Evidence map›Paper›PMID 41128955›Full record

ArticleAnnals of surgical oncology2026

Accuracy of Predicting Residual Disease and Disease Progression During Active Surveillance for Esophageal Cancer.

Sanjiv S G Gangaram Panday, David van Klaveren, Sjoerd M Lagarde, Hester F Lingsma, Bianca Mostert, Peter-Paul L O Coene, Jan Willem T Dekker, Henk H Hartgrink, Joos Heisterkamp, Merlijn Hutteman and 9 more

Abstract read
In one paragraph

Article in Annals of surgical oncology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed, 1 pooled it
–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

6 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Trial
  3. Article
  4. Article
  5. Article
  6. 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

19 authors.

Sanjiv S G Gangaram PandayDepartment of Surgery, Erasmus MC Cancer Institute, University Medical Centre, Rotterdam, The Netherlands. s.gangaram-panday@erasmusmc.nl.
David van KlaverenDepartment of Public Health, Erasmus MC, University Medical Centre, Rotterdam, The Netherlands.
Sjoerd M LagardeDepartment of Surgery, Erasmus MC Cancer Institute, University Medical Centre, Rotterdam, The Netherlands.
Hester F LingsmaDepartment of Public Health, Erasmus MC, University Medical Centre, Rotterdam, The Netherlands.
Bianca MostertDepartment of Medical Oncology, Erasmus MC Cancer Institute, University Medical Centre, Rotterdam, The Netherlands.
Peter-Paul L O CoeneDepartment of Surgery, Maasstad Hospital, Rotterdam, The Netherlands.
Jan Willem T DekkerDepartment of Surgery, Reinier de Graaf Gasthuis, Delft, The Netherlands.
Henk H HartgrinkDepartment of Surgery, Leiden University Medical Centre, Leiden, The Netherlands.
Joos HeisterkampDepartment of Surgery, Elisabeth Tweesteden Hospital, Tilburg, The Netherlands.
Merlijn HuttemanDepartment of Surgery, Radboud University Medical Centre, Nijmegen, The Netherlands.
Ewout A KouwenhovenDepartment of Surgery, ZGT Hospital, Almelo, The Netherlands.
Grard A P NieuwenhuijzenDepartment of Surgery, Catharina Hospital, Eindhoven, The Netherlands.
Jean-Pierre PierieDepartment of Surgery, Medical Centre Leeuwarden, Leeuwarden, The Netherlands.
Johanna W van SandickDepartment of Surgical Oncology, The Netherlands Cancer Institute, Amsterdam, The Netherlands.
Meindert N SosefDepartment of Surgery, Zuyderland Medical Centre, Heerlen, The Netherlands.
Edwin S van der ZaagDepartment of Surgery, Gelre Hospital, Apeldoorn, The Netherlands.
J Jan B van LanschotDepartment of Surgery, Erasmus MC Cancer Institute, University Medical Centre, Rotterdam, The Netherlands.
Bas P L WijnhovenDepartment of Surgery, Erasmus MC Cancer Institute, University Medical Centre, Rotterdam, The Netherlands.
SANO Study Group

Funding

KWF Kankerbestrijding 10825ZonMw 843004104
6 · The paper itself

Abstract

backgroundTo date, active surveillance has been non-inferior to standard surgery for patients with esophageal cancer, achieving a clinical complete response (CCR) after neoadjuvant chemoradiotherapy (nCRT). However, two thirds of patients have residual disease detected 12 weeks after nCRT and undergo surgery. At 12 weeks, nearly half of the patients with CCR will experience locoregional regrowth. This study aimed to identify routine predictive factors for achieving (sustained) CCR to improve patient selection for active surveillance.

methodsData from the SANO trial were analyzed, including data of patients who underwent nCRT for esophageal cancer. Logistic regression assessed predictors of CCR at 12 weeks, with potential factors including age, sex, WHO performance status, clinical T and N categories, histology, differentiation grade, tumor location, and tumor length. For patients with CCR in active surveillance, cause-specific proportional hazards regression identified predictors of sustained CCR (no locoregional regrowth, dissemination, or death) during a minimum 3-year follow-up period. Discrimination was quantified using the concordance statistic (c-statistic) with bootstrap validation.

resultsOf 750 patients, 274 (37 %) achieved CCR at 12 weeks. Higher cN category was associated with lower likelihood of CCR (cN2-3 vs cN0: odds ratio [OR], 0.57; 95 % confidence interval [CI], 0.37-0.88; P < 0.01; c-statistic, 0.56). Among 198 patients in active surveillance, 25 % had sustained CCR after a median follow-up period of 54 months (interquartile range [IQR],46-58 months). Higher cN category (cN2-3 vs cN0; HR, 2.08; 95 % CI, 1.25-3.48; P < 0.01) was associated with non-sustained CCR (c-statistic, 0.58).

conclusionStandard clinical parameters poorly predict clinical response after nCRT. Additional predictive parameters and better diagnostic tests are needed to improve patient selection for active surveillance.

Indexed as

AdenocarcinomaCarcinoma, Squamous CellEsophageal NeoplasmsNeoadjuvant TherapyNeoplasm, ResidualWatchful WaitingAgedDisease ProgressionFemaleFollow-Up StudiesHumansMaleMiddle AgedPrognosisSurvival Rate

Identifiers

PMID41128955
PMCPMC12765740

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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.