Javascript must be enabled to continue!
A Link Between Hypercholesterolemia and Chronic Lymphocytic Leukemia
View through CrossRef
Abstract
Background
Dyslipidemia and metabolic syndrome are risk factors for cancer, and clinically aggressive CLL cells are believed to rely on lipid metabolism. Statins promote apoptosis and inhibit CLL cell growth in pre-clinical models, and statin use during salvage therapy for CLL may confer a survival advantage.
Methods
To investigate the prevalence of hyperlipidemia and the effect of statin therapy, lipid profiling was performed on 238 consecutive patients presenting to a specialized CLL clinic between January 2012 and February 2014. Demographics, timing of diagnosis and initiation of chemoimmunotherapy was ascertained from clinical records. Prognostic information was obtained from pathology or flow cytometeric reports. The first lipid profile following CLL diagnosis was recorded. RAI stage was determined from blood counts and radiology or clinical examination at the time of lipid profiling. Patients were grouped according to statin therapy (yes/no) and hyperlipidemia.
Results
Of 281 patients reviewed, 238 were evaluable with a lipid profile. 110 patients (46.2%) were either taking statins at the time of their CLL diagnosis (27.3%) or prescribed a statin during the study period (18.5%) and an additional 11 (4.2%) had a diagnosis of dyslipidemia not on therapy. Of the remaining 117 patients, 18 had LDL ³ 3.5mmol/L, giving a total of 139 patients (58.4%) with abnormal lipid profiles. The statin-exposed group was significantly older (median age 69.5 vs 65, p=0.03) and there were a larger proportion of males (68.6% vs. 53.9%, p=0.02). There were no significant differences in RAI staging, cytogenetics, beta-2-microglobulin levels, or CD38 expression between groups. (Table 1)
59.7% of all patients were treatment-free by the end of the study period and there were no differences between statin/no-statin groups. Of those requiring treatment, median time to first treatment (TFT) was 48 (IQR, 24-85.3) months. TFT was significantly longer with statins (57.5 (IQR, 32-77) vs. 36 (IQR, 11-100) months, p<0.02. Initiation of statins following diagnosis of CLL was associated with further prolongation of TFT compared to those on statins at diagnosis (74 (IQR, 62-96) vs. 45 (IQR, 30-64) months, p<0.02). Two cases of spontaneous remission were noted with statin initiation. (Figure 1)
Conclusions
There is an increased prevalence of hyperlipidemia in CLL patients (58.4%) compared to the general population (35-39%). Statin therapy is associated with a prolonged TFT despite a significantly older population and a higher proportion of male patients in this group. CLL patients should be screened for hyperlipidemia and statin therapy may be an adjunct to CLL treatment.
Patient Characteristics by Lipid Abnormalities Abstract 5630. Table 1.Time to First Treatment (TFT) by Statin UseTotal N (%)No statin N (%)Statin Use/Dyslipidemia N (%)p -valueTotal238117121Male146 (61.3)63 (53.9)83 (68.6)0.02Median age (Q1, Q3)67 (60, 74)65 (58, 73)69 (63, 76)0.01RAI Stage0.64N1178 (74.8%)78 (66.7%)99 (81.8%)MBL73407135361341618232102232081241477Lipid profile (Mean ± Std Dev)HDL (mM)1.23 ± 0.471.33 ± 0.491.14 ± 0.420.001LDL (mM)2.55 ± 1.032.69 ± 0.872.42 ± 1.160.05TC/HDL3.92 ± 1.433.80 ± 1.254.03 ± 1.570.21Non HDL-C (mM)3.22 ± 1.143.29 ± 0.993.14 ± 1.270.29B2M (N = 0.6-2.3 m g/ml)0.52Mean ± Std Dev3.20 ± 2.143.19 ± 2.363.21 ± 1.92CD38 status0.86Unknown74 (31.1%)37 (31.6%)37 (30.6%)CD38+331419CD38-1226260Partial945Cytogenetics20.32Unknown125 (52.5%)61 (52.1%)63 (52.1%)13q-62283511q-1367+122081217p-1275normal24159>1 abnormality201010
1stage determined from those untreated at time of lipid profiling
2counted in all pertinent groups if more than one abnormality
Abstract 5630. Table 2. Time to First Treatment (TFT) by Statin Initiation Total (N=238) No statin (N=128) Statin Use (N=110) P-value W&W1 (%) 142 (59.7) 74 (58.8) 68 (61.8) 0.53 Available TFT data/Total Treated2 89/96 51/54 38/42 Median TFT (IQR) (mo) 48 (24, 83) 36 (11, 100) 57.5 (32, 77) 0.02
1watch & wait
2could not determine TFT for some patients.
Abstract 5630. Table 3. No statin (N=128) Statin Started (N=43) Statin Previous (N=67) P-value W&W1 (%) 74 (58.8) 29 (67.4) 39 (58.2) 0.55 Available TFT data/Total Treated2 51/54 13/14 25/28 Median TFT (IQR) (mo) 36 (11, 100) 74 (62, 96) 45 (30, 64) 0.04
1watch & wait
2could not determine TFT for some
Figure 1 Figure 1.
[1]Spaner DE, Lee E, Shi Y, Wen F, Li Y et al. Leukemia 2013; 27:1090-1099.
[2]Chae YK, Trinh L, Jain P, Wang X, Rozovski U et al. Blood 2014; 123: 1424-1426.
Disclosures
No relevant conflicts of interest to declare.
Title: A Link Between Hypercholesterolemia and Chronic Lymphocytic Leukemia
Description:
Abstract
Background
Dyslipidemia and metabolic syndrome are risk factors for cancer, and clinically aggressive CLL cells are believed to rely on lipid metabolism.
Statins promote apoptosis and inhibit CLL cell growth in pre-clinical models, and statin use during salvage therapy for CLL may confer a survival advantage.
Methods
To investigate the prevalence of hyperlipidemia and the effect of statin therapy, lipid profiling was performed on 238 consecutive patients presenting to a specialized CLL clinic between January 2012 and February 2014.
Demographics, timing of diagnosis and initiation of chemoimmunotherapy was ascertained from clinical records.
Prognostic information was obtained from pathology or flow cytometeric reports.
The first lipid profile following CLL diagnosis was recorded.
RAI stage was determined from blood counts and radiology or clinical examination at the time of lipid profiling.
Patients were grouped according to statin therapy (yes/no) and hyperlipidemia.
Results
Of 281 patients reviewed, 238 were evaluable with a lipid profile.
110 patients (46.
2%) were either taking statins at the time of their CLL diagnosis (27.
3%) or prescribed a statin during the study period (18.
5%) and an additional 11 (4.
2%) had a diagnosis of dyslipidemia not on therapy.
Of the remaining 117 patients, 18 had LDL ³ 3.
5mmol/L, giving a total of 139 patients (58.
4%) with abnormal lipid profiles.
The statin-exposed group was significantly older (median age 69.
5 vs 65, p=0.
03) and there were a larger proportion of males (68.
6% vs.
53.
9%, p=0.
02).
There were no significant differences in RAI staging, cytogenetics, beta-2-microglobulin levels, or CD38 expression between groups.
(Table 1)
59.
7% of all patients were treatment-free by the end of the study period and there were no differences between statin/no-statin groups.
Of those requiring treatment, median time to first treatment (TFT) was 48 (IQR, 24-85.
3) months.
TFT was significantly longer with statins (57.
5 (IQR, 32-77) vs.
36 (IQR, 11-100) months, p<0.
02.
Initiation of statins following diagnosis of CLL was associated with further prolongation of TFT compared to those on statins at diagnosis (74 (IQR, 62-96) vs.
45 (IQR, 30-64) months, p<0.
02).
Two cases of spontaneous remission were noted with statin initiation.
(Figure 1)
Conclusions
There is an increased prevalence of hyperlipidemia in CLL patients (58.
4%) compared to the general population (35-39%).
Statin therapy is associated with a prolonged TFT despite a significantly older population and a higher proportion of male patients in this group.
CLL patients should be screened for hyperlipidemia and statin therapy may be an adjunct to CLL treatment.
Patient Characteristics by Lipid Abnormalities Abstract 5630.
Table 1.
Time to First Treatment (TFT) by Statin UseTotal N (%)No statin N (%)Statin Use/Dyslipidemia N (%)p -valueTotal238117121Male146 (61.
3)63 (53.
9)83 (68.
6)0.
02Median age (Q1, Q3)67 (60, 74)65 (58, 73)69 (63, 76)0.
01RAI Stage0.
64N1178 (74.
8%)78 (66.
7%)99 (81.
8%)MBL73407135361341618232102232081241477Lipid profile (Mean ± Std Dev)HDL (mM)1.
23 ± 0.
471.
33 ± 0.
491.
14 ± 0.
420.
001LDL (mM)2.
55 ± 1.
032.
69 ± 0.
872.
42 ± 1.
160.
05TC/HDL3.
92 ± 1.
433.
80 ± 1.
254.
03 ± 1.
570.
21Non HDL-C (mM)3.
22 ± 1.
143.
29 ± 0.
993.
14 ± 1.
270.
29B2M (N = 0.
6-2.
3 m g/ml)0.
52Mean ± Std Dev3.
20 ± 2.
143.
19 ± 2.
363.
21 ± 1.
92CD38 status0.
86Unknown74 (31.
1%)37 (31.
6%)37 (30.
6%)CD38+331419CD38-1226260Partial945Cytogenetics20.
32Unknown125 (52.
5%)61 (52.
1%)63 (52.
1%)13q-62283511q-1367+122081217p-1275normal24159>1 abnormality201010
1stage determined from those untreated at time of lipid profiling
2counted in all pertinent groups if more than one abnormality
Abstract 5630.
Table 2.
Time to First Treatment (TFT) by Statin Initiation Total (N=238) No statin (N=128) Statin Use (N=110) P-value W&W1 (%) 142 (59.
7) 74 (58.
8) 68 (61.
8) 0.
53 Available TFT data/Total Treated2 89/96 51/54 38/42 Median TFT (IQR) (mo) 48 (24, 83) 36 (11, 100) 57.
5 (32, 77) 0.
02
1watch & wait
2could not determine TFT for some patients.
Abstract 5630.
Table 3.
No statin (N=128) Statin Started (N=43) Statin Previous (N=67) P-value W&W1 (%) 74 (58.
8) 29 (67.
4) 39 (58.
2) 0.
55 Available TFT data/Total Treated2 51/54 13/14 25/28 Median TFT (IQR) (mo) 36 (11, 100) 74 (62, 96) 45 (30, 64) 0.
04
1watch & wait
2could not determine TFT for some
Figure 1 Figure 1.
[1]Spaner DE, Lee E, Shi Y, Wen F, Li Y et al.
Leukemia 2013; 27:1090-1099.
[2]Chae YK, Trinh L, Jain P, Wang X, Rozovski U et al.
Blood 2014; 123: 1424-1426.
Disclosures
No relevant conflicts of interest to declare.
Related Results
Are Cervical Ribs Indicators of Childhood Cancer? A Narrative Review
Are Cervical Ribs Indicators of Childhood Cancer? A Narrative Review
Abstract
A cervical rib (CR), also known as a supernumerary or extra rib, is an additional rib that forms above the first rib, resulting from the overgrowth of the transverse proce...
Myosin-IIa Is Required for Leukemia Cell Extravasation and Its Inhibition Reduces Leukemia Dissemination and Prolongs Survival in a Mouse Model of Acute Lymphoblastic Leukemia
Myosin-IIa Is Required for Leukemia Cell Extravasation and Its Inhibition Reduces Leukemia Dissemination and Prolongs Survival in a Mouse Model of Acute Lymphoblastic Leukemia
Abstract
Background: Leukemia affects approximately 45,000 people each year in the USA with more than 20,000 fatalities. Many leukemia patients experience initial re...
STAT3 Mutations in Large Granular Lymphocytic Leukemia
STAT3 Mutations in Large Granular Lymphocytic Leukemia
Abstract
Abstract 1606
Introduction:
Large granular lymphocytic leukemia (LGL leukemia) is a rare lymphoprolifera...
ROR1 Expression Accelerates Leukemia Development in RORxTCL1 Transgenic Mice,
ROR1 Expression Accelerates Leukemia Development in RORxTCL1 Transgenic Mice,
Abstract
Abstract 3905
ROR1 is a receptor tyrosine kinase-like orphan receptor and an oncofetal protein that is expressed on chronic lymphocytic leuke...
/r/philosophy 2016-2017 AMA Series Recap + Survey!
/r/philosophy 2016-2017 AMA Series Recap + Survey!
This past academic year the moderators of /r/philosophy organised an
ongoing AMA series with 18 different philosophers working on a variety
of different topics, from metaphysics to...
Nature Products Enhance NKG2D Ligands Expression of CD123+CD34+CD38− Leukemia Stem Cells for Stimulating Cytotoxicity of NKG2D+ Cells to Themselves
Nature Products Enhance NKG2D Ligands Expression of CD123+CD34+CD38− Leukemia Stem Cells for Stimulating Cytotoxicity of NKG2D+ Cells to Themselves
Abstract
CD123+CD34+CD38− leukemia cells regarded as leukemia stem cells, not only refractory to chemotherapeutics but also resistant to immune response such as cyto...
Aktivitas Makrofag Meningkat Pada Aorta Tikus Hiperkolesterolemia
Aktivitas Makrofag Meningkat Pada Aorta Tikus Hiperkolesterolemia
Aterosklerosis merupakan, kondisi inflamasi kronik, faktor resiko penyakit kardiovaskular disebabkan oleh tingginya kadar kolesterol. Tujuan penelitian ini mengevaluasi peran mielo...
Abstract 132: African polyherbal formulation alleviates benzene-induced leukemia in Wistar rats
Abstract 132: African polyherbal formulation alleviates benzene-induced leukemia in Wistar rats
Abstract
Background: Chemotherapy and radiotherapy are effective cancer treatment options but they are accompanied by serious side effects. Therefore, more effective...

