Evidence map›Paper›PMID 25326159›Full record

SynthesisThe oncologist2014

Targeted therapies in metastatic colorectal cancer: a systematic review and assessment of currently available data.

Martha M Kirstein, Ansgar Lange, Anne Prenzler, Michael P Manns, Stefan Kubicka, Arndt Vogel

Registry-linked trialOpen access · bronzeAbstract readMeta-AnalysisSystematic Review
In one paragraph

Synthesis in The oncologist, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04395612 (A Clinical Proof-of-concept Study Evaluating Efficacy and Safety of ZL-2306), which is not on this map. Cited by 48 papers, 6 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
48citing papers in PubMed, 6 pooled it
7.5field-weighted citation impact, top 2% 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.

NCT04395612 phase2unknown statusnot on this mapstarted 2020, after this paper: background citation

A Clinical Proof-of-concept Study Evaluating Efficacy and Safety of ZL-2306 (Niraparib) Combined With Brivanib or Toripalimab in Patients With Metastatic, Recurrent, and Persistent Cervical Cancer

TypeinterventionalSponsorChongqing University Cancer HospitalRan2020 to 2022Enrolled38ConditionsCervical CancerArmsniraparib combined with brivanib, niraparib combined with toripalimab
3 · Its place in the literature

Who cites it

48 citing papers in PubMed, 6 syntheses or guidelines pooled it, 105 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Pooled it
  5. Second-line systemic therapy for metastatic colorectal cancer.The Cochrane database of systematic reviews · 2017
    Pooled it
  6. Pooled it
  7. Trial
  8. Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Molecules (Basel, Switzerland) · 2021
    Article
  17. Article
  18. Review
  19. Article
  20. Multimodal immune activation abilities and characteristics of reovirus.American journal of translational research · 2021
    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

6 authors at 3 institutions in 1 country.

Martha M KirsteinDepartment of Gastroenterology, Hepatology and Endocrinology, Hannover Medical School, Hannover, Germany; Leibniz University Hannover, Center for Health Economics Research Hannover, Hannover, Germany; Cancer Center Reutlingen, Reutlingen, Germany.
Ansgar LangeDepartment of Gastroenterology, Hepatology and Endocrinology, Hannover Medical School, Hannover, Germany; Leibniz University Hannover, Center for Health Economics Research Hannover, Hannover, Germany; Cancer Center Reutlingen, Reutlingen, Germany.
Anne PrenzlerDepartment of Gastroenterology, Hepatology and Endocrinology, Hannover Medical School, Hannover, Germany; Leibniz University Hannover, Center for Health Economics Research Hannover, Hannover, Germany; Cancer Center Reutlingen, Reutlingen, Germany.
Michael P MannsDepartment of Gastroenterology, Hepatology and Endocrinology, Hannover Medical School, Hannover, Germany; Leibniz University Hannover, Center for Health Economics Research Hannover, Hannover, Germany; Cancer Center Reutlingen, Reutlingen, Germany.
Stefan KubickaDepartment of Gastroenterology, Hepatology and Endocrinology, Hannover Medical School, Hannover, Germany; Leibniz University Hannover, Center for Health Economics Research Hannover, Hannover, Germany; Cancer Center Reutlingen, Reutlingen, Germany.
Arndt VogelDepartment of Gastroenterology, Hepatology and Endocrinology, Hannover Medical School, Hannover, Germany; Leibniz University Hannover, Center for Health Economics Research Hannover, Hannover, Germany; Cancer Center Reutlingen, Reutlingen, Germany vogel.arndt@mh-hannover.de.
Medizinische Hochschule Hannover · DELeibniz University Hannover · DEReutlingen University · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSurvival of patients with metastatic colorectal cancer (mCRC) has been significantly improved with the introduction of the monoclonal antibodies targeting the vascular endothelial growth factor (VEGF) and the epidermal growth factor receptor (EGFR). Novel molecular-targeted agents such as aflibercept and regorafenib have recently been approved. The aim of this review is to summarize and assess the effects of molecular agents in mCRC based on the available phase II and III trials, pooled analyses, and meta-analyses/systematic reviews.

methodsA systematic literature search was conducted using the meta-database of the German Institute of Medical Documentation and Information. Criteria of the Scottish Intercollegiate Guidelines Network were used to assess the quality of the controlled trials and systematic reviews/meta-analyses.

resultsOf the 806 retrieved records, 40 publications were included. For bevacizumab, efficacy in combination with fluoropyrimidine-based chemotherapy in first- and subsequent-line settings has been shown. The benefit of continued VEGF targeting has also been demonstrated with aflibercept and regorafenib. Cetuximab is effective with fluoropyrimidine, leucovorin, and irinotecan (FOLFIRI) in first-line settings and as a single agent in last-line settings. Efficacy for panitumumab has been shown with oxaliplatin with fluoropyrimidine in first-line settings, with FOLFIRI in second-line settings, and as monotherapy in last-line settings. Treatment of anti-EGFR antibodies is restricted to patients with tumors that do not harbor mutations in Kirsten rat sarcoma and in neuroblastoma RAS.

conclusionAmong various therapeutic options, the future challenge will be a better selection of the population that will benefit the most from specific anti-VEGF or anti- EGFR treatment and a careful consideration of therapy sequence.

Indexed as

Antibodies, MonoclonalAntibodies, Monoclonal, HumanizedAntineoplastic Combined Chemotherapy ProtocolsBevacizumabCamptothecinColorectal NeoplasmsErbB ReceptorsFluorouracilHumansIrinotecanLeucovorinMolecular Targeted TherapyOrganoplatinum CompoundsOxaliplatinPanitumumabVascular Endothelial Growth Factor AAntibodies, MonoclonalAntibodies, Monoclonal, HumanizedBevacizumabCamptothecinEGFR protein, humanErbB ReceptorsFluorouracilIrinotecanLeucovorinOrganoplatinum CompoundsOxaliplatinPanitumumabVascular Endothelial Growth Factor AVEGFA protein, humanAfliberceptBevacizumabCetuximabColorectal cancerPanitumumabRegorafenib

Identifiers

PMID25326159
PMCPMC4221380
OpenAlexW2131794175

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.