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Children's Oncology Group's 2013 blueprint for research: Bone tumors
被引:152
|作者:
Gorlick, Richard
[1
,2
]
Janeway, Katherine
[3
]
Lessnick, Stephen
[4
]
Randall, R. Lor
[5
,6
]
Marina, Neyssa
[7
,8
]
机构:
[1] Yeshiva Univ, Albert Einstein Coll Med, Dept Pediat & Mol Pharmacol, Bronx, NY 10467 USA
[2] Childrens Hosp Montefiore, Div Pediat Hematol Oncol, Bronx, NY 10467 USA
[3] Dana Farber Childrens Hosp Canc Ctr, Dept Pediat Hematol Oncol, Boston, MA USA
[4] Univ Utah, Sch Med, Dept Oncol Sci,Div Pediat Hematol Oncol, Ctr Childrens Canc Res,Huntsman Canc Inst, Salt Lake City, UT USA
[5] Univ Utah, Orthopaed Huntsman Canc Inst, Salt Lake City, UT USA
[6] Univ Utah, Primary Childrens Med Ctr, Salt Lake City, UT USA
[7] Lucile Packard Childrens Hosp, Palo Alto, CA USA
[8] Stanford Univ, Palo Alto, CA 94304 USA
关键词:
blueprint;
bone sarcoma;
Ewing sarcoma;
osteosarcoma;
FACTOR-I-RECEPTOR;
EWING SARCOMA FAMILY;
PRIMITIVE NEUROECTODERMAL TUMOR;
ONCOGENIC TRANSCRIPTION FACTOR;
MONOCLONAL-ANTIBODY;
GENE-EXPRESSION;
MURAMYL TRIPEPTIDE;
PROGNOSTIC-FACTORS;
PHASE-II;
METASTATIC OSTEOSARCOMA;
D O I:
10.1002/pbc.24429
中图分类号:
R73 [肿瘤学];
学科分类号:
100214 ;
摘要:
In the US, approximately 650 children are diagnosed with osteosarcoma and Ewing sarcoma (ES) each year. Five-year survival ranges from 65% to 75% for localized disease and <30% for patients with metastases. Recent findings include interval-compressed five drug chemotherapy improves survival with localized ES. In osteosarcoma a large international trial investigating the addition of ifosfamide/etoposide or interferon to standard therapy has completed accrual. For ES an ongoing trial explores the addition of cyclophosphamide/topotecan to interval-compressed chemotherapy. Trials planned by the Children's Oncology Group will investigate new target(s) including IGF-1R and mTOR in ES, and RANKL and GD2 in osteosarcoma. Pediatr Blood Cancer 2013; 60: 10091015. (c) 2012 Wiley Periodicals, Inc.
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页码:1009 / 1015
页数:7
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