High-Dose Chemotherapy Followed by Autologous Stem Cell Transplantation for Metastatic Rhabdomyosarcoma-A Systematic Review

被引:14
|
作者
Peinemann, Frank [1 ]
Kroeger, Nicolaus [2 ]
Bartel, Carmen [1 ]
Grouven, Ulrich [1 ,3 ]
Pittler, Max [4 ]
Erttmann, Rudolf [5 ]
Kulig, Michael [1 ,6 ]
机构
[1] Inst Qual & Efficiency Hlth Care IQWiG, Cologne, Germany
[2] Univ Hosp Hamburg Eppendorf, Interdisciplinary Clin Stem Cell Transplantat, Hamburg, Germany
[3] Hannover Med Sch, D-3000 Hannover, Germany
[4] Univ Freiburg, German Cochrane Ctr, Freiburg, Germany
[5] Univ Hosp Hamburg Eppendorf, Dept Pediat Hematol & Oncol, Hamburg, Germany
[6] German Hlth Care Syst G BA, Fed Joint Comm, Berlin, Germany
来源
PLOS ONE | 2011年 / 6卷 / 02期
关键词
BONE-MARROW-TRANSPLANTATION; SOFT-TISSUE SARCOMA; RISK SOLID TUMORS; SMALL ROUND-CELL; INTENSIVE CHEMOTHERAPY; ALVEOLAR RHABDOMYOSARCOMA; MULTIAGENT CHEMOTHERAPY; COMPLETE REMISSION; PEDIATRIC BONE; EWINGS-SARCOMA;
D O I
10.1371/journal.pone.0017127
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Introduction: Patients with metastatic rhabdomyosarcoma (RMS) have a poor prognosis. The aim of this systematic review is to investigate whether high-dose chemotherapy (HDCT) followed by autologous hematopoietic stem cell transplantation (HSCT) in patients with metastatic RMS has additional benefit or harm compared to standard chemotherapy. Methods: Systematic literature searches were performed in MEDLINE, EMBASE, and The Cochrane Library. All databases were searched from inception to February 2010. PubMed was searched in June 2010 for a last update. In addition to randomized and non-randomized controlled trials, case series and case reports were included to complement results from scant data. The primary outcome was overall survival. A meta-analysis was performed using the hazard ratio as primary effect measure, which was estimated from Cox proportional hazard models or from summary statistics of Kaplan Meier product-limit estimations. Results: A total of 40 studies with 287 transplant patients with metastatic RMS (age range 0 to 32 years) were included in the assessment. We identified 3 non-randomized controlled trials. The 3-year overall survival ranged from 22% to 53% in the transplant groups vs. 18% to 55% in the control groups. Meta-analysis on overall survival in controlled trials showed no difference between treatments. Result of meta-analysis of pooled individual survival data of case series and case reports, and results from uncontrolled studies with aggregate data were in the range of those from controlled data. The risk of bias was high in all studies due to methodological flaws. Conclusions: HDCT followed by autologous HSCT in patients with RMS remains an experimental treatment. At present, it does not appear justifiable to use this treatment except in appropriately designed controlled trials.
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页数:11
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