I read with great interest the study conducted by Fong et al. published in this issue of Annals, which evaluated psychological symptoms and health-related quality of life (HRQOL) among a cohort of 143 young adult survivors of childhood cancer in Singapore.1 Almost 1 in 4 survivors demonstrated significant psychological distress and poor mental well-being (relative to population norms) at more than 15 years post-cancer diagnosis. Other than being the first in Singapore to characterise the psychological burden experienced by survivors, the notable strengths of this study are (1) the inclusion of siblings as comparators to minimise the potential confounding effects of genetics, family environment and socioeconomic factors on the study outcomes; (2) the use of validated self-reported measures that enable cross-comparison with studies from other countries; and (3) the use of International Classification of Diseases, Ninth Edition diagnosis codes to capture clinical chronic conditions and late effects of cancer. The authors conclude their paper by calling for regular surveillance and timely interventions to improve mental health functioning and HRQOL in cancer survivorship programmes in Singapore. Taken together, this study contributes to the existing literature that highlights the unique needs that survivors of childhood cancer face as they advance to young adulthood, which include the need for ongoing psychosocial support, transition from child-centred to adult-oriented health-care systems, and age-appropriate education on their personal health risks.