Clonal Upregulation of Effector Cytotoxic T Lymphocytes in a Patient with Multiple Tyrosine Kinase Inhibitor-Refractory Chronic Myeloid Leukemia with Long-Term Survival

• Published in: Case reports in oncology 2021-01, Vol.14 (1), p.493-499
• Main Authors: Jo, Tatsuro, Sakai, Takahiro, Matsuzaka, Kaori, Noguchi, Kazuhiro, Hayashi, Shizuka, Matsuo, Masatoshi, Taguchi, Jun
• Format: Article
• Language: English
• Subjects: Biomarkers; Blood; Blood platelets; Bone marrow; Case Report; Case reports; Chromosomes; chronic myeloid leukemia; cytotoxic t lymphocyte; Cytotoxicity; Flow cytometry; Hemoglobin; Inhibitor drugs; Kinases; Laboratories; Leukemia; Mutation; Patients; Stem cells; t-cell receptor repertoire; Targeted cancer therapy; tyrosine kinase inhibitor
• ISSN: 1662-6575; 1662-6575
• DOI: 10.1159/000514631

We present the case of a patient with multiple tyrosine kinase inhibitor (TKI)-refractory chronic phase chronic myeloid leukemia (CP-CML) with a T315I mutation of abl1. Dasatinib, a second-generation TKI, was administered as the initial treatment but achieved neither a cytogenetic nor molecular response. A mutational analysis of abl1 revealed that the patient had a T315I mutation. The patient was then administered ponatinib, a third-generation TKI, which is thought to be effective against T315I; however, the complete blood counts became within normal limits, and neither a cytogenetic nor molecular response was achieved. However, the patient has maintained a healthy chronic phase (with no blast crises) for more than 5½ years since the diagnosis of CP-CML. T-cell receptor (TCR) repertoire analyses using peripheral blood revealed a remarkable clonal expansion of effector cytotoxic T lymphocytes (CTLs) that contained TCR V beta 13.6. We observed the clonal expansion of naïve CTLs with TCR V beta 13.6; however, no clonality was observed in the memory CTLs. The naïve and effector CTLs persisted at very high percentages since the seventh month after starting dasatinib. The CTLs could not have led to the molecular response; therefore, there might be plenty of CML stem cells remaining in the bone marrow. Therefore, although the CTLs might have prevented the disease from developing blast crises over more than 5 years, the CTLs might not have been able to become memory CTLs.