Evidence map›Paper›PMID 42174414›Full record

Observational studyBMC gastroenterology2026

Comparison of surgical safety among different comprehensive treatment models for adenocarcinoma of esophagogastric junction: a single-center cohort study.

Hongmei Dai, Yinkui Wang, Fei Shan, Shuangxi Li, Yongning Jia, Kan Xue, Rulin Miao, Zhemin Li, Xiaolei Xiu, Ziyu Li and 1 more

Abstract readComparative StudyObservational StudyComparative Study
In one paragraph

Observational study in BMC gastroenterology, 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

11 authors.

Hongmei Dai *Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education/Beijing), Gastrointestinal Cancer Center, Peking University Cancer Hospital & Institute, Haidian District, 52 Fucheng Road, Beijing, 100142, China.
Yinkui Wang *Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education/Beijing), Gastrointestinal Cancer Center, Peking University Cancer Hospital & Institute, Haidian District, 52 Fucheng Road, Beijing, 100142, China.
Fei ShanState Key Laboratory of Holistic Integrative Management of Gastrointestinal Cancers, Gastrointestinal Cancer Center, Peking University Cancer Hospital & Institute, Beijing, 100142, China.
Shuangxi LiKey Laboratory of Carcinogenesis and Translational Research (Ministry of Education/Beijing), Gastrointestinal Cancer Center, Peking University Cancer Hospital & Institute, Haidian District, 52 Fucheng Road, Beijing, 100142, China.
Yongning JiaState Key Laboratory of Holistic Integrative Management of Gastrointestinal Cancers, Gastrointestinal Cancer Center, Peking University Cancer Hospital & Institute, Beijing, 100142, China.
Kan XueKey Laboratory of Carcinogenesis and Translational Research (Ministry of Education/Beijing), Gastrointestinal Cancer Center, Peking University Cancer Hospital & Institute, Haidian District, 52 Fucheng Road, Beijing, 100142, China.
Rulin MiaoKey Laboratory of Carcinogenesis and Translational Research (Ministry of Education/Beijing), Gastrointestinal Cancer Center, Peking University Cancer Hospital & Institute, Haidian District, 52 Fucheng Road, Beijing, 100142, China.
Zhemin LiKey Laboratory of Carcinogenesis and Translational Research (Ministry of Education/Beijing), Gastrointestinal Cancer Center, Peking University Cancer Hospital & Institute, Haidian District, 52 Fucheng Road, Beijing, 100142, China.
Xiaolei XiuInstitute of Medical Information/Library, Chinese Academy of Medical Sciences & Peking Union Medical College, Chaoyang District, 3 Yabao Road, Beijing, 100020, China.
Ziyu LiKey Laboratory of Carcinogenesis and Translational Research (Ministry of Education/Beijing), Gastrointestinal Cancer Center, Peking University Cancer Hospital & Institute, Haidian District, 52 Fucheng Road, Beijing, 100142, China. ziyu_li@hsc.pku.edu.cn.
Jiafu JiState Key Laboratory of Holistic Integrative Management of Gastrointestinal Cancers, Gastrointestinal Cancer Center, Peking University Cancer Hospital & Institute, Beijing, 100142, China.

Funding

Beijing Hospitals Authority Innovation Studio of Young Staff Funding Support No. 202123Beijing Municipal Administration of Hospitals Incubating Program No. PX2021043Clinical Research Fund For Distinguished Young Scholars of Peking University Cancer Hospital No. QNJJ2022016Clinical Research United Fund of Peking University Cancer Hospital No. LHJJ2023003Science Foundation of Peking University Cancer Hospital No. PY202320Science Foundation of Peking University Cancer Hospital No. PY202335Sponsored by Beijing Nova Program No. 20220484111
6 · The paper itself

Abstract

backgroundNeoadjuvant chemotherapy (NAC) and neoadjuvant chemoradiotherapy (nCRT) are increasingly used to treat adenocarcinoma of the esophagogastric junction (AEG). However, there is insufficient clinical evidence to compare surgical safety among the three comprehensive treatment models, including the surgery‑first model, NAC model, and nCRT model. Therefore, this study was designed to compare surgical safety of the three comprehensive treatment models.

methodsThis is a retrospective cohort study. From January 2012 to December 2018, 276 consecutive patients with Siewert II and III AEG (cT2-4NxM0) in the Gastrointestinal Cancer Center, Peking University Cancer Hospital & Institute were enrolled in this study. All these patients underwent surgery and were categorized into three groups: surgery‑first group, NAC group and nCRT group. Inverse probability of treatment weighting (IPTW) was applied to balance baseline characteristics between the three groups.

resultsThe overall postoperative complication rate in nCRT groups was 59.6%, which was significantly higher than that in the surgery-first group (42.2%, P = 0.040) and the NAC group (39.3%, P = 0.027). Moreover, the rate of major postoperative complications differed significantly among the three groups (P = 0.011), with the nCRT group showing a notably higher incidence than the surgery-first group (P = 0.008) and the NAC group (P = 0.043). No significant differences in postoperative complication rates were found between the surgery-first group and the NAC group. After IPTW, nCRT was significantly associated with increased postoperative complication (weighed OR = 2.25, 95% CI: 1.13-4.50, P = 0.022), and major postoperative complications (weighed OR:3.27, 95% CI: 1.45-7.39, P = 0.005). Thoracoabdominal approach (weighed OR = 6.47, 95% CI: 1.44-29.13, P = 0.015), combined organ resection (weighed OR = 5.08, 95% CI: 1.66-15.51, P = 0.004), and operative time exceeding 240 min (weighed OR = 2.23, 95% CI: 1.20-4.12, P = 0.011) were also identified as independent risk factors for postoperative complications.

conclusionsNeoadjuvant chemotherapy did not increase the risk of postoperative complications. In contrast, nCRT was associated with worse postoperative complications. We should pay more attention to AEG patients receiving neoadjuvant chemoradiotherapy.

Indexed as

AdenocarcinomaEsophageal NeoplasmsEsophagectomyNeoadjuvant TherapyPostoperative ComplicationsAgedChemotherapy, AdjuvantEsophagogastric JunctionFemaleHumansMaleMiddle AgedRadiotherapy, AdjuvantRetrospective StudiesTreatment OutcomeAdenocarcinoma of the esophagogastric junctionNeoadjuvant chemoradiotherapyNeoadjuvant chemotherapyPostoperative complicationSurgical safety

Identifiers

PMID42174414
PMCPMC13390464

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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.