Decitabine plus CLAG chemotherapy as a bridge to haploidentical transplantation in the setting of acute myeloid leukemia relapse after HLA-matched sibling transplantation: a case report
Mengqi Jin,
Yongxian Hu,
Wenjun Wu,
Yi Luo,
Yamin Tan,
Jian Yu,
Aiyun Jin,
Luxin Yang,
He Huang,
Guoqing Wei
Affiliations
Mengqi Jin
Bone Marrow Transplantation Center, The First Affiliated Hospital, School of Medicine, Zhejiang University
Yongxian Hu
Bone Marrow Transplantation Center, The First Affiliated Hospital, School of Medicine, Zhejiang University
Wenjun Wu
Bone Marrow Transplantation Center, The First Affiliated Hospital, School of Medicine, Zhejiang University
Yi Luo
Bone Marrow Transplantation Center, The First Affiliated Hospital, School of Medicine, Zhejiang University
Yamin Tan
Bone Marrow Transplantation Center, The First Affiliated Hospital, School of Medicine, Zhejiang University
Jian Yu
Bone Marrow Transplantation Center, The First Affiliated Hospital, School of Medicine, Zhejiang University
Aiyun Jin
Bone Marrow Transplantation Center, The First Affiliated Hospital, School of Medicine, Zhejiang University
Luxin Yang
Bone Marrow Transplantation Center, The First Affiliated Hospital, School of Medicine, Zhejiang University
He Huang
Bone Marrow Transplantation Center, The First Affiliated Hospital, School of Medicine, Zhejiang University
Guoqing Wei
Bone Marrow Transplantation Center, The First Affiliated Hospital, School of Medicine, Zhejiang University
Abstract Background Patients with relapsed/refractory acute myeloid leukemia after hematopoietic stem cell transplantation (HSCT) have a poor prognosis, with a 2-year survival rate of 14%. The optimal treatment for these patients remains unclear. To treat these patients, we designed a new salvage regimen consisting of decitabine, cladribine, cytarabine, and granulocyte-stimulating factor (D-CLAG). Case presentation Here, we describe a case of acute monocytic leukemia with a complex karyotype in a 38-year-old female patient who relapsed after her first HSCT, which was performed using a matched sibling donor. The patient did not respond to standard induction chemotherapy and subsequently achieved complete remission with the D-CLAG regimen. No severe hematological or extramedullary toxicity was observed. Subsequently, the patient received a second D-CLAG regimen as a bridge therapy and directly underwent haploidentical related HSCT. Following HSCT, the marrow showed complete hematologic and cytogenetic remission. Currently, 1 year after transplantation, the patient’s general condition remains good. Conclusions This case suggests that the D-CLAG regimen can be an option for reinduction in relapsed refractory AML patients as a bridge to transplantation. Nevertheless, further research will be required in the future as this report describes only a single case.