Evidence map›Paper›PMID 37855688›Full record

ArticleClinical cancer research : an official journal of the American Association for Cancer Research2024

PET/CT Biomarkers Enable Risk Stratification of Patients with Relapsed/Refractory Diffuse Large B-cell Lymphoma Enrolled in the LOTIS-2 Clinical Trial.

Juan Pablo Alderuccio, Isildinha M Reis, Mehdi Hamadani, Muthiah Nachiappan, Salman Leslom, Brad S Kahl, Weiyun Z Ai, John Radford, Melhem Solh, Kirit M Ardeshna and 11 more

Registry-linked trialOpen access · greenAbstract read
In one paragraph

Article in Clinical cancer research : an official journal of the American Association for Cancer Research, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03589469 (A Phase 2 Open-Label Single-Arm Study to Evaluate the Efficacy and Safety of Loncastuximab Tesirine in Patients With Relapsed or Refractory Diffuse Large B-Cell Lymphoma), which is not on this map. Cited by 8 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 2 pooled it
2.3field-weighted citation impact, top 12% 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.

NCT03589469 phase2completednot on this map

A Phase 2 Open-Label Single-Arm Study to Evaluate the Efficacy and Safety of Loncastuximab Tesirine in Patients With Relapsed or Refractory Diffuse Large B-Cell Lymphoma (DLBCL) (LOTIS-2)

TypeinterventionalSponsorADC Therapeutics S.A.Ran2018 to 2022Enrolled145ConditionsDiffuse Large B-Cell Lymphoma Refractory, Diffuse Large B-cell Lymphoma RecurrentArmsLoncastuximab tesirine
3 · Its place in the literature

Who cites it

8 citing papers in PubMed, 2 syntheses or guidelines pooled it, 9 citations in OpenAlex.

  1. Pooled it
  2. The prognostic utility ofFrontiers in immunology · 2024
    Pooled it
  3. Imaging the efficacy and side effects of CAR T-cell therapy in children and young adults.Cancer imaging : the official publication of the International Cancer Imaging Society · 2026
    Review
  4. Article
  5. Association of [Diagnostics (Basel, Switzerland) · 2025
    Article
  6. Clinical scoring systems, molecular subtypes and baseline [Cancer imaging : the official publication of the International Cancer Imaging Society · 2024
    Review
  7. Article
  8. Semiquantitative 2-[Frontiers in medicine · 2024
    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

21 authors at 13 institutions in 4 countries.

Juan Pablo AlderuccioSylvester Comprehensive Cancer Center, University of Miami Miller School of Medicine, Miami, Florida.ORCID 0000-0002-2690-3377
Isildinha M ReisSylvester Comprehensive Cancer Center, University of Miami Miller School of Medicine, Miami, Florida.ORCID 0000-0002-7695-8771
Mehdi HamadaniMedical College of Wisconsin, Milwaukee, Wisconsin.ORCID 0000-0001-5372-510X
Muthiah NachiappanSylvester Comprehensive Cancer Center, University of Miami Miller School of Medicine, Miami, Florida.ORCID 0000-0002-1335-4620
Salman LeslomSylvester Comprehensive Cancer Center, University of Miami Miller School of Medicine, Miami, Florida.ORCID 0009-0007-6210-4322
Brad S KahlWashington University, St. Louis, Missouri.ORCID 0000-0003-0459-6609
Weiyun Z AiHelen Diller Family Comprehensive Cancer Center, University of California, San Francisco, California.ORCID 0000-0001-5757-6949
John RadfordNIHR Clinical Research Facility, University of Manchester and the Christie NHS Foundation Trust, Manchester Academic Health Science Centre, Manchester, United Kingdom.ORCID 0000-0001-7898-2786
Melhem SolhBlood and Marrow Transplant Program at Northside Hospital, Atlanta, Georgia.ORCID 0000-0003-3766-5623
Kirit M ArdeshnaUniversity College London Hospitals NHS Foundation Trust, London, United Kingdom.ORCID 0000-0002-8938-7875
Brian T HessMedical University of South Carolina, Charleston, South Carolina.ORCID 0000-0003-0176-2050
Matthew A LunningUniversity of Nebraska Medical Center- Fred and Pamela Buffett Cancer Center, Omaha, Nebraska.ORCID 0000-0002-2761-7612
Pier Luigi ZinzaniIRCCS Azienda Ospedaliero-Universitaria di Bologna, Istituto di Ematologia "Seràgnoli"; Dipartimento di Scienze Mediche e Chirurgiche, Università di Bologna, Bologna, Italy.ORCID 0000-0002-2112-2651
Anastasios StathisOncology Institute of Southern Switzerland, EOC, Bellinzona, Switzerland.ORCID 0000-0002-2859-7529
Carmelo Carlo-StellaDepartment of Biomedical Sciences, Humanitas University, Milano, Italy.ORCID 0000-0003-3144-0124
Izidore S LossosSylvester Comprehensive Cancer Center, University of Miami Miller School of Medicine, Miami, Florida.ORCID 0000-0002-9346-9013
Paolo F CaimiCleveland Clinic Taussig Cancer Center, Cleveland, Ohio.ORCID 0000-0003-1436-0464
Sunwoo HanSylvester Comprehensive Cancer Center, University of Miami Miller School of Medicine, Miami, Florida.ORCID 0000-0001-6874-2471
Fei YangSylvester Comprehensive Cancer Center, University of Miami Miller School of Medicine, Miami, Florida.ORCID 0000-0001-6260-9020
Russ A Kuker *Sylvester Comprehensive Cancer Center, University of Miami Miller School of Medicine, Miami, Florida.ORCID 0000-0002-0074-6596
Craig H Moskowitz *Sylvester Comprehensive Cancer Center, University of Miami Miller School of Medicine, Miami, Florida.ORCID 0000-0002-9189-3152
Sylvester Comprehensive Cancer Center · USCleveland Clinic · USHumanitas University · ITInstitute of Oncology Research · CHIstituto di Ematologia di Bologna · ITManchester Academic Health Science Centre · GBMedical College of Wisconsin · USMedical University of South Carolina · USNorthside Hospital · USUCSF Helen Diller Family Comprehensive Cancer Center · USUniversity College London Hospitals NHS Foundation Trust · GBUniversity of Missouri–St. Louis · USUniversity of Nebraska Medical Center · US

Funding

Tumor Biology Research ProgramP30CA240139 · NCI · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI Stephen D. Nimer · 2019 to 2026
$24.1M
The Lymphoma Epidemiology of Outcomes (LEO) Cohort Study (Supplement)U01CA195568 · NCI · MAYO CLINIC ROCHESTER · PI CERHAN, JAMES R, FLOWERS, CHRISTOPHER R · 2015 to 2025
$22.1M
Identify the Mechanisms of LMO2-Mediated Inhibition of Homologous Recombination and Establish PARP-Targeted Synthetic Lethality as a New Therapy for DLBCLR01CA233945 · NCI · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI LOSSOS, IZIDORE S, VERDUN, RAMIRO ERNESTO · 2019 to 2023
$1.8M
NCI NIH HHS P30 CA240139NCI NIH HHS R01 CA233945NCI NIH HHS U01 CA195568
6 · The paper itself

Abstract

purposeSignificant progress has occurred in developing quantitative PET/CT biomarkers in diffuse large B-cell lymphoma (DLBCL). Total metabolic tumor volume (MTV) is the most extensively studied, enabling assessment of FDG-avid tumor burden associated with outcomes. However, prior studies evaluated the outcome of cytotoxic chemotherapy or chimeric antigen receptor T-cell therapy without data on recently approved FDA agents. Therefore, we aimed to assess the prognosis of PET/CT biomarkers in patients treated with loncastuximab tesirine. EXPERIMENTAL

designWe centrally reviewed screening PET/CT scans of patients with relapsed/refractory DLBCL enrolled in the LOTIS-2 (NCT03589469) study. MTV was obtained by computing individual volumes using the SUV ≥4.0 threshold. Other PET/CT metrics, clinical factors, and the International Metabolic Prognostic Index (IMPI) were evaluated. Logistic regression was used to assess the association between biomarkers and treatment response. Cox regression was used to determine the effect of biomarkers on time-to-event outcomes. We estimated biomarker prediction as continuous and binary variables defined by cutoff points.

resultsAcross 138 patients included in this study, MTV with a cutoff point of 96 mL was the biomarker associated with the highest predictive performance in univariable and multivariable models to predict failure to achieve complete metabolic response (OR, 5.42; P = 0.002), progression-free survival (HR, 2.68; P = 0.002), and overall survival (HR, 3.09; P < 0.0001). IMPI demonstrated an appropriate performance, however, not better than MTV alone.

conclusionsPretreatment MTV demonstrated robust risk stratification, with those patients demonstrating high MTV achieving lower responses and survival to loncastuximab tesirine in relapsed/refractory DLBCL.

Indexed as

Lymphoma, Large B-Cell, DiffusePositron Emission Tomography Computed TomographyBiomarkersClinical Trials as TopicFluorodeoxyglucose F18HumansPositron-Emission TomographyPrognosisRetrospective StudiesRisk AssessmentTumor BurdenBiomarkersFluorodeoxyglucose F18

Identifiers

PMID37855688
PMCPMC10872617
OpenAlexW4387764403

What OpenQuestion holds

Textmetadata
LicenceTDM
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.