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1.
Ann Hematol ; 90(7): 827-35, 2011 Jul.
Article in English | MEDLINE | ID: mdl-21212952

ABSTRACT

An independent clinical assessment was compared with flow cytometry (FCM) and cytomorphology results obtained on 227 cerebrospinal fluids investigated for hematologic malignancy, in a retrospective longitudinal study with a median observation time of 11 months. A combined method assessment (CMA), defining "positive" a sample if at least one method gave "positive" results, was also tested. Eleven out of 55 screening samples and 53 out of 166 follow-up samples resulted positive at clinical evaluation. FCM and CM were concordant with positive clinical assessment in 68.5% and 51.5% of cases, respectively. According to CMA, 10.5% of samples (resulting false negative by either FCM or cytomorphology) were rescued as true positive. FCM retained significantly higher accuracy than cytomorphology (p=0.0065) and 100% sensitivity when at least 220 leukocytes were acquired. CMA accuracy was higher than FCM accuracy and significantly higher than cytomorphology accuracy in the analysis of all samples (p<0.0001), samples from mature B/T cell neoplasms (p=0.0021), and samples drawn after intrathecal treatment (p=0.0001). When acquiring ≤220 leukocytes, FCM accuracy was poor, and combining cytomorphology added statistically significant diagnostic advantage (p=0.0043). Although FCM is the best diagnostic tool for evaluating CSF, morphology seems helpful especially when clinically positive follow-up samples are nearly acellular.


Subject(s)
Cerebrospinal Fluid/cytology , Cytodiagnosis/methods , Flow Cytometry/methods , Hematologic Neoplasms/cerebrospinal fluid , Hematologic Neoplasms/diagnosis , Hematologic Neoplasms/pathology , Cytodiagnosis/standards , Female , Flow Cytometry/standards , Humans , Immunophenotyping , Male , Retrospective Studies , Sensitivity and Specificity , Treatment Outcome
2.
Leuk Res ; 34(8): 1027-34, 2010 Aug.
Article in English | MEDLINE | ID: mdl-20206995

ABSTRACT

Flow cytometry and cytomorphology results on 92 body cavity fluids [61 effusions and 31 bronchoalveolar lavage fluids (BALF)] from hematologic malignancy were compared with retrospective clinical outcome. We observed double true positive/negative results in 67 cases (73%), and double false negative results in 2 cases (2%). Immunophenotyping accounted for true positive/negative results in 22 out of 23 mismatched cases (25%), and retained significantly higher accuracy than that of cytomorphology especially in effusions and differentiated lymphoma. In BALF analysis, immunophenotyping and cytomorphology sensitivity was 75% and 0%, respectively. Flow cytometry retains the highest accuracy in detecting neoplastic cells in body cavity fluids.


Subject(s)
Biomarkers, Tumor , Body Fluids , Flow Cytometry , Hematologic Neoplasms/diagnosis , Immunophenotyping , Aged , Bronchoalveolar Lavage Fluid/chemistry , Cell Count , False Positive Reactions , Female , Humans , Longitudinal Studies , Male , Middle Aged , Prognosis , Retrospective Studies
3.
Leuk Res ; 32(11): 1715-23, 2008 Nov.
Article in English | MEDLINE | ID: mdl-18456323

ABSTRACT

We studied circulating (C)CD34(+) cells by flow cytometry in 96 patients with myelodysplastic syndromes (MDS) at diagnosis, and in a subset of 35 cases during follow-up. CCD34(+) counts were stratified within both International Prognostic Scoring System (IPSS) and World Health Organization (WHO) categories. Counts >10/microl were associated with poorer leukemia-free survival, a prognostic value for evolution independent from that of WHO, and a higher progression probability within intermediate-risk IPSS and WHO classes. When serial measurements were performed, counts >10/microl more frequently correlated to evolution. Separating newly diagnosed patients on the basis of 10/microl cut-off of circulating CD34(+) cells retains prognostic utility, especially in intermediate-risk MDS.


Subject(s)
Antigens, CD34/blood , Myelodysplastic Syndromes/blood , Aged , Female , Flow Cytometry , Follow-Up Studies , Humans , Immunophenotyping , Karyotyping , Male , Neoplasm Staging , Prognosis , Retrospective Studies , Risk Factors , Survival Rate
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