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

被引:38
作者
Orbach, Daniel [1 ]
Sparber-Sauer, Monika [2 ]
Laetsch, Theodore W. [3 ,4 ]
Minard-Colin, Veronique [5 ]
Bielack, Stefan S. [2 ,6 ]
Casanova, Michela [7 ]
Corradini, Nadege [8 ]
Koscielniak, Ewa [2 ,9 ]
Scheer, Monika [2 ]
Hettmer, Simone [10 ]
Bisogno, Gianni [11 ]
Hawkins, Douglas S. [12 ]
Ferrari, Andrea [7 ]
机构
[1] PSL Res Univ, Inst Curie, SIREDO Oncol Ctr, Care Innovat & Res Children & AYA Canc, Paris, France
[2] Olga Hosp, Zentrum Kinder Jugend & Frauenmed, Stuttgart Canc Ctr, Klinikum Stuttgart,Padiatrie Onkol Hamatol Immuno, Stuttgart, Germany
[3] Univ Texas Southwestern Med Ctr Dallas, Dept Pediat, Childrens Hlth, Dallas, TX USA
[4] Univ Texas Southwestern Med Ctr Dallas, Childrens Hlth, Harold C Simmons Comprehens Canc Ctr, Dallas, TX 75390 USA
[5] Univ Paris Saclay, Gustave Roussy, Dept Pediat & Adolescent Oncol, Villejuif, France
[6] Univ Munster, Dept Pediat Hematol & Oncol, Munster, Germany
[7] Fdn IRCCS Ist Nazl Tumori Milano, Pediat Oncol Unit, Milan, Italy
[8] Ctr Leon Berard, Dept Paediat Haematol & Oncol, Lyon, France
[9] Univ Tubingen, Dept Pediat Oncol, Tubingen, Germany
[10] Univ Freiburg, Fac Med, Div Pediat Hematol & Oncol, Dept Pediat & Adolescent Med, Freiburg, Germany
[11] Univ Padua, Dept Womens & Childrens Hlth, Hematol & Oncol Div, Padua, Italy
[12] Univ Washington, Fred Hutchinson Canc Res Ctr, Seattle Childrens Hosp, Div Hematol Oncol, Seattle, WA 98195 USA
关键词
Infantile fibrosarcoma; Chemotherapy; Conservative surgery; NTRK inhibitors; Targeted therapy; POSITIVE SOLID TUMORS; SOFT-TISSUE SARCOMAS; PREOPERATIVE CHEMOTHERAPY; CONGENITAL FIBROSARCOMA; NTRK FUSION; LAROTRECTINIB; TRK; ENTRECTINIB; MANAGEMENT; ROS1;
D O I
10.1016/j.ejca.2020.06.028
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
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. (c) 2020 Elsevier Ltd. All rights reserved.
引用
收藏
页码:183 / 192
页数:10
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