Pediatric Hodgkin lymphoma: Maximizing efficacy and minimizing toxicity

被引:60
作者
Hodgson, David. C.
Hudson, Melissa M.
Constine, Louis S.
机构
[1] Univ Toronto, Dept Radiat Oncol, Toronto, ON M5G 2M9, Canada
[2] Univ Hlth Network, Princess Margaret Hosp, Radiat Med Program, Toronto, ON, Canada
[3] Univ Tennessee, St Jude Childrens Res Hosp, Coll Med, Dept Clin Oncol, Memphis, TN USA
[4] Univ Rochester, Med Ctr, James P Wilmot Canc Ctr, Dept Radiat Oncol, Rochester, NY 14642 USA
[5] Univ Rochester, Med Ctr, James P Wilmot Canc Ctr, Dept Pediat, Rochester, NY 14642 USA
关键词
D O I
10.1016/j.semradonc.2007.02.009
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Historically, both adult and childhood Hodgkin lymphoma (HL) were treated with full-dose (35-45 Gy) extended-field radiation therapy (RT). Although this treatment was the first to produce reliable disease control, the resulting late toxicity led pediatric oncologists to pioneer the use of combined chemotherapy and low-dose (15-25 Gy) involved-field RT for all stages of HL. Currently, standard treatment of childhood HL is risk adapted; those with favorable risk disease typically receive 2 to 4 cycles of multi-agent chemotherapy with low-dose IFRT, whereas those with higher-risk disease receive more intensive chemotherapy before IFRT. This approach produces long-term survival rates >90% while limiting exposure to anthracyclines, alkylators, and radiation to normal tissues. In contrast to adult HL, IFRT remains an important component of the treatment of advanced-stage HL in pediatric patients. Current clinical trials for children with HL aim to further segregate patients into risk strata such that those who are highly curable can receive less toxic therapy, whereas high-risk patients can receive augmented therapy. Response-adapted therapy, in which overall treatment intensity is modified according to the initial response to chemotherapy, is emerging as a potential means of further reducing therapy for some while maintaining high cure rates. The challenge is to refine therapy in a rare disease in which long-time intervals are necessary to observe an adequate number of events (treatment failure or late effects) to answer judicious questions. © 2007 Elsevier Inc. All rights reserved.
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收藏
页码:230 / 242
页数:13
相关论文
共 111 条
[1]   Cardiovascular status in long-term survivors of Hodgkin's disease treated with chest radiotherapy [J].
Adams, MJ ;
Lipsitz, SR ;
Colan, SD ;
Tarbell, NJ ;
Treves, ST ;
Diller, L ;
Greenbaum, N ;
Mauch, P ;
Lipshultz, SE .
JOURNAL OF CLINICAL ONCOLOGY, 2004, 22 (15) :3139-3148
[2]   Involved-field radiotherapy for advanced Hodgkin's lymphoma [J].
Aleman, BMP ;
Raemaekers, JMM ;
Tirelli, U ;
Bortolus, R ;
van't Veer, MB ;
Lybeert, MLM ;
Keuning, JJ ;
Carde, P ;
Girinsky, T ;
van der Maazen, RWM ;
Tomsic, R ;
Vovk, M ;
van Hoof, A ;
Demeestere, G ;
Lugtenburg, PJ ;
Thomas, J ;
Schroyens, W ;
De Boeck, K ;
Baars, JW ;
Kluin-Nelemans, JC ;
Carrie, C ;
Aoudjhane, M ;
Bron, D ;
Eghbali, H ;
Smit, WGJM ;
Meerwaldt, JH ;
Hagenbeek, A ;
Pinna, A ;
Henry-Amar, M .
NEW ENGLAND JOURNAL OF MEDICINE, 2003, 348 (24) :2396-2406
[3]   Long-term cause-specific mortality of patients treated for Hodgkin's disease [J].
Aleman, BMP ;
van den Belt-Dusebout, AW ;
Klokman, WJ ;
van't Veer, MB ;
Bartelink, H ;
van Leeuwen, FE .
JOURNAL OF CLINICAL ONCOLOGY, 2003, 21 (18) :3431-3439
[4]   Risk factors for Hodgkin's disease by Epstein-Barr virus (EBV) status: Prior infection by EBV and other agents [J].
Alexander F.E. ;
Jarrett R.F. ;
Lawrence D. ;
Armstrong A.A. ;
Freeland J. ;
Gokhale D.A. ;
Kane E. ;
Taylor G.M. ;
Wright D.H. ;
Cartwright R.A. .
British Journal of Cancer, 2000, 82 (5) :1117-1121
[5]   An epidemiologic study of index and family infectious mononucleosis and adult Hodgkin's disease (HD):: Evidence for a specific association with EBV+ve HD in young adults [J].
Alexander, FE ;
Lawrence, DJ ;
Freeland, J ;
Krajewski, AS ;
Angus, B ;
Taylor, GM ;
Jarrett, RF .
INTERNATIONAL JOURNAL OF CANCER, 2003, 107 (02) :298-302
[6]  
Andersson Jan, 2006, Herpes, V13, P12
[7]   Epstein-Barr virus and Hodgkin's disease: Further evidence for the three disease hypothesis [J].
Armstrong, AA ;
Alexander, FE ;
Cartwright, R ;
Angus, B ;
Krajewski, AS ;
Wright, DH ;
Lee, F ;
Kane, E ;
Jarrett, RF .
LEUKEMIA, 1998, 12 (08) :1272-1276
[8]  
BADER SB, 1993, CANCER-AM CANCER SOC, V72, P249, DOI 10.1002/1097-0142(19930701)72:1<249::AID-CNCR2820720144>3.0.CO
[9]  
2-8
[10]  
BAYLEWEISGERBER C, 1984, CANCER, V54, P215, DOI 10.1002/1097-0142(19840715)54:2<215::AID-CNCR2820540207>3.0.CO