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Inflammatory Myofibroblastic Tumor With ROS1 Gene Fusions in Children and Young Adolescents.

Authors :
Schoot RA
Orbach D
Minard Colin V
Alaggio R
Di Carlo D
Corradini N
Mercolini F
Milano GM
van Noesel MM
Rome A
Dall'Igna P
Pajtler K
Sparber-Sauer M
Ferrari A
Casanova M
Source :
JCO precision oncology [JCO Precis Oncol] 2023 Sep; Vol. 7, pp. e2300323.
Publication Year :
2023

Abstract

Purpose: Inflammatory myofibroblastic tumors (IMTs) are often driven by anaplastic lymphoma kinase fusions and less frequently by alternative fusions such as ROS1 . We describe the clinical characteristics, treatment approach, and outcome for a series of young patients with IMTs and ROS1 alterations.<br />Methods: This was a retrospective, international, multicenter study analyzing young patients (younger than 21 years) with ROS1 -altered IMTs treated in 10 European referral centers between 2014 and 2022. Patients were included in the European pediatric Soft tissue sarcoma Study Group NRSTS-2005 protocol or registered in the Soft Tissue Sarcoma Registry. Primary surgery was recommended if a microscopic radical resection was feasible without mutilation. No standard systemic treatment protocol was available, but several medical options were recommended.<br />Results: A total of 19 patients (median age 8.3 years) were included. Most patients had a biopsy at diagnosis (Intergroup Rhabdomyosarcoma Study [IRS] I; n = 2, IRS II; n = 1, IRS III biopsy; n = 11, IRS III resection; n = 3, IRS IV; n = 2). Twelve patients received neoadjuvant systemic therapy in first line (four received multiple treatments): high-dose steroids (n = 2), vinorelbine/vinblastine with methotrexate (n = 6), or ROS1 inhibitors (n = 8). After a median follow-up of 2.8 years (range, 0.2-13.4), seven patients developed an event. The 3-year event-free survival was 41% (95% CI, 11 to 71), and the 3-year overall survival was 100%.<br />Conclusion: Outcome for ROS1 -altered IMTs appears excellent. A complete resection at diagnosis was often not feasible, and most patients needed neoadjuvant therapy. Patients who developed a tumor event could be cured with reinitiation of systemic therapy and/or surgery. This approach illustrates a switch in treatment philosophy moving from immediate, often mutilating, surgery to systemic (targeted) therapy as a bridge to more conservative surgery later in the treatment course.

Details

Language :
English
ISSN :
2473-4284
Volume :
7
Database :
MEDLINE
Journal :
JCO precision oncology
Publication Type :
Academic Journal
Accession number :
37856763
Full Text :
https://doi.org/10.1200/PO.23.00323