Translocation t(1;19)(q23;p13) in adult acute lymphoblastic leukemia - a distinct subtype with favorable prognosis.
Musa YilmazHagop M KantarjianGokce TorunerC Cameron YinRashmi Kanagal-ShamanaJorge E CortesGhayyas IssaNicholas J ShortJoseph D KhouryGuillermo Garcia-ManeroFarhad RavandiTapan KadiaMarina KonoplevaWilliam G WierdaNitin JainZeev E EstrovKoji SasakiSherry PierceSusan M O'BrienElias J JabbourPublished in: Leukemia & lymphoma (2020)
The recurring translocation t(1;19) (q23;p13) with TCF3-PBX1 rearrangements are uncommon in adult acute lymphoblastic leukemia (ALL), and their prognostic impact remains to be described in the era of modern chemotherapies. We investigated 427 adult patients with newly diagnosed pre-B ALL, 16 (4%) had t(1;19)(q23;p13) at diagnosis. All 16 patients achieved complete remission after induction with intensive chemotherapy, and with a median of 7-year follow-up, 2 relapsed. The 5-year cumulative incidence of relapse and overall survival rates were 14% and 82%, respectively. Our analysis showed that adult patients with t(1;19)(q23;p13) positive ALL had favorable prognosis with intensive chemotherapy regimens.
Keyphrases
- acute lymphoblastic leukemia
- newly diagnosed
- allogeneic hematopoietic stem cell transplantation
- end stage renal disease
- ejection fraction
- chronic kidney disease
- risk factors
- prognostic factors
- peritoneal dialysis
- systemic lupus erythematosus
- rheumatoid arthritis
- diffuse large b cell lymphoma
- disease activity
- patient reported outcomes
- childhood cancer
- chemotherapy induced
- high resolution
- single molecule