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p27kip1 Expression Is Associated With Tumor Response to Preoperative Chemoradiotherapy in Rectal Cancer

  • Esposito, Giovanni1, 2, 3
  • Pucciarelli, Salvatore4
  • Alaggio, Rita5
  • Giacomelli, Luciano5
  • Marchiori, Elisabetta4
  • Iaderosa, Gaetano Antonio5
  • Friso, Maria Luisa6
  • Toppan, Paola4
  • Chieco-Bianchi, Luigi1, 2
  • Lise, Mario4
  • 1 Department of Oncology and Surgery of the University of Padova, Sections of Oncology (GE, LC-B), Padova, Italy , Padova
  • 2 City Hospital of Padova, Department of the Molecular Diagnostic Oncology Service (GE, LC-B), Padova, Italy , Padova
  • 3 Servizio Citodiagnostica Molecolare Oncologica, Via Gattamelata, 64, Padova, 35128, Italy , Padova
  • 4 Department of Oncology and Surgery of the University of Padova, Sections of II Clinical Surgery (SP, EM, PT, ML), Padova, Italy , Padova
  • 5 Department of Oncology and Surgery of the University of Padova, Sections of Pathology (RA, LG, GAI), Padova, Italy , Padova
  • 6 City Hospital of Padova, Division of Radiology (MLF), Padova, Italy , Padova
Published Article
Annals of Surgical Oncology
Springer - Society of Surgical Oncology
Publication Date
May 01, 2001
DOI: 10.1007/s10434-001-0311-2
Springer Nature


Background Our aim was to ascertain whether or not the response to preoperative chemoradiotherapy for rectal cancer is associated with p27kip1 and p53 protein expression. Methods: Thirty-eight patients (27 male, 11 female) with a mean age of 59 years (age range 33–87) and stage II-III rectal cancer received preoperative chemoradiotherapy (45–50.4 Gy; 5-FU 350 mg/m2/day and leucovorin 10 mg/m2/day). Thirty-one underwent low anterior resection; seven underwent abdominoperineal excision. Endoscopic tumor biopsies, performed before adjuvant therapy, were evaluated for: histologic type, tumor differentiation, mitotic index, and p27kip1 and p53 protein expression which were immunohistochemically determined. p53 expression was graded as: a) absent or present in ≤10% of tumor cells; b) present in 11–25%; c) present in 26–75%; and d) present in >75% of tumor cells. p27kip1 expression was assessed using both light microscopy (percent of stained cells x10 HPF) and cytometry with an image analysis workstation. Tumor response, ascertained with histology, was classified using a scale from 0 (no response) to 6 (complete pathologic response). Results: The mitotic index for the endoscopic biopsies was low in 14 cases, moderate in 17 cases, and high in 7 cases. p53 protein expression was found in 21 (a), 3 (b), 3 (c), and 11 (d) cases. The mean percentage of cells expressing the p27kip1 protein was 34 (range 0–77.14%). A close correlation was found between cytometric and light microscopy findings for p27kip1 (r2 = 0.92, P = .0001). Tumor differentiation was good in 5 cases, poor in 2 cases, and moderate in the remaining 31 cases. While the response to adjuvant therapy was good/complete in 25 (65.78%) cases, it was absent/poor in 13 (34.21%) cases. Univariate analysis associated type of adjuvant therapy (chemoradiotherapy, P = .0428) and p27kip1 protein lower expression (P = .0148) with a poor response to adjuvant treatment. Stepwise linear regression found overexpression of p53 and p27kip1 and young age to be independent variables that were linked to a good response to adjuvant therapy. Conclusions:Lack of p27kip1 and p53 protein expression in rectal cancer is associated with a poor response to preoperative adjuvant therapy.

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