Evidence map›Paper›PMID 31007870›Full record

ReviewComputational and structural biotechnology journal2019

Treatment According to Molecular Profiling in Relapsed/Refractory Cancer Patients: A Review Focusing on Latest Profiling Studies.

Kai Zimmer, Florian Kocher, Gilbert Spizzo, Mohamed Salem, Guenther Gastl, Andreas Seeber

Open access · goldAbstract readReview
In one paragraph

Review in Computational and structural biotechnology journal, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.1field-weighted citation impact, top 26% 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

16 citing papers in PubMed, 28 citations in OpenAlex.

  1. Precision oncology: transforming cancer care through personalized medicine.Medical oncology (Northwood, London, England) · 2025
    Review
  2. Article
  3. Article
  4. Review
  5. Review
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Review
  12. Genomic profiling in oncology clinical practice.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2020
    Review
  13. Moving Molecular Profiling to Routine Clinical Practice: A Way Forward?Journal of the National Cancer Institute · 2020
    Article
  14. Article
  15. Article
  16. Precision Oncology-The Quest for Evidence.Journal of personalized medicine · 2019
    Review
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 2 institutions in 2 countries.

Kai ZimmerDepartment of Haematology and Oncology, Medical University of Innsbruck, Austria.
Florian KocherDepartment of Haematology and Oncology, Medical University of Innsbruck, Austria.
Gilbert SpizzoDepartment of Haematology and Oncology, Medical University of Innsbruck, Austria.
Mohamed SalemLevine Cancer Institute, Carolinas HealthCare System, Charlotte, USA.
Guenther GastlDepartment of Haematology and Oncology, Medical University of Innsbruck, Austria.
Andreas SeeberDepartment of Haematology and Oncology, Medical University of Innsbruck, Austria.
Innsbruck Medical University · ATCarolinas Healthcare System · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In this review we aim to summarize studies investigating the impact of a molecular profiling (MP)-guided treatment approach in heavily pretreated cancer patients. In summary, many independent single- and multicenter studies showed a significant benefit of MP-guided treatment regarding response rates and survival. However, in the only randomized trial conducted so far, no benefit of MP-guided targeted therapy was observed. Notably, various profiling approaches were conducted in the respective studies: some studies used a single analytic approach (i.e. next-generation sequencing), others applied multiple analytic methods to perform comprehensive molecular profiling. It seems that multiplatform profiling analyses, detected an increased number of druggable molecular targets or signaling pathway alterations and that a higher proportion of patients was treated according to the molecular cancer profile. Even though no randomized study has shown a benefit of molecular profiling so far, many studies indicate that MP-guided treatment can be beneficial in patients with relapsed and/or refractory cancer. Currently ongoing large randomized trials (i.e. NCI-MATCH, TAPUR) will add evidence to the role of profiling-guided cancer treatment.

Indexed as

Abl, Abelson murine leukemia viral oncogene homolog 1ASCO, American Society of Clinical OncologyBcr, Breakpoint cluster regionCGH, Comparative genomic hybridizationCISH, Chromogenic in-situ hybridizationCR, Complete responseDNA, Deoxyribonucleic acidFDA, Food and Drug AdministrationFGFR, Fibroblast growth factor receptorFISH, Fluorescence in-situ hybridizationHER2, Human epidermal growth factor receptor 2HR, Hazard RatioIHC, ImmunohistochemistryMEK, Mitogen-activated protein kinaseMetastatic cancerMolecular profilingMP, Molecular profileMSI, Microsatellite InstabilitymTOR, Mammalian target of RapamycinNCI, National Cancer InstituteNGS, Next generation sequencingORR, Overall response rateOS, Overall SurvivalPCR, Polymerase chain reactionPersonalized medicinePFS, Progression-free survivalPIK3CA, Phosphatidylinositol-4,5-bisphosphate-3-kinase catalytic subunit alphaPrecision oncologyPR, Partial ResponsePTEN, Phosphatase and tensin homologRAF, Rapidly growing fibrosarcoma - proteinRNA, Ribonucleic acidR/R, Refractory/RelapsedSD, Stable DiseaseTTF, Time to treatment failureWES, Whole-exome sequencing

Identifiers

PMID31007870
PMCPMC6453774
OpenAlexW2924092569

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.