RESECTION FOR SOLITARY BRAIN METASTASIS - ROLE OF ADJUVANT RADIATION AND PROGNOSTIC VARIABLES IN 229 PATIENTS

被引:121
作者
SMALLEY, SR
LAWS, ER
OFALLON, JR
SHAW, EG
SCHRAY, MF
机构
[1] MAYO CLIN & MAYO FDN, DEPT NEUROL SURG, DIV RADIAT ONCOL, ROCHESTER, MN 55905 USA
[2] MAYO CLIN & MAYO FDN, CANC STAT UNIT, ROCHESTER, MN 55905 USA
关键词
BRAIN NEOPLASM; METASTASIS; CRANIOTOMY; RADIATION THERAPY; PROGNOSIS;
D O I
10.3171/jns.1992.77.4.0531
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
The authors reviewed 229 consecutive patients treated intramurally by resection of solitary cerebral metastasis. Patients were classified into four groups on the basis of whether a gross total resection or subtotal resection was performed and whether systemic disease was present or absent at the time of craniotomy. Group 1 had gross total resection and no systemic disease; Group 2 had subtotal resection and no systemic disease; Group 3 had subtotal resection and systemic disease; and Group 4 had gross total resection and systemic disease. All four groups were further subdivided into Subgroup A (adjuvant whole-brain radiation therapy) or Subgroup B (no adjuvant radiation). Data were collected regarding multiple patient and tumor variables for multivariate analysis. Survival data for the 46 patients in Group IA (median 1.3 years, 2-year survival rate 41%, 5-year survival rate 21%) were markedly better than those for the 75 in Group 1B (median 0.7 year, 2-year survival rate 19%, 5-year survival rate 4%). The 20 patients in Group 2A also had superior survival data (median 1.1 years, 2-year survival rate 30%, 3-year survival rate 30%) when compared with the eight patients in Group 2B (median 3 months, 1-year survival rate 0%). However, the 16 and 22 patients in Groups 3A and 4A, respectively, had no discernible differences compared to the seven and 35 patients in their Group 3B and 4B counterparts. Multivariate analyses were performed to assess the association of survival with multiple patient, disease, and treatment variables. Poor neurological status and systemic disease were significantly associated with inferior survival, while longer (> 36 months) intervals between primary diagnosis and craniotomy were significantly associated with improved survival. After adjusting for the effects of other patient, disease, and treatment characteristics, adjuvant whole-brain radiotherapy was significantly associated with improved survival times. These data support the continued use of craniotomy followed by adjuvant whole-brain radiation therapy for treatment of solitary brain metastasis. However, this aggressive therapy appears relatively contraindicated in the face of either systemic disease or substantial neurological deficit.
引用
收藏
页码:531 / 540
页数:10
相关论文
共 55 条
[1]  
AZAB M, 1989, CANCER-AM CANCER SOC, V64, P1829, DOI 10.1002/1097-0142(19891101)64:9<1829::AID-CNCR2820640912>3.0.CO
[2]  
2-G
[3]  
BASTRON JA, 1963, CLIN EXAMINATIONS NE
[4]   BLOOD-FLOW AND OXYGEN UTILIZATION IN THE CONTRALATERAL CEREBRAL-CORTEX OF PATIENTS WITH UNTREATED INTRACRANIAL TUMORS AS STUDIED BY POSITRON EMISSION TOMOGRAPHY, WITH OBSERVATIONS ON THE EFFECT OF DECOMPRESSIVE SURGERY [J].
BEANEY, RP ;
BROOKS, DJ ;
LEENDERS, KL ;
THOMAS, DGT ;
JONES, T ;
HALNAN, KE .
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 1985, 48 (04) :310-319
[5]  
Breiman L, 2017, CLASSIFICATION REGRE, P368, DOI 10.1201/9781315139470
[6]   SURGICAL-TREATMENT OF PRIMARY LUNG-CANCER AND SOLITARY INTRACRANIAL METASTASIS [J].
CATINELLA, FP ;
KITTLE, CF ;
FABER, LP ;
MILLOY, FJ ;
WARREN, WH ;
VONROENN, KA .
CHEST, 1989, 95 (05) :972-975
[7]   INTERSTITIAL IR-192 IMPLANTATION FOR MALIGNANT BRAIN-TUMORS .2. CLINICAL-EXPERIENCE [J].
CHUN, M ;
MCKEOUGH, P ;
WU, A ;
KASDON, D ;
HEROS, D ;
CHANG, H .
BRITISH JOURNAL OF RADIOLOGY, 1989, 62 (734) :158-162
[8]  
COX DR, 1972, J R STAT SOC B, V34, P187
[9]   THE ROLE OF POSTOPERATIVE RADIOTHERAPY AFTER RESECTION OF SINGLE BRAIN METASTASES [J].
DEANGELIS, LM ;
MANDELL, LR ;
THALER, HT ;
KIMMEL, DW ;
GALICICH, JH ;
FUKS, Z ;
POSNER, JB .
NEUROSURGERY, 1989, 24 (06) :798-805
[10]  
DEANGELIS LM, 1989, J NEURO-ONCOL, V7, P241