Evidence map›Paper›PMID 36149968›Full record

Trial reportBlood advances2022

Health-related quality of life with lisocabtagene maraleucel vs standard of care in relapsed or refractory LBCL.

Jeremy S Abramson, Patrick B Johnston, Manali Kamdar, Sami Ibrahimi, Koji Izutsu, Jon Arnason, Bertram Glass, Pim Mutsaers, Matthew Lunning, Julia Braverman and 7 more

Open access · goldAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Blood advances, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed, 1 pooled it
2.8field-weighted citation impact, top 8% 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

20 citing papers in PubMed, 1 synthesis or guideline pooled it, 21 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Trial
  4. Article
  5. Quality of Life in CAR-T Cell Therapy.Hematology reports · 2026
    Review
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  7. Review
  8. Article
  9. Article
  10. Review
  11. Review
  12. Review
  13. Article
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  16. Article
  17. Article
  18. Review
  19. Article
  20. CAR-T Cell Therapy in Large B Cell Lymphoma.Mediterranean journal of hematology and infectious diseases · 2023
    Review
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 at 13 institutions in 5 countries.

Jeremy S AbramsonLymphoma Program, Massachusetts General Hospital Cancer Center, Boston, MA.ORCID 0000-0001-8467-9257
Patrick B JohnstonDivision of Hematology, Mayo Clinic, Rochester, MN.
Manali KamdarDivision of Hematology, Hematologic Malignancies and Stem Cell Transplantation, University of Colorado Cancer Center, Aurora, CO.
Sami IbrahimiTransplant and Cellular Therapy Clinic, University of Oklahoma Stephenson Cancer Center, Oklahoma City, OK.
Koji IzutsuDepartment of Hematology, National Cancer Center Hospital, Tokyo, Japan.
Jon ArnasonDepartment of Hematology/Oncology, Beth Israel Deaconess Medical Center, Boston, MA.
Bertram GlassDepartment of Hematology and Cell Therapy, Helios Klinikum Berlin-Buch, Berlin, Germany.
Pim MutsaersDepartment of Hematology, Erasmus University Medical Center, Rotterdam, The Netherlands.
Matthew LunningHematology/Oncology Division, University of Nebraska Medical Center, Omaha, NE.
Julia BravermanBristol Myers Squibb, Princeton, NJ.
Fei Fei LiuBristol Myers Squibb, Princeton, NJ.ORCID 0000-0003-3364-0808
Alessandro CrottaCelgene, a Bristol-Myers Squibb Company, Boudry, Switzerland.
Sandrine MontheardCelgene, a Bristol-Myers Squibb Company, Boudry, Switzerland.
Alessandro PrevitaliCelgene, a Bristol-Myers Squibb Company, Boudry, Switzerland.
Shien GuoClinical Outcome Assessment, Evidera, Waltham, MA.
Ling ShiClinical Outcome Assessment, Evidera, Waltham, MA.
Scott R SolomonTransplant and Cellular Immunotherapy Program, Northside Hospital Cancer Institute, Atlanta, GA.
Bristol-Myers Squibb (Switzerland) · CHBristol-Myers Squibb (United States) · USCenter for Assessment · USBeth Israel Deaconess Medical Center · USErasmus MC · NLHelios Hospital Berlin-Buch · DEMassachusetts General Hospital · USMayo Clinic · USNebraska Medical Center · USNorthside Hospital · USOklahoma State University Oklahoma City · USTokyo National Hospital · JPUniversity of Colorado Cancer Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Lisocabtagene maraleucel (liso-cel) has shown promising efficacy in clinical trials for patients with relapsed/refractory large B-cell lymphoma (LBCL). We present health-related quality of life (HRQOL) results from the TRANSFORM study, the first comparative analysis of liso-cel vs standard of care (SOC) as second-line therapy in this population. Adults with LBCL refractory or relapsed ≤12 months after first-line therapy and eligible for autologous stem cell transplantation were randomized 1:1 to the liso-cel or SOC arms (3 cycles of immunochemotherapy in which responders proceeded to high-dose chemotherapy and autologous stem cell transplantation). HRQOL was assessed by European Organisation for Research and Treatment of Cancer Quality of Life Questionnaire - 30 items and the Functional Assessment of Cancer Therapy-Lymphoma subscale. Patients with baseline and ≥1 postbaseline assessment were analyzed (liso-cel, n = 47; SOC, n = 43). The proportion of patients with meaningful improvement in global health status/quality of life (QOL) was higher, whereas deterioration was lower in the liso-cel arm vs SOC arm from day 126 to month 6. Mean change scores showed meaningful worsening in global health status/QOL at month 6, fatigue at day 29 and month 6, and pain at month 6 with SOC; mean scores for other domains were maintained or improved in both arms. Time to confirmed deterioration favored the liso-cel arm vs SOC arm in global health status/QOL (median: not reached vs 19.0 weeks, respectively; hazard ratio, 0.47; 95% confidence interval, 0.24-0.94). HRQOL was either improved or maintained from baseline in patients with relapsed/refractory LBCL in the liso-cel arm vs SOC arm as second-line treatment. This study is registered at clinicaltrials.gov as #NCT0357531.

Indexed as

Hematopoietic Stem Cell TransplantationLymphoma, Large B-Cell, DiffuseAdultAntineoplastic Combined Chemotherapy ProtocolsHumansQuality of LifeStandard of CareTransplantation, Autologous

Identifiers

PMID36149968
PMCPMC9713278
OpenAlexW4297016769

What OpenQuestion holds

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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.