Evidence map›Paper›PMID 24087880›Full record

ArticlePediatric hematology and oncology2014

Pediatric Burkitt's lymphoma and diffuse B-cell lymphoma: are surveillance scans required?

H M Eissa, C E Allen, K Kamdar, S Simko, P Goradia, Z Dreyer, P Steuber, K L McClain, R P Guillerman, Catherine M Bollard

Abstract read
In one paragraph

Article in Pediatric hematology and oncology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 2 pooled it
1.6field-weighted citation impact, top 18% 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

10 citing papers in PubMed, 2 syntheses or guidelines pooled it, 27 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Article
  4. Patients undergoing multipleThe British journal of radiology · 2022
    Article
  5. Review
  6. Review
  7. Article
  8. Cancer research in India: Challenges & opportunities.The Indian journal of medical research · 2018
    Article
  9. Article
  10. Pediatric lymphomas and histiocytic disorders of childhood.Pediatric clinics of North America · 2015
    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

10 authors at 4 institutions in 1 country.

H M EissaTexas Children's Cancer Center, Texas Children's Hospital , Houston, Texas , USA.
C E Allen
K Kamdar
S Simko
P Goradia
Z Dreyer
P Steuber
K L McClain
R P Guillerman
Catherine M Bollard
Baylor College of Medicine · USTexas Children's Hospital · USChildren's Cancer Center · USUniversity of Pennsylvania · US

Funding

Tissue ResourceP50CA126752 · NCI · BAYLOR COLLEGE OF MEDICINE · PI MALCOLM K. BRENNER, HELEN E HESLOP · 2007 to 2026
$51.4M
PEDIATRIC ONCOLOGY CLINICAL RESEARCH TRAINING PROGRAMK12CA090433 · NCI · BAYLOR COLLEGE OF MEDICINE · PI CARL E ALLEN, Donald W. Parsons · 2002 to 2026
$18.5M
NCI NIH HHS K12 CA090433NCI NIH HHS P50 CA126752
6 · The paper itself

Abstract

Outcomes in pediatric B-Non-Hodgkin Lymphoma (B NHL) have improved with intensive chemotherapy protocols, with long-term survival now over 80%. However, long-term adverse effects of therapy and poor outcomes for patients who relapse remain challenges. In this study, we aimed to evaluate the potential risks and benefits of routine relapse surveillance imaging after the completion of therapy. We reviewed 44 B NHL patients diagnosed and treated at Texas Children's Cancer Center in the period between 2000 to 2011. All cross-sectional diagnostic imaging examinations performed for disease assessment after completion of chemotherapy were reviewed and cumulative radiation dosage from these examinations and the frequency of relapse detection by these examinations were recorded. Only 3 patients of the 44 relapsed (6.8%), though none of the relapses were initially diagnosed by computed tomography (CT) or fludeoxyglucose positron emission tomography (FDG-PET) scans. Median effective dose of ionizing radiation per patient was 40.3 mSv with an average of 49.1 mSv (range 0-276 mSv). This single-institution study highlights the low relapse rate in pediatric B-NHL with complete response at the end of therapy, the low sensitivity of early detection of relapse with surveillance CT or FDG-PET imaging, and the costs and potential increased risk of secondary malignancies from cumulative radiation exposure from surveillance imaging. We propose that routine surveillance CT or FDG-PET scans for these patients may not be necessary.

Indexed as

Fluorodeoxyglucose F18Positron-Emission TomographyTomography, X-Ray ComputedAdolescentAntineoplastic Combined Chemotherapy ProtocolsBurkitt LymphomaChemoradiotherapyChildChild, PreschoolCohort StudiesCross-Sectional StudiesFemaleFollow-Up StudiesHumansLymphoma, B-CellMaleFluorodeoxyglucose F18Radiopharmaceuticals

Identifiers

PMID24087880
PMCPMC4133356
OpenAlexW1992897464

What OpenQuestion holds

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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.