Evidence map›Paper›PMID 25915155›Full record

ArticleOncotarget2015

HER-2 and HER-3 expression in liver metastases of patients with colorectal cancer.

Hanna Styczen, Iris Nagelmeier, Tim Beissbarth, Manuel Nietert, Kia Homayounfar, Thilo Sprenger, Ute Boczek, Kathrin Stanek, Julia Kitz, Hendrik A Wolff and 5 more

Registry-linked trialOpen access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03034473 (Translational Validation Study to Examine KFO179-1 Biomarker Scores for the Prediction and Prognosis of Advanced Primary Resectable Rectal Cancer Stages UICC II-IV, With a 5-FU-based Standard Radiochemotherapy Followed by Total Mesorectal Excision.), which is not on this map. Cited by 22 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed, 1 pooled it
1.6field-weighted citation impact, top 18% 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.

NCT03034473 naunknown statusnot on this map

Translational Validation Study to Examine KFO179-1 Biomarker Scores for the Prediction and Prognosis of Advanced Primary Resectable Rectal Cancer Stages UICC II-IV, With a 5-FU-based Standard Radiochemotherapy Followed by Total Mesorectal Excision.

TypeinterventionalSponsorUniversity Medical Center GoettingenRan2011 to 2024Enrolled200ConditionsLocally Advanced Rectal CancerArmsTranslational Research and multimodal treatment
3 · Its place in the literature

Who cites it

22 citing papers in PubMed, 1 synthesis or guideline pooled it, 29 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Review
  5. Review
  6. Article
  7. Article
  8. Article
  9. Cell Therapy as Target Therapy against Colon Cancer Stem Cells.International journal of molecular sciences · 2023
    Review
  10. Review
  11. Review
  12. Article
  13. Review
  14. Article
  15. [Influence of molecular markers on oncological surgery of colorectal cancer].Der Chirurg; Zeitschrift fur alle Gebiete der operativen Medizen · 2021
    Review
  16. Review
  17. Thirty Years of HER3: From Basic Biology to Therapeutic Interventions.Clinical cancer research : an official journal of the American Association for Cancer Research · 2021
    Review
  18. Article
  19. Article
  20. 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

15 authors at 2 institutions in 1 country.

Hanna StyczenDepartment of General, Visceral and Pediatric Surgery, University Medical Center, Göttingen, Germany.
Iris NagelmeierTargos Molecular Pathology, Pathology Nordhessen, Kassel, Germany.
Tim BeissbarthDepartment of Medical Statistics, University Medical Center, Göttingen, Germany.
Manuel NietertDepartment of Medical Statistics, University Medical Center, Göttingen, Germany.
Kia HomayounfarDepartment of General, Visceral and Pediatric Surgery, University Medical Center, Göttingen, Germany.
Thilo SprengerDepartment of General, Visceral and Pediatric Surgery, University Medical Center, Göttingen, Germany.
Ute BoczekDepartment of General, Visceral and Pediatric Surgery, University Medical Center, Göttingen, Germany.
Kathrin StanekDepartment of General, Visceral and Pediatric Surgery, University Medical Center, Göttingen, Germany.
Julia KitzDepartment of Pathology, University Medical Center, Göttingen, Germany.
Hendrik A WolffDepartment of Radiotherapy and Radiooncology, University Medical Center, Göttingen, Germany.
B Michael GhadimiDepartment of General, Visceral and Pediatric Surgery, University Medical Center, Göttingen, Germany.
Peter MiddelTargos Molecular Pathology, Pathology Nordhessen, Kassel, Germany.
Torsten LierschDepartment of General, Visceral and Pediatric Surgery, University Medical Center, Göttingen, Germany.
Josef RüschoffTargos Molecular Pathology, Pathology Nordhessen, Kassel, Germany.
Lena-Christin ConradiDepartment of General, Visceral and Pediatric Surgery, University Medical Center, Göttingen, Germany.
Universitätsmedizin Göttingen · DEUniversity of Göttingen · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveIn this study, we evaluate the frequency of HER-2 and HER-3 expression in liver metastases from patients with colorectal cancer (CRLM). We analyzed the potential of HER-2 and HER-3 as therapeutic targets and evaluated their prognostic value. PATIENTS AND

methodsOverall 208 patients with CRLM were enrolled. HER-2 and HER-3 expression were determined in metastatic tissue of diagnostic punch biopsies (n = 29) or resection specimens (n = 179). The results of immunohistochemistry (IHC) scoring and In-situ-hybridization (ISH)-amplification were correlated with clinical parameters and for the 179 resected patients with cancer-specific (CSS) and overall survival (OS). The mean follow-up time was 56.7 months.

resultsPositivity of HER-2 status (IHC score 2+/ISH+ and IHC 3+) was found in 8.2% of CRLM. High expression of HER-3 (IHC score 2+ and IHC 3+) was detected in 75.0% of liver metastases. CSS after liver surgery was determined and was independent from the HER-2 status (p = 0.963); however HER-3 was prognostic with a favorable course for patients showing an overexpression of HER-3 (p = 0.037).

conclusionsHER-2 overexpression occurs in only 8% of patients with CRLM but with 75% of cases HER-3 is frequently overexpressed in CRLM. Therefore, HER-2 and particularly HER-3 could serve as novel targets to be addressed within multimodal treatment approaches.

Indexed as

Gene Expression Regulation, NeoplasticAdultAgedAged, 80 and overColonColorectal NeoplasmsErb-b2 Receptor Tyrosine KinasesFemaleFollow-Up StudiesHumansImmunohistochemistryIn Situ HybridizationKaplan-Meier EstimateLiverLiver NeoplasmsMaleERBB2 protein, humanErb-b2 Receptor Tyrosine KinasesReceptor, ErbB-3colorectal cancerHER-2HER-3liver metastasestargeted therapy

Identifiers

PMID25915155
PMCPMC4558136
OpenAlexW1829134241

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Registered trials

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.