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Immunoglobulin Gene Sequence Analysis In Chronic Lymphocytic Leukemia: From Patient Material To Sequence Interpretation
Published on: November 26, 2018
Single-institutional retrospective analysis of Japanese patients with chronic lymphocytic leukemia
Risa Hashida1, Sumiko Kohashi1, Jun Kato1
1Division of Hematology, Department of Medicine, Keio University School of Medicine.
Insights
Chronic lymphocytic leukemia (CLL) is rare in Japan. This study of 29 Japanese patients found clinical courses comparable to Western countries, with a 5-year overall survival rate of 83%.
Area of Science:
- Hematology
- Oncology
- Epidemiology
Background:
- Chronic lymphocytic leukemia (CLL) is a rare lymphoid malignancy in Japan.
- Clinical features of CLL in the Japanese population require further elucidation.
Purpose of the Study:
- To retrospectively analyze the clinical features and outcomes of Japanese CLL patients.
- To compare the clinical course of Japanese CLL patients with those in Western countries.
Main Methods:
- Retrospective analysis of 29 newly diagnosed Japanese CLL patients.
- Median follow-up of 69 months.
- Evaluation of treatment, survival rates, and outcomes after allogeneic hematopoietic stem cell transplantation.
Main Results:
- Median age was 62 years, with 59% males.
- Five-year overall survival rate was 83%; treatment-free survival was 67%.
- Two patients underwent allogeneic stem cell transplantation for refractory disease with no relapse.
Conclusions:
- The clinical course of Japanese CLL patients appears comparable to Western populations.
- Larger studies are needed to fully understand CLL features and long-term outcomes in Japan.
Abstract:
Unlike in Western countries, chronic lymphocytic leukemia (CLL) is a rare lymphoid malignancy in Japan, and its clinical features remain to be elucidated in the Japanese population. Therefore, we retrospectively analyzed 29 Japanese CLL patients newly diagnosed at our institute. Seventeen (59%) were male, and their median age was 62 years. With a median follow-up period from diagnosis of 69 months (range, 3-170 months), 9 patients received some form of treatment for CLL. Three patients died of disease progression with or without infection (n=2) or skin cancer (n=1). Five-year overall and treatment-free survival rates were 83% (95%CI, 46-96%) and 67% (95%CI, 45-81%), respectively. Two patients received allogeneic hematopoietic stem cell transplantation for refractory disease, and both were alive without disease relapse at 53 and 110 months, respectively, after transplantation. These results suggest the clinical courses of Japanese patients with CLL to be comparable to those in Western countries. However, future studies of larger numbers of patients are needed to further elucidate the features and long-term clinical courses of CLL in the Japanese population.
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