Evidence map›Paper›PMID 29472376›Full record

ArticleEndocrine connections2018

Clinical relevance of different WHO grade 3 pancreatic neuroendocrine neoplasms based on morphology.

Xu Han, Xuefeng Xu, Hongyun Ma, Yuan Ji, Dansong Wang, Tiantao Kuang, Wenchuan Wu, Bin Song, Gang Li, Gang Jin and 1 more

Abstract read
In one paragraph

Article in Endocrine connections, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing 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

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

  1. Pooled it
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  5. Article
  6. Review
  7. Article
  8. Review
  9. Review
  10. Neuroendocrine Tumors in Pediatrics.Global pediatric health · 2019
    Review
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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.

Xu HanDepartment of Pancreatic SurgeryZhongshan Hospital, Fudan University, Shanghai, China.
Xuefeng XuDepartment of Pancreatic SurgeryZhongshan Hospital, Fudan University, Shanghai, China.
Hongyun MaDepartment of Pancreatic SurgeryChanghai Hospital, Second Military Medical University, Shanghai, China.
Yuan JiDepartment of PathologyZhongshan Hospital, Fudan University, Shanghai, China.
Dansong WangDepartment of Pancreatic SurgeryZhongshan Hospital, Fudan University, Shanghai, China.
Tiantao KuangDepartment of Pancreatic SurgeryZhongshan Hospital, Fudan University, Shanghai, China.
Wenchuan WuDepartment of Pancreatic SurgeryZhongshan Hospital, Fudan University, Shanghai, China.
Bin SongDepartment of Pancreatic SurgeryChanghai Hospital, Second Military Medical University, Shanghai, China.
Gang LiDepartment of Pancreatic SurgeryChanghai Hospital, Second Military Medical University, Shanghai, China.
Gang JinDepartment of Pancreatic SurgeryChanghai Hospital, Second Military Medical University, Shanghai, China lou.wenhui@zs-hospital.sh.cn jingangchh@163.com.
Wenhui LouDepartment of Pancreatic SurgeryZhongshan Hospital, Fudan University, Shanghai, China lou.wenhui@zs-hospital.sh.cn jingangchh@163.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeEmerging evidence suggests G3 pancreatic neuroendocrine neoplasms (pNENs) present heterogeneous morphology and biology. The 2017 WHO classification has introduced a new category of well-differentiated pancreatic neuroendocrine tumors (WD-pNETs) G3, compared with poorly differentiated pancreatic neuroendocrine carcinomas (PD-pNECs) G3. We aim to analysis the demographics and outcomes of patients with resectable 2017 WHO G3 pNENs to facilitate the distinction between two entities.

methodsThe multi-institutional retrospective cohort involving 57 surgically treated patients affected by 2017 WHO G3 pNENs were morphologically identified and clinically analyzed. Patients having WD-pNETs G3 and those having PD-pNECs G3 were compared.

resultsThirty patients had WD-pNETs and 27 patients had PD-pNECs. The distributions of Ki-67 and mitotic count in patients with PD-pNECs or WD-pNETs showed remarkable disparities. ROC indicated cut-off value of Ki-67 was 45. PD-pNECs were more common in patients with elevated Ki-67 and mitotic count, advanced AJCC TNM stage, vascular invasion, regional lymph-node metastases, elevated NSE and decreased CgA levels compared with WD-pNETs (

conclusionsPD-pNECs G3 presented malignant biological behavior and dismal outcome compared with WD-pNETs G3. These findings challenge 2010 WHO classification and suggest the categorization can be improved by refined tumor grading.

Indexed as

grade 3pancreatic neuroendocrine neoplasmspoorly differentiated pancreatic neuroendocrine carcinomasprognosiswell-differentiated pancreatic neuroendocrine tumors

Identifiers

PMID29472376
PMCPMC5825924

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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.