Condition: Acute Promyelocytic Leukemia (APL) · Sponsor: Instituto do Cancer do Estado de São Paulo
It is a non-randomized, multicenter, prospective study, aiming to treat patients with newly diagnosed acute promyelocytic leukemia with a combination of oral arsenic and atra, with low dose chemotherapy for those with high-risk disease (white blood cell count above 10x10a9/L). The primary objective is to assess the 2-year overall survival (OS) in these patients, comparing with the historical control group of patients treated with ATRA/chemotherapy according to the IC-APL 2006 protocol.
This description comes directly from the study's public registry record.
Elaine Uehara · 55 38933535 · elaine.uuehara@hc.fm.usp.br
Always discuss trial participation with your own doctor first.
| Instituto do Cancer do Estado de Sao Paulo | São Paulo, São Paulo, Brazil | Recruiting |
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Source record: clinicaltrials.gov/study/NCT06982274