Survival and neurodevelopmental outcome of young children with medulloblastoma at St Jude Children's Research Hospital

被引:168
作者
Walter, AW
Mulhern, RK
Gajjar, A
Heideman, RL
Reardon, D
Sanford, RA
Xiong, XP
Kun, LE
机构
[1] St Jude Childrens Res Hosp, Dept Hematol Oncol, Memphis, TN 38105 USA
[2] St Jude Childrens Res Hosp, Dept Behav Med, Memphis, TN 38105 USA
[3] St Jude Childrens Res Hosp, Dept Radiat Oncol, Memphis, TN 38105 USA
[4] St Jude Childrens Res Hosp, Dept Biostat, Memphis, TN 38105 USA
[5] Univ Tennessee, Coll Med, Dept Pediat, Memphis, TN USA
[6] Univ Tennessee, Coll Med, Dept Radiat Oncol, Memphis, TN USA
[7] Univ Tennessee, Coll Med, Dept Pediat Neurosurg, Memphis, TN USA
关键词
D O I
10.1200/JCO.1999.17.12.3720
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: Young children treated for medulloblastoma are at especially high risk for morbidity and mortality from their disease and therapy. This study sought to assess the relationship, if any, between patient outcome and M stage. Neuropsychologic and endocrine outcomes were also assessed. Patients and Methods: Twenty-nine consecutively diagnosed infants and young children were treated for medulloblastoma at St Jude Children's Research Hospital between November 1984 and December 1995. All patients were treated with the intent of using postoperative chemotherapy to delay planned irradiation, Results: The median age at diagnosis wets 2.6 years. Six patients completed planned chemotherapy without progressive disease and underwent irradiation a, completion of chemotherapy. Twenty-three children experienced disease progression during chemotherapy and underwent irradiation at the lime of progression. The 5-year overall survival rate for the entire cohort was 51% +/- 10%. The 5-year progression-free survival rate was 21% +/- 8%. M stage did naf impact survival. All patients lost cognitive function during and after therapy at a rate of -3.9 intelligence quotient points per year (P =.0028). Sensory functions declined significantly after therapy (P =.007). All long-term survivors required hormone replacement therapy and had growth abnormalities. Conclusion: The majority of infants created for medulloblastoma experienced disease progression during initial chemotherapy. However, more than half of these patients can be cured with salvage radiation therapy, regardless of M stage. The presence of metastatic disease did not increase the risk of dying from medulloblastoma. All patients treated in this fashion have significant neuropsychologic deficits. Our experience demonstrates that medulloblastoma in infancy is a curable disease, albeit at a significant cost. J Clin Oncol 17:3720-3728. (C) 1999 by American Society of Clinical Oncology.
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页码:3720 / 3728
页数:9
相关论文
共 52 条
[1]  
AGESTI A, 1990, CATEGORICAL DATA ANA
[2]   Effects of medulloblastoma resections on outcome in children: A report from the children's cancer group [J].
Albright, AL ;
Wisoff, JH ;
Zeltzer, PM ;
Boyett, JM ;
Rorke, LB ;
Stanley, P .
NEUROSURGERY, 1996, 38 (02) :265-270
[3]   MOPP chemotherapy without irradiation as primary postsurgical therapy for brain tumors in infants and young children [J].
Ater, JL ;
vanEys, J ;
Woo, SY ;
Moore, B ;
Copeland, DR ;
Bruner, J .
JOURNAL OF NEURO-ONCOLOGY, 1997, 32 (03) :243-252
[4]  
BARAM TZ, 1987, CANCER, V60, P173, DOI 10.1002/1097-0142(19870715)60:2<173::AID-CNCR2820600209>3.0.CO
[5]  
2-F
[6]  
Bayley N., 1969, BAYLEY SCALES INFANT
[7]   TREATMENT AND PROGNOSIS OF MEDULLOBLASTOMA IN CHILDREN - A STUDY OF 82 VERIFIED CASES [J].
BLOOM, HJG ;
WALLACE, ENK ;
HENK, JM .
AMERICAN JOURNAL OF ROENTGENOLOGY RADIUM THERAPY AND NUCLEAR MEDICINE, 1969, 105 (01) :43-&
[8]   NEUROBEHAVIORAL AND NEUROLOGIC OUTCOME IN LONG-TERM SURVIVORS OF POSTERIOR-FOSSA BRAIN-TUMORS - ROLE OF AGE AND PERIOPERATIVE FACTORS [J].
CHAPMAN, CA ;
WABER, DP ;
BERNSTEIN, JH ;
POMEROY, SL ;
LAVALLY, B ;
SALLAN, SE ;
TARBELL, N .
JOURNAL OF CHILD NEUROLOGY, 1995, 10 (03) :209-212
[9]   OTOTOXIC EFFECT OF CISPLATIN IN CHILDREN WITH BRAIN-TUMORS [J].
COHEN, BH ;
ZWEIDLER, P ;
GOLDWEIN, JW ;
MOLLOY, J ;
PACKER, RJ .
PEDIATRIC NEUROSURGERY, 1991, 16 (06) :292-296
[10]   HYPOTHALAMIC PITUITARY DYSFUNCTION AFTER RADIATION FOR BRAIN-TUMORS [J].
CONSTINE, LS ;
WOOLF, PD ;
CANN, D ;
MICK, G ;
MCCORMICK, K ;
RAUBERTAS, RF ;
RUBIN, P .
NEW ENGLAND JOURNAL OF MEDICINE, 1993, 328 (02) :87-94