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CAR-T Therapy Followed by Hematopoietic Stem Cell Transplantation Can Improve Survival in Children Relapsed/Refractory Philadelphia Chromosome-positive B-cell Acute Lymphoblastic Leukemia.
Li, Yao; Hu, Guan-Hua; Xu, Lan-Ping; Zhang, Xiao-Hui; Liu, Kai-Yan; Suo, Pan; Wang, Yu; Cheng, Yi-Fei; Huang, Xiao-Jun.
Affiliation
  • Li Y; Beijing Key Laboratory of Hematopoietic Stem Cell Transplantation, Peking University People's Hospital, Peking University Institute of Hematology, National Clinical Research Center for Hematologic Disease, Peking-Tsinghua Center for Life Science, Research Unit of Key Technique for Diagnosis and Treatment of Hematologic Malignancies, Chinese Academic of Medical Sciences, Beijing, China.
J Pediatr Hematol Oncol ; 46(5): 241-247, 2024 07 01.
Article de En | MEDLINE | ID: mdl-38652054
ABSTRACT

BACKGROUND:

Philadelphia chromosome (Ph)-positive B-cell acute lymphoblastic leukemia (ALL) has a high complete remission (CR) rate, but relapse and prolonged measurable residual disease remain serious problems. We sought to describe the CR rate measurable residual disease negative rate and address the results and safety of pediatric patients who underwent after receiving chimeric antigen receptor (CAR) specific for CD19 (CAR-19) followed by hematopoietic stem cell transplantation (HSCT) for the treatment of Ph-positive ALL.

METHODS:

A descriptive study was conducted at Peking University People's Hospital from September 2013 to January 2021. 13 patients with relapsed/refractory Ph-positive B-ALL who received CAR-T therapy followed by allo-HSCT were included. We concentrated on the overall patient survival and CR rate.

RESULTS:

The median time between CAR-T therapy and allo-HSCT was 58 days. Among all the patients, the CR rate was 100%, the flow cytometry negativity rate was 84.62%, and the BCR-ABL negativity rate was 53.85% at 1 month after CAR-T infusion. All the patients achieved a major molecular response in 6 months after HSCT. After a median follow-up of 45 months, the 3-year OS rate was 66.7%, and the 3-year DFS rate was 61.5%. The 3-year OS rate of patients with BCR-ABL-positive pre-HSCT was significantly lower than that in the BCR-ABL-negative group (40.0% vs. 85.7%, P =0.042). Also, the same trend was observed for the 3-year DFS rate but did not differ significantly (40.0% vs. 75.0%, P =0.233).

CONCLUSIONS:

CAR-T therapy followed by allo-HSCT can be a safe and effective treatment for Ph-positive B-ALL pediatric patients.
Sujet(s)

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Chromosome Philadelphie / Immunothérapie adoptive / Transplantation de cellules souches hématopoïétiques Limites: Adolescent / Child / Child, preschool / Female / Humans / Male Langue: En Journal: J Pediatr Hematol Oncol Sujet du journal: HEMATOLOGIA / NEOPLASIAS / PEDIATRIA Année: 2024 Type de document: Article Pays d'affiliation: Chine Pays de publication: États-Unis d'Amérique

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Chromosome Philadelphie / Immunothérapie adoptive / Transplantation de cellules souches hématopoïétiques Limites: Adolescent / Child / Child, preschool / Female / Humans / Male Langue: En Journal: J Pediatr Hematol Oncol Sujet du journal: HEMATOLOGIA / NEOPLASIAS / PEDIATRIA Année: 2024 Type de document: Article Pays d'affiliation: Chine Pays de publication: États-Unis d'Amérique