TY - JOUR
T1 - All‐trans retinoic acid followed by chemotherapy for salvage of refractory or relapsed acute promyelocytic leukemia
AU - Cortes, Jorge E.
AU - Kantarjian, Hagop
AU - O'Brien, Susan
AU - Robertson, L. E.
AU - Koller, Charles
AU - Hirsh‐Ginsberg, Cheryl
AU - Stass, Sanford
AU - Keating, Michael
AU - Estey, Elihu
PY - 1994/6/15
Y1 - 1994/6/15
N2 - Background. All‐trans retinoic acid (ATRA) is effective in the treatment of relapsed or refractory acute promyelocytic leukemia (APL), but relapse is the rule if response is unmaintained. Methods. Seventeen patients with APL were salvaged with ATRA at a dosage of 50 mg/m2/day for 3 months or until complete remission (CR) was achieved; idarubicin (12 mg/m2/day for 4 days) was added if blast plus promyelocyte count either was or reached ≥10 × 103/μl. After CR was achieved, patients received three courses of idarubicin (12 mg/m2 daily for 3 days) followed by three courses of mitoxantrone (5 mg/m2 daily for 3 days) and etoposide (250 mg/m2 daily for 3 days). Maintenance was with 6‐mercaptopurine and methotrexate. Results. A CR was achieved in 14 patients (82%), the disease was refractory in 2 patients, and one patient died during induction. Three patients underwent allogeneic bone marrow transplant during CR. After a median follow‐up of 26 weeks, six patients remain in CR. Median CR duration is 40 weeks (range 8–56+). Patients treated with ATRA plus chemotherapy in first salvage, when compared to a historic control group treated with chemotherapy alone, had a significantly better CR rate (87% vs. 57%; P = 0.04) and a lower induction death rate (7% vs. 29%; P = 0.08), resulting in longer median survival (26 vs. 17 weeks; P = 0.13). Four patients developed the „retinoic acid syndrome”, which was fatal in one case. Three patients developed thrombotic events. Conclusions. ATRA followed by chemotherapy is effective treatment for patients with APL who relapse after conventional therapy, and it may be superior to chemotherapy alone. Cancer 1994; 73:2946–52.
AB - Background. All‐trans retinoic acid (ATRA) is effective in the treatment of relapsed or refractory acute promyelocytic leukemia (APL), but relapse is the rule if response is unmaintained. Methods. Seventeen patients with APL were salvaged with ATRA at a dosage of 50 mg/m2/day for 3 months or until complete remission (CR) was achieved; idarubicin (12 mg/m2/day for 4 days) was added if blast plus promyelocyte count either was or reached ≥10 × 103/μl. After CR was achieved, patients received three courses of idarubicin (12 mg/m2 daily for 3 days) followed by three courses of mitoxantrone (5 mg/m2 daily for 3 days) and etoposide (250 mg/m2 daily for 3 days). Maintenance was with 6‐mercaptopurine and methotrexate. Results. A CR was achieved in 14 patients (82%), the disease was refractory in 2 patients, and one patient died during induction. Three patients underwent allogeneic bone marrow transplant during CR. After a median follow‐up of 26 weeks, six patients remain in CR. Median CR duration is 40 weeks (range 8–56+). Patients treated with ATRA plus chemotherapy in first salvage, when compared to a historic control group treated with chemotherapy alone, had a significantly better CR rate (87% vs. 57%; P = 0.04) and a lower induction death rate (7% vs. 29%; P = 0.08), resulting in longer median survival (26 vs. 17 weeks; P = 0.13). Four patients developed the „retinoic acid syndrome”, which was fatal in one case. Three patients developed thrombotic events. Conclusions. ATRA followed by chemotherapy is effective treatment for patients with APL who relapse after conventional therapy, and it may be superior to chemotherapy alone. Cancer 1994; 73:2946–52.
KW - acute promyelocytic leukemia
KW - all‐trans retinoic acid
KW - salvage
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U2 - 10.1002/1097-0142(19940615)73:12<2946::AID-CNCR2820731211>3.0.CO;2-Q
DO - 10.1002/1097-0142(19940615)73:12<2946::AID-CNCR2820731211>3.0.CO;2-Q
M3 - Article
C2 - 8199992
AN - SCOPUS:0028271821
SN - 0008-543X
VL - 73
SP - 2946
EP - 2952
JO - Cancer
JF - Cancer
IS - 12
ER -