TY - JOUR
T1 - Spotlight on the treatment of infantile fibrosarcoma in the era of neurotrophic tropomyosin receptor kinase inhibitors
T2 - International consensus and remaining controversies
AU - Orbach, Daniel
AU - Sparber-Sauer, Monika
AU - Laetsch, Theodore W.
AU - Minard-Colin, Veronique
AU - Bielack, Stefan S.
AU - Casanova, Michela
AU - Corradini, Nadege
AU - Koscielniak, Ewa
AU - Scheer, Monika
AU - Hettmer, Simone
AU - Bisogno, Gianni
AU - Hawkins, Douglas S.
AU - Ferrari, Andrea
N1 - Funding Information:
D.O. reports doing consultant work for the French Larotrectinib transparency committee (consultancy agreement signed with the institution). An independent translational research project conducted by him is partially supported by Bayer (Investigation Supported research). He also reports consulting for Roche (consultancy agreement signed with the institution). M.S.S. reports consulting for Roche (hemophilia, emicizumab) and Sobi (hemophilia).D.S.H. reports receiving reimbursement for travel and accommodations to attend medical advisory boards for Bayer, Celgene, LOXO Oncology, and AstraZeneca. His institution has received funding to support clinical trial research for which he was the institutional principal investigator from Amgen, Seattle Genetics, Eisai, Merck Sharp & Dohme, Incyte, Jazz Pharmaceuticals, Eli Lilly, and E R Squibb & Sons. T.W.L. reports consulting for Bayer, Loxo Oncology, Novartis, and Eli Lilly, and receivingresearch funding from Bayer, Novartis, and Pfizer. S.S.B. reports advisory board/consultancy positions for Bayer, Boehringer Ingelheim, Clinigen, Ipsen, Isofol, Lilly, Pfizer, Novartis, Roche, and Sensorion. V.M.C. reports receiving reimbursement for travel and accommodations to attend medical advisory boards for Roche, BMS, Celgene, and Novartis. Her institution has received funding to support clinical trial research for which he was the institutional principal investigator from Roche and BMS. G.B. reports receiving reimbursement for travel and accommodations to attend medical advisory boards for Bayer and Loxo. M.S. has consulted for Bayer, and Eli Lilly.N.C. has consulted for Roche and BMS, and received reimbursement for travel and accommodations to attend medical congress and advisory boards. E.K./A.F./S.H have no conflicts of interests. M.C. reports advisory board/consultancy position for Bayer, Roche, EISA, Lilly, Merck, Tesaro, Halozyme.The ExPO-r-Net project was cofounded and financed by the European Union's health program within ERN PaedCan network. The CWS-81 trial was supported by the Federal Ministry of Research and Technology no. 01ZP0831, the CWS-86, -91, -96, and -2002P trials were supported by grants from the German Cancer Aid Foundation, Bonn, Germany (CWS-86: no. M34/87/Tr1, CWS-91: no. M76/91/Tr2, CWS-96: T9/96/TrI, CWS-2002P: 50-2721-Tr2), SoTiSaR with grant no. A2007/13DKS2009.08 from the Deutsche Kinderkrebsstiftung, Bonn, Germany, and the Foerderkreis krebskranke Kinder Stuttgart, Germany. T.W.L. is supported by the Norma and Jim Smith Professorship of Clinical Excellence and Eugene P. Frenkel, M.D. Scholarship in Clinical Medicine.
Funding Information:
D.O. reports doing consultant work for the French Larotrectinib transparency committee (consultancy agreement signed with the institution). An independent translational research project conducted by him is partially supported by Bayer (Investigation Supported research). He also reports consulting for Roche (consultancy agreement signed with the institution). M.S.S. reports consulting for Roche (hemophilia, emicizumab) and Sobi (hemophilia).D.S.H. reports receiving reimbursement for travel and accommodations to attend medical advisory boards for Bayer, Celgene, LOXO Oncology, and AstraZeneca. His institution has received funding to support clinical trial research for which he was the institutional principal investigator from Amgen , Seattle Genetics , Eisai , Merck Sharp & Dohme , Incyte, Jazz Pharmaceuticals , Eli Lilly , and E R Squibb & Sons. T.W.L. reports consulting for Bayer , Loxo Oncology, Novartis , and Eli Lilly , and receivingresearch funding from Bayer , Novartis , and Pfizer . S.S.B. reports advisory board/consultancy positions for Bayer, Boehringer Ingelheim, Clinigen, Ipsen, Isofol, Lilly, Pfizer, Novartis, Roche, and Sensorion. V.M.C. reports receiving reimbursement for travel and accommodations to attend medical advisory boards for Roche, BMS, Celgene, and Novartis. Her institution has received funding to support clinical trial research for which he was the institutional principal investigator from Roche and BMS. G.B. reports receiving reimbursement for travel and accommodations to attend medical advisory boards for Bayer and Loxo. M.S. has consulted for Bayer, and Eli Lilly.N.C. has consulted for Roche and BMS, and received reimbursement for travel and accommodations to attend medical congress and advisory boards. E.K./A.F./S.H have no conflicts of interests. M.C. reports advisory board/consultancy position for Bayer, Roche, EISA, Lilly, Merck, Tesaro, Halozyme.
Funding Information:
The ExPO-r-Net project was cofounded and financed by the European Union's health program within ERN PaedCan network. The CWS-81 trial was supported by the Federal Ministry of Research and Technology no. 01ZP0831, the CWS-86, -91, -96, and -2002P trials were supported by grants from the German Cancer Aid Foundation , Bonn, Germany (CWS-86: no. M34/87/Tr1, CWS-91: no. M76/91/Tr2, CWS-96: T9/96/TrI, CWS-2002P: 50-2721-Tr2), SoTiSaR with grant no. A2007/13DKS2009.08 from the Deutsche Kinderkrebsstiftung , Bonn, Germany, and the Foerderkreis krebskranke Kinder Stuttgart , Germany. T.W.L. is supported by the Norma and Jim Smith Professorship of Clinical Excellence and Eugene P. Frenkel, M.D. Scholarship in Clinical Medicine.
Publisher Copyright:
© 2020 Elsevier Ltd
PY - 2020/9
Y1 - 2020/9
N2 - 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.
AB - 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.
KW - Chemotherapy
KW - Conservative surgery
KW - Infantile fibrosarcoma
KW - NTRK inhibitors
KW - Targeted therapy
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UR - http://www.scopus.com/inward/citedby.url?scp=85089198330&partnerID=8YFLogxK
U2 - 10.1016/j.ejca.2020.06.028
DO - 10.1016/j.ejca.2020.06.028
M3 - Article
C2 - 32784118
AN - SCOPUS:85089198330
SN - 0959-8049
VL - 137
SP - 183
EP - 192
JO - European Journal of Cancer
JF - European Journal of Cancer
ER -