Sustained Complete Response to Metronomic Chemotherapy in a Child with Refractory Atypical Teratoid Rhabdoid Tumor: A Case Report

被引:9
作者
Berland, Mahe [1 ]
Padovani, Laetitia [2 ]
Rome, Angelique [1 ]
Pech-Gourg, Gregoire [3 ]
Figarella-Branger, Dominique [4 ,5 ]
Andre, Nicolas [1 ,5 ,6 ]
机构
[1] La Timone Hosp, AP HM, Dept Pediat Hematol Oncol, Marseille, France
[2] La Timone Hosp, AP HM, Dept Radiat Oncol & Pediat, Marseille, France
[3] La Timone Hosp, AP HM, Dept Neurosurg, Marseille, France
[4] Aix Marseille Univ, La Timone Hosp, AP HM, Dept Pathol, Marseille, France
[5] Aix Marseille Univ, Ctr Rech Oncol Biol & Oncopharmacol, INSERM, UMR 79 911, Marseille, France
[6] Metron Global Hlth Initiat, Marseille, France
来源
FRONTIERS IN PHARMACOLOGY | 2017年 / 8卷
关键词
pharmaceutical preparations; metronomic chemotherapy; drug repurposing; brain tumor; ATRT; pediatric oncology; CENTRAL-NERVOUS-SYSTEM; CANCER;
D O I
10.3389/fphar.2017.00792
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Atypical teratoid rhabdoid tumor (ATRT) is a rare and highly aggressive embryonal tumor of the central nervous system with a dismal prognosis and no definitive guidelines for treatment, especially at relapse or in case of refractory disease. Metronomic chemotherapy (MC) has emerged as a new treatment option in solid malignancies, with lower toxicity and is frequently combined with drug repositioning. We report a case of ATRT in an 8-year-old boy who progressed during multimodal therapy including surgical resection, chemotherapy and radiotherapy. He was treated with MC involving continuous oral celecoxib with alternating metronomic etoposide and cyclophosphamide, in combination with biweekly bevacizumab and monthly intrathecal liposomal cytarabine. To date, he remains clinically and symptomatically disease-free with a follow-up of 10 months. The treatment was well-tolerated. Metronomics represent a possible alternative regimen for children with recurrent or progressive ATRT.
引用
收藏
页数:4
相关论文
共 15 条
[11]   Metronomic chemotherapy: new rationale for new directions [J].
Pasquier, Eddy ;
Kavallaris, Maria ;
Andre, Nicolas .
NATURE REVIEWS CLINICAL ONCOLOGY, 2010, 7 (08) :455-465
[12]   Antiangiogenic metronomic therapy for children with recurrent embryonal brain tumors [J].
Peyrl, Andreas ;
Chocholous, Monika ;
Kieran, Mark W. ;
Azizi, Amedeo A. ;
Prucker, Christina ;
Czech, Thomas ;
Dieckmann, Karin ;
Schmook, Maria-Theresa ;
Haberler, Christine ;
Leiss, Ulrike ;
Slavc, Irene .
PEDIATRIC BLOOD & CANCER, 2012, 59 (03) :511-517
[13]   Metronomic therapy can increase quality of life during paediatric palliative cancer care, but careful patient selection is essential [J].
Porkholm, Mikaela ;
Toiviainen-Salo, Sanna ;
Seuri, Raija ;
Lonnqvist, Tuula ;
Vepsalainen, Kaisa ;
Saarinen-Pihkala, Ulla M. ;
Pentikainen, Virve ;
Kivivuori, Sanna-Maria .
ACTA PAEDIATRICA, 2016, 105 (08) :946-951
[14]   A Phase II Trial of a Multi-Agent Oral Antiangiogenic (Metronomic) Regimen in Children With Recurrent or Progressive Cancer [J].
Robison, Nathan J. ;
Campigotto, Federico ;
Chi, Susan N. ;
Manley, Peter E. ;
Turner, Christopher D. ;
Zimmerman, Mary Ann ;
Chordas, Christine A. ;
Werger, Annette M. ;
Allen, Jeffrey C. ;
Goldman, Stewart ;
Rubin, Joshua B. ;
Isakoff, Michael S. ;
Pan, Wilbur J. ;
Khatib, Ziad A. ;
Comito, Melanie A. ;
Bendel, Anne E. ;
Pietrantonio, Jay B. ;
Kondrat, Laura ;
Hubbs, Shannon M. ;
Neuberg, Donna S. ;
Kieran, Mark W. .
PEDIATRIC BLOOD & CANCER, 2014, 61 (04) :636-642
[15]   Multimodal therapy in children and adolescents with newly diagnosed atypical teratoid rhabdoid tumor: individual pooled data analysis and review of the literature [J].
Schrey, D. ;
Lechon, F. Carceller ;
Malietzis, G. ;
Moreno, L. ;
Dufour, C. ;
Chi, S. ;
Lafay-Cousin, L. ;
von Hoff, K. ;
Athanasiou, T. ;
Marshall, L. V. ;
Zacharoulis, S. .
JOURNAL OF NEURO-ONCOLOGY, 2016, 126 (01) :81-90