A systematic review of p53 as a biomarker of survival in patients with osteosarcoma

被引:68
作者
Fu, Hai-Liang [1 ]
Shao, Lin [1 ]
Wang, Qiang [1 ]
Jia, Tao [1 ]
Li, Ming [1 ]
Yang, Da-Ping [2 ]
机构
[1] Harbin Med Univ, Affiliated Hosp 2, Dept Orthopaed Surg, Harbin 150001, Heilongjiang, Peoples R China
[2] Harbin Med Univ, Affiliated Hosp 2, Dept Plast Surg, Harbin 150001, Heilongjiang, Peoples R China
关键词
Osteosarcoma; p53; Survival; Systematic review; PROGNOSTIC VALUE; EXPRESSION; TUMOR; BCL-2; METAANALYSIS; PROTEINS; TP53;
D O I
10.1007/s13277-013-0966-x
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Osteosarcoma is the most common malignant bone tumor, and the prognosis of patients with osteosarcoma is still unsatisfactory with low survival rates. There are many studies assessing the prognostic role of upregulated p53 in patients presenting osteosarcoma, and there is no consistent finding. To summarize the existing evidence about whether the presence of upregulated p53 was a biomarker of survival in patients with osteosarcoma, we performed a systematic review and meta-analysis of relevant publications. We assessed the effect of upregulated p53 on the 3-year overall survival and the 3-year disease-free survival by calculating the pooled odds ratio (OR) with corresponding 95 % confidence interval (95 %CI). Fifteen studies with a total of 609 patients with osteosarcoma were finally included into the systematic review and meta-analysis. Compared with osteosarcoma patients with low or undetectable p53, patients with upregulated p53 were obviously associated with decreased 3-year overall survival (OR = 0.29, 95 %CI 0.19-0.43, P < 0.001). In addition, patients with upregulated p53 were obviously associated with decreased 3-year disease-free survival (OR = 0.06, 95 %CI 0.02-0.23, P < 0.001). The results from the systematic review and meta-analysis highlight that p53 is an effective biomarker of survival in patients with osteosarcoma. In addition, more studies with a large sample size are needed to identify the effect of p53 expression in osteosarcoma patients.
引用
收藏
页码:3817 / 3821
页数:5
相关论文
共 30 条
[1]
Novel therapeutic strategy for osteosarcoma targeting osteoclast differentiation, bone-resorbing activity, and apoptosis pathway [J].
Akiyama, Toru ;
Dass, Crispin R. ;
Choong, Peter F. M. .
MOLECULAR CANCER THERAPEUTICS, 2008, 7 (11) :3461-3469
[2]
[Anonymous], J MOD ONCOL
[3]
[Anonymous], ACTA ACAD MED CPAPF
[4]
[Anonymous], ZHEJIANG MED J
[5]
Osteosarcoma: ESMO Clinical Recommendations for diagnosis, treatment and follow-up [J].
Bielack, S. ;
Carrle, D. ;
Casali, P. G. .
ANNALS OF ONCOLOGY, 2009, 20 :137-139
[6]
Expression of Molecular Markers in the Tumor and Survival Prognosis in Osteosarcoma [J].
Boulytcheva, I. V. ;
Soloviev, Yu. N. ;
Kushlinskii, N. E. ;
Mahson, A. N. .
BULLETIN OF EXPERIMENTAL BIOLOGY AND MEDICINE, 2010, 150 (02) :237-242
[7]
de Oliveira CRGCM, 2007, CLINICS, V62, P167, DOI 10.1590/S1807-59322007000200012
[8]
METAANALYSIS IN CLINICAL-TRIALS [J].
DERSIMONIAN, R ;
LAIRD, N .
CONTROLLED CLINICAL TRIALS, 1986, 7 (03) :177-188
[9]
Bias in meta-analysis detected by a simple, graphical test [J].
Egger, M ;
Smith, GD ;
Schneider, M ;
Minder, C .
BMJ-BRITISH MEDICAL JOURNAL, 1997, 315 (7109) :629-634
[10]
Clinicopathological significance of cathepsin D expression in non-small cell lung cancer is conditional on apoptosis-associated protein phenotype: an immunohistochemistry study [J].
Fan, Chuifeng ;
Lin, Xuyong ;
Wang, Enhua .
TUMOR BIOLOGY, 2012, 33 (04) :1045-1052