Related Experiment Video
Updated: Jul 27, 2026

10:52
Tumor Engraftment in a Xenograft Mouse Model of Human Mantle Cell Lymphoma
Published on: March 30, 2018
Solid tumors after chronic lymphocytic leukemia.
M Hisada1, R J Biggar, M H Greene
1Division of Cancer Epidemiology and Genetics, National Cancer Institute, Bethesda, MD 20852, USA. mh280i@nih.gov
Blood
|September 6, 2001
Summary
Patients with chronic lymphocytic leukemia (CLL) face a higher risk of developing second cancers. This includes Kaposi sarcoma, melanoma, and cancers of the lung, larynx, brain, stomach, and bladder.
Area of Science:
- Oncology
- Epidemiology
Background:
- Chronic lymphocytic leukemia (CLL) is associated with an increased risk of subsequent neoplasms.
- Understanding these risks is crucial for patient management and surveillance.
Purpose of the Study:
- To quantify the risk of second cancers in a large cohort of patients diagnosed with CLL.
- To identify specific cancer types with elevated risks following a CLL diagnosis.
Main Methods:
- Utilized data from the population-based Surveillance, Epidemiology and End Results (SEER) Program.
- Analyzed a cohort of 16,367 patients with CLL to calculate observed/expected (O/E) ratios for second cancers.
- Compared cancer risks between patients who received chemotherapy and those who did not.
Main Results:
- An overall increased risk of second cancers was observed (O/E = 1.20).
- Significant excesses in risk were noted for Kaposi sarcoma (O/E = 5.09), malignant melanoma (O/E = 3.18), lung cancer (O/E = 1.66), and laryngeal cancer (O/E = 1.72).
- Elevated risks were also found for brain cancer in men (O/E = 1.91) and stomach (O/E = 1.76) and bladder cancers (O/E = 1.52) in women.
Conclusions:
- Patients with CLL have a statistically significant increased risk of developing various secondary cancers.
- The findings suggest potential roles for immunologic impairment or other etiologic factors in the development of these subsequent neoplasms.
- Further research is warranted to elucidate the underlying mechanisms driving these increased cancer risks post-CLL.

