CHRONIC LYMPHOCYTIC
LEUKEMIA (CLL)

Exploring dysfunctional pathways, mechanisms, and biomarkers in CLL to
discover new insights into the progression of the disease.1

of leukemia cases diagnosed globally are CLL.2

of patients with CLL overexpress the BCL-2 protein.3

INCIDENCE AND MORTALITY

  • An estimated 18,740 people in the US were diagnosed during 2023, and 4,490 people died from the disease.15
  • Five-year survival rate is 88.0% in the US.15
  • CLL is most frequently diagnosed among people aged 65 to 74 years 15
  • In the US, 98% of CLL cases are diagnosed in people older than 44 years.15
  • The median age at diagnosis is 70 years.15

CLL is a slow-progressing cancer in which mature clonal B lymphocytes accumulate in the bone marrow, blood, and other lymphoid tissues.

Complications associated with CLL include recurrent infection and autoimmune diseases, risk of secondary malignancy, and transformation to diffuse large B-cell lymphoma (DLBCL).4

CLL is a slow-progressing cancer in which mature clonal B lymphocytes accumulate in the bone marrow, blood, and other lymphoid tissues.

Complications associated with CLL include recurrent infection and autoimmune diseases, risk of secondary malignancy, and transformation to diffuse large B-cell lymphoma (DLBCL).4

CLL is a slow-progressing cancer in which mature clonal B lymphocytes accumulate in the bone marrow, blood, and other lymphoid tissues.

Complications associated with CLL include recurrent infection and autoimmune diseases, risk of secondary malignancy, and transformation to diffuse large B-cell lymphoma (DLBCL).4

CLL is a slow-progressing cancer in which mature clonal B lymphocytes accumulate in the bone marrow, blood, and other lymphoid tissues.

Complications associated with CLL include recurrent infection and autoimmune diseases, risk of secondary malignancy, and transformation to diffuse large B-cell lymphoma (DLBCL).4

CLL is a slow-progressing cancer in which mature clonal B lymphocytes accumulate in the bone marrow, blood, and other lymphoid tissues.

Complications associated with CLL include recurrent infection and autoimmune diseases, risk of secondary malignancy, and transformation to diffuse large B-cell lymphoma (DLBCL).4

Relevant Cancer Targets

BCL-2

Learn about how BCL-2 plays a role in tumor survival and is a rational target for therapeutic intervention.MORE>


BTK

Learn about BTK and B cell signalingMORE>


MALT1

Learn about MALT1 and NF-κB signalingMORE>

CD3xCD20 BISPECIFICS

Learn about CD3 on T cells and bispecific targeting of CD20. MORE>


CD19

Learn about CD19 and B cell signalingMORE>

Explore AbbVie's Work

Learn More About Our Investigational Agents in CLL

Learn More About Our Clinical Research in CLL

  1. Anderson MA, Huang D, Roberts A. Targeting BCL2 for the treatment of lymphoid malignancies. Semin Hematol. 2014;51(3):219-227.
  2. Global Burden of Disease Cancer Collaboration, Fitzmaurice C, Allen C, et al. Global, regional, and national cancer incidence, mortality, years of life lost, years lived with disability, and disability-adjusted life-years for 32 cancer groups, 1990 to 2015: a systematic analysis for the Global Burden of Disease Study. JAMA Oncol. 2017;3(4):524-548
  3. Howlader N, Noone AM, Krapcho M, et al (eds). National Cancer Institute. SEER Cancer Statistics Review, 1975-2017. Updated April 2020 based on November 2019 SEER data submission. Accessed March 2024. https://seer.cancer.gov/csr/1975_2017/.
  4. Stilgenbauer S, Furman RR, Zent CS. Management of chronic lymphocytic leukemia. Am Soc Clin Oncol Educ Book. 2015:164-175.
  5. Zhang S, Kipps TJ. The pathogenesis of chronic lymphocytic leukemia. Annu Rev Pathol. 2014;9:103-118.
  6. Guieze R, Wu CJ. Genomic and epigenomic heterogeneity in chronic lymphocytic leukemia. Blood. 2015;23:445-453.
  7. Hamblin TJ, et al. Unmutated Ig V(H) genes are associated with a more aggressive form of chronic lymphocytic leukemia. Blood. 1999;94(6):1848-1854.
  8. Hallek M, et al. iwCLL guidelines for diagnosis, indications for treatment, response assessment, and supportive management of CLL. Blood. 2018 ;131(25):2745-2760.
  9. Stilgenbauer S, Schnaiter A, Paschka P, et al. Gene mutations and treatment outcome in chronic lymphocytic leukemia: results from the CLL8 trial. Blood. 2014;123(21):3247-3254.
  10. Hallek M, Cheson BD, Catovsky D, et al. Guidelines for the diagnosis and treatment of chronic lymphocytic leukemia: a report from the International Workshop on Chronic Lymphocytic Leukemia updating the National Cancer Institute–Working Group 1996 guidelines. Blood. 2008;111(12):5446-5456.
  11. Bewarder M, et al. Current Treatment Options in CLL. Cancers (Basel). 2021;13(10):2468.
  12. Davids MS. How should we sequence and combine novel therapies in CLL? Hematology Am Soc Hematol Educ Program. 2017 ;2017(1):346-353.
  13. Bose P, Gandhi V. Recent therapeutic advances in chronic lymphocytic leukemia. F1000Res. 2017;6:1924.
  14. Lu K, Wang X. Therapeutic advancement of chronic lymphocytic leukemia. J Hematol Oncol. 2012;5(55).
  15. NCI. Cancer Stat Facts: Chronic Lymphocytic Leukemia (CLL).Accessed March 2024.
  16. Scarfo L. Novel therapies and combinations in CLL refractory to BTK inhibitors and venetoclax. Hematology Am Soc Hematol Educ Program (2022) 2022 (1): 316–322.