Treatment of relapsed acute lymphoblastic leukemia in children: an observational study of the Japan Children's Cancer Group.
Hiroaki GotoAkiko KadaChitose OgawaRitsuo NishiuchiJunko YamanakaAkihiro IguchiMasanori NishiKimiyoshi SakaguchiTadashi KumamotoShinji MochizukiHideaki UekiYoshiyuki KosakaAkiko M SaitoHidemi ToyodaPublished in: International journal of hematology (2024)
The Japan Children's Cancer Group Relapsed Acute Lymphoblastic Leukemia (ALL) Committee conducted a prospective observational study (ALL-R14) to explore promising reinduction therapy regimens for relapsed ALL to investigate in future trials. In Japan, clofarabine- and bortezomib-based regimens were of interest since they were newly introduced for ALL in the study period (2015-2018). Seventy-five pediatric patients were enrolled in total. The 2-year event-free/overall survival rates in patients with first (n = 59) or second (n = 11) relapse were 40.1% (95% confidence interval [CI]: 25.5-52.3%)/66.3% (95% CI 52.3-77.0%) and 34.1% (95% CI 9.1-61.6%)/62.3% (95% CI 27.7-84.0%), respectively. Clofarabine- or bortezomib-based regimens were used only in patients with high-risk disease. The first reinduction therapy used in the 41 patients with early or multiple relapsed B-cell precursor ALL was clofarabine in 7 patients and bortezomib in 9 patients. The odds ratio for reinduction failure risk with a clofarabine- or bortezomib-based regimen compared with other regimens was 9.0 (95% CI 0.9-86.4, P = 0.057) or 1.9 (95% CI 0.4-8.7, P = 0.42), respectively. Thus, clofarabine- or bortezomib-based regimens had no obvious advantage as reinduction therapy for relapsed ALL in children.
Keyphrases
- acute lymphoblastic leukemia
- multiple myeloma
- newly diagnosed
- acute myeloid leukemia
- end stage renal disease
- young adults
- diffuse large b cell lymphoma
- hodgkin lymphoma
- allogeneic hematopoietic stem cell transplantation
- chronic kidney disease
- ejection fraction
- peritoneal dialysis
- prognostic factors
- papillary thyroid
- stem cells
- smoking cessation
- cell therapy