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Natural history of colorectal carcinoma: Can the tumor volume doubling time be predicted by radiologic findings or immunohistochemical variables?
Author(s) -
Iwashita Ikuko,
Ueyama Toshihiko,
Iwashita Akinori,
Kawamoto Kenji,
Kitagawa Shinji,
Motooka Makoto,
Utsunomiya Takashi,
Masuda Kouji
Publication year - 1998
Publication title -
journal of surgical oncology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.201
H-Index - 111
eISSN - 1096-9098
pISSN - 0022-4790
DOI - 10.1002/(sici)1096-9098(199808)68:4<215::aid-jso3>3.0.co;2-7
Subject(s) - immunohistochemistry , doubling time , medicine , colorectal cancer , carcinoma , proliferating cell nuclear antigen , pathology , oncology , cell , cancer , biology , genetics
Abstract Background and Objectives: The factors influencing the growth rate of colorectal carcinoma have not been determined. The aim of this study was to clarify the relationship between the doubling time (DT), morphology, and proliferating cell nuclear antigen, Ki‐67 and p53 immunohistochemistry in colorectal carcinoma. Methods Thirty‐three patients (37 lesions) were studied retrospectively. The DT was calculated and correlated with the initial and final tumor size, morphologic shape, and immunohistochemical results. Results The DT ranged from 2.4 to 48.0 months (mean: 12.0 months). The mean DT of the early‐stage carcinomas was significantly longer than that of the advanced carcinomas. In the latter group, both slowly growing and rapidly growing tumors were observed. The DT showed no correlation with the initial or final size and shape of the tumors on radiographs, or with the immunohistochemical results. Conclusions Our data revealed that it is not possible to evaluate the growth rate of colorectal carcinomas based on their morphological shape, cellular proliferative activity, or tumor suppressor gene activity. J. Surg. Oncol. 68:215–224, 1998 . © 1998 Wiley‐Liss, Inc.