Clinical presentation, diagnosis, and pharmacotherapy of patients with primary brain tumors

被引:30
作者
Newton, HB
Turowski, RC
Stroup, TJ
McCoy, LK
机构
[1] Ohio State Univ, Dept Neurol, Div Neurooncol, Columbus, OH 43210 USA
[2] James Canc Hosp, Outpatient Chemotherapy Clin, Columbus, OH USA
[3] Columbus Childrens Hosp, Dept Pharm, Columbus, OH USA
关键词
primary brain tumors; malignant; benign; chemotherapy;
D O I
10.1345/aph.18353
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
OBJECTIVE: TO briefly review the clinical presentation and diagnosis of patients with primary brain tumors, followed by an in-depth; sun;ey of the pertinent pharmacotherapy. DATA SOURCES: A detailed search of the neurologic, neurosurgical, and oncologic literature for basic science research, clinical studies, and review articles related to chemotherapy and pharmacotherapy of primary brain tumors. STUDY SELECTION: Relevant studies on tissue culture systems, animals, and humans examining the mechanisms of action, pharmacokinetics, clinical pharmacology, and treatment results of chemotherapeutic agents for primary brain tumors. In addition, studies of pharmacologic agents administered for supportive care and symptom control are reviewed. DATA SYNTHESIS: Primary brain tumors derive from cells within the intracranial cavity and generally present with headache, seizure activity, cognitive changes, and weakness. They are diagnosed most efficiently with magnetic resonance imaging. After diagnosis, the most common supportive medications include corticosteroids, gastric acid inhibitors, and anticonvulsants. Chemotherapy is adjunctive treatment for patients with malignant tumors and selected recurrent or progressive benign neoplasms. In general, the most effective chemotherapeutic drugs are alkylating agents such as the nitrosoureas, procarbazine, cisplatin, and carboplatin. Other agents used include cyclophosphamide, methotrexate. vincristine, and etoposide. Angiogenesis inhibitors and gene therapy comprise some of the novel therapeutic strategies under investigation. CONCLUSIONS: The efficacy of chemotherapy for primary brain tumors remains modest. Novel agents must be discovered that are more specific and attack tumor cells at the molecular level of tumorigenesis. Furthermore, strategies must be developed to counteract the pervasive problem of brain tumor chemoresistance.
引用
收藏
页码:816 / 832
页数:17
相关论文
共 165 条
[31]   Recurrent supratentorial malignant gliomas in children - Long-term salvage therapy with oral etoposide [J].
Chamberlain, MC .
ARCHIVES OF NEUROLOGY, 1997, 54 (05) :554-558
[32]   Salvage chemotherapy with paclitaxel for recurrent oligodendrogliomas [J].
Chamberlain, MC ;
Kormanik, PA .
JOURNAL OF CLINICAL ONCOLOGY, 1997, 15 (12) :3427-3432
[33]   Phase I study of paclitaxel in patients with recurrent malignant glioma: A North American brain tumor consortium report [J].
Chang, SM ;
Kuhn, JG ;
Rizzo, J ;
Robins, HI ;
Schold, SC ;
Spence, AM ;
Berger, MS ;
Mehta, MP ;
Bozik, ME ;
Pollack, I ;
Gilbert, M ;
Fulton, D ;
Rankin, C ;
Malec, M ;
Prados, MD .
JOURNAL OF CLINICAL ONCOLOGY, 1998, 16 (06) :2188-2194
[34]   High dose oral tamoxifen and subcutaneous interferon alpha-2a for recurrent glioma [J].
Chang, SM ;
Barker, FG ;
Huhn, SL ;
Nicholas, MK ;
Page, M ;
Rabbitt, J ;
Prados, MD .
JOURNAL OF NEURO-ONCOLOGY, 1998, 37 (02) :169-176
[35]  
Chauveinc L, 1996, J NEURO-ONCOL, V27, P141
[36]  
Cheng AL, 1998, CANCER, V82, P1946, DOI 10.1002/(SICI)1097-0142(19980515)82:10<1946::AID-CNCR19>3.0.CO
[37]  
2-T
[38]  
Chu E., 1996, CANC CHEMOTHERAPY BI, P109
[39]   CISPLATIN, ARA-C AND ETOPOSIDE (PAE) IN THE TREATMENT OF RECURRENT CHILDHOOD BRAIN-TUMORS [J].
CORDEN, BJ ;
STRAUSS, LC ;
KILLMOND, T ;
CARSON, BS ;
WHARAM, MD ;
KUMAR, AJ ;
PIANTADOSI, S ;
ROBB, PA ;
PHILLIPS, PC .
JOURNAL OF NEURO-ONCOLOGY, 1991, 11 (01) :57-63
[40]   CLINICAL AND RADIOGRAPHIC RESPONSE IN A MINORITY OF PATIENTS WITH RECURRENT MALIGNANT GLIOMAS TREATED WITH HIGH-DOSE TAMOXIFEN [J].
COULDWELL, WT ;
WEISS, MH ;
DEGIORGIO, CM ;
WEINER, LP ;
HINTON, DR ;
EHRESMANN, GR ;
CONTI, PS ;
APUZZO, MLJ ;
KORNBLITH, P ;
DETRIBOLET, N ;
TAOA, M ;
LEVIN, VA ;
OLDFIELD, EH .
NEUROSURGERY, 1993, 32 (03) :485-490