| Literature DB >> 30728138 |
Koichi Miyamura1, Takuya Yamashita2, Yoshiko Atsuta3,4, Tatsuo Ichinohe5, Koji Kato6, Naoyuki Uchida7, Takahiro Fukuda8, Kazuteru Ohashi9, Hiroyasu Ogawa10, Tetsuya Eto11, Masami Inoue12, Satoshi Takahashi13, Takehiko Mori14, Heiwa Kanamori15, Hiromasa Yabe16, Asahito Hama6, Shinichiro Okamoto14, Yoshihiro Inamoto8.
Abstract
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.Entities:
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Year: 2019 PMID: 30728138 PMCID: PMC6373751 DOI: 10.1182/bloodadvances.2018026039
Source DB: PubMed Journal: Blood Adv ISSN: 2473-9529