Conservative strategy in infantile fibrosarcoma is possible: The European paediatric Soft tissue sarcoma Study Group experience

被引:72
作者
Orbach, Daniel [1 ]
Brennan, Bernadette [2 ]
De Paoli, Angela [3 ]
Gallego, Soledad [4 ]
Mudry, Peter [5 ]
Francotte, Nadine [6 ]
van Noesel, Max [7 ]
Kelsey, Anna [8 ]
Alaggio, Rita [9 ]
Ranchere, Dominique [10 ]
De Salvo, Gian Luca [3 ]
Casanova, Michela [11 ]
Bergeron, Christophe [12 ]
Merks, Johannes H. M. [13 ]
Jenney, Meriel [14 ]
Stevens, Michael C. G. [15 ]
Bisogno, Gianni [16 ]
Ferrari, Andrea [11 ]
机构
[1] Inst Curie, Dept Pediat Adolescent & Young Adult Oncol, Paris, France
[2] Royal Manchester Childrens Hosp, Dept Pediat Oncol, Manchester M27 1HA, Lancs, England
[3] IRCCS Ist Oncol Veneto, Clin Trials & Biostat Unit, Padua, Italy
[4] Hosp Univ Vall dHebron, Paediat Oncol, Barcelona, Spain
[5] Univ Childrens Hosp, Dept Pediat Oncol, Brno, Czech Republic
[6] CHC Clin Esperance, Dept Pediat, Montegnee, Belgium
[7] Princess Maxima Ctr Pediat Oncol, Utrecht, Netherlands
[8] Royal Manchester Childrens Hosp, Dept Diagnost Paediat Histopathol, Manchester M27 1HA, Lancs, England
[9] Univ Padua, Dept Pathol, I-35100 Padua, Italy
[10] Ctr Leon Berard, Inst Hematol & Oncol Pediat, Dept Pathol, F-69373 Lyon, France
[11] Fdn IRCCS Ist Nazl Tumori, Pediat Oncol Unit, Milan, Italy
[12] Ctr Leon Berard, Inst Hematol & Oncol Pediat, Dept Pediat Oncol, F-69373 Lyon, France
[13] Univ Amsterdam, Acad Med Ctr, Emma Childrens Hosp, Dept Pediat Oncol, Meibergdreef 9, NL-1105 AZ Amsterdam, Netherlands
[14] Childrens Hosp Wales, Dept Pediat Oncol, Heath Pk, Cardiff, S Glam, Wales
[15] Univ Bristol, Royal Hosp Children, Dept Pediat Oncol, Bristol BS8 1TH, Avon, England
[16] Univ Padua, Pediat Hematol & Oncol Div, Padua, Italy
关键词
Infantile fibrosarcoma; Newborn; Infant; Cancer; Chemotherapy; ETV6-NTRK3; transcript; INTERGROUP RHABDOMYOSARCOMA; CONGENITAL FIBROSARCOMA; INTERNATIONAL-SOCIETY; CHILDHOOD-CANCER; ONCOLOGY SIOP; 1ST YEAR; TUMORS; LIFE;
D O I
10.1016/j.ejca.2015.12.028
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Infantile fibrosarcoma (IFS) is a very rare disease occurring in young infants characterised by a high local aggressiveness but overall with a favourable survival. To try to reduce the total burden of therapy, the European pediatric Soft tissue sarcoma Study Group has developed conservative therapeutic recommendations according to initial resectability. Material and methods: Between 2005 and 2012, children with localised IFS were prospectively registered. Initial surgery was suggested only if possible without mutilation. Patients with initial complete (IRS-group I/R0) or microscopic incomplete (group II/R1) resection had no further therapy. Patients with initial inoperable tumour (group III/R2) received first-line vincristine-actinomycin-D chemotherapy (VA). Delayed conservative surgery was planned after tumour reduction. Aggressive local therapy (mutilating surgery or external radiotherapy) was discouraged. Results: A total of 50 infants (median age 1.4 months), were included in the study. ETV6-NTRK3 transcript was present in 87.2% of patients where investigation was performed. According to initial surgery, 11 patients were classified as group I, 8 as group II and 31 as group III. VA chemotherapy was first delivered to 25 children with IRS-III/R2 and one with IRS-II/R1 disease. Response rate to VA was 68.0%. Mutilating surgery was only performed in three cases. After a median follow-up of 4.7 years (range 1.9-9.0), 3-year event-free survival and overall survival were respectively 84.0% (95% confidence interval [CI] 70.5-91.7) and 94.0% (95% CI 82.5-98.0). Conclusions: Conservative therapy is possible in IFS as only three children required mutilating surgery, and alkylating or anthracycline based chemotherapy was avoided in 71.0% of patients needing chemotherapy. VA regimen should be first line therapy in order to reduce long term effects. (C) 2016 Elsevier Ltd. All rights reserved.
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页码:1 / 9
页数:9
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