TY - JOUR
T1 - High probability of follow-up termination among AYA survivors after allogeneic hematopoietic cell transplantation
AU - Miyamura, Koichi
AU - Yamashita, Takuya
AU - Atsuta, Yoshiko
AU - Ichinohe, Tatsuo
AU - Kato, Koji
AU - Uchida, Naoyuki
AU - Fukuda, Takahiro
AU - Ohashi, Kazuteru
AU - Ogawa, Hiroyasu
AU - Eto, Tetsuya
AU - Inoue, Masami
AU - Takahashi, Satoshi
AU - Mori, Takehiko
AU - Kanamori, Heiwa
AU - Yabe, Hiromasa
AU - Hama, Asahito
AU - Okamoto, Shinichiro
AU - Inamoto, Yoshihiro
N1 - Publisher Copyright:
© 2019 by The American Society of Hematology
PY - 2019/2/12
Y1 - 2019/2/12
N2 - The need for long-term follow-up (LTFU) after allogeneic hematopoietic cell transplantation (HCT) has been increasingly recognized for managing late effects such as subsequent cancers and cardiovascular events. A substantial population, however, has already terminated LTFU at HCT centers. To better characterize follow-up termination, we analyzed the Japanese transplant registry database. The study cohort included 17 980 survivors beyond 2 years who underwent their first allogeneic HCT between 1974 and 2013. The median patient age at HCT was 34 years (range, 0-76 years). Follow-up at their HCT center was terminated in 4987 patients. The cumulative incidence of follow-up termination was 28% (95% confidence interval [CI], 27%-29%) at 10 years, increasing to 67% (95% CI, 65%-69%) at 25 years after HCT. Pediatric patients showed the lowest probability of follow-up termination for up to 16 years after HCT, whereas adolescent and young adult (AYA) patients showed the highest probability of follow-up termination throughout the period. Follow-up termination was most often made by physicians based on the patient’s good physical condition. Multivariate analysis identified 6 factors associated with follow-up termination: AYA patients, female patients, standard-risk malignancy or nonmalignant disease, unrelated bone marrow transplantation, HCT between 2000 and 2005, and absence of chronic graft-versus-host disease. These results suggest the need for education of both physicians and patients about the importance of LTFU, even in survivors with good physical condition. The decreased risk for follow-up termination after 2005 may suggest the increasing focus on LTFU in recent years.
AB - The need for long-term follow-up (LTFU) after allogeneic hematopoietic cell transplantation (HCT) has been increasingly recognized for managing late effects such as subsequent cancers and cardiovascular events. A substantial population, however, has already terminated LTFU at HCT centers. To better characterize follow-up termination, we analyzed the Japanese transplant registry database. The study cohort included 17 980 survivors beyond 2 years who underwent their first allogeneic HCT between 1974 and 2013. The median patient age at HCT was 34 years (range, 0-76 years). Follow-up at their HCT center was terminated in 4987 patients. The cumulative incidence of follow-up termination was 28% (95% confidence interval [CI], 27%-29%) at 10 years, increasing to 67% (95% CI, 65%-69%) at 25 years after HCT. Pediatric patients showed the lowest probability of follow-up termination for up to 16 years after HCT, whereas adolescent and young adult (AYA) patients showed the highest probability of follow-up termination throughout the period. Follow-up termination was most often made by physicians based on the patient’s good physical condition. Multivariate analysis identified 6 factors associated with follow-up termination: AYA patients, female patients, standard-risk malignancy or nonmalignant disease, unrelated bone marrow transplantation, HCT between 2000 and 2005, and absence of chronic graft-versus-host disease. These results suggest the need for education of both physicians and patients about the importance of LTFU, even in survivors with good physical condition. The decreased risk for follow-up termination after 2005 may suggest the increasing focus on LTFU in recent years.
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U2 - 10.1182/bloodadvances.2018026039
DO - 10.1182/bloodadvances.2018026039
M3 - Article
C2 - 30728138
AN - SCOPUS:85061134713
SN - 2473-9529
VL - 3
SP - 397
EP - 405
JO - Blood Advances
JF - Blood Advances
IS - 3
ER -