R. Wiggenraad et al., THE PROGNOSTIC-SIGNIFICANCE OF P53 EXPRESSION FOR SURVIVAL AND LOCAL-CONTROL IN RECTAL-CARCINOMA TREATED WITH SURGERY AND POSTOPERATIVE RADIOTHERAPY, International journal of radiation oncology, biology, physics, 41(1), 1998, pp. 29-35
Citations number
43
Categorie Soggetti
Oncology,"Radiology,Nuclear Medicine & Medical Imaging
Purpose: To investigate whether p53 immunoreactivity is a prognostic f
actor for survival and pelvic control in rectal carcinoma treated with
surgery and postoperative radiotherapy. Methods and Materials: From 1
981 through 1989, 146 patients with rectal carcinoma received postoper
ative radiotherapy and were followed for at least 5 years or until dea
th. The specimens of 123 of these 146 patients could be retrieved and
examined immunohistochemically for p53 expression. The prognostic valu
e for survival and pelvic control of p53 expression and other patient
and treatment factors was examined by univariate and multivariate anal
yses. Results: p53 expression has no prognostic significance for overa
ll survival in this group of 123 patients. The only prognostic factor
for survival in this material is tumor stage (p < 0.01). The actuarial
pelvic recurrence rates of p53- and p53+ cases are different in favor
of the p53- ones. In the univariate analysis this difference is signi
ficant (p = 0.05). However, in the multivariate analysis the influence
of p53 expression, additional to stage, becomes nonsignificant (p = 0
.10). This indicates that p53 expression is not a strong independant p
rognostic factor for pelvic recurrence. In the multivariate analysis s
tage turns out to be the only predictor of pelvic recurrence (p = 0.03
). When only recurrences inside the radiation field are considered, th
ere is no difference between p53+ and p53- cases. Conclusion: Based on
this material, we have found no convincing evidence that p53 expressi
on is an important predictor of survival or local control in rectal ca
ncer treated with surgery and postoperative radiotherapy. We have foun
d no evidence that possible differences in radiosensitivity between p5
3+ and p53- tumors have clinical significance for this group of patien
ts. (C) 1998 Elsevier Science Inc.