Wells W A, Carney P A, Eliassen M S, Tosteson A N, Greenberg E R
Department of Pathology, Dartmouth Medical School, Hanover, NH 03756, USA.
J Natl Cancer Inst. 1998 Jan 21;90(2):142-5. doi: 10.1093/jnci/90.2.142.
This study assessed the degree of diagnostic agreement among community-based general pathologists reading slides of representative breast tissue specimens and tested whether diagnostic variability is associated with type of breast specimen (e.g., core needle or excisional biopsy) or slide quality.
Twenty-six of the 44 eligible pathologists working at community-based pathology practices in New Hampshire participated. Each pathologist evaluated slides of breast tissue obtained from 30 case subjects randomly selected from a statewide breast pathology database. The diagnostic categories used were benign, benign with atypia, noninvasive malignant, and invasive malignant. The levels of agreement (i.e., kappa coefficients) for the diagnoses were assessed.
Agreement was high among pathologists for assignment of diagnostic category (kappa coefficient = 0.71) and was nearly perfect for their selection of benign versus malignant categories (kappa coefficient = 0.95). There was less agreement for the categories of noninvasive malignant and benign with atypia (kappa coefficients of 0.59 and 0.22, respectively). There was no apparent relationship between levels of diagnostic agreement and specimen type or perceived slide quality.
Diagnostic agreement for breast tissue specimens is high overall among community-based pathologists, but clinically relevant disagreements may occur in the assessment of noninvasive malignant diagnoses. The establishment of reread policies for certain diagnostic categories may reduce the possibility that diagnostic misclassification will lead to overtreatment or undertreatment. The high degree of diagnostic reproducibility for invasive cancerous lesions of the breast suggests that it is unnecessary for a central review of these lesions in national cancer trials.
本研究评估了社区普通病理学家在阅读代表性乳腺组织标本玻片时的诊断一致性程度,并测试了诊断变异性是否与乳腺标本类型(如粗针活检或切除活检)或玻片质量相关。
新罕布什尔州社区病理实践机构中44名符合条件的病理学家中有26名参与了研究。每位病理学家评估了从全州乳腺病理数据库中随机选取的30例受试者的乳腺组织玻片。使用的诊断类别为良性、非典型性良性、非侵袭性恶性和侵袭性恶性。评估了诊断的一致性水平(即kappa系数)。
病理学家在诊断类别分配上的一致性较高(kappa系数 = 0.71),在良性与恶性类别的选择上几乎达到完美(kappa系数 = 0.95)。在非侵袭性恶性和非典型性良性类别上的一致性较低(kappa系数分别为0.59和0.22)。诊断一致性水平与标本类型或感知的玻片质量之间没有明显关系。
社区病理学家对乳腺组织标本的诊断总体一致性较高,但在非侵袭性恶性诊断评估中可能会出现临床相关的分歧。为某些诊断类别制定重新阅读政策可能会降低诊断错误分类导致过度治疗或治疗不足的可能性。乳腺浸润性癌病变的高度诊断可重复性表明,在国家癌症试验中对这些病变进行中央审查是不必要的。