Evidence map›Paper›PMID 42703514›Full record

ArticleJournal of gastrointestinal oncology2026

Prediction of histological response by PET-CT after 2 weeks of neoadjuvant chemo-radiotherapy for rectal cancer: a prospective clinical trial.

Daniel Reinhorn, Yulia Kundel, Noa Gordon, Judit Prus, Sara Morgenstern, Nir Wasserberg, David Groshar, Hanna Bernstine, Baruch Brenner

Abstract read
In one paragraph

Article in Journal of gastrointestinal oncology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

9 authors.

Daniel Reinhorn *Davidoff Cancer Center, Rabin Medical Center, Petah Tikva, Israel.
Yulia Kundel *Davidoff Cancer Center, Rabin Medical Center, Petah Tikva, Israel.
Noa GordonDavidoff Cancer Center, Rabin Medical Center, Petah Tikva, Israel.
Judit PrusDavidoff Cancer Center, Rabin Medical Center, Petah Tikva, Israel.
Sara MorgensternFaculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
Nir WasserbergFaculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
David GrosharFaculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
Hanna BernstineFaculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
Baruch BrennerDavidoff Cancer Center, Rabin Medical Center, Petah Tikva, Israel.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Early prediction of pathological response to neoadjuvant chemoradiotherapy (nCRT) in locally advanced rectal cancer (LARC) may help guide individualized treatment strategies. This prospective clinical trial aimed to evaluate whether interim Methods: Twenty-one LARC patients receiving nCRT followed by surgery were included. Results: No significant differences in ΔSUV-mean%, ΔSUV-max%, and ΔMTV% were found between pCR and non-pCR groups or between TRG I-II and TRG III-V groups. Absolute SUV-mean and SUV-max values at baseline, and SUV-max and MTV values at 2 weeks, differed significantly between pCR and non-pCR groups. ROC analyses demonstrated discriminatory ability for predicting pCR, with area under the curve (AUC) values of 0.79-0.82. Conclusions: Early metabolic response after 2 weeks of nCRT did not correlate with pCR or TRG in LARC. Absolute SUV-mean and SUV-max values at baseline and absolute SUV-max and MTV values at 2 weeks showed predictive value for pCR.

Indexed as

chemoradiotherapypathological complete response (pCR)positron emission tomography-computed tomography (PET-CT)Rectal cancer

Identifiers

PMID42703514
PMCPMC13546572

What OpenQuestion holds

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Registered trials

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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.