首页 | 本学科首页   官方微博 | 高级检索  
     


Long-term outcomes after high dose therapy and autologous haematopoietic cell rescue for refractory/relapsed Hodgkin lymphoma
Authors:Ann Y. Minn  Elyn Riedel  Jerry Halpern  Laura J. Johnston  Sandra J. Horning  Richard T. Hoppe  Karyn A. Goodman
Affiliation:1. Department of Radiation Oncology, Stanford University, Palo Alto, CA, USA;2. Department of Radiation Oncology, Memorial Sloan Kettering Cancer Center, New York, NY, USA;3. Department of Health Research and Policy, Stanford University, Palo Alto, CA, USA;4. Department of Medicine, Division of Bone Marrow Transplantation, Stanford University, Palo Alto, CA, USA;5. Clinical Development Hematology/Oncology, Genentech, Inc., South San Francisco, CA, USA;6. Department of Radiation Oncology, Stanford University, Palo Alto, CA, USA

Department of Radiation Oncology, Memorial Sloan Kettering Cancer Center, New York, NY, USA

Correspondence: Karyn A. Goodman, MD, Department of Radiation Oncology, Memorial Sloan-Kettering Cancer Center, 1275 York Ave., New York, NY 10065, USA.

E-mail: goodmank@mskcc.org

Abstract:
The standard treatment for patients with refractory or relapsed Hodgkin lymphoma (HL) is high-dose chemotherapy and/or radiation with autologous haematopoietic cell rescue (AHCR). In this study, we assessed quality of life and evaluated the risk of late morbidity and mortality for HL patients who underwent AHCR. One hundred and fifty-four patients who underwent AHCR at Stanford University from 1988 to 2002 and survived ≥2 years were evaluated. Median follow-up was 10·2 years. There were 54 deaths, 34 from HL, 20 from other causes. The 10-year cumulative incidence of death from HL or other causes was 21·7% and 12·7%, respectively. Thirteen deaths were from second malignancies. The risk ratio of second malignancies was 8·0 [95% confidence interval (CI), 4·7–12·6] compared with the general population, and 3·0 (95% CI, 1·8–4·8) compared with HL patients not undergoing AHCR. The risk ratio of second malignancies was 1·5 (95% CI, 0·9–2·4) compared with HL patients receiving non-AHCR therapy. Overall quality of life did not differ from the general population, but AHCR survivors did note reduced functioning and some worse symptoms. AHCR survivors may be at increased risk of death from HL and other causes compared with the general population, but not compared with the HL population as a whole.
Keywords:Hodgkins lymphoma  hsc transplantation  radiotherapy  bmt  high dose therapy
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号