Evidence map›Paper›PMID 25188872›Full record

ArticleGenetics in medicine : official journal of the American College of Medical Genetics2015

Good survival outcome of metastatic SDH-deficient gastrointestinal stromal tumors harboring SDHA mutations.

Maria A Pantaleo, Cristian Lolli, Margherita Nannini, Annalisa Astolfi, Valentina Indio, Maristella Saponara, Milena Urbini, Stefano La Rovere, Antony Gill, David Goldstein and 13 more

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Article in Genetics in medicine : official journal of the American College of Medical Genetics, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed, 1 pooled it
3.1field-weighted citation impact, top 9% 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

26 citing papers in PubMed, 1 synthesis or guideline pooled it, 68 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Review
  4. Article
  5. Review
  6. Article
  7. Review
  8. Review
  9. Genes · 2023
    Review
  10. Article
  11. Article
  12. Review
  13. Review
  14. Targeted therapy inTherapeutic advances in medical oncology · 2021
    Review
  15. Frontiers in oncology · 2021
    Article
  16. Medicina (Kaunas, Lithuania) · 2020
    Article
  17. Article
  18. The Emerging Role of the FGF/FGFR Pathway in Gastrointestinal Stromal Tumor.International journal of molecular sciences · 2020
    Review
  19. The Emerging Role of Succinate Dehyrogenase Genes (SDHx) in Tumorigenesis.International journal of hematology-oncology and stem cell research · 2019
    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

23 authors at 10 institutions in 3 countries.

Maria A Pantaleo1] Department of Specialized, Experimental and Diagnostic Medicine, Sant'Orsola-Malpighi Hospital, University of Bologna, Bologna, Italy [2] "Giorgio Prodi" Cancer Research Center, University of Bologna, Bologna, Italy.
Cristian LolliDepartment of Specialized, Experimental and Diagnostic Medicine, Sant'Orsola-Malpighi Hospital, University of Bologna, Bologna, Italy.
Margherita NanniniDepartment of Specialized, Experimental and Diagnostic Medicine, Sant'Orsola-Malpighi Hospital, University of Bologna, Bologna, Italy.
Annalisa Astolfi8220;Giorgio Prodi" Cancer Research Center, University of Bologna, Bologna, Italy.
Valentina Indio8220;Giorgio Prodi" Cancer Research Center, University of Bologna, Bologna, Italy.
Maristella SaponaraDepartment of Specialized, Experimental and Diagnostic Medicine, Sant'Orsola-Malpighi Hospital, University of Bologna, Bologna, Italy.
Milena Urbini8220;Giorgio Prodi" Cancer Research Center, University of Bologna, Bologna, Italy.
Stefano La RovereNIER Ingegneria SpA, Bologna, Italy.
Antony GillDepartment of Anatomical Pathology, Royal North Shore Hospital, Australia and University of Sydney, Sydney, Australia.
David Goldstein1] Prince of Wales Hospital, Sydney, Australia [2] Prince of Wales Clinical School, University of New South Wales, New South Wales, Australia.
Claudio CeccarelliPathology Unit, Sant'Orsola-Malpighi Hospital, University of Bologna, Bologna, Italy.
Donatella SantiniPathology Unit, Sant'Orsola-Malpighi Hospital, University of Bologna, Bologna, Italy.
Giulio RossiSection of Pathologic Anatomy and Division of Oncology, Modena University Hospital Trust, Modena, Italy.
Michelangelo FiorentinoLaboratory of Oncological and Transplant Molecular Pathology, Pathology Unit, Sant'Orsola-Malpighi Hospital, University of Bologna, Bologna, Italy.
Valerio Di ScioscioDepartment of Radiology, Sant'Orsola Malpighi Hospital, Bologna University, Bologna, Italy.
Pietro FusaroliGI Unit, Department of Medical and Surgical Sciences, University of Bologna/Hospital of Imola , Bologna, Italy.
Anna MandrioliDepartment of Specialized, Experimental and Diagnostic Medicine, Sant'Orsola-Malpighi Hospital, University of Bologna, Bologna, Italy.
Lidia GattoDepartment of Specialized, Experimental and Diagnostic Medicine, Sant'Orsola-Malpighi Hospital, University of Bologna, Bologna, Italy.
Fausto CatenaDepartment of Surgery and Transplantation, Sant'Orsola-Malpighi Hospital, University of Bologna, Bologna, Italy.
Umberto BassoMedical Oncology 1, Veneto Oncology Institute, IRCCS, Padua, Italy.
Giorgio ErcolaniDepartment of Surgery and Transplantation, Sant'Orsola-Malpighi Hospital, University of Bologna, Bologna, Italy.
Antonio Daniele PinnaDepartment of Surgery and Transplantation, Sant'Orsola-Malpighi Hospital, University of Bologna, Bologna, Italy.
Guido Biasco1] Department of Specialized, Experimental and Diagnostic Medicine, Sant'Orsola-Malpighi Hospital, University of Bologna, Bologna, Italy [2] "Giorgio Prodi" Cancer Research Center, University of Bologna, Bologna, Italy.
IRCCS Azienda Ospedliero-Universitaria di Bologna Policlinico di Sant'Orsola · ITIRCCS Materno Infantile Burlo Garofolo · ITUniversity of Trieste · ITOasi Maria SS · ITCasa Sollievo della Sofferenza · ITIngegneria dei Sistemi (Italy) · ITIstituto Oncologico Veneto · ITRoyal North Shore Hospital · AUUniversity of Bologna · ITUniversity of Turin · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeA subset of patients with KIT/PDGFRA wild-type gastrointestinal stromal tumors show loss of function of succinate dehydrogenase, mostly due to germ-line mutations of succinate dehydrogenase subunits, with a predominance of succinate dehydrogenase subunit A. The clinical outcome of these patients seems favorable, as reported in small series in which patients were individually described. This work evaluates a retrospective survival analysis of a series of patients with metastatic KIT/PDGFRA wild-type succinate dehydrogenase-deficient gastrointestinal stromal tumors.

methodsSixty-nine patients with metastatic gastrointestinal stromal tumors were included in the study (11 KIT/PDGFRA wild-type, of whom 6 were succinate dehydrogenase deficient, 5 were non-succinate dehydrogenase deficient, and 58 were KIT/PDGFRA mutant). All six succinate dehydrogenase-deficient patients harbored SDHA mutations. Kaplan-Meier curves and log-rank tests were used to compare the survival of patients with succinate dehydrogenase subunit A-mutant gastrointestinal stromal tumors with that of KIT/PDGFRA wild-type patients without succinate dehydrogenase deficiency and patients with KIT/PDGFRA-mutant gastrointestinal stromal tumors.

resultsFollow-up ranged from 8.5 to 200.7 months. The difference between succinate dehydrogenase subunit A-mutant gastrointestinal stromal tumors and KIT/PDGFRA-mutant or KIT/PDGFRA wild-type non-succinate dehydrogenase deficient gastrointestinal stromal tumors was significant considering different analyses (P = 0.007 and P = 0.033, respectively, from diagnosis of gastrointestinal stromal tumor for the whole study population; P = 0.005 and P = 0.018, respectively, from diagnosis of metastatic disease for the whole study population; P = 0.007 for only patients who were metastatic at diagnosis).

conclusionPatients with metastatic KIT/PDGFRA wild-type succinate dehydrogenase-deficient gastrointestinal stromal tumors harboring succinate dehydrogenase subunit A mutations present an impressively long survival. These patients should be identified in clinical practice to better tailor treatments and follow-up over time.

Indexed as

MutationAdultAgedElectron Transport Complex IIExonsFemaleFollow-Up StudiesGastrointestinal Stromal TumorsHumansKaplan-Meier EstimateMaleMiddle AgedNeoplasm MetastasisPatient Outcome AssessmentPrognosisProto-Oncogene Proteins c-kitElectron Transport Complex IIProto-Oncogene Proteins c-kitReceptor, Platelet-Derived Growth Factor alphaSDHA protein, human

Identifiers

PMID25188872
OpenAlexW1988975026

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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.