Evidence map›Paper›PMID 23187748›Full record

Trial reportAnnals of surgery2013

Neither FDG-PET Nor CT can distinguish between a pathological complete response and an incomplete response after neoadjuvant chemoradiation in locally advanced rectal cancer: a prospective study.

José G Guillem, Jeannine A Ruby, Tobias Leibold, Timothy J Akhurst, Henry W Yeung, Marc J Gollub, Michelle S Ginsberg, Jinru Shia, Arief A Suriawinata, Elyn R Riedel and 8 more

Open access · greenAbstract readClinical Trial
In one paragraph

Trial report in Annals of surgery, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 50 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
50citing papers in PubMed, 2 pooled it
5.9field-weighted citation impact, top 3% 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

50 citing papers in PubMed, 2 syntheses or guidelines pooled it, 100 citations in OpenAlex.

  1. Pooled it
  2. Rectal Cancer, Version 2.2018, NCCN Clinical Practice Guidelines in Oncology.Journal of the National Comprehensive Cancer Network : JNCCN · 2018
    Guideline
  3. Trial
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. New Opportunities for Minimizing Toxicity in Rectal Cancer Management.American Society of Clinical Oncology educational book. American Society of Clinical Oncology. Annual Meeting · 2023
    Article
  11. Review
  12. Article
  13. Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Article
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

18 authors at 7 institutions in 4 countries.

José G GuillemDepartment of Surgery, Memorial Sloan-Kettering Cancer Center, New York, NY 10065, USA. guillemj@mskcc.org
Jeannine A Ruby
Tobias Leibold
Timothy J Akhurst
Henry W Yeung
Marc J Gollub
Michelle S Ginsberg
Jinru Shia
Arief A Suriawinata
Elyn R Riedel
Madhu Mazumdar
Leonard B Saltz
Bruce D Minsky
Garrett M Nash
Philip B Paty
Larissa K Temple
Martin R Weiser
Steven M Larson
Memorial Sloan Kettering Cancer Center · USCancer Research And Biostatistics · USCornell University · USDartmouth Cancer CenterDartmouth–Hitchcock Medical Center · USPeter MacCallum Cancer Centre · AURobert Bosch Hospital · DE

Funding

Tumor Hypoxia Imaging - Laboratory and Clinical StudiesP01CA115675 · NCI · SLOAN-KETTERING INST CAN RESEARCH · PI LING, CLIFTON C · 2006 to 2010
$9.5M
PET IMAGING IN MULTIMODALITY MANAGEMENT OF RECTAL CANCERR01CA082534 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI GUILLEM, JOSE G · 1999 to 2001
$507k
NCI NIH HHS P01 CA115675NCI NIH HHS R01 CA082534NCI NIH HHS R01 CA 82534
6 · The paper itself

Abstract

objectiveTo prospectively compare the ability of flourodeoxyglucose-positron emission tomography (FDG-PET) and computed tomography (CT) to identify a pathological complete response (pCR) in patients with rectal cancer treated by chemoradiation.

backgroundA major obstacle in pursuing nonoperative management in patients with rectal cancer after chemoradiation is the inability to identify a pCR preoperatively.

methodsA total of 121 patients with rectal cancer were prospectively enrolled. FDG-PET scans and helical CT scans were obtained before and after neoadjuvant chemoradiation. Consensus readings of PET and CT scans were used to classify certainty of disease (5-point confidence rating scale). The ability of PET and CT scans to accurately distinguish a pCR (ypT0) from an incomplete response (ypT1-4) was estimated using the area under the receiver operating characteristic curve (AUC).

resultsOf the 121 patients, 26 (21%) had a pCR. PET and CT scans were equally inadequate at distinguishing a pCR from an incomplete response (AUC = 0.64 for both, P = 0.97). Among the 26 patients with a pCR, 14 (54%) and 5 (19%) were classified as complete responders on PET and CT scans, respectively. Among the 95 patients with an incomplete pathological response, 63 (66%) and 90 (95%) were classified as incomplete responders on PET and CT scans, respectively. None of the individual PET parameters, including visual response score, mean standard uptake value (SUVmean), maximum SUV (SUVmax), and total lesion glycolysis, accurately distinguished a pCR (AUCs = 0.57-0.73).

conclusionsNeither PET nor CT scans have adequate predictive value to be clinically useful in distinguishing a pCR from an incomplete response and, therefore, should not be obtained for the purpose of attempting to predict a pCR after neoadjuvant chemoradiation for rectal cancer.

Indexed as

Chemoradiotherapy, AdjuvantNeoadjuvant TherapyPositron-Emission TomographyTomography, Spiral ComputedAdenocarcinomaAdultAgedAged, 80 and overFemaleFluorodeoxyglucose F18HumansMaleMiddle AgedProspective StudiesRadiopharmaceuticalsRectal NeoplasmsFluorodeoxyglucose F18Radiopharmaceuticals

Identifiers

PMID23187748
PMCPMC12432588
OpenAlexW2321626327

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.