ETV6::RUNX1 Acute Lymphoblastic Leukemia: how much therapy is needed for cure?
Anna ØstergaardMarta FioccoHester de Groot-KrusemanAnthony V MoormanAjay VoraMartin ZimmermannMartin SchrappeAndrea BiondiGabriele EscherichJan StaryChihaya ImaiToshihiko ImamuraMats HeymanKjeld SchmiegelowRob PietersPublished in: Leukemia (2024)
Recent trials show 5-year survival rates >95% for ETV6::RUNX1 Acute Lymphoblastic Leukemia (ALL). Since treatment has many side effects, an overview of cumulative drug doses and intensities between eight international trials is presented to characterize therapy needed for cure. A meta-analysis was performed as a comprehensive summary of survival outcomes at 5 and 10 years. For drug dose comparison in non-high risk trial arms, risk group distribution was applied to split the trials into two groups: trial group A with ~70% (range: 63.5-75%) of patients in low risk (LR) (CCLSG ALL2004, CoALL 07-03, NOPHO ALL2008, UKALL2003) and trial group B with ~45% (range: 38.7-52.7%) in LR (AIEOP-BFM ALL 2000, ALL-IC BFM ALL 2002, DCOG ALL10, JACLS ALL-02). Meta-analysis did not show evidence of heterogeneity between studies in trial group A LR and medium risk (MR) despite differences in treatment intensity. Statistical heterogeneity was present in trial group B LR and MR. Trials using higher cumulative dose and intensity of asparaginase and pulses of glucocorticoids and vincristine showed better 5-year event-free survival but similar overall survival. Based on similar outcomes between trials despite differences in therapy intensity, future trials should investigate, to what extent de-escalation is feasible for ETV6::RUNX1 ALL.
Keyphrases
- acute lymphoblastic leukemia
- phase iii
- study protocol
- free survival
- phase ii
- clinical trial
- systematic review
- open label
- allogeneic hematopoietic stem cell transplantation
- high intensity
- end stage renal disease
- transcription factor
- stem cells
- newly diagnosed
- chronic kidney disease
- single cell
- ejection fraction
- current status
- combination therapy
- insulin resistance
- skeletal muscle
- case control
- type diabetes
- drug induced
- patient reported outcomes
- double blind