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Poster Display Session (ID 63)
- Event: ELCC 2017
- Type: Poster Display Session
- Presentations: 1
- Coordinates: 5/07/2017, 12:30 - 13:00, Hall 1
38P - Flow cytometry immunophenotyping of pleural fluid cytology in patients with diffuse large B-cell lymphoma (DLBCL) and malignant pleural effusion (ID 377)
12:30 - 13:00 | Author(s): S.C. Sulfaro
Diffuse large B-cell lymphoma (DLBCL) is the most common subtype of NHL and comprises up to 35% of cases. In patients with DLBCL the clinical presentation varies widely. Malignant pleural effusion (MPE) represents a common occurrence in cancer patients with either thoracic and extra-thoracic malignancies, often requiring invasive diagnostic procedures, including video-assisted thoracoscopic surgery (VATS)-guided biopsy. Approximately 20% of patients with DLBCL may develop MPE. The aim of this study was to demonstrate the usefulness of flow cytometry phenotyping (FCP) of pleural cytology (PC) in patients with MPE due to DLBCL.
A retrospective chart review of 40 (15 (37.5%) males and 25 (62.5%) females, median age 69 tears, range 46-85 years) patients with histologically confirmed MPE was performed at a tertiary referral Medical Center. All patients underwent PC and FCP before VATS-guided biopsy. For the FCP, the FACSCanto II system and the FACSDiva software (BD Biosciences, Franklin Lakes, USA) were used. Compensation beads were obtained with single stains of each antibody to determine the compensation settings, and the settings were applied in FlowJo software (Tree Star, Ashland, USA) after data collection. Sample cells were stained with a panel of antibodies, including CD5, CD10, CD19, CD23, Kappa, Lambda, and CD45 (Dako, Glostrup, Denmark). In the presence of a T-cell population with aberrant phenotypes or a B-cell population with monotypic light chains, the diagnosis of DLBCL-related pleural effusion was made.
Final histology showed 5 (12.5%) patients with DLBCL and 35 (87.5%) with MPE from other malignancies (mainly breast cancer and lung cancer). The age (68.0±10.1 vs. 67.5±14.2 years; p = 0.94) and the male to female ratio (p = 0.64) did not differ between groups. The results are reported in the Table. The sensitivity and negative predictive value of FCP reached 100%, the specificity was the same as obtained with the PC alone, but the accuracy was superior (97.5% vs. 85%; p = 0.003).rnTable: 38PResults of flow cytometry phenotyping and pleural cytologyrn
rnrnrn Resultsrn Flow cytometry immunophenotypingrn Pleural fluid cytologyrn rnrn Sensitivityrn 100%rn 0%rn rnrn Specificityrn 97.1% (95% CI: 91.6-100)rn 97.1% (95% CI: 91.6-100)rn rnrn Negative predictive valuern 100%rn 97.2%rn rnrn Clinical accuracyrn 97.5%rn 85.0%rn rnrn Prevalencern 12.5%rn 12.5%rn rnrn False positive ratern 2.9%rn 2.9%rn rnrn False negative ratern 0%rn 14.3%rn rnrn Likelihood ratio positivern 35rn 0rn rnrnrn Likelihood ratio negativern 0rn 1.3rn
FCP of PC has great value in confirming (or excluding) the relationship between pleural effusion and malignancy, including lymphoma, exhibiting a significantly higher accuracy that that of PC alone. FCP should be performed in all patients with a history of DLBCL who exhibit suspicious MPE.
Clinical trial identification:
Legal entity responsible for the study:
Università degli Studi di Padova
Università degli Studi di Padova
All authors have declared no conflicts of interest.