Difference between revisions of "Inflammatory myofibroblastic tumor"

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<big>Note: this is a rare cancer, see [https://www.cancer.gov/pediatric-adult-rare-tumor/rare-tumors/rare-soft-tissue-tumors/inflammatory-myofibroblastic-tumor this page] for more information. These are regimens tested in subtype-specific populations, please see the '''[[Soft_tissue_sarcoma|main soft tissue sarcoma page]]''' for other regimens.</big>
 
<big>Note: this is a rare cancer, see [https://www.cancer.gov/pediatric-adult-rare-tumor/rare-tumors/rare-soft-tissue-tumors/inflammatory-myofibroblastic-tumor this page] for more information. These are regimens tested in subtype-specific populations, please see the '''[[Soft_tissue_sarcoma|main soft tissue sarcoma page]]''' for other regimens.</big>
 
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Revision as of 20:21, 11 August 2023

Section editor
Elizabethdavis2.jpg
Elizabeth J. Davis, MD
Vanderbilt University
Nashville, TN, USA

Note: this is a rare cancer, see this page for more information. These are regimens tested in subtype-specific populations, please see the main soft tissue sarcoma page for other regimens.

1 regimens on this page
1 variants on this page


All lines of therapy

Crizotinib monotherapy

Regimen

Study Dates of enrollment Evidence
Gambacorti-Passerini et al. 2018 (PROFILE 1013) 2011-03 to 2013-10 Phase 1b, fewer than 20 pts in this subgroup (RT)

Biomarker eligibility criteria

  • ALK+

Targeted therapy

Continued indefinitely

References

  1. PROFILE 1013: Gambacorti-Passerini C, Orlov S, Zhang L, Braiteh F, Huang H, Esaki T, Horibe K, Ahn JS, Beck JT, Edenfield WJ, Shi Y, Taylor M, Tamura K, Van Tine BA, Wu SJ, Paolini J, Selaru P, Kim TM. Long-term effects of crizotinib in ALK-positive tumors (excluding NSCLC): A phase 1b open-label study. Am J Hematol. 2018 May;93(5):607-614. Epub 2018 Feb 8. link to original article link to PMC article PubMed NCT01121588