Improving survival in recurrent medulloblastoma:: earlier detection, better treatment or still an impasse?

被引:60
作者
Bouffet, E
Doz, F
Demaille, MC
Tron, P
Roche, H
Plantaz, D
Thyss, A
Stephan, JL
Lejars, O
Sariban, E
Buclon, M
Zücker, JM
Brunat-Mentigny, M
Bernard, JL
Gentet, JC
机构
[1] Ctr Leon Berard, Dept Paediat Oncol, F-69373 Lyon 08, France
[2] Ctr Leon Berard, Unite Biostat & Evaluat Therapeut, F-69373 Lyon 08, France
[3] Inst Curie, Dept Paediat Oncol, Paris, France
[4] Ctr Oscar Lambret, Dept Paediat Oncol, F-59020 Lille, France
[5] Hop Charles Nicolle, Dept Paediat, Rouen, France
[6] Ctr Cladius Regaud, Dept Paediat Oncol, Toulouse, France
[7] Hop Tronche, Dept Paediat Oncol, Grenoble, France
[8] Ctr Antoine Lacassagne, Dept Paediat Oncol, F-06054 Nice, France
[9] Nop Nord, Dept Paediat Oncol, St Etienne, France
[10] Hop Reine Fabiola, Dept Paediat Haematol Oncol, Brussels, Belgium
[11] CHU Tours, Dept Paediat, Tours, France
[12] Hop Enfants La Timone, Dept Paediat Oncol, Marseille, France
关键词
medulloblastoma; relapse; prognosis; salvage therapy;
D O I
10.1038/bjc.1998.220
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Early detection of relapse has been advocated to improve survival in children with recurrent medulloblastoma. However, the prognostic factors and the longer term outcome of these patients remains unclear. Pattern of recurrences were analysed in three consecutive protocols of the Societe Francaise d'Oncologie Pediatrique (1985-91). A uniform surveillance programme including repeated lumbar puncture combined with computerized tomography (CT) or magnetic resonance imaging (MRI) scan was applied for ail registered patients. Forty-six out of 116 patients had progressive or recurrent disease. The median time from diagnosis to recurrence was 10.5 months and 76% relapses occurred during the first 2 years. Seventeen patients had asymptomatic relapses that were detected by the surveillance protocol. Forty-one patients were treated at time of progression. Twenty-three responded to salvage therapy and 11 achieved a second complete remission. The median survival time after progression was 5 months (<1-41 months), and only two patients remained alive at time of follow-up. Length of survival is primarily related to some specific patterns of relapse (time from diagnosis to recurrence, circumstances of relapse, extent of relapse) and to the response to salvage therapy. No evidence of long-term benefit appeared from any form of treatment.
引用
收藏
页码:1321 / 1326
页数:6
相关论文
共 33 条
[1]   Response of recurrent medulloblastoma to low-dose oral etoposide [J].
Ashley, DM ;
Meier, L ;
Zalduondo, FM ;
Friedman, HS ;
Gajjar, A ;
Kun, L ;
Duffner, PK ;
Smith, S ;
Longee, D .
JOURNAL OF CLINICAL ONCOLOGY, 1996, 14 (06) :1922-1927
[2]   PROSPECTIVE RANDOMIZED TRIAL OF CHEMOTHERAPY GIVEN BEFORE RADIOTHERAPY IN CHILDHOOD MEDULLOBLASTOMA - INTERNATIONAL-SOCIETY-OF-PEDIATRIC-ONCOLOGY (SIOP) AND THE (GERMAN)-SOCIETY-OF-PEDIATRIC-ONCOLOGY (GPO) - SIOP-II [J].
BAILEY, CC ;
GNEKOW, A ;
WELLEK, S ;
JONES, M ;
ROUND, C ;
BROWN, J ;
PHILLIPS, A ;
NEIDHARDT, MK .
MEDICAL AND PEDIATRIC ONCOLOGY, 1995, 25 (03) :166-178
[3]   PHASE-II STUDY OF IFOSFAMIDE IN CHILDHOOD BRAIN-TUMORS - A REPORT BY THE FRENCH-SOCIETY-OF-PEDIATRIC-ONCOLOGY (SFOP) [J].
CHASTAGNER, P ;
SOMMELETOLIVE, D ;
KALIFA, C ;
BRUNATMENTIGNY, M ;
ZUCKER, JM ;
DEMEOCQ, F ;
BARANZELLI, MC ;
TRON, P ;
BERGERON, C ;
PEIN, F ;
DELUMLEY, L .
MEDICAL AND PEDIATRIC ONCOLOGY, 1993, 21 (01) :49-53
[4]   Will high dose chemotherapy followed by autologous bone marrow transplantation supplant cranio-spinal irradiation in young children treated for medulloblastoma? [J].
DupuisGirod, S ;
Hartmann, O ;
Benhamou, E ;
Doz, F ;
Mechinaud, F ;
Bouffet, E ;
Coze, C ;
Kalifa, C .
JOURNAL OF NEURO-ONCOLOGY, 1996, 27 (01) :87-98
[5]  
ELSON PJ, 1988, CANCER RES, V48, P7310
[6]   THE TREATMENT OF MEDULLOBLASTOMA - RESULTS OF A PROSPECTIVE RANDOMIZED TRIAL OF RADIATION-THERAPY WITH AND WITHOUT CCNU, VINCRISTINE, AND PREDNISONE [J].
EVANS, AE ;
JENKIN, RDT ;
SPOSTO, R ;
ORTEGA, JA ;
WILSON, CB ;
WARA, W ;
ERTEL, IJ ;
KRAMER, S ;
CHANG, CH ;
LEIKIN, SL ;
HAMMOND, GD .
JOURNAL OF NEUROSURGERY, 1990, 72 (04) :572-582
[7]  
FINLAY JL, 1987, AM J PEDIAT HEMATOL, V9, P264
[8]   Pilot study of high-dose thiotepa and etoposide with autologous bone marrow rescue in children and young adults with recurrent CNS tumors [J].
Finlay, JL ;
Goldman, S ;
Wong, MC ;
Cairo, M ;
Garvin, J ;
August, C ;
Cohen, BH ;
Stanley, P ;
Zimmerman, RA ;
Bostrom, B ;
Geyer, JR ;
Harris, RE ;
Sanders, J ;
Yates, AJ ;
Boyett, JM ;
Packer, RJ .
JOURNAL OF CLINICAL ONCOLOGY, 1996, 14 (09) :2495-2503
[9]   MORE ON SURVEILLANCE OF CHILDREN WITH MEDULLOBLASTOMA [J].
FRIEDMAN, HS ;
KUN, LE .
NEW ENGLAND JOURNAL OF MEDICINE, 1995, 332 (03) :191-191
[10]   PREIRRADIATION CHEMOTHERAPY INCLUDING 8-DRUGS-IN-1-DAY REGIMEN AND HIGH-DOSE METHOTREXATE IN CHILDHOOD MEDULLOBLASTOMA - RESULTS OF THE M7 FRENCH COOPERATIVE STUDY [J].
GENTET, JC ;
BOUFFET, E ;
DOZ, F ;
TRON, P ;
ROCHE, H ;
THYSS, A ;
PLANTAZ, D ;
STEPHAN, JL ;
MOTTOLESE, C ;
PONVERT, D ;
CARRIE, C ;
RAYBAUD, C ;
BRUNATMENTIGNY, M ;
CHOUX, M ;
PHILIP, T ;
ZUCKER, JM ;
BERNARD, JL .
JOURNAL OF NEUROSURGERY, 1995, 82 (04) :608-614