Serum thymidine kinase 1 concentration in Chinese patients with chronic lymphocytic leukemia and its correlation with other prognostic factors

2009 ◽  
Vol 90 (2) ◽  
pp. 205-211 ◽  
Author(s):  
Wei Xu ◽  
Xin Cao ◽  
Kou-Rong Miao ◽  
Chun Qiao ◽  
Yu-Jie Wu ◽  
...  
2010 ◽  
Vol 134 (3) ◽  
pp. 472-477 ◽  
Author(s):  
Sergej N. Konoplev ◽  
Herbert A. Fritsche ◽  
Susan O’Brien ◽  
William G. Wierda ◽  
Michael J. Keating ◽  
...  

Blood ◽  
2008 ◽  
Vol 112 (11) ◽  
pp. 4189-4189
Author(s):  
Jianyong Li ◽  
Wei Xu ◽  
Hui Yu ◽  
Hongxia Qiu ◽  
Chun Qiao ◽  
...  

Abstract Objective To investigate serum thymidine kinase (TK) level in Chineses patients with chronic lymphocytic leukemia (CLL) and its correlation with other prognostic factors, including Binet stages, absolute lymphocyte count (ALC), lactate dehydrogenase (LDH), immunoglobulin heavy-chain variable region (IgVH) gene mutation status, ZAP-70 protein and CD38 expression level, and cytogenetic aberrations. Methods Serum TK1 level in 39 CLL patients was detected by TK monoclonal antibody (Anti-TK mAb) and enhanced chemiluminecence (ECL). IgVH mutation status was detected by multiplex PCR and sequencing of purified PCR amplification products. A panel of monoclonal antibodies and multiparametic flow cytometry were employed to immunophenotype and determine the expression of ZAP-70 protein and CD38. A panel of probes and interphase fluorescence in stu hybridization (FISH) were used to detect cytogenetic aberrations including 6q-, 11q-, +12, 13q-,17p- and IgH translocation. Results The level of TK1 was higher in CLL patients that in normal control (P<0.05). TK1 level was not signifigantly correlated with sex, age, Binet stages, CD38, and cytogenetic aberrations. Patients with higher level of ALC, LDH, ZAP-70 and unmutated IgVH genes had higher levels of TK1 than those with lower level of ALC, LDH, ZAP-70 and mutated IgVH genes (P=0.018, P=0.018, P=0.038 and P=0.030, respectively). Conclusions Serum TK1 level significantly correlates with ALC, LDH, ZAP-70 and IgVH mutational status, and could be a predictive marker of IgVH mutation status. Serum TK1 might be applied for the assessment of prognosis in Chinese patients with CLL.


Blood ◽  
2008 ◽  
Vol 112 (11) ◽  
pp. 4183-4183
Author(s):  
Wei Xu ◽  
Jianyong Li ◽  
Xin Cao ◽  
DAN-Xia Zhu ◽  
Lin Yao ◽  
...  

Abstract Chronic lymphocytic leukemia (CLL) is the most common type of adult leukemias in the Western countries, however, infrequent in the Eastern. Autoimmune hemolytic anemia (AHA) is a complication in chronic lymphocytic leukemia (CLL). The direct antiglobulin test (DAT) may be positive at some time during the disease course in up to 35% of cases, but overt AHA occurs less frequently. The aim of the study was to explore the prognostic impact of positive DAT in Chinese patients with CLL and its correlation with other prognostic factors, including Binet stages, lymphocyte count in peripheral blood, lactate dehydrogenase (LDH), β2-microglobulin (β2-MG), IgVH mutation status, ZAP-70, CD38 and cytogenetic abnormalities. Out of the 80 Chinese patients with CLL, positive DAT was found in 21 (30.6%) cases. The incidence of positive was 12.5% in Binet A, 23.8% and 44.4% in Binet B and C, respectively. The incidence of positive DAT was significantly increased at Binet C, compared with Binet A (P=0.006), and the presence of higher LDH and β2-MG levels correlated strongly with positive DAT (P=0.006 and P=0.004, respectively). Patients with unmutated IgVH genes had higher incidence of positive DAT than did patients with IgVH mutations (P=0.042), and positive DAT was also associated with higher level of ZAP-70 and CD38 (P=0.004 and P<0.001, respectively). We also analyzed positive DAT in different cytogenetic subgroups. Higher incidence of positive DAT was found in patients with unfavorable cytogenetic aberrations (deletion in 17p13 or 11q22) in contrast to lower level in good risk cytogenetics (deletion in 13q as the sole abnormality) (P = 0.002). Positive DAT was associated with poor outcome. Survival analysis showed that the patients with positive DAT had significantly shorter OS (mean, 106.3 months) (95% CI, 74.7 to 137.8 months) than the patients negative DAT (mean, 151.5 months) (95% CI, 122.3 to 180.6 months) (P=0.024). Patients treated with fludarabine were not likely to remain DAT positive and to change from negative to positive (P=0.209). In conclusion, DAT status provides a new prognostic indicator and correlates with other clinical or laboratory prognostic factors, and might be applied for the assessment of prognosis in patients with CLL.


Blood ◽  
2009 ◽  
Vol 114 (22) ◽  
pp. 4387-4387
Author(s):  
Jianyong Li ◽  
Wei Xu ◽  
Chun Qiao ◽  
Yu-Jie Wu ◽  
Kourong Miao ◽  
...  

Abstract Abstract 4387 Chronic lymphocytic leukemia (CLL) is one of the most common lymphoid malignancies in the Western countries, however, infrequent in Asian populations. Although the median survival is around 10 years, CLL is a disease with an extremely variable clinical course with overall survival times ranging from months to decades; some patients never need treatment, while others require intensive treatment early after diagnosis. Some factors, such as clinical stages, IGHV mutational status, cytogenetic abnormalities, ZAP-70, and the expression of CD38 in leukaemic cells, were strong indicator of prognosis in CLL. However, the prognostic factors of Chinese patients with CLL compared with the Western countries have not yet been clarified. The aim of this study was to explore the influence of factors on the prognosis of Chinese patients with CLL. One hundred and twenty-nine patients with CLL were enrolled in this study. Multiplex PCR and sequencing, fluorescence in situ hybridization (FISH), and flow cytometry were used to detect IGHV mutational status, cytogenetic abnormalities, and the expression of ZAP-70 and CD38, respectively. A panel of FISH probes included 13q14 (D13S319), 17p13 (p53 gene), 11q23 (ATM gene), 6q23(MYB gene), the centromere of chromosome 12 (D12Z3) and 14q32 (IGHC/IGHV). In 129 CLL patients, according to the Binet clinical staging system, 65 (50.4 %) patients were in Binet A, 28 (21.7 %) in Binet B and 36 (27.9 %) in Binet C. Eighty-four (65.1%) patients had mutated IGHV, and 45 (34.9%) had unmutated IGHV. The most frequently expressed VH gene family was found to be VH3 (50.4%) followed by VH4 (32.6%), VH1 (10.9%), VH2 (2.3%), VH5(2.3%) and VH7 (1.6%), with no expression of VH6 gene families. VH1-69 and VH3-21 which commonly overused in Western CLL patients were very low in our cohort (0.8% and 3.1%, respectively). Molecular cytogenetic aberrations were found in 94 patients (72.9%) and 36 patients (27.9%) with more than two abnormalities. The most frequent abnormalities detected in our patients was del(13q14), with an incidence of 53.0%, followed by 14q32 translocation of 20.2%, +12 of 18.3%, del(11q23) of 10.8%, del(17p13) of 10.o%, and del(6q23) of 6.1%. Forty-one patients (31.8%) were positive for ZAP-70 (≥20%), and 51 patients (39.5%) were positive for CD38 (≥30%). With a median follow-up of 32 months (range, 4-58 months), eight patients (6.2%) died (CLL-related deaths). In univariate analysis for survival, advanced Binet stage (P=0.023), unmutated IGHV status (P=0.002), deletions of 17p13 or 11q23 (P=0.003), high expression of ZAP-70 (P=0.034), and high expression of CD38 (P=0.046) were poor prognostic factors. The prognostic factors with statistical significance were further used in a two-variables Cox analysis, which comparing unmutated IGHV status to other prognostic factors individually to show prognostic independence. The unmutated IGHV status were the independent prognostic factors and strongly associated with OS. This study demonstrates that the frequencies of IGHV gene families indicated significant difference in Chinese CLL patients compared with Western patients, suggesting involvement of ethnic and/or environmental factors in CLL disease initiation. The unmutated IGHV status, Binet clinical stages, Chromosomal aberrations of del(17p13) and del(11q23), high expression of ZAP-70 and CD38 have been shown highly predictive prognostic value for Chinese patients with CLL. Disclosures: No relevant conflicts of interest to declare.


2020 ◽  
pp. 28-34
Author(s):  
D. V. Kravchenko ◽  
V. N. Martinkov ◽  
J. N. Pugacheva ◽  
Y. I. Yarets ◽  
A. E. Silin ◽  
...  

Objective: to determine a complex of the most significant prognostic factors in chronic lymphocytic leukemia (CLL) for the purpose of evaluation of the probability of the disease progression. Material and methods. The study included 127 CLL patients whose clinical and laboratory parameters (sizes of the lymph nodes, liver and spleen, general and biochemical blood tests, β2-microglobulin, thymidine kinase, tissue polypeptide antigen (TPA), immunophenotypic markers) had been evaluated at the setting of the diagnosis. As a result of a dynamic followup, the patients were divided into 2 groups: 71 patients who had been observed in the outpatient setting and had had no signs of CLL progression within 3 years of the followup (group 1), and 56 patients with clinical signs of the disease progression that had manifested themselves after 3 years of the followup (group 2). Results. The study has revealed statistically considerable differences (Mann-Whitney test) between the groups in the size of the lymph nodes, liver and spleen, in the Binet stages, leukocyte count, absolute values of lymphocytes, the counts of red blood cells, hemoglobin and platelets, as well as the levels of β2-microglobulin, thymidine kinase, TPA, and immunophenotypic markers of CD24, ZAP-70, and CD38 in the blood, which indicates the interconnection of the levels of these parameters at the setting of the diagnosis with subsequent rapid CLL progression. According to the results of the use of logistic regression and Cox regression analysis, 10 parameters showing the strongest interconnection between the progression and 3-year progression free survival (PFS) have been selected. The use of the step-by-step selection of variables has made it possible to formulate a qualitative Cox regression equation including 5 main parameters: β2-microglobulin, thymidine kinase, TPA, ZAP-70, and CD38, which is indicative of the possibility to use this combination of the markers to predict CLL progression. Conclusion: The prognostic value of the complex of the laboratory parameters (β2-microglobulin, thymidine kinase, TPA, ZAP-70, and CD38) has been determined to assess the probability of CLL progression at the setting of the diagnosis, which can be used for the determination of the management tactics and selection of the treatment scheme for these patients.


2007 ◽  
Vol 148 (16) ◽  
pp. 737-743
Author(s):  
Béla Kajtár ◽  
Pál Jáksó ◽  
László Kereskai ◽  
Ágnes Lacza ◽  
Gábor Méhes ◽  
...  

Bevezetés: Az utóbbi években felfedezett számos új prognosztikai faktor segítséget nyújthat a várható túlélés meghatározásához krónikus lymphocytás leukémia esetében. Célok: Jelen tanulmány célja e prognosztikai faktorok gyakoriságának, valamint egymással való összefüggésének meghatározása volt 419 beteg mintáin. Módszerek: 160 esetben végezték el az immunglobulin-nehézláncgén mutációs vizsgálatát. Eredmények: Az esetek 62%-ában nem mutált immunglobulin gént találtak, a nehézlánc géncsaládok használata különbözött a mutációs státusz függvényében. A CD38 expresszió 78%-os konkordanciát mutatott a mutációs státusszal, a ZAP-70-expresszió tekintetében korrelációt nem figyeltek meg. Citogenetikai abnormalitást 76%-ban láttak, a leggyakoribb eltérések a del(13q) (57%), a 12-es triszómia (15%), a del(11q) (12%) és a del(17p) (6%) voltak. A del(11q)-t hordozó esetek 95%-a nem mutált, az egyedül del(13q)-t hordozó esetek 74%-a mutált IgH-gént tartalmazott. Következtetések: A vizsgált paraméterek nem függetlenek egymástól, ezért alkalmazásuk a klinikai gyakorlatban gondos tervezést igényel.


ESMO Open ◽  
2021 ◽  
Vol 6 (2) ◽  
pp. 100076
Author(s):  
A. Matikas ◽  
K. Wang ◽  
E. Lagoudaki ◽  
B. Acs ◽  
I. Zerdes ◽  
...  

2009 ◽  
Vol 38 (2) ◽  
pp. 123-130 ◽  
Author(s):  
Amos Pines ◽  
Isaac Ben-Bassat ◽  
Michaela Modan ◽  
Tzvia Blumstein ◽  
Bracha Ramot

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