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Volume 41, Issue 2, Pages 262-270 (February 2010)


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p53 expression in tumor-stromal fibroblasts is closely associated with the nodal metastasis and outcome of patients with invasive ductal carcinoma who received neoadjuvant therapy

Takahiro Hasebe, MD, PhDaCorresponding Author Informationemail address, Nobuko Tamura, MDb, Nao Okada, MDb, Takashi Hojo, MDb, Sadako Akashi-Tanaka, MD, PhDb, Chikako Shimizu, MDc, Histoshi Tsuda, MD, PhDd, Tatsuhiro Shibata, MD, PhDe, Yuko Sasajima, MD, PhDd, Motoki Iwasaki, MD, PhDf, Takayuki Kinoshita, MD, PhDb

Received 10 April 2009; received in revised form 27 July 2009; accepted 30 July 2009. published online 16 October 2009.

Summary 

The purpose of this study was to determine whether p53 immunoreactivity in tumor-stromal fibroblasts assessed by the Allred scoring system in biopsy specimens obtained before neoadjuvant therapy and assessed in surgical specimens obtained after neoadjuvant therapy is significantly associated with nodal metastasis by invasive ductal carcinoma and with the outcome of 318 patients with invasive ductal carcinoma who received neoadjuvant therapy, according to UICC pathologic TNM stage, in multivariate analyses with well-known clinicopathologic factors. The Allred scores for p53 in tumor-stromal fibroblasts in the surgical specimens were significantly associated with the presence of nodal metastasis. The Allred scores for p53 in the tumor-stromal fibroblasts of biopsy and surgical specimens were a very important outcome predictive factor for patients who received neoadjuvant therapy, independent of UICC pathologic TNM status, but the outcome predictive power of the Allred scores for p53 in tumor-stromal fibroblasts assessed in the surgical specimens was superior to that of the Allred scores for p53 in tumor-stromal fibroblasts in the biopsy specimens. The results indicated a close association between p53 protein expression in tumor-stromal fibroblasts, especially in surgical specimens, and both the presence of nodal metastasis and the outcome of invasive ductal carcinoma patients who received neoadjuvant therapy.

a Clinical Trials and Practice Support Division, Pathology Consultation Service, Center for Cancer Control and Information Services, National Cancer Center, Tokyo 104-0045, Japan

b Department of Breast Surgery, National Cancer Center Hospital, Tokyo 104-0045, Japan

c Division of Breast and Medical Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan

d Clinical Laboratory Division, National Cancer Center Hospital, Tokyo 104-0045, Japan

e Cancer Genomics Project, National Cancer Center Research Institute, Tokyo 104-0045, Japan

f Epidemiology and Prevention Division, Research Center for Cancer Prevention and Screening, National Cancer Center, Tokyo 104-0045, Japan

Corresponding Author InformationCorresponding author.

 This study was supported in part by a Grant-in-Aid for Scientific Research (KAKENHI) (C) (19590378, 21590393) from Japan Society for the Promotion of Science and in part by a Grant-in-Aid for Cancer Research from the Ministry of Health, Labor and Welfare (20-16) of Japan.

PII: S0046-8177(09)00284-6

doi:10.1016/j.humpath.2009.07.021


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