Karyotype evolution on fluorescent in situ hybridization analysis is associated with short survival in patients with chronic lymphocytic leukemia and is related to CD49d expression - PubMed (original) (raw)
Karyotype evolution on fluorescent in situ hybridization analysis is associated with short survival in patients with chronic lymphocytic leukemia and is related to CD49d expression
Tait D Shanafelt et al. J Clin Oncol. 2008.
No abstract available
Conflict of interest statement
AUTHORS’ DISCLOSURES OF POTENTIAL CONFLICTS OF INTEREST
The author(s) indicated no potential conflicts of interest.
Figures
Fig 1
Karyotype evolution and survival. (A) Overall survival from date of repeat fluorescent in situ hybridization (FISH) analysis based on whether or not patients had clonal evolution (n = 63). (B) Overall survival from date of clonal evolution based on the type of cytogenetic defect acquired (n = 17).
Fig 2
Stability and reproducibility of CD49d evaluated by flow cytometry. (A) Comparison of CD49d expression on chronic lymphocytic leukemia peripheral blood samples tested as either fresh samples or on thawing after storage at −80°C (n = 14). The intraclass correlation coefficient between the two assays was 0.983 (95% CI, 0.948 to 0.995). (B) Expression of CD49d over time on sequential samples from patients (n = 32) who had samples at multiple time points over a 3-month to 4-year interval. The intraclass correlation coefficient between the two assays was 0.952 (95% CI, 0.908 to 0.976). Dotted horizontal line represents the 45% threshold used to separate patients expressing and not expressing CD49d. One (3%) of 32 patients had a change in CD49d classification over time. (C) Comparison of a two-color (CD19, CD49d) verses three-color (CD19, CD5, CD49d) flow cytometry strategy for evaluating CD49d. (○) Fresh specimens (n = 35); (+) frozen specimens (n = 34). The solid line represents the x = y line (ie, for values on this line, two-color and three-color results are the same). Dotted lines indicate a 5% difference between x and y values. The two assays yielded nearly identical results in all cases, with an intraclass correlation coefficient of 0.999 (95% CI, 0.999 to 1.000) for comparisons on both fresh and frozen samples.
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