High-dose chemotherapy followed by autologous haematopoietic cell transplantation for children, adolescents, and young adults with first recurrence of Ewing sarcoma

被引:6
作者
Haveman, Lianne M. [1 ]
van Ewijk, Roelof [1 ]
van Dalen, Elvira C. [1 ]
Breunis, Willemijn B. [2 ,3 ,4 ]
Kremer, Leontien C. M. [1 ,2 ]
van den Berg, Henk [2 ]
Dirksen, Uta [5 ]
Merks, Johannes H. M. [1 ,2 ]
机构
[1] Princess Maxima Ctr Pediat Oncol, Utrecht, Netherlands
[2] Univ Amsterdam, Emma Childrens Hosp, Dept Paediat Oncol, Amsterdam UMC, Amsterdam, Netherlands
[3] Univ Childrens Hosp Zurich, Dept Oncol, Zurich, Switzerland
[4] Univ Childrens Hosp Zurich, Childrens Res Ctr, Zurich, Switzerland
[5] Univ Hosp Essen, Sarcoma Ctr, Pediat 3, West German Canc Ctr, Essen, Germany
来源
COCHRANE DATABASE OF SYSTEMATIC REVIEWS | 2021年 / 09期
关键词
PROGNOSTIC-FACTORS; BONE-MARROW; RISK; FAMILY; TUMORS; RESCUE; EXPERIENCE; SURVIVAL; THERAPY; RELAPSE;
D O I
10.1002/14651858.CD011406.pub2
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background Ewing sarcoma is a solid tumour, which is the second most common primary bone malignancy in children, oGen occurring in the long bones and pelvis. An incidence rate of 4.5 per million a year is reported, with a peak incidence of 11 per million at the age of 12 years. Despite more intensive chemotherapy, 30% to 40% of young people with Ewing sarcoma will have recurrence of the disease. Less than 30% of young people with a recurrence of Ewing sarcoma are alive at 24 months, and less than 10% are alive at 48 months. High-dose chemotherapy (HDC), followed by autologous haematopoietic cell transplantation (AHCT), is used in a variety of paediatric groups with diverse solid tumours. The hypothesis is that HDC regimens may overcome resistance to standard polychemotherapy, and this way may eradicate minimal residual disease, leading to improved survival aGer a first recurrence of disease. Objectives To assess the eKicacy of HDC with AHCT versus conventional chemotherapy in improving event-free survival, overall survival, qualityadjusted survival, and progression-free survival in children, adolescents, and young adults with first recurrence of Ewing sarcoma, and to determine the toxicity of the treatment. Search methods We searched CENTRAL, MEDLINE, Embase, conference proceedings from the SIOP, ASPHO, CTOS, ASBMT, EBMT, and EMSOS, and two trial registries in January 2020. We also searched reference lists of relevant articles and review articles. Selection criteria We planned to include randomised controlled trials (RCTs) or (historical) controlled clinical trials (CCTs) comparing the eKectiveness of HDC plus AHCT with conventional chemotherapy for children, adolescents, and young adults (up to 30 years old at the date of diagnostic biopsy) with a first recurrence of Ewing sarcoma. Data collection and analysis We used standard methodological procedures expected by Cochrane. Main results We did not identify any eligible studies. Authors' conclusions Since we did not identify any eligible studies, we are unable to draw any conclusions about the eKicacy and toxicity of HDC with AHCT versus conventional chemotherapy in children, adolescents, and young adults with a first recurrence of Ewing sarcoma. Further highquality research is urgently needed.
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页数:20
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