CELL TYPE ACCURACY OF BRONCHIAL BIOPSY SPECIMENS IN PRIMARY LUNG-CANCER

Citation
Jjs. Cataluna et al., CELL TYPE ACCURACY OF BRONCHIAL BIOPSY SPECIMENS IN PRIMARY LUNG-CANCER, Chest, 109(5), 1996, pp. 1199-1203
Citations number
23
Categorie Soggetti
Respiratory System
Journal title
ChestACNP
ISSN journal
00123692
Volume
109
Issue
5
Year of publication
1996
Pages
1199 - 1203
Database
ISI
SICI code
0012-3692(1996)109:5<1199:CTAOBB>2.0.ZU;2-F
Abstract
Study objectives: To evaluate the diagnostic accuracy of bronchial bio psy (BE) specimens in establishing the specific cell type in primary l ung cancer (LC), and to study the influence of several factors an this accuracy. Setting: Tertiary health-care center. Patients: One hundred forty-six patients with LC diagnosed by BE specimens who underwent th oracotomy (T). Measurements: We have studied the specific LC cell type observed in the BE specimen and compared it with the T specimen (refe rence diagnosis). Age, location and type of bronchial lesion, number a nd size of the biopsy fragments, tumoral size, sample necrosis, degree of cell differentiation , tumoral stage, pathologist's experience, an d the presence of other diagnostic tests with the same cell type were analyzed to assess their influence on the concordance between the two diagnoses. Results: The overall concordance between BE and T histologi c diagnosis was 0.70 (kappa coefficient [K]). Of the different histolo gic types, the worst result was obtained in large cell carcinoma (LLC) (K, 0.49). Squamous carcinoma and adenocarcinoma gave similar results (0.74 and 0.77, respectively), while small cell lung cancer (SCLC) on ly reached a value of 0.60. The degree of cell differentiation, the ab sence of necrosis, and presence of other preoperative diagnoses were t he variables that most influenced the histologic accuracy of BB specim ens. Therefore, the probability of BB accuracy was 2.7, 7.7, and 25 ti mes higher in cell-differentiated, than in poorly differentiated, mode rately differentiated, or undifferentiated carcinomas; 5.2 times highe r when there was no necrosis in the sample; and 7.43 higher when there was another preoperative diagnosis. Conclusions: The histologic resul ts of BE must be examined carefully, especially in cellular subtypes l ike LLC. The absence of differentiation and presence of necrosis in BE samples were the factors that require the greatest caution in ascerta ining the cell type. When they are involved and also in all cases in w hich identifying the specific cell type has important implications, we prefer to classify the patients as having SCLC or non-small cell lung cancer, and then reclassify them later after using a second diagnosti c technique.