Methods in Pathology

Mod Pathol 2002;15(12):1366–1373

Tissue Micro-Array: A Cost and Time-Effective Method for Correlative Studies by Regional and National Cancer Study Groups

This research was presented in part at the 2001 Annual Meeting of the United States and Canadian Academy of Pathology, Atlanta, GA, March 2001.

Martha Milanes-Yearsley M.D.1, M Elizabeth H Hammond M.D.2, Thomas F Pajak Ph.D.3, Jay S Cooper M.D.4, Chu Chang M.D.5, Thomas Griffin M.D.6, Diana Nelson M.D.7, George Laramore M.D.8 and Milijenko Pilepich M.D.9

  1. 1Department of Pathology, Ohio State University, Columbus, Ohio
  2. 2Department of Pathology, LDS Hospital, Salt Lake City, Utah
  3. 3Radiation Therapy Oncology Group, Statistical Unit, Philadelphia, Pennsylvania
  4. 4Department of Radiation Oncology, New York University Medical Center, New York, New York
  5. 5Department of Radiation Oncology, Columbia Presbyterian Medical Center, New York, New York
  6. 6Griffin Corporation, Seattle, Washington
  7. 7Department of Radiation Oncology, Mayo Clinic, Rochester, Minnesota
  8. 8Department of Radiation Oncology, University of Washington Medical Center, Seattle, Washington
  9. 9Department of Radiation Oncology, St. Joseph Mercy Hospital, Ann Arbor, Michigan

Correspondence: M. Elizabeth H. Hammond, M.D., Department of Pathology, LDS Hospital. 8th Avenue and "C" Street, Salt Lake City, UT 84143; e-mail: ldehammo@ihc.com; fax: 801-408-5020.

Accepted 21 August 2002.

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Abstract

Tissue micro-arrays have been used for molecular and immunohistochemical studies. We sought to evaluate whether such arrays could substitute for whole sections in correlative studies performed by the Radiation Therapy Oncology Group. Four multitumor 150-sample arrays were built using formalin-fixed, paraffin-embedded, archival prostate, brain, and head/neck tumor blocks from RTOG tissue bank. p53 immunostaining of arrays and whole sections was done. Blind evaluation of each slide was made, and agreement rates between the two techniques were determined in various scenarios. Cost was also evaluated. Results demonstrate excellent agreement for p53 between slides and arrays. Agreement improved when three or four replicate arrays were used. Findings based on one to four arrays agree well with those obtained from analysis of the whole tissue samples. Minimal tissue damage, improved tissue salvage, cost reduction, ease of interpretation, and significant time savings were realized by using the arrays. Tissue micro array technique is a valuable tool for evaluation of patient materials associated with clinical trials.

Keywords:

Clinical trials, Immunohistochemistry, p53, Tissue bank, Tissue microarray

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