Evidence map›Paper›PMID 34211840›Full record

ArticleFrontiers in oncology2021

Outstanding Response in a Patient With ROS1-Rearranged Inflammatory Myofibroblastic Tumor of Soft Tissues Treated With Crizotinib: Case Report.

Danila Comandini, Fabio Catalano, Massimiliano Grassi, Guido Pesola, Rossella Bertulli, Antonio Guadagno, Bruno Spina, Matteo Mascherini, Franco De Cian, Federico Pistoia and 1 more

Abstract readCase Reports
In one paragraph

Article in Frontiers in oncology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing 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

14 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Oncogenic gene fusions in cancer: from biology to therapy.Signal transduction and targeted therapy · 2025
    Review
  5. Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. 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

11 authors.

Danila ComandiniMedical Oncology Unit 1, IRCCS Ospedale Policlinico San Martino, Genova, Italy.
Fabio CatalanoMedical Oncology Unit 1, IRCCS Ospedale Policlinico San Martino, Genova, Italy.
Massimiliano GrassiMedical Oncology Unit 1, IRCCS Ospedale Policlinico San Martino, Genova, Italy.
Guido PesolaClinic of Medical Oncology, Oncology Institute of Southern Switzerland, Bellinzona, Switzerland.
Rossella BertulliAdult Mesenchymal Tumor Medical Oncology Unit, Fondazione IRCCS Istituto Nazionale Tumori, Milan, Italy.
Antonio GuadagnoAnatomic Pathology Unit, IRCCS Ospedale Policlinico San Martino, Genova, Italy.
Bruno SpinaAnatomic Pathology Unit, IRCCS Ospedale Policlinico San Martino, Genova, Italy.
Matteo MascheriniSurgical Clinic Unit 1, IRCCS Ospedale Policlinico San Martino, Genova, Italy.
Franco De CianSurgical Clinic Unit 1, IRCCS Ospedale Policlinico San Martino, Genova, Italy.
Federico PistoiaDepartment of Health Sciences (DISSAL), University of Genova, Genova, Italy.
Sara Elena RebuzziMedical Oncology Unit 1, IRCCS Ospedale Policlinico San Martino, Genova, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Inflammatory myofibroblastic tumor (IMT) is a very rare subtype of sarcoma, which frequently harbor chromosomal rearrangements, including anaplastic lymphoma kinase (ALK) rearrangements (almost 50% of the IMTs) and other kinase fusions such as ROS1. ROS1 fusions are present in about 10% of IMT, almost half of the ALK-negative IMT patients. Apart from radical surgery for resectable tumors, there is no standard-of-care therapy for advanced IMTs. Nonetheless, the use of tyrosine kinase inhibitors has shown promising efficacy in IMT patients with targetable genomic alterations. We report the case of a 24-year-old patient with chemotherapy-refractory metastatic IMT harboring ROS1 kinase fusion, who experienced a significant clinical and pathological response to crizotinib. This clinical case highlights the need to assess all patients with unresectable IMTs for chromosomal abnormalities and gene mutations and address them to targeted agents as well as clinical trials.

Indexed as

crizotinibinflammatory myofibroblastic tumorinflammatory pseudotumorretreatmentROS1sarcomatarget therapy

Identifiers

PMID34211840
PMCPMC8239351

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.