Evidence map›Paper›PMID 28050231›Full record

ArticleGenes & cancer2016

Treatment of patients with refractory metastatic cancer according to molecular profiling on tumor tissue in the clinical routine: an interim-analysis of the ONCO-T-PROFILE project.

Andreas Seeber, Guenther Gastl, Christian Ensinger, Gilbert Spizzo, Wolfgang Willenbacher, Florian Kocher, Christoph Leitner, Ella Willenbacher, Arno Amann, Normann Steiner and 4 more

Abstract read
In one paragraph

Article in Genes & cancer, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
–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. Trial
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Bioinformatics for precision oncology.Briefings in bioinformatics · 2019
    Review
  9. Article
  10. Review
  11. Article
  12. 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

14 authors.

Andreas SeeberDepartment of Haematoloy and Oncology, Innsbruck Medical University, Austria; Laboratory for Experimental Oncogenomics, Tyrolean Cancer Research Institute, Austria.
Guenther GastlDepartment of Haematoloy and Oncology, Innsbruck Medical University, Austria.
Christian EnsingerDepartment of Pathology, Innsbruck Medical University, Austria.
Gilbert SpizzoHaematooncological Day Hospital, Hospital of Merano, Italy.
Wolfgang WillenbacherDepartment of Haematoloy and Oncology, Innsbruck Medical University, Austria.
Florian KocherDepartment of Haematoloy and Oncology, Innsbruck Medical University, Austria.
Christoph LeitnerDepartment of Haematoloy and Oncology, Innsbruck Medical University, Austria.
Ella WillenbacherDepartment of Haematoloy and Oncology, Innsbruck Medical University, Austria.
Arno AmannDepartment of Haematoloy and Oncology, Innsbruck Medical University, Austria.
Normann SteinerDepartment of Haematoloy and Oncology, Innsbruck Medical University, Austria.
Wolfgang EistererDepartment of Haematoloy and Oncology, Innsbruck Medical University, Austria.
Andreas VossCaris Life Sciences, Basel, Switzerland.
Kenneth RussellCaris Life Sciences, Basel, Switzerland.
Heinz ZwierzinaDepartment of Haematoloy and Oncology, Innsbruck Medical University, Austria.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionPatients with refractory metastatic cancer have been shown to benefit from molecular profiling of tumor tissue. The ONCO-T-PROFILE project was launched in March 2014 at the Innsbruck Medical University. Within 2 years our project aims to recruit 110 patients with stage IV cancer refractory to standard therapy. Our data presented here are based on an interim-analysis.

methodsTumor tissue specimens were submitted for molecular profiling to the certified laboratory (Caris Life Science, USA). Druggable tumor targets were selected based on biomarker status to agents with potential clinical benefit. Clinical benefit was defined as a PFS ratio (=PFS upon treatment according to the molecular profile/ PFS upon the last prior therapy) ≥ 1.3.

resultsAs of April 2015, tumors from 50 patients have been molecularly profiled and one or more targets were detectable in 48 specimens (98%). So far, 19 (38%) patients have been treated according to their molecular tumor profile. To date, 8 (42%) patients have reached a PFS ratio of ≥ 1.3.

conclusionsWe could show that molecular profiling is feasible in the clinical routine. A proportion of patients might benefit from an individualized treatment approach based on molecular profiling. As a result, we will proceed to enroll patients in ONCO-T-PROFILE.

Indexed as

cancercaris life sciencesmolecular profilingnext generation sequencingpersonalized medicine

Identifiers

PMID28050231
PMCPMC5115171

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.