0000-0002-0863-8573
Samantha JaglowskiComprehensive Cancer Center, Blood and Marrow Transplant Program, The Ohio State University, Columbus, OH.ORCID 0000-0002-4335-2554
John RadfordDivision of Cancer Sciences, The Christie NHS Foundation Trust and the University of Manchester, Manchester, United Kingdom.ORCID 0000-0001-7898-2786
Franck MorschhauserGroupe de Recherche sur les formes Injectables et les Technologies Associées, University of Lille, CHU Lille, Lille, France.ORCID 0000-0002-3714-9824
David CunninghamThe Royal Marsden NHS Foundation Trust, London, United Kingdom.ORCID 0000-0001-5158-1069
Alejandro Martin Garcia-SanchoHematology Department, Salamanca University Hospital, Institute of Biomedical Research of Salamanca (IBSAL), Centro de Investigación Biomédica en Red Cáncer (CIBERONC), Salamanca, Spain.ORCID 0000-0001-6330-1028
Dimitrios TzachanisMoores Cancer Center, University of California, San Diego, La Jolla, CA.ORCID 0000-0003-4515-4428
Matthew L UlricksonBanner MD Anderson Cancer Center, Gilbert, AZ.
Reem KarmaliDivision of Hematology and Oncology, Robert H. Lurie Comprehensive Cancer Center, Northwestern University, Chicago, IL.ORCID 0000-0003-0984-4376
Natasha KekreThe Ottawa Hospital, Ottawa, ON, Canada.ORCID 0000-0001-8394-0855
Catherine ThieblemontUniversity of Paris, Hôpital Saint-Louis, Hemato-Oncology, DMU DHI, Paris, France.
Gunilla EnbladDepartment of Immunology, Genetics and Pathology, Uppsala University, Uppsala, Sweden.
Peter DregerDepartment of Medicine, University of Heidelberg, Heidelberg, Germany.
Ram MalladiCambridge University Hospitals NHS Foundation Trust, Cambridge, United Kingdom.
Namita JoshiOPEN Health, Bethesda, MD.
Wei-Jhih WangOPEN Health, Bethesda, MD.
Caitlyn T SolemOPEN Health, Bethesda, MD.ORCID 0000-0002-4914-8052
Julia Thornton SniderKite, a Gilead Company, Santa Monica, CA.ORCID 0000-0003-0017-4863
Paul ChengKite, a Gilead Company, Santa Monica, CA.
Christina ToKite, a Gilead Company, Santa Monica, CA.
Marie José KerstenCancer Center Amsterdam, Department of Hematology, Amsterdam UMC on behalf of Stichting Hemato-Oncologie voor Volwassenen Nederland (HOVON)/ Lunenburg Lymphoma Phase 1 / II Consortium (LLPC), University of Amsterdam, Amsterdam, Netherlands.
Centro de Investigación Biomédica en Red · ESDalhousie University · CAHeidelberg University · DEHôpital de l'Enfant-Jésus · CAHovon · NLIcahn School of Medicine at Mount Sinai · USInnsbruck Medical University · ATMoffitt Cancer Center · USNational Health Service · GBNorthwestern University · USOttawa Hospital · CARoyal Marsden NHS Foundation Trust · GBRoyal Victoria Regional Health Centre · CATel Aviv University · ILThe Ohio State University · USThe University of Texas MD Anderson Cancer Center · USUniversità della Svizzera italiana · CHUniversité de Lille · FRUniversité Paris Cité · FRUniversity Hospitals Birmingham NHS Foundation Trust · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Here, we report the first comparative analysis of patient-reported outcomes (PROs) with chimeric antigen receptor T-cell therapy vs standard-of-care (SOC) therapy in second-line relapsed/refractory large B-cell lymphoma (R/R LBCL) from the pivotal randomized phase 3 ZUMA-7 study of axicabtagene ciloleucel (axi-cel) vs SOC. PRO instruments were administered at baseline, day 50, day 100, day 150, month 9, and every 3 months from randomization until 24 months or an event-free survival event. The quality of life (QoL) analysis set comprised patients with a baseline and ≥1 follow-up PRO completion. Prespecified hypotheses for Quality of Life Questionnaire-Core 30 (QLQ-C30) physical functioning, global health status/QoL, and EQ-5D-5L visual analog scale (VAS) were tested using mixed-effects models with repeated measures. Clinically meaningful changes were defined as 10 points for QLQ-C30 and 7 for EQ-5D-5L VAS. Among 359 patients, 296 (165 axi-cel, 131 SOC) met inclusion criteria for QoL analysis. At day 100, statistically significant and clinically meaningful differences in mean change of scores from baseline were observed favoring axi-cel over SOC for QLQ-C30 global health status/QoL (estimated difference 18.1 [95% confidence interval (CI), 12.3-23.9]), physical functioning (13.1 [95% CI, 8.0-18.2]), and EQ-5D-5L VAS (13.7 [95% CI, 8.5-18.8]; P < .0001 for all). At day 150, scores significantly favored axi-cel vs SOC for global health status/QoL (9.8 [95% CI, 2.6-17.0]; P = .0124) and EQ-5D-5L VAS (11.3 [95% CI, 5.4-17.1]; P = .0004). Axi-cel showed clinically meaningful improvements in QoL over SOC. Superior clinical outcomes and favorable patient experience with axi-cel should help inform treatment choices in second-line R/R LBCL. This trial was registered at www.clinicaltrials.gov as #NCT03391466.

Indexed as

Lymphoma, Large B-Cell, DiffuseQuality of LifeAntigens, CD19Biological ProductsHumansImmunotherapy, AdoptivePatient Reported Outcome MeasuresAntigens, CD19axicabtagene ciloleucelBiological Products

Identifiers

PMID35839452
PMCPMC10653042
OpenAlexW4285492548

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.