ArticleBritish journal of cancer1994
p53 protein in low-grade astrocytomas: a study with long-term follow-up.
Article in British journal of cancer, 1994. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers, 1 of them a synthesis that pooled it.
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Who cites it
9 citing papers in PubMed, 1 synthesis or guideline pooled it.
- P53 immunoexpression as a prognostic marker for human astrocytomas: a meta-analysis and review of the literature.Journal of neuro-oncology · 2010Pooled it
- Mutant, wild type, or overall p53 expression: freedom from clinical progression in tumours of astrocytic lineage.British journal of cancer · 2004Article
- Proliferation and apoptosis in long-term surviving low grade gliomas in relation to radiotherapy.Journal of neuro-oncology · 2002Article
- Clinicopathological features, MIB-1 labeling index and apoptotic index in recurrent astrocytic tumors.Pathology oncology research : POR · 2001Article
- Cells with TP53 mutations in low grade astrocytic tumors evolve clonally to malignancy and are an unfavorable prognostic factor.Oncogene · 1999Article
- Simultaneous alterations of retinoblastoma and p53 protein expression in astrocytic tumors.Pathology oncology research : POR · 1999Article
- p53 protein in pediatric malignant astrocytomas: a study of 21 patients.Journal of neuro-oncology · 1997Article
- Computer-assisted microscope characterization of BCNU-induced modifications in the collective behavior of 12 human brain cancer cell lines.Journal of neuro-oncology · 1996Article
- Mutations and immunohistochemistry of p53 and proliferation markers in astrocytic tumors of childhood.Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery · 1995Article
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7 authors.
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Abstract
The immunohistochemical expression of p53 protein (p53) was examined in 52 patients out of a series of 66 patients with low-grade astrocytomas with long-term follow-up. All patients were also evaluated for several clinical and histological features, among which only preoperative Karnofsky score and the extent of surgery were statistically significant parameters to predict outcome on multivariate analysis. p53 accumulation was seen in 46.1% of patients, with a wide range of percentage of positive cells. Median survival for p53-positive and p53-negative patients was 41 and 37 months respectively. The survival curves of p53-positive and -negative patients were not statistically different. However, the curves showed a trend towards a more aggressive course in p53-positive patients beginning 3-4 years after surgery. Five years after diagnosis the survival estimate with the Kaplan-Meier method was 21.2% for patients with p53-positive tumours and 45.9% for patients with p53-negative tumours. This trend is not due to different distribution of major clinical prognostic factors (age, incomplete resection or Karnofsky status). The trend could be related to the time needed by the p53-positive clone to outgrow the rest of the p53-negative neoplastic cell population. This hypothesis is further supported by the fact that the five recurrences which were surgically removed (one anaplastic astrocytoma and four glioblastomas) derived from p53-positive tumours and were themselves intensely p53 positive.
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