Evidence map›Paper›PMID 35476549›Full record

ArticleJCO precision oncology2022

ALK Inhibitors in Patients With ALK Fusion-Positive GI Cancers: An International Data Set and a Molecular Case Series.

Margherita Ambrosini, Marzia Del Re, Paolo Manca, Andrew Hendifar, Alexander Drilon, Guilherme Harada, Anne Hansen Ree, Samuel Klempner, Gunhild Mari Mælandsmo, Kjersti Flatmark and 11 more

Open access · hybridAbstract read
In one paragraph

Article in JCO precision oncology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
3.8field-weighted citation impact, top 5% 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

22 citing papers in PubMed, 29 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Leptomeningeal carcinomatosis in gastric cancer: a single-center retrospective analysis of 86 cases.Gastric cancer : official journal of the International Gastric Cancer Association and the Japanese Gastric Cancer Association · 2026
    Article
  5. Article
  6. Review
  7. Oncogenic gene fusions in cancer: from biology to therapy.Signal transduction and targeted therapy · 2025
    Review
  8. Review
  9. Article
  10. Review
  11. Article
  12. Review
  13. Article
  14. Fusion genes in pancreatic tumors.Trends in cancer · 2024
    Review
  15. Review
  16. Review
  17. Review
  18. Review
  19. Article
  20. 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

21 authors at 9 institutions in 3 countries.

Margherita AmbrosiniMedical Oncology Department, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.ORCID 0000-0003-4131-2409
Marzia Del ReClinical Pharmacology and Pharmacogenetics Unit, Department of Clinical and Experimental Medicine, University Hospital of Pisa, Pisa, Italy.ORCID 0000-0001-7343-6161
Paolo MancaMedical Oncology Department, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.ORCID 0000-0002-3813-6339
Andrew HendifarDivision of Hematology and Oncology, Cedars-Sinai Medical Center, Los Angeles, CA.ORCID 0000-0002-2079-9177
Alexander DrilonMemorial Sloan Kettering Cancer Center, New York, NY.ORCID 0000-0001-6806-9061
Guilherme HaradaMemorial Sloan Kettering Cancer Center, New York, NY.ORCID 0000-0003-4012-3251
Anne Hansen ReeDepartment of Oncology, Akershus University Hospital, Lorenskog, Norway.ORCID 0000-0002-8264-3223
Samuel KlempnerMassachusetts General Hospital Cancer Center, Boston, MA.ORCID 0000-0002-4062-0808
Gunhild Mari MælandsmoDepartment of Tumor Biology, Institute for Cancer Research, Oslo University Hospital, The Norwegian Radium Hospital, Oslo, Norway.
Kjersti FlatmarkDepartment of Gastroenterological Surgery, Norwegian Radium Hospital, Oslo University Hospital, Oslo, Norway.ORCID 0000-0001-7409-0780
Hege G RussnesDivision of Laboratory Medicine, Department of Pathology, Oslo University Hospital, Norway.ORCID 0000-0001-8724-1891
James M ClearyDepartment of Medical Oncology, Dana-Farber Cancer Institute,Boston, MA.ORCID 0000-0001-7213-3951
Harshabad SinghDepartment of Medical Oncology, Dana-Farber Cancer Institute,Boston, MA.
Elisa SottotettiMedical Oncology Department, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.
Antonia MartinettiMedical Oncology Department, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.
Giovanni RandonMedical Oncology Department, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.
Andrea Sartore-BianchiDepartment of Oncology and Hemato-Oncology, University of Milano (La Statale), Milan, Italy.ORCID 0000-0003-0780-0409
Iolanda CaponePathology Department, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.
Massimo MilionePathology Department, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.
Maria Di BartolomeoMedical Oncology Department, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.
Filippo PietrantonioMedical Oncology Department, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.ORCID 0000-0002-8530-8420
Fondazione IRCCS Istituto Nazionale dei Tumori · ITOslo University Hospital · NODana-Farber Cancer Institute · USMemorial Sloan Kettering Cancer Center · USAzienda Ospedaliera Universitaria Pisana · ITCedars-Sinai Medical Center · USMassachusetts General Hospital · USUniversity of Milan · ITUniversity of Oslo · NO

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Hongbiao Carl Lekaye · 1985 to 2026
$347.4M
NCI NIH HHS P30 CA008748
6 · The paper itself

Abstract

purposeIn GI cancers, anaplastic lymphoma kinase ( MATERIALS AND

methodsWe assembled a clinical and molecular international data set of pretreated patients with metastatic or nonresectable cancers of GI primary tumor origin with documented

resultsPrimary tumor sites were distributed as follows: 5 (38%) pancreas, 3 (23%) right colon, and 1 (8%) for each one of gastric, duodenal, rectal, left colon, and biliary tract sites. Seven patients (54%) were treated with alectinib, 5 (38%) with crizotinib, and 1 (8%) with entrectinib. After disease progression, five patients (38%) received a subsequent ALKi treatment line, and at the time of data cutoff date, treatment was still ongoing in two patients. Five of 12 evaluable patients (41%) achieved a partial response to first-line ALKi, five patients (41%) had stable disease, and 2 (17%) had progressive disease. No complete responses were registered. At a median follow-up of 39.6 months (interquartile range: 19.8-59.5), the median progression-free survival was 5.0 months (95% CI, 3.68 to no response) and the median overall survival was 9.3 months (95% CI, 5.46 to no response).

conclusionTreatment with ALKi provides remarkable responses and clinical benefit in pretreated patients with ALK fusion-positive GI malignancies. Despite the rarity,

Indexed as

Carcinoma, Non-Small-Cell LungGastrointestinal NeoplasmsLung NeoplasmsCrizotinibHumansProspective StudiesProtein Kinase InhibitorsCrizotinibProtein Kinase Inhibitors

Identifiers

PMID35476549
PMCPMC9200393
OpenAlexW4224930739

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.