The concept of the GPOH-HD 2003 therapy study for pediatric Hodgkin's disease:: Evolution in the tradition of the DALJGPOH studies

被引:50
作者
Körholz, D
Claviez, A
Hasenclever, D
Kluge, R
Hirsch, W
Kamprad, F
Dörffel, W
Wickmann, L
Papsdorf, K
Dieckmann, K
Kahn, T
Mauz-Körholz, C
Dannenberg, C
Pötter, R
Brosteanu, O
Schellong, G
Sabri, O
机构
[1] Univ Leipzig, Med Ctr, Clin & Policlin Children & Adolescents, Div Pediat Hematol & Oncol, D-04317 Leipzig, Germany
[2] Univ Leipzig, Med Ctr, Dept Radiol, D-04317 Leipzig, Germany
[3] Univ Leipzig, Med Ctr, Dept Nucl Med, D-04317 Leipzig, Germany
[4] Univ Leipzig, Med Ctr, Dept Radiotherapy, D-04317 Leipzig, Germany
[5] Univ Leipzig, Inst Biomath & Epidemiol, D-04317 Leipzig, Germany
[6] Univ Leipzig, Ctr Coordinat Clin Studies, D-04317 Leipzig, Germany
[7] Vienna Gen Hosp, Dept Radiotherapy, Vienna, Austria
[8] HELIOS Klinikum Berlin Buch, Dept Pediat, Berlin, Germany
[9] Univ Kiel, Dept Pediat, D-24098 Kiel, Germany
[10] Univ Munster, Med Ctr, Dept Pediat, D-4400 Munster, Germany
来源
KLINISCHE PADIATRIE | 2004年 / 216卷 / 03期
关键词
Hodgkin's disease; children; GPOH; FDG-PET radiotherapy; dacarbazine;
D O I
10.1055/s-2004-822627
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Today it is possible to cure more than 90% of children and adolescents with Hodgkin's disease with a combination of radiotherapy and chemotherapy. Since the DAL-HD 82 study, the main scientific focus has been on avoiding late effects such as the OPSI syndrome, late complications involving the heart, lungs, thyroid and/or gonads particularly sterility in men and premature onset of menopause in women, and the prevention of secondary malignancies. The GPOH-HD 2003 study will introduce FDG-PET to the initial diagnostic program and the assessment of response to therapy in order to evaluate further possibilities for reducing therapy. In this context, the central review of all clinical and radiological findings, systematically done since the DAL-HD 90 study, will be increasingly relevant in maintaining standardised stage classification and therapy group assignment which was established by the preceding studies. Continuing in the direction of the earlier studies, the indications for radiotherapy will be restricted even further. In the early stages (treatment group I) patients with CR or a negative FDG-PET at the end of chemotherapy will receive no radiotherapy in order to reduce the risk of a secondary malignancy. In a randomized comparison, procarbazine will be replaced by dacarbazine in the COPP cycles to determine whether sterility in men and premature onset of menopause in women can be avoided by elimination of procarbazine while retaining the same clinical efficacy. Finally, relapse therapy is to be tailored according to the time of relapse, the initial therapy group, and the patient's response to the relapse therapy with more patients receiving autologous transplantation in order to further improve the results of relapse treatment.
引用
收藏
页码:150 / 156
页数:7
相关论文
共 46 条
[1]   Autologous hematopoietic stem-cell transplantation for relapsed or refractory Hodgkin's disease in children and adolescents [J].
Baker, KS ;
Gordon, BG ;
Gross, TG ;
Abromowitch, MA ;
Lyden, ER ;
Lynch, JC ;
Vose, JM ;
Armitage, JO ;
Coccia, PF ;
Bierman, PJ .
JOURNAL OF CLINICAL ONCOLOGY, 1999, 17 (03) :825-831
[2]   Positron emission tomography with [18F]2-fluoro-D-2-deoxyglucose (FDG-PET) predicts relapse of malignant lymphoma after high-dose therapy with stem cell transplantation [J].
Becherer, A ;
Mitterbauer, M ;
Jaeger, U ;
Kalhs, P ;
Greinix, HT ;
Karanikas, G ;
Pötzi, C ;
Raderer, M ;
Dudczak, R ;
Kletter, K .
LEUKEMIA, 2002, 16 (02) :260-267
[3]   High risk of subsequent neoplasms continues with extended follow-up of childhood Hodgkin's disease: Report from the late effects study group [J].
Bhatia, S ;
Yasui, Y ;
Robison, LL ;
Birch, JM ;
Bogue, MK ;
Diller, L ;
DeLaat, C ;
Fossati-Bellani, F ;
Morgan, E ;
Oberlin, O ;
Reaman, G ;
Ruymann, FB ;
Tersak, J ;
Meadows, AT .
JOURNAL OF CLINICAL ONCOLOGY, 2003, 21 (23) :4386-4394
[4]   Breast cancer and other second neoplasms after childhood Hodgkin's disease [J].
Bhatia, S ;
Robison, LL ;
Oberlin, O ;
Greenberg, M ;
Bunin, G ;
FossatiBellani, F ;
Meadows, AT .
NEW ENGLAND JOURNAL OF MEDICINE, 1996, 334 (12) :745-751
[5]  
BRAMSWIG JH, 1990, CANCER-AM CANCER SOC, V65, P1298, DOI 10.1002/1097-0142(19900315)65:6<1298::AID-CNCR2820650607>3.0.CO
[6]  
2-W
[7]  
Buchmann I, 2001, CANCER, V91, P889
[8]   EARLY MENOPAUSE IN LONG-TERM SURVIVORS OF CANCER DURING ADOLESCENCE [J].
BYRNE, J ;
FEARS, TR ;
GAIL, MH ;
PEE, D ;
CONNELLY, RR ;
AUSTIN, DF ;
HOLMES, GF ;
HOLMES, FF ;
LATOURETTE, HB ;
MEIGS, JW ;
STRONG, LC ;
MYERS, MH ;
MULVIHILL, JJ .
AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY, 1992, 166 (03) :788-793
[9]  
Cremerius U, 2001, NUKLEARMED-NUCL MED, V40, P23
[10]   18FDG-PET following treatment as valid predictor for disease-free survival in Hodgkin's lymphoma [J].
de Wit, M ;
Bohuslavizki, KH ;
Buchert, R ;
Bumann, D ;
Clausen, M ;
Hossfeld, DK .
ANNALS OF ONCOLOGY, 2001, 12 (01) :29-37