Sw. Kang et al., HISTOLOGIC REGRESSION IN MALIGNANT-MELANOMA - AN INTEROBSERVER CONCORDANCE STUDY, Journal of cutaneous pathology, 20(2), 1993, pp. 126-129
Histologic evidence for regression as a prognostic indicator in melano
ma has shown conflicting results. To assess if melanoma regression is
a consistently identifiable histologic feature, an interobserver conco
rdance study was undertaken. Fifty histologic slides of melanoma with
Breslow thickness of 1 mm or less were non-randomly selected from the
Massachusetts General Hospital Melanoma Registry. The selection was in
favor of those with regression present in 44 of 50 slides (88%). Two
dermatopathologists working independently evaluated a 2 mm wide bracke
ted area in each tissue section and then the remainder of the non-brac
keted tissue section for regression. Before and after each slide revie
w, the evaluators were required to read criteria for early, intermedia
te, and late regression explicitly outlined. The overall concordance r
ate for the presence and absence of regression was 96% (48/50) in the
bracketed area and 90% for the outside area. When the group with regre
ssion was subdivided into three stages, interobserver agreement fell t
o 86% for the bracketed, and 66% for the outside area. In at least 30%
of cases where regression was detected in the bracketed area, both re
viewers observed two or more stages of regression in the remainder of
tissue section. Therefore, subdividing the process is impractical and
unrealistic. Consistent histologic identification of regression in mel
anoma requires a simple and systematic approach which should be applie
d to future studies that include melanoma regression as a prognostic f
actor.