scholarly journals Leukemia Cutis As an Early Presentation or Relapsing Manifestation of Chronic Lymphocytic Leukemia

Blood ◽  
2019 ◽  
Vol 134 (Supplement_1) ◽  
pp. 5461-5461
Author(s):  
Mahmood B Aldapt ◽  
Mohamed A Yassin

Introduction Cutaneous infiltration (Leukemia cutis) by CLL is regarded as specific sign of skin involvement, these findings can vary in presentations; they can be localized or generalized in the form of erythematous papules, plaques, nodules, and large tumors, however ulceration is uncommon. Skin lesions in general can be seen in 25% of patients with CLL. It is unclear what is the impact of cutaneous infiltration by CLL on prognosis, mainly because most cases are sporadic, either in case reports or series, with no consistency in the modality of treatment. Patients and methods A systematic search of the Medline database (PubMed), Google Scholar was performed to identify English language articles published from Jan 2000 to June 2019 with the following search terms: Leukemia cutis - CLL, cutaneous - CLL, skin - CLL, cutaneous - chronic lymphocytic leukemia, skin - chronic lymphocytic leukemia. Only patients with confirmed CLL Leukemia cutis were included in this analysis. Results A total of 56 cases were identified, with median age of 66 years (range from 39-90), of these cases 43 (76.8%) were males and 12 (21.4%) were females, with ratio of 3.6 : 1. Head and neck were the most common involved sites, interestingly it was very common on the earlobes, followed by trunk and extremities. The most common clinical presentation was papulonodular skin lesions, others like erythematous patches were seen, but ulceration was uncommon. Most cases had leukemia cutis as the initial presentation of CLL. The median time before relapse with skin involvement was 5.5 years (range 1 to 21 years). Most patients were diagnosed at early stage. Majority were treated with chemotherapy, others managed by observation, local radiotherapy or chemoimmunotherapy. In general, 35 (62.5%) cases had cutaneous response to treatment (25 CR and 10 PR). Discussion CLL skin infiltration is not uncommon, but it is not well described in the literature, here in our review we revisited specific cutaneous infiltration by CLL, we emphasized on Leukemia cutis rather than general secondary skin manifestations in CLL. Many cases had CLL skin involvement at the site of old herpetic lesions, which raises the hypothesis of monoclonal B-cells antigenic recruitment, rather than true metastasis. Most presentations came as first sign of the disease, and mostly in early stage. It was also observed that skin infiltration by CLL does not affect prognosis, as most patients attained complete or partial remission with very low progression rate. Because of the rarity of the disease, treatment modalities varied widely, and there was no consensus on treatment, yet all treatment modalities resulted in cutaneous response rate of 62.5%. The best modality of treatment in cutaneous CLL is based on the staging, lesions distribution (localized vs. generalized) and co-morbidities. Conclusion Leukemia cutis is rare but rather a recognized complication of CLL, most likely presents as papulonodular lesions as initial sign of the disease, furthermore most patients present in early stage, it is observed that all patients ≤60 year old had early stage disease, patients with early stage and localized leukemia cutis can benefit from observation alone strategy, on the other hand all patients with advanced stage were >60 year old, and intervention in these patients is warranted, in other situations treatment is individualized based on staging, lesions distribution (localized vs. generalized) and comorbidities. Leukemia cutis did not affect the prognosis of the disease. Disclosures No relevant conflicts of interest to declare.

Blood ◽  
2013 ◽  
Vol 122 (21) ◽  
pp. 672-672 ◽  
Author(s):  
Pietro Bulian ◽  
Tait D Shanafelt ◽  
Chris Fegan ◽  
Antonella Zucchetto ◽  
Lilla Cro ◽  
...  

Abstract Purpose Although CD49d is an unfavorable prognostic marker in chronic lymphocytic leukemia (CLL), definitive validation evidence is lacking. A worldwide multi-center analysis was performed using published and unpublished CLL series to evaluate the impact of CD49d as overall survival (OS) and treatment free survival (TFS) predictor. Patients and Methods A training/validation strategy was chosen to find the optimal CD49d cut-off. The hazard ratio (HR) for death and treatment imposed by CD49d was estimated by pooled analysis of 2,972 CLL, and Cox analysis stratified by center and stage was used to adjust for confounding variables. The importance of CD49d over other flow cytometry-based prognosticators (CD38, ZAP-70) was ranked by recursive partitioning. Results Patients with ≥30% of neoplastic cells expressing CD49d were considered CD49d+. The decrease in OS at 5 and 10-years among CD49d+ cases was 7% and 23% (decrease in TFS 26% and 25% respectively). The pooled HR of CD49d for OS was 2.5 (2.3 for TFS) in univariate analysis. This HR remained significant and of similar magnitude (HR=2.0) in a Cox model adjusted for clinical and biological prognosticators. Hierarchical trees including all cases, or restricted to early stage or patients ≤65 years, always selected CD49d as the most important flow-cytometry-based biomarker, with negligible additional prognostic information added by CD38 or ZAP-70. Consistently, by bivariate analysis, CD49d reliably identified patients' subsets with poorer outcome independent of CD38 and ZAP-70. Conclusions In this analysis of ∼3000 patients, CD49d emerged as the strongest flow cytometry-based predictor of OS and TFS in CLL. Disclosures: Shanafelt: Genentech: Research Funding; Glaxo-Smith-Kline: Research Funding; Cephalon: Research Funding; Hospira: Research Funding; Celgene: Research Funding; Polyphenon E International: Research Funding. Burger:Pharmacyclics: Research Funding.


2014 ◽  
Vol 32 (9) ◽  
pp. 897-904 ◽  
Author(s):  
Pietro Bulian ◽  
Tait D. Shanafelt ◽  
Chris Fegan ◽  
Antonella Zucchetto ◽  
Lilla Cro ◽  
...  

Purpose Although CD49d is an unfavorable prognostic marker in chronic lymphocytic leukemia (CLL), definitive validation evidence is lacking. A worldwide multicenter analysis was performed using published and unpublished CLL series to evaluate the impact of CD49d as an overall (OS) and treatment-free survival (TFS) predictor. Patients and Methods A training/validation strategy was chosen to find the optimal CD49d cutoff. The hazard ratio (HR) for death and treatment imposed by CD49d was estimated by pooled analysis of 2,972 CLLs; Cox analysis stratified by center and stage was used to adjust for confounding variables. The importance of CD49d over other flow cytometry–based prognosticators (eg, CD38, ZAP-70) was ranked by recursive partitioning. Results Patients with ≥ 30% of neoplastic cells expressing CD49d were considered CD49d+. Decrease in OS at 5 and 10 years among CD49d+ patients was 7% and 23% (decrease in TFS, 26% and 25%, respectively). Pooled HR of CD49d for OS was 2.5 (2.3 for TFS) in univariate analysis. This HR remained significant and of similar magnitude (HR, 2.0) in a Cox model adjusted for clinical and biologic prognosticators. Hierarchic trees including all patients or restricted to those with early-stage disease or those age ≤ 65 years always selected CD49d as the most important flow cytometry–based biomarker, with negligible additional prognostic information added by CD38 or ZAP-70. Consistently, by bivariate analysis, CD49d reliably identified patient subsets with poorer outcome independent of CD38 and ZAP-70. Conclusion In this analysis of approximately 3,000 patients, CD49d emerged as the strongest flow cytometry–based predictor of OS and TFS in CLL.


2021 ◽  
Vol 9 (7) ◽  
Author(s):  
Maria Dimou ◽  
Theodoros Iliakis ◽  
Vasileios Paradalis ◽  
Aikaterini Bitsani ◽  
Marie‐Christine Kyrtsonis ◽  
...  

Cells ◽  
2021 ◽  
Vol 10 (5) ◽  
pp. 1088
Author(s):  
Katarzyna Lipska ◽  
Agata Filip ◽  
Anna Gumieniczek

Malignant cells in chronic lymphocytic leukemia (CLL) show resistance to apoptosis, as well as to chemotherapy, which are related to deletions or mutations of TP53, high expression of MCL1 and BCL2 genes and other abnormalities. Thus, the main goal of the present study was to assess the impact of chlorambucil (CLB) combined with valproic acid (VPA), a known antiepileptic drug and histone deacetylation inhibitor, on apoptosis of the cells isolated from 17 patients with CLL. After incubation with CLB (17.5 µM) and VPA (0.5 mM), percentage of apoptosis, as well as expression of two TP53 target genes (p21 and HDM2) and two genes from Bcl-2 family (BCL2 and MCL1), were tested. As a result, an increased percentage of apoptosis was observed for CLL cells treated with CLB and VPA, and with CLB alone. Under the treatment with the drug combination, the expression of p21 gene was visibly higher than under the treatment with CLB alone. At the same time, the cultures under CLB treatment showed visibly higher expression of BCL2 than the cultures with VPA alone. Thus, the present study strongly suggests further investigations on the CLB and VPA combination in CLL treatment.


2020 ◽  
Vol 38 (3) ◽  
pp. 406-408 ◽  
Author(s):  
Marta Lionetti ◽  
Marzia Barbieri ◽  
Vanessa Favasuli ◽  
Elisa Taiana ◽  
Sonia Fabris ◽  
...  

Blood ◽  
1996 ◽  
Vol 88 (11) ◽  
pp. 4259-4264 ◽  
Author(s):  
M Sarfati ◽  
S Chevret ◽  
C Chastang ◽  
G Biron ◽  
P Stryckmans ◽  
...  

Abstract Prognosis of B-cell chronic lymphocytic leukemia (CLL) is based on clinical staging whose limitation is the failure to assess whether the disease will progress or remain stable in early stage (Binet A, or Rai 0, I, II) patients. We previously reported that soluble CD23 (sCD23), a protein derived from the B-cell membrane CD23 Ag, is selectively elevated in the serum of CLL patients. This prospective study assessed the predictive value of serum sCD23 level measured at study entry on the overall survival of all CLL patients and on disease progression of stage Binet A patients. Prognostic value of repeated measurements of sCD23 over time in stage A patients was also analyzed. One hundred fifty-three CLL patients were prospectively followed with a median follow-up of 78 months. Eight clinical or biological parameters were collected from the date of the first sCD23 measurement. At study entry, by Cox model, Binet staging (P = .0001) and serum sCD23 level (P = .03) appeared as prognostic factors for survival. Patients with sCD23 level above median value (> 574 U/mL) had a significantly worse prognosis than those with lower values (median survival of 53 v 100+ months, P = .0001). During follow-up, sCD23 doubling time increased by 3.2 the risk of death (P = .001). Among stage A patients (n = 100), sCD23 determination at study entry was the sole variable predictive of disease progression, patients with sCD23 level above 574 U/mL had a median time progression of 42 months versus 88 months for those with lower levels (P = .0001). Stage A patients who doubled their sCD23 level exhibited a 15-fold increased risk of progression (P = .0001) and, in addition, the sCD23 increase preceded by 48 months disease progression. We conclude that in CLL patients, serum sCD23 level provides significant additional prognostic information in terms of overall survival. Most interestingly, among early stage patients, sCD23 determination at diagnosis and during the course of the disease may help to the early identification of patients who will rapidly progress to upper stages.


2018 ◽  
Vol 35 (2) ◽  
pp. 367-368
Author(s):  
Abhenil Mittal ◽  
Ajay Gogia ◽  
Saumyaranjan Mallick ◽  
Ritu Gupta

2017 ◽  
Vol 59 (6) ◽  
pp. 1348-1355 ◽  
Author(s):  
Craig Mescher ◽  
David Gilbertson ◽  
Nicole M. Randall ◽  
Gobind Tarchand ◽  
Julie Tomaska ◽  
...  

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