Brain metastases during follow-up of children and adolescents with extracranial malignant germ cell tumors: Risk adapted management decision tree analysis based on data of the MAHO/MAKEI-registry

被引:3
作者
Goebel, Ulrich [2 ]
von Kries, Ruediger [1 ,2 ]
Teske, Carmen [3 ]
Schneider, Dominik T. [4 ]
Beyerlein, Andreas [1 ]
Bernbeck, Benedikt [4 ]
Calaminus, Gabriele [3 ]
机构
[1] Univ Munich, Inst Social Paediat & Adolescent Med, D-81377 Munich, Germany
[2] Univ Dusseldorf, ESPED Surveillance Unit Rare Pediat Dis Germany, Coordinat Ctr Clin Studies, D-40225 Dusseldorf, Germany
[3] Univ Munster, Clin Pediat Hematol & Oncol, Munster, Germany
[4] Klinikum Dortmund, Pediat Clin, Dortmund, Germany
关键词
adolescents; children; decision tree analysis; high-risk group; malignant germ cell tumor; secondary brain metastases; surveillance strategy; HIGH-DOSE CHEMOTHERAPY; TESTICULAR CANCER; CHILDHOOD; CISPLATIN; ETOPOSIDE; THERAPY; TESTIS; GPO;
D O I
10.1002/pbc.24229
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background The overall risk for brain metastases among children and adolescents with extracranial malignant germ cell tumors (mGCT) is low but may vary between subgroups. Early identification of subgroups with an increased risk for brain metastasis is therefore important. Procedure We analyzed 900/2,160 patients from the German MAHO/MAKEI registry on children and adolescents with malignant extracranial GCT (pure teratomas (grade 03) were not included). For follow-up evaluation, patients with brain metastases at diagnosis and those with a follow-up shorter than 32 months after diagnosis (longest interval to brain metastases in our cohort) were excluded. Patients were censored at detection of brain metastases or death due to other causes. A decision tree analysis considering age, gender, site of primary tumor, and presence of other metastases at diagnosis as risk factors for brain metastases was performed. Results Among 838 eligible patients, 9 acquired brain metastases during follow-up, accounting for death in 5. There were no brain metastases in absence of extracranial metastases at diagnosis. If extracranial metastases were detected in absence of mediastinal mGCT the risk for brain metastases was 1.2% (95% CI: 0.23.5.%). In contrast, risk was increased to 37.5 (95% CI 15.264.6%) in patients with mediastinal GCTs and extracranial metastases. Conclusion A high-risk subgroup is detected with a decision tree analysis approach. These patients may benefit from an intensified chemotherapy. Close surveillance for CNS-metastases is warranted in this high-risk group while less close monitoring in low-risk patients is justified. Pediatr Blood Cancer 2013;60:217223. (c) 2012 Wiley Periodicals, Inc.
引用
收藏
页码:217 / 223
页数:7
相关论文
共 27 条
[1]  
Atkinson E, 1997, TECHNICAL REPORT, P61
[2]  
Bussey KJ, 1999, GENE CHROMOSOME CANC, V25, P134, DOI 10.1002/(SICI)1098-2264(199906)25:2<134::AID-GCC9>3.3.CO
[3]  
2-P
[4]   Prognostic value of tumor size, metastases, extension into bone, and increased tumor marker in children with malignant sacrococcygeal germ cell tumors:: A prospective evaluation of 71 patients treated in the German cooperative protocols maligne Keimzelltumoren (MAKEI) 83/86 and MAKEI 89 [J].
Calaminus, G ;
Schneider, DT ;
Bökkerink, JPM ;
Gadner, H ;
Harms, D ;
Willers, R ;
Göbel, U .
JOURNAL OF CLINICAL ONCOLOGY, 2003, 21 (05) :781-786
[5]   Randomized comparison of combination chemotherapy with etoposide, bleomycin, and either high-dose or standard-dose cisplatin in children and adolescents with high-risk malignant germ cell tumors: A pediatric intergroup study - Pediatric Oncology Group 9049 and Children's Cancer Group 8882 [J].
Cushing, B ;
Giller, R ;
Cullen, JW ;
Marina, NM ;
Lauer, SJ ;
Olson, TA ;
Rogers, PC ;
Colombani, P ;
Rescorla, F ;
Billmire, DF ;
Vinocur, CD ;
Hawkins, EP ;
Davis, MM ;
Perlman, EJ ;
Castleberry, RP .
JOURNAL OF CLINICAL ONCOLOGY, 2004, 22 (13) :2691-2700
[6]   The Cohort of Long-term Survivors at the German Childhood Cancer Registry [J].
Debling, D. ;
Spix, C. ;
Blettner, M. ;
Michaelis, J. ;
Kaatsch, P. .
KLINISCHE PADIATRIE, 2008, 220 (06) :371-377
[7]   High-dose chemotherapy and stem-cell rescue for metastatic germ-cell tumors [J].
Einhorn, Lawrence H. ;
Williams, Stephen D. ;
Chamness, Amy ;
Brames, Mary J. ;
Perkins, Susan M. ;
Abonour, Rafat .
NEW ENGLAND JOURNAL OF MEDICINE, 2007, 357 (04) :340-348
[8]   IMPROVED CHEMOTHERAPY IN DISSEMINATED TESTICULAR CANCER [J].
EINHORN, LH ;
DONOHUE, JP .
JOURNAL OF UROLOGY, 1977, 117 (01) :65-69
[9]   TREATMENT STRATEGY IN NON-TESTICULAR MALIGNANT GERM-CELL TUMORS IN CHILDREN AND ADOLESCENTS - CONCEPT OF THE COOPERATIVE THERAPY STUDY MAKEI-83 OF THE GPO [J].
GOBEL, U ;
HAAS, RJ ;
HARMS, D ;
JANKA, G ;
BRAMSWIG, J ;
JURGENS, H ;
WEISSBACH, L ;
FABER, P ;
MULLER, E .
KLINISCHE PADIATRIE, 1983, 195 (03) :201-206
[10]   Germ-cell tumors in childhood and adolescence [J].
Göbel, U ;
Schneider, DT ;
Calaminus, G ;
Haas, RJ ;
Schmidt, P ;
Harms, D .
ANNALS OF ONCOLOGY, 2000, 11 (03) :263-271