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Non-invasive early detection of malignant pulmonary nodules by FISH-based sputum test.
Shlomi, Dekel; Peled, Nir; Schwarz, Yehuda A; Soo Hoo, Guy W; Batra, Raj K; Fink, Gershon; Kaplan, Tal; Cohen, Lahav; Mollan, Scott; Burfeind, William R.
Afiliação
  • Shlomi D; Pulmonary Clinic, Dan Petah-Tiqwa District, Clalit Health Services, Israel. Electronic address: dekels1@zahav.net.il.
  • Peled N; The Cancer Institute, Soroka Medical Center & Ben-Gurion University, Beer-Sheva, Israel.
  • Schwarz YA; Pulmonary Institute, Tel-Aviv Sourasky Medical Center & Sackler Faculty of Medicine, Tel-Aviv, Israel.
  • Soo Hoo GW; Pulmonary and Critical Care Section, West Los Angeles VA Healthcare Center, Los Angeles, CA, USA.
  • Batra RK; Pulmonary and Critical Care Section, West Los Angeles VA Healthcare Center, Los Angeles, CA, USA.
  • Fink G; Clinical Trials Research Institute, Kaplan Medical Center, Rehovot, Israel.
  • Kaplan T; BioView Ltd, Rehovot, Israel.
  • Cohen L; BioView Ltd, Rehovot, Israel.
  • Mollan S; Biostatistics and Programming, ICON Clinical Research LLC, Durham, NC, USA.
  • Burfeind WR; Department of Surgery, St. Luke's University Health Network, Bethlehem & Temple University Medical School, PA, USA.
Cancer Genet ; 226-227: 1-10, 2018 10.
Article em En | MEDLINE | ID: mdl-30005848
BACKGROUND: Early detection decreases lung cancer mortality. The Target-FISH Lung Cancer Detection (LCD) Test is a non-invasive test designed to detect chromosomal changes (deletion or amplification) via Fluorescence in situ Hybridization (FISH) in sputum specimens from persons suspected of having lung cancer. We evaluated the performance of the LCD test in patients with highly suspicious pulmonary nodules who were scheduled for a biopsy procedure. METHODS: Induced sputum was collected from patients who were scheduled for biopsy of a solitary pulmonary nodule (0.8-3 cm) in one of 6 tertiary medical centers in the US and Israel. The lung cancer detection (LCD) Test combined sputum cytology and Target-FISH analysis on the same target cells and the results were compared to the pathology. Participants with non-surgical negative biopsy results were followed for 2 years to determine their final diagnosis. RESULTS: Of the 173 participants who were evaluated, 112 were available for analysis. Overall, the LCD test had a sensitivity of 85.5% (95% CI, 76.1-92.3), specificity of 69% (95% CI, 49.2-84.7) and an accuracy of 81.3% (95% CI, 72.8-88). The positive and negative predictive values (PPV, NPV) were 88.8% and 62.5%, respectively. The LCD test was positive in 9 of 11 lung cancer patients who had an initial negative biopsy. CONCLUSIONS: In a cohort of patients with highly suspicious lung nodules, the LCD test is a non-invasive option with good sensitivity and a high positive predictive value. A positive LCD test reinforces the need to aggressively pursue a definitive diagnosis of suspicious nodules.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Escarro / Hibridização in Situ Fluorescente / Citodiagnóstico / Detecção Precoce de Câncer / Neoplasias Pulmonares Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Escarro / Hibridização in Situ Fluorescente / Citodiagnóstico / Detecção Precoce de Câncer / Neoplasias Pulmonares Idioma: En Ano de publicação: 2018 Tipo de documento: Article