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Early Evaluation of the Apoptotic Index Ratio is Useful in Predicting the Efficacy of Chemoradiotherapy in Esophageal Squamous Cell Carcinoma

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Journal Oncol Lett
Specialty Oncology
Date 2012 Jun 29
PMID 22740896
Citations 1
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Abstract

Chemoradiotherapy for advanced esophageal cancer is a standard treatment alongside surgical treatment. Although numerous investigators have attempted to identify the predictive markers for chemoradiosensitivity, there appear to be few candidates that can be applied in clinical use. Using biopsy specimens, we investigated the apoptotic index (AI) prior to treatment and following a radiation dose of 10 Gy to detect the early response to chemoradiotherapy in 28 patients with esophageal squamous cell carcinoma. Molecular markers, including p53, p21, bax, bcl-2, HSP27, HSP70, HSP90, Ku70, Ku86 and HIF-1α, were also examined by immunohistochemical staining. The patients were divided into two groups depending on the response to chemoradiotherapy: a responder group (RG) (n=19) that included the patients with complete or partial response, and a non-responder group (NRG) (n=9), that included patients with stable or progressive disease. In the RG and NRG, the AI of pretreatment was 4.7±5.3 (mean ± SD, cells/1,000 cells) and 5.9±3.7, respectively. The apoptotic index ratio (AIR), which was determined by dividing the AI following 10 Gy radiation by the pretreatment AI, was higher in the RG compared to the NRG (4.7±4.5 versus 1.9±1.4, p=0.03). When the cut-off value of AIR was set at 2.4, the sensitivity, specificity and accuracy were 74, 78 and 76%, respectively. Among the molecular markers we examined immunohistochemically, a positive p53 expression in the pretreatment evaluation was associated with the efficacy of chemoradiotherapy (p=0.08). Regarding the expression of other molecular markers, no significant correlations were found in RG and NRG. In the present study, the results indicated that AIR is useful for the prediction of chemoradiosensitivity in esophageal squamous cell carcinoma.

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References
1.
Shimoyama S, Konishi T, Kawahara M, Aoki F, Harada N, Shimizu S . Expression and alteration of p53 and p21(waf1/cip1) influence the sensitivity of chemoradiation therapy for esophageal cancer. Hepatogastroenterology. 1998; 45(23):1497-504. View

2.
Oka K, Suzuki Y, Nakano T . High growth fraction at 9 grays of radiotherapy is associated with a good prognosis for patients with cervical squamous cell carcinoma. Cancer. 2000; 89(7):1526-31. View

3.
Fiorica F, Di Bona D, Schepis F, Licata A, Shahied L, Venturi A . Preoperative chemoradiotherapy for oesophageal cancer: a systematic review and meta-analysis. Gut. 2004; 53(7):925-30. PMC: 1774092. DOI: 10.1136/gut.2003.025080. View

4.
Hefferin M, Tomkinson A . Mechanism of DNA double-strand break repair by non-homologous end joining. DNA Repair (Amst). 2005; 4(6):639-48. DOI: 10.1016/j.dnarep.2004.12.005. View

5.
Theisen J, Krause B, Peschel C, Schmid R, Geinitz H, Friess H . Early response evaluation and prediction in neoadjuvant-treated patients with esophageal cancer. World J Gastrointest Surg. 2010; 1(1):30-7. PMC: 2999119. DOI: 10.4240/wjgs.v1.i1.30. View