Literature DB >> 32784118

Spotlight on the treatment of infantile fibrosarcoma in the era of neurotrophic tropomyosin receptor kinase inhibitors: International consensus and remaining controversies.

Daniel Orbach1, Monika Sparber-Sauer2, Theodore W Laetsch3, Veronique Minard-Colin4, Stefan S Bielack5, Michela Casanova6, Nadege Corradini7, Ewa Koscielniak8, Monika Scheer2, Simone Hettmer9, Gianni Bisogno10, Douglas S Hawkins11, Andrea Ferrari6.   

Abstract

Targeted neurotrophic tropomyosin receptor kinase (TRK) inhibitors offer a highly specific therapeutic option for patients with infantile fibrosarcoma (IFS) carrying the NTRK gene translocation. International recommendations are needed to define the role of TRK inhibitors (TRKI) for infants with IFS. We analysed retrospective data for all published patients with IFS in the European Paediatric Soft tissue sarcoma Study Group and Cooperative Weichteilsarkomstudiengruppe (CWS) experience and developed a consensus strategy with the Children's Oncology Group. Therapies consisted of tumour resection and/or perioperative chemotherapy for extensive tumours. Among the 172 European patients treated, 162 were alive at the end of the follow-up. Sixty-five patients (40% of all survivors) were treated with surgery alone and 64 patients (39%) with surgery combined with chemotherapy. Radiotherapy was delivered to 3% of survivors (five patients). In addition, 28 survivors (17%) exclusively received chemotherapy. Among the 129 patients treated with surgery, 91% had conservative surgery (118 cases). Overall, nine patients died of disease, one from toxicity (6%) and 20 patients (12%) survived with major functional deficits or had mutilating surgery. Overall, conventional conservative strategies before the era of targeted therapy, even in the case of extensive tumours, demonstrate efficacy in IFS, but are associated with acute and some chronic side effects. TRKI have demonstrated very rapid responses in the vast majority of children with IFS with limited acute toxicity. With the current state of our knowledge, both conventional chemotherapy and TRKI should be regarded as options for patients with localised disease at the physician's and parent's discretion. TRKI should be considered in patients with metastatic disease, and before mutilating surgery when conventional chemotherapy fails. Outside a clinical trial, additional data are needed to resolve the lack of consensus about front-line use of conventional chemotherapy versus TRKI in patients with localised disease.
Copyright © 2020 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  Chemotherapy; Conservative surgery; Infantile fibrosarcoma; NTRK inhibitors; Targeted therapy

Mesh:

Substances:

Year:  2020        PMID: 32784118     DOI: 10.1016/j.ejca.2020.06.028

Source DB:  PubMed          Journal:  Eur J Cancer        ISSN: 0959-8049            Impact factor:   9.162


  3 in total

Review 1.  Malignant Superficial Mesenchymal Tumors in Children.

Authors:  Philippe Drabent; Sylvie Fraitag
Journal:  Cancers (Basel)       Date:  2022-04-26       Impact factor: 6.575

Review 2.  Pediatric Non-Rhabdomyosarcoma Soft Tissue Sarcomas: Standard of Care and Treatment Recommendations from the European Paediatric Soft Tissue Sarcoma Study Group (EpSSG).

Authors:  Andrea Ferrari; Bernadette Brennan; Michela Casanova; Nadege Corradini; Pablo Berlanga; Reineke A Schoot; Gema L Ramirez-Villar; Akmal Safwat; Gabriela Guillen Burrieza; Patrizia Dall'Igna; Rita Alaggio; Lisa Lyngsie Hjalgrim; Susanne Andrea Gatz; Daniel Orbach; Max M van Noesel
Journal:  Cancer Manag Res       Date:  2022-09-23       Impact factor: 3.602

3.  Prevalence of NTRK Fusions in Canadian Solid Tumour Cancer Patients.

Authors:  Ronald Carter; Harriet Feilotter; Timothy Feltis; Joshua D Silvertown; Connie Lisle; Laura Semenuk; Colleen Knapp; Jillann Jaynes; Doreen Berg; Nabodita Kaul; Josianne Lachapelle; Leslie Richardson; Marsha Speevak; Haya Sarras; David M Berman
Journal:  Mol Diagn Ther       Date:  2022-10-04       Impact factor: 4.476

  3 in total

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