Evidence map›Paper›PMID 26719374›Full record

Trial reportJournal of nuclear medicine : official publication, Society of Nuclear Medicine2016

Prospective Study of 3'-Deoxy-3'-18F-Fluorothymidine PET for Early Interim Response Assessment in Advanced-Stage B-Cell Lymphoma.

Heiko Schöder, Andrew D Zelenetz, Paul Hamlin, Somali Gavane, Steven Horwitz, Matthew Matasar, Alison Moskowitz, Ariela Noy, Lia Palomba, Carol Portlock and 5 more

Open access · bronzeAbstract readClinical Trial
In one paragraph

Trial report in Journal of nuclear medicine : official publication, Society of Nuclear Medicine, 2016. 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
4.9field-weighted citation impact, top 4% 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, 47 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Emerging Role of [Hematology reports · 2024
    Review
  5. Article
  6. Prognostic Role of Interim 18-Fluorodeoxyglucose-PET in Diffuse Large B Cell Lymphoma: Experience from a Tertiary Care Centre in North India.Indian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion · 2022
    Article
  7. Review
  8. Molecular imaging with FLT: a case of Cassandra's curse?European journal of nuclear medicine and molecular imaging · 2021
    Article
  9. Article
  10. MRI and PET/MRI in hematologic malignancies.Journal of magnetic resonance imaging : JMRI · 2020
    Review
  11. Tumour necrosis as assessed withEuropean radiology · 2019
    Observational
  12. Article
  13. Article
  14. Ultra-early response assessment in lymphoma treatment: [European journal of nuclear medicine and molecular imaging · 2018
    Article
  15. Article
  16. Interim FDG-PET in lymphoma, a questionable practice in hematology.European journal of nuclear medicine and molecular imaging · 2017
    Article
  17. Article
  18. Article
  19. Metabolic Tumor Volume in Lymphoma: Hype or Hope?Journal of clinical oncology : official journal of the American Society of Clinical Oncology · 2016
    Article
  20. 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

15 authors at 1 institution in 1 country.

Heiko SchöderMolecular Imaging and Therapy Service, Department of Radiology, Memorial Sloan Kettering Cancer Center, New York, New York schoderh@mskcc.org.
Andrew D ZelenetzLymphoma Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York; and.
Paul HamlinLymphoma Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York; and.
Somali GavaneMolecular Imaging and Therapy Service, Department of Radiology, Memorial Sloan Kettering Cancer Center, New York, New York.
Steven HorwitzLymphoma Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York; and.
Matthew MatasarLymphoma Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York; and.
Alison MoskowitzLymphoma Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York; and.
Ariela NoyLymphoma Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York; and.
Lia PalombaLymphoma Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York; and.
Carol PortlockLymphoma Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York; and.
David StrausLymphoma Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York; and.
Ravinder GrewalMolecular Imaging and Therapy Service, Department of Radiology, Memorial Sloan Kettering Cancer Center, New York, New York.
Jocelyn C MigliacciDepartment of Surgery, Memorial Sloan Kettering Cancer Center, New York.
Steven M LarsonMolecular Imaging and Therapy Service, Department of Radiology, Memorial Sloan Kettering Cancer Center, New York, New York.
Craig H MoskowitzLymphoma Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York; and.
Memorial Sloan Kettering Cancer Center · US

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Hongbiao Carl Lekaye · 1985 to 2026
$347.4M
NCI NIH HHS P30 CA008748
6 · The paper itself

Abstract

unlabelledCurrent clinical and imaging tools remain suboptimal for early assessment of prognosis and treatment response in aggressive lymphomas. PET with 3'-deoxy-3'-(18)F-fluorothymidine ((18)F-FLT) can be used to measure tumor cell proliferation and treatment response. In a prospective study in patients with advanced-stage B-cell lymphoma, we investigated the prognostic and predictive value of (18)F-FLT PET in comparison to standard imaging with (18)F-FDG PET and clinical outcome.

methodsSixty-five patients were treated with an induction/consolidation regimen consisting of 4 cycles of R-CHOP-14 (rituximab, cyclophosphamide, doxorubicin, vincristine, prednisone) followed by 3 cycles of ICE (ifosfamide, carboplatin, etoposide). (18)F-FLT PET was performed at baseline and at interim (iPET) after 1-2 cycles of therapy. (18)F-FDG PET was performed at baseline, after cycle 4, and at the end of therapy. The relationship between PET findings, progression-free survival (PFS) and overall survival (OS) was investigated.

resultsWith a median follow-up of 51 mo, PFS and OS were 71% and 86%, respectively. (18)F-FLT iPET, analyzed visually (using a 5-point score) or semiquantitatively (using SUV and ΔSUV) predicted both PFS and OS (P < 0.01 for all parameters). Residual (18)F-FLT SUVmax on iPET was associated with an inferior PFS (hazard ratio, 1.26, P = 0.001) and OS (hazard ratio, 1.27, P = 0.002). When (18)F-FDG PET was used, findings in the end of treatment scan were better predictors of PFS and OS than findings on the interim scan. Baseline PET imaging parameters, including SUV, proliferative volume, or metabolic tumor volume, did not correlate with outcome.

conclusion(18)F-FLT PET after 1-2 cycles of chemotherapy predicts PFS and OS, and a negative (18)F-FLT iPET result may potentially help design risk-adapted therapies in patients with aggressive lymphomas. In contrast, the positive predictive value of (18)F-FLT iPET remains too low to justify changes in patient management.

Indexed as

DideoxynucleosidesPositron Emission Tomography Computed TomographyAdultAgedDisease-Free SurvivalFemaleHumansLymphoma, Large B-Cell, DiffuseMaleMiddle AgedNeoplasm StagingProspective StudiesTime FactorsTreatment OutcomeYoung AdultalovudineDideoxynucleosidesB-cell cell lymphomaFDG PETFLT PEToutcome

Identifiers

PMID26719374
PMCPMC4854760
OpenAlexW2342566523

What OpenQuestion holds

Textmetadata
LicenceTDM
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.