論文

査読有り 国際誌
2012年2月

New criteria for histologic grading of colorectal cancer.

The American journal of surgical pathology
  • Hideki Ueno
  • Yoshiki Kajiwara
  • Hideyuki Shimazaki
  • Eiji Shinto
  • Yojiro Hashiguchi
  • Kuniaki Nakanishi
  • Kazunari Maekawa
  • Yuka Katsurada
  • Takahiro Nakamura
  • Hidetaka Mochizuki
  • Junji Yamamoto
  • Kazuo Hase
  • 全て表示

36
2
開始ページ
193
終了ページ
201
記述言語
英語
掲載種別
研究論文(学術雑誌)
DOI
10.1097/PAS.0b013e318235edee
出版者・発行元
LIPPINCOTT WILLIAMS & WILKINS

Conventional tumor grading systems based on the degree of tumor differentiation may not always be optimal because of difficulty in objective assessment and insufficient prognostic value for decision making in colorectal cancer (CRC) treatment. This study aimed to determine the importance of assessing the number of poorly differentiated clusters as the primary criterion for histologic grading of CRC. Five hundred consecutive patients with curatively resected stage II and III CRCs (2000 to 2005) were pathologically reviewed. Cancer clusters of ≥5 cancer cells and lacking a gland-like structure were counted under a ×20 objective lens in a field containing the highest number of clusters. Tumors with <5, 5 to 9, and ≥10 clusters were classified as grade (G)1, G2, and G3, respectively (n=156, 198, and 146 tumors, respectively). Five-year disease-free survival rates were 96%, 85%, and 59% for G1, G2, and G3, respectively (P<0.0001). Poorly differentiated clusters affected survival outcome independent of T and N stages and could help in more effective stratification of patients by survival outcome compared with tumor staging (Akaike information criterion, 1086.7 vs. 1117.0; Harrell concordance index, 0.73 vs. 0.67). The poorly differentiated cluster-based grading system showed a higher weighted κ coefficient for interobserver variability (5 observers) compared with conventional grading systems (mean, 0.66 vs. 0.52; range, 0.55 to 0.73 vs. 0.39 to 0.68). Our novel histologic grading system is expected to be less subjective and more informative for prognostic prediction compared with conventional tumor grading systems and TNM staging. It could be valuable in determining individualized postoperative CRC treatment.

リンク情報
DOI
https://doi.org/10.1097/PAS.0b013e318235edee
PubMed
https://www.ncbi.nlm.nih.gov/pubmed/22251938
Web of Science
https://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=JSTA_CEL&SrcApp=J_Gate_JST&DestLinkType=FullRecord&KeyUT=WOS:000299316800004&DestApp=WOS_CPL
ID情報
  • DOI : 10.1097/PAS.0b013e318235edee
  • ISSN : 0147-5185
  • PubMed ID : 22251938
  • Web of Science ID : WOS:000299316800004

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