Evidence map›Paper›PMID 37014660›Full record

Trial reportClinical cancer research : an official journal of the American Association for Cancer Research2023

KIT and PDGFRA Mutations and Survival of Gastrointestinal Stromal Tumor Patients Treated with Adjuvant Imatinib in a Randomized Trial.

Heikki Joensuu, Eva Wardelmann, Mikael Eriksson, Annette Reichardt, Kirsten Sundby Hall, Jochen Schütte, Silke Cameron, Peter Hohenberger, Harri Sihto, Philipp J Jost and 6 more

Open access · hybridAbstract readMulticenter StudyRandomized Controlled Trial
In one paragraph

Trial report in Clinical cancer research : an official journal of the American Association for Cancer Research, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed, 1 pooled it
5.8field-weighted citation impact, top 3% 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

20 citing papers in PubMed, 1 synthesis or guideline pooled it, 21 citations in OpenAlex.

  1. Guideline
  2. Trial
  3. Review
  4. Article
  5. Article
  6. Observational
  7. Review
  8. Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Review
  15. Article
  16. [Gastrointestinal stromal tumors : Where do we stand?]Pathologie (Heidelberg, Germany) · 2024
    Review
  17. The impact of contour maps on estimating the risk of gastrointestinal stromal tumor recurrence: indications for adjuvant therapy: an analysis of the Kinki GIST registry.Gastric cancer : official journal of the International Gastric Cancer Association and the Japanese Gastric Cancer Association · 2024
    Article
  18. Article
  19. Cancers · 2023
    Review
  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

16 authors at 14 institutions in 5 countries.

Heikki JoensuuDepartment of Oncology, Helsinki University Hospital and University of Helsinki, Helsinki, Finland.ORCID 0000-0003-0281-2507
Eva WardelmannGerhard-Domagk-Institute of Pathology, University of Münster, Münster, Germany.ORCID 0000-0001-6788-4910
Mikael ErikssonDepartment of Oncology, Skåne University Hospital and Lund University, Lund, Sweden.ORCID 0000-0003-0463-0678
Annette ReichardtHelios Klinikum Berlin-Buch, Sarkomzentrum Berlin-Brandenburg, Berlin, Germany.ORCID 0009-0006-9451-4097
Kirsten Sundby HallDepartment of Oncology, The Norwegian Radium Hospital, Oslo University Hospital, Oslo, Norway.ORCID 0000-0002-2126-8255
Jochen SchütteAlfried Krupp Krankenhaus, Essen Rüttenscheid, Germany.ORCID 0009-0005-3692-0719
Silke CameronDepartment of Gastroenterology, University of Göttingen, Göttingen, Germany.ORCID 0000-0003-2761-0960
Peter HohenbergerDivision of Surgical Oncology & Thoracic Surgery, Mannheim University Medical Center, Mannheim, Germany.ORCID 0000-0001-5359-5923
Harri SihtoDepartment of Pathology, University of Helsinki and Helsinki University Hospital, Helsinki, Finland.ORCID 0000-0001-5265-5509
Philipp J JostMedical Department III, Klinikum rechts der Isar, Technical University of Munich, Munich, Germany.ORCID 0000-0003-2454-0362
Lars H LindnerDepartment of Medicine III, University Hospital, LMU Munich, Munich, Germany.ORCID 0000-0003-3708-8264
Sebastian BauerSarcoma Center, West German Cancer Center, Essen, Germany.ORCID 0000-0001-5949-8120
Bengt NilssonDepartment of Surgery, Sahlgrenska University Hospital, Gothenburg, Sweden.ORCID 0009-0003-0919-0656
Raija KallioDepartment of Oncology and Radiotherapy, Oulu University Hospital, Oulu, Finland.ORCID 0000-0002-5912-496X
Tommi Pesonen4Pharma Ltd, Turku, Finland.ORCID 0009-0009-3513-8345
Peter ReichardtHelios Klinikum Berlin-Buch, Sarkomzentrum Berlin-Brandenburg, Berlin, Germany.ORCID 0009-0008-1410-3111
Helios Hospital Berlin-Buch · DEUniversity of Helsinki · FIAlfried Krupp Hospital · DEHeidelberg University · DELMU Klinikum · DEOslo University Hospital · NOOulu University Hospital · FISahlgrenska University Hospital · SESkåne University Hospital · SETUM Klinikum · DETurku City Hospital · FIUniversitätsmedizin Göttingen · DEUniversity of Münster · DEWest Cancer Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeLimited data are available about the influence of KIT and PDGFRA mutations on overall survival (OS) of patients with gastrointestinal stromal tumor (GIST) treated with adjuvant imatinib. PATIENTS AND

methodsThe Scandinavian Sarcoma Group XVIII/AIO multicenter trial accrued 400 patients with a high risk for GIST recurrence after macroscopically complete surgery between February 4, 2004, and September 29, 2008. The patients received adjuvant imatinib 400 mg/day for either 1 year or 3 years based on random allocation. We analyzed using conventional sequencing KIT and PDGFRA mutations centrally from 341 (85%) patients who had localized, centrally confirmed GIST, and correlated the results with recurrence-free survival (RFS) and OS in exploratory analyses.

resultsDuring a median follow-up time of 10 years, 164 RFS events and 76 deaths occurred. Most patients were re-treated with imatinib when GIST recurred. Patients with KIT exon 11 deletion or indel mutation treated with 3 years of adjuvant imatinib survived longer than patients treated for 1 year [10-year OS 86% versus 64%, respectively; HR, 0.34; 95% confidence interval (CI), 0.15-0.72; P = 0.007], and also had longer RFS (10-year RFS 47% versus 29%; HR, 0.48; 95% CI, 0.31-0.74; P < 0.001). Patients with KIT exon 9 mutation had unfavorable OS regardless of the duration of adjuvant imatinib.

conclusionsCompared with 1 year of imatinib, 3 years of adjuvant imatinib led to 66% reduction in the estimated risk of death and a high 10-year OS rate in the subset of patients with a KIT exon 11 deletion/indel mutation.

Indexed as

Antineoplastic AgentsGastrointestinal Stromal TumorsChemotherapy, AdjuvantHumansImatinib MesylateMutationReceptor Protein-Tyrosine KinasesAntineoplastic AgentsImatinib MesylateReceptor Protein-Tyrosine Kinases

Identifiers

PMID37014660
PMCPMC10472091
OpenAlexW4362522227

What OpenQuestion holds

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LicenceCC BY-NC-ND
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Registered trials

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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.