LAUSR

Simple Summary The history of the treatment of APL has shown remarkable success. However, it is not clear whether it is necessary to monitor long-term toxicity in “cured” patients who survive for more than five years, which is critical to ensuring maximum survival in APL patients. To answer this question, we performed a comprehensive analysis of 1952 APL 5-year survivors and 5973 non-APL acute myeloid leukemia (AML) 5-year survivors from the Surveillance, Epidemiology, and End Results (SEER) database. We found that the overall mortality risk in >5-year survivors of APL was 1.41 times than that of the general population due to a significant increase in mortality from AML (SMR, 87.67) and other second malignant neoplasms (SMR, 1.56) only at 60–119 months. This result indicated long-term survivors of APL are safe after 10 years, which may help clinicians make future risk assessment, health guidance, and follow-up plans for APL long-term survivors. Abstract Background: Acute promyelocytic leukemia (APL) is a highly curable cancer, but it is not clear whether it is also necessary to monitor long-term toxicity in “cured” patients who survive for more than five years, which is critical to ensuring maximum survival in APL patients. Methods: A total of 1952 APL 5-year survivors and 5973 non-APL acute myeloid leukemia (AML) 5-year survivors were included from the Surveillance, Epidemiology, and End Results (SEER) database. The standardized mortality ratio (SMR) was calculated to measure the risk of death. Cumulative mortality is calculated as the incidence of specific causes of death under competing risk events. Results: The SMR of all causes of death in >5-year survivors of APL was higher than that of the general population only at 60–119 months (SMR, 1.41). This was mainly because a significant increase in mortality from AML (SMR, 87.67) and second malignant neoplasms (SMNs) (SMR, 1.56) was found only at 60–119 months. However, there was no higher risk of death from non-cancer-related disease in >5-year survivors of APL than that of the general population (SMR, 0.89). The SMR of all-cause deaths in >5-year survivors of non-APL AML decreased year by year and was no higher than that of the general population until after 216 months. The cumulative incidence of AML-related death, SMN-related death, and non-cancer-related death was significantly lower in APL patients than in non-APL AML patients throughout the follow-up period. Conclusions: Compared with the general population, the risk of death of patients with APL was higher within 5 to 10 years but not higher over 10 years. Therefore, we believe that long-term survivors of APL are safe after 10 years.