Evidence map›Paper›PMID 42498744›Full record

ArticleBritish journal of cancer2026

Chinese expert consensus on precision testing and molecular diagnosis of pancreatic cancer (2025).

Dan Cao, Jianhui Wu, Jiujie Cui, Chen Xun, Jun Zhou, Wei Li, Jinghua Sun, Liu Yang, Ke Cheng, Huanji Xu and 10 more

Abstract readConsensus Statement
In one paragraph

Article in British journal of cancer, 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

20 authors.

Dan Cao *Division of Abdominal Tumor Multimodality Treatment, West China Hospital of Sichuan University, Chengdu, China.ORCID http://orcid.org/0000-0003-2755-7258
Jianhui Wu *Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education), Department of Hepato-Pancreato-Biliary Surgery, Peking University Cancer Hospital and Institute, Beijing, China.ORCID http://orcid.org/0000-0003-3482-3876
Jiujie Cui *Department of Oncology and State Key Laboratory of Systems Medicine for Cancer of Shanghai Cancer Institute, Renji Hospital, School of Medicine, Shanghai Jiaotong University, Shanghai, China.
Chen Xun *Hepatobiliary and Pancreatic Tumor Department, Nanjing Tianyinshan Hospital Affiliated to China Pharmaceutical University, Nanjing, China.ORCID http://orcid.org/0009-0007-7237-0245
Jun ZhouKey Laboratory of Carcinogenesis and Translational Research (Ministry of Education), Department of Gastrointestinal Oncology, Peking University Cancer Hospital & Institute, Beijing, China.
Wei LiDepartment of Oncology, The First Affiliated Hospital of Soochow University, Suzhou, China.
Jinghua SunDepartment of Medical Oncology, The Second Hospital of Dalian Medical University, Dalian, China.ORCID http://orcid.org/0000-0001-8121-9685
Liu YangDepartment of Medical Oncology, The First Affiliated Hospital of Zhejiang University, Hangzhou, China.
Ke ChengDepartment of Medical Oncology, Cancer Center, West China Hospital, Sichuan University, Chengdu, China.ORCID http://orcid.org/0000-0002-6034-8872
Huanji XuDepartment of Medical Oncology, West China Hospital, Sichuan University, Chengdu, China.
Guanghai DaiDepartment of Medical Oncology, Chinese PLA General hospital, Beijing, China.ORCID http://orcid.org/0000-0001-7508-274X
Kuirong JiangPancreas Center & Department of General Surgery, The First Affiliated Hospital of Nanjing Medical University, Nanjing, China.
Qi LiDepartment of Oncology, Shanghai General Hospital, Shanghai, China.
Guang TanDepartment of Hepatobiliary surgery, The First Affiliated Hospital of Dalian Medical University, Dalian, China.
Hongmei ZhangDepartment of Oncology, Xijing Hospital, The Air Force Military Medical University, Xi'an, China.
Tao ZhangCancer Center, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.ORCID http://orcid.org/0000-0003-4018-3393
Zhihong ZhangDepartment of Pathology, The First Affiliated Hospital of Nanjing Medical University, Nanjing, China.
Chunyi HaoHepato-Pancreato-Biliary Surgery, Peking University Cancer Hospital, Beijing, China. haochunyi@bjmu.edu.cn.ORCID http://orcid.org/0000-0002-1233-1689
Liwei WangOncology Department and State Key Laboratory of Systems Medicine for Cancer of Shanghai Cancer Institute, Renji Hospital, School of Medicine, Shanghai Jiaotong University, Shanghai, China. liweiwang@shsmu.edu.cn.ORCID http://orcid.org/0000-0002-8304-3115
Shukui QinCancer Center, Tianyinshan Hospital, China Pharmaceutical University, Nanjing, China. qinsk@csco.org.cn.ORCID http://orcid.org/0000-0003-2289-1521

Funding

National Natural Science Foundation of China (National Science Foundation of China) 82573943
6 · The paper itself

Abstract

This consensus by the CSCO Pancreatic Cancer Expert Committee establishes evidence-based guidelines for molecular testing in pancreatic ductal adenocarcinoma. It details recommendations for biomarkers (e.g., KRAS, BRCA, MSI), liquid biopsy, and precision imaging to direct targeted therapies and immunotherapy, aiming to standardize diagnosis and optimize individualized patient care. Pancreatic ductal adenocarcinoma (PDAC) is the most common pathological type of primary pancreatic malignancy, accounting for ~95% of cases and generally referred to as pancreatic cancer [1]. Its prognosis is extremely poor and its incidence continues to rise [2]. According to the most recent global cancer statistics, the incidence of pancreatic cancer ranks 12th among all cancers, and its mortality ranks 6th, making it one of the deadliest malignancies worldwide [3]. Approximately 57% of patients have metastatic disease at diagnosis and require systemic therapy, for which chemotherapy remains the standard first-line option [1]. However, the overall response rate to currently available systemic regimens is low, and the 5-year survival rate for patients with metastatic disease remains below 5% [3]. Although most pancreatic cancers harbor canonical driver mutations, they exhibit marked heterogeneity at the molecular level. Whole-genome sequencing (WGS) and integrative genomic analyses have identified molecular subtypes of PDAC with potential clinical relevance [4-9]. With the increasing implementation of precision oncology, the Chinese Society of Clinical Oncology (CSCO) Guidelines for the Diagnosis and Treatment of Pancreatic Cancer give a level 1 recommendation to perform genetic and other molecular testing on tissue or cytologic specimens as part of the pathological diagnostic work-up, in order to guide individualized treatment, including targeted therapy and immunotherapy [10]. To further promote the use of genetic and molecular testing in the precision treatment of pancreatic cancer, the CSCO Pancreatic Cancer Expert Committee convened a multidisciplinary panel to develop the present Chinese Expert Consensus on Precision Testing and Molecular Diagnosis of Pancreatic Cancer (2025), aiming to provide clinicians with an authoritative reference for precision diagnostics and treatment decision-making.

Indexed as

Carcinoma, Pancreatic DuctalMolecular Diagnostic TechniquesPancreatic NeoplasmsPrecision MedicineBiomarkers, TumorChinaHumansPrognosisBiomarkers, Tumor

Identifiers

PMID42498744
PMCPMC13534480

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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.