Evidence map›Paper›PMID 27026089›Full record

ArticleInternational journal of colorectal disease2016

Colorectal cancer in Crohn's colitis is comparable to sporadic colorectal cancer.

Jochen K Lennerz, Kimberley W J van der Sloot, Long Phi Le, Julie M Batten, Jae Young Han, Kenneth C Fan, Corey A Siegel, Amitabh Srivastava, Do Youn Park, Jey-Hsin Chen and 8 more

Abstract readComparative Study
PubMed Publisher
In one paragraph

Article in International journal of colorectal disease, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed, 1 pooled it
4.5field-weighted citation impact, top 6% of its field
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

19 citing papers in PubMed, 1 synthesis or guideline pooled it, 33 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Intratumor microbiota and colorectal cancer: Comprehensive and lucid review.Chinese journal of cancer research = Chung-kuo yen cheng yen chiu · 2024
    Article
  4. Review
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Review
  13. Review
  14. Crohn's Disease and the Risk of Cancer.Clinics in colon and rectal surgery · 2019
    Review
  15. Review
  16. Review
  17. Dynamics of Genome Alterations in Crohn's Disease-Associated Colorectal Carcinogenesis.Clinical cancer research : an official journal of the American Association for Cancer Research · 2018
    Article
  18. Mutational Analysis Identifies Therapeutic Biomarkers in Inflammatory Bowel Disease-Associated Colorectal Cancers.Clinical cancer research : an official journal of the American Association for Cancer Research · 2018
    Article
  19. 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

18 authors at 7 institutions in 2 countries.

Jochen K LennerzDepartment of Pathology, Massachusetts General Hospital/Harvard Medical School, Boston, MA, 02116, USA. JLennerz@partners.org.
Kimberley W J van der SlootDivision of Gastroenterology, Massachusetts General Hospital/Harvard Medical School, Boston, MA, USA.
Long Phi LeDepartment of Pathology, Massachusetts General Hospital/Harvard Medical School, Boston, MA, 02116, USA.
Julie M BattenDepartment of Pathology, Massachusetts General Hospital/Harvard Medical School, Boston, MA, 02116, USA.
Jae Young HanDepartment of Pathology, Massachusetts General Hospital/Harvard Medical School, Boston, MA, 02116, USA.
Kenneth C FanDepartment of Pathology, Massachusetts General Hospital/Harvard Medical School, Boston, MA, 02116, USA.
Corey A SiegelDartmouth-Hitchcock Inflammatory Bowel Disease Center, Dartmouth-Hitchcock Medical Center, Lebanon, NH, USA.
Amitabh SrivastavaDepartment of Pathology, Brigham and Women's Hospital, Boston, MA, USA.
Do Youn ParkDepartment of Pathology, Pusan National University Hospital and Pusan National University School of Medicine, Busan, Republic of Korea.
Jey-Hsin ChenSwedish Medical Center, CellNetix Pathology and Laboratories, Seattle, WA, USA.
Bruce E SandsDr. Henry D. Janowitz Division of Gastroenterology, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Joshua R KorzenikDivision of Gastroenterology, Hepatology and Endoscopy, Brigham and Women's Hospital, Boston, MA, USA.
Robert D OdzeDepartment of Pathology, Brigham and Women's Hospital, Boston, MA, USA.
Dora Dias-SantagataDivision of Gastroenterology, Massachusetts General Hospital/Harvard Medical School, Boston, MA, USA.
Darrell R BorgerDepartment of Hematology/Oncology, Massachusetts General Hospital/Harvard Medical School, Boston, MA, USA.
Hamed KhaliliDivision of Gastroenterology, Massachusetts General Hospital/Harvard Medical School, Boston, MA, USA.
A John IafrateDepartment of Pathology, Massachusetts General Hospital/Harvard Medical School, Boston, MA, 02116, USA.
Gregory Y LauwersDepartment of Pathology, Massachusetts General Hospital/Harvard Medical School, Boston, MA, 02116, USA.
Harvard University · USBrigham and Women's Hospital · USMassachusetts General Hospital · USDartmouth–Hitchcock Medical Center · USIcahn School of Medicine at Mount Sinai · USPusan National University Hospital · KRSwedish Medical Center · US

Funding

Oral Contraceptives in the Etiopathogenesis of Crohn's DiseaseK23DK099681 · NIDDK · MASSACHUSETTS GENERAL HOSPITAL · PI KHALILI, HAMED · 2013 to 2017
$946k
NIDDK NIH HHS K23 DK099681
6 · The paper itself

Abstract

purposeIt is now recognized that Crohn's disease (CD), similar to ulcerative colitis (UC), carries an up to 20-fold higher cancer risk, and the development of colorectal carcinoma (CRC) is a major long-term complication. Once CRC is present, molecular profiling is one of the components in selecting appropriate treatment strategies; however, in contrast to UC, genetic alterations in Crohn's colitis-associated CRC are poorly understood.

methodsIn a series of 227 patients with Crohn's colitis, we identified 33 cases of CRC (~14 %) and performed targeted mutational analysis of BRAF/KRAS/NRAS and determined microsatellite status as well as immunophenotype of the tumors.

resultsIn the CRC cohort, the median age at time of cancer diagnosis was 58 (range 34-77 vs. 59.5 in sporadic; P = 0.81) and the median CD duration was 29 years (range 6-45). As a group, CRC complicating Crohn's colitis is BRAF (97 %) and NRAS (100 %) wild type and the vast majority is microsatellite stable (94 %); KRAS-mutations were found in six cases (18 %). Stage grouping, anatomic distribution, and overall survival were similar to sporadic CRC; however, long-standing CD (≥25 years) as well as gastric-immunophenotype (MUC5AC+) was associated with significantly shorter overall survival (P = 0.0029; P = 0.036, respectively).

conclusionIn summary, the clinicopathological and molecular profile of CD-associated CRC is similar to that observed in sporadic CRC.

Indexed as

AdultAgedColorectal NeoplasmsCrohn DiseaseDNA MethylationFemaleFollow-Up StudiesGenetic Association StudiesGTP PhosphohydrolasesHumansImmunophenotypingMaleMembrane ProteinsMicrosatellite RepeatsMiddle AgedMutationBRAF protein, humanGTP PhosphohydrolasesKRAS protein, humanMembrane ProteinsMLH1 protein, humanMutL Protein Homolog 1NRAS protein, humanProto-Oncogene Proteins B-rafProto-Oncogene Proteins p21(ras)Colorectal cancerCrohn’s colitisSNaPshotTargeted re-sequencing

Identifiers

PMID27026089
OpenAlexW2335387331

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.