For adult patients with ALL which regimen you prefer (1) Pediatric type or BFM-like protocols or (2) Hyper-CVAD? Does anybody think that Hyper-CVAD is more toxic and associated with unnecessary prolonged meylosuppression?
For patients under 40 either BFM or a pediatric protocol are the preferred regimens because these regimens have L-asparaginase which has shown to improve the outcome of these patients. Unfortunately, L-asparaginase (or the peggylated form) is not well tolerated in older patients (40-60y) and Hyper-CVAD +/- rituximab (if lymphobalsts express CD20 (>20%)) or Hyper-CVAD + TKI (preferably dasatinib because of higher CNS penetration) for PH + ALL are most commonly used. For patients > 60y of age, Hyper-CVAD is very toxic and other less toxic regimens may be used.
Thank you for your reply. I think H-CVAD is more myelosuppressive than BFM-like regimens and is associated with more morbidity and mortality. We use PEG-Asparaginase with our USC ALL regimen, which is BFM-like (Dan Douer, JCO 2014), and it is well tolerated. However, I am not sure if patients who are Ph+ need that.
I prefer BFM-like protocol for adolescents and young adults under 30 years,and tolerance of Peg Aspa is better than other Aspa and tolerable for young.
Bellow 40 yrs BFM-like protocol is more preferable but in case of Ph+cromosome patient add TKI like imatinib or dasatinib. Hyper -CVAD is more toxic, so after 40yrs it may use but cautiously.
Augmented hyper-CVAD based on dose-intensified vincristine, dexamethasone, and asparaginase in adult acute lymphoblastic leukemia salvage therapy. But not sure if anybody used as frontline.