Title | Outcome of children and adolescents with relapsed Hodgkin lymphoma treated with high-dose therapy and autologous stem cell transplantation: the Memorial Sloan Kettering Cancer Center experience. |
Publication Type | Journal Article |
Year of Publication | 2018 |
Authors | Giulino-Roth L, O'Donohue T, Chen Z, Trippett TM, Klein E, Kernan NA, Kobos R, Prockop SE, Scaradavou A, Shukla N, Steinherz PG, Moskowitz AJ, Moskowitz CH, Boulad F |
Journal | Leuk Lymphoma |
Volume | 59 |
Issue | 8 |
Pagination | 1861-1870 |
Date Published | 2018 Aug |
ISSN | 1029-2403 |
Keywords | Adolescent, Antineoplastic Combined Chemotherapy Protocols, Child, Dose-Response Relationship, Drug, Female, Hematopoietic Stem Cell Transplantation, Hodgkin Disease, Humans, Kaplan-Meier Estimate, Male, Neoplasm Recurrence, Local, Prognosis, Retrospective Studies, Transplantation, Autologous, Treatment Outcome, Young Adult |
Abstract | To evaluate outcomes and prognostic markers among children with relapsed Hodgkin lymphoma (HL) treated with autologous stem cell transplant (ASCT), we conducted a retrospective analysis of 36 consecutive pediatric patients treated at Memorial Sloan Kettering Cancer Center from 1989 to 2013. With a median follow-up of 9.6 years, the 10-year overall survival (OS) and event-free survival (EFS) were 74.1 and 67.1% respectively. Absence of B-symptoms, chemotherapy-sensitive disease, and transplant date after 1997 were each associated with superior EFS [HR 0.12 (p = .0015), 0.18 (p = .0039), and 0.17 (p = .0208), respectively]. Childhood Hodgkin International Prognostic Score at relapse (R-CHIPS) was calculated in a subset of patients (n = 22) and a lower score was associated with improved OS (HR 0.29, p = .0352) and a trend toward improved EFS (HR 0.38, p = .0527). In summary, ASCT results in durable remission for the majority of pediatric patients with relapsed HL. R-CHIPS should be evaluated in larger cohorts as a potential predictive tool. |
DOI | 10.1080/10428194.2017.1403601 |
Alternate Journal | Leuk Lymphoma |
PubMed ID | 29183202 |
PubMed Central ID | PMC6637236 |
Grant List | P30 CA008748 / CA / NCI NIH HHS / United States |