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Inflammatory Myofibroblastic Tumor With ROS1 Gene Fusions in Children and Young Adolescents.
Schoot, Reineke A; Orbach, Daniel; Minard Colin, Veronique; Alaggio, Rita; Di Carlo, Daniela; Corradini, Nadege; Mercolini, Federico; Milano, Giuseppe Maria; van Noesel, Max M; Rome, Angelique; Dall'Igna, Patrizia; Pajtler, Kristian; Sparber-Sauer, Monika; Ferrari, Andrea; Casanova, Michela.
Affiliation
  • Schoot RA; Princess Máxima Center for Pediatric Oncology, Utrecht, the Netherlands.
  • Orbach D; SIREDO Oncology Center (Care, Innovation and Research for Children, Adolescents and Young Adults with Cancer), Institut Curie, PSL University, Paris, France.
  • Minard Colin V; Department of Pediatric and Adolescent Oncology, Gustave-Roussy, Université Paris-Saclay, Villejuif, France.
  • Alaggio R; Pathology Unit, Department of Laboratories, Bambino Gesu Children's Hospital, IRCCS, Rome, Italy.
  • Di Carlo D; Pediatric Hematology-Oncology Division, University Hospital of Padova, Padova, Italy.
  • Corradini N; Department of Pediatric Oncology, Institut d'Hematologie et d'Oncologie Pédiatrique, Centre Léon Bérard, Lyon, France.
  • Mercolini F; Pediatric Oncology and Hematology "Lalla Seràgnoli", Istituto di Ricovero e Cura a Carattere Scientifico, Azienda Ospedaliero-Universitaria di Bologna, Bologna, Italy.
  • Milano GM; Department of Hematology/Oncology, Cell and Gene Therapy, Bambino Gesù Children's Hospital, Istituto di Ricovero e Cura a Carattere Scientifico (IRCSS), Rome, Italy.
  • van Noesel MM; Princess Máxima Center for Pediatric Oncology, Utrecht, the Netherlands.
  • Rome A; Department of Pediatric Oncology, Timone Children's Hospital, Marseille, France.
  • Dall'Igna P; Pediatric Surgery, Department of Precision and Regenerative Medicine and Jonic Area, Pediatric Hospital Giovanni XXIII, University of Bari, Bari, Italy.
  • Pajtler K; Hopp Children's Cancer Center Heidelberg (KiTZ), Heidelberg University, Heidelberg, Germany.
  • Sparber-Sauer M; Division of Pediatric Neurooncology, German Cancer Research Center (DKFZ) and German Cancer Consortium (DKTK), Heidelberg University, Heidelberg, Germany.
  • Ferrari A; Department of Pediatric Oncology, Hematology, and Immunology, Heidelberg University Hospital, Heidelberg, Germany.
  • Casanova M; Stuttgart Cancer Center, Zentrum für Kinder-, Jugend- und Frauenmedizin (Olgahospital), Pädiatrie 5 (Pädiatrische Onkologie, Hämatologie, Immunologie), Klinikum der Landeshauptstadt Stuttgart, Stuttgart, Germany.
JCO Precis Oncol ; 7: e2300323, 2023 09.
Article in En | MEDLINE | ID: mdl-37856763
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.

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.

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%.

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.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Rhabdomyosarcoma / Sarcoma Limits: Adolescent / Child / Humans Country/Region as subject: Europa Language: En Journal: JCO Precis Oncol Year: 2023 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Rhabdomyosarcoma / Sarcoma Limits: Adolescent / Child / Humans Country/Region as subject: Europa Language: En Journal: JCO Precis Oncol Year: 2023 Document type: Article