Majhail Navneet S, Chitphakdithai Pintip, Logan Brent, King Roberta, Devine Steven, Rossmann Susan N, Hale Gregory, Hartzman Robert J, Karanes Chatchada, Laport Ginna G, Nemecek Eneida, Snyder Edward L, Switzer Galen E, Miller John, Navarro Willis, Confer Dennis L, Levine John E
Blood & Marrow Transplant Program, Cleveland Clinic, Cleveland, Ohio; National Marrow Donor Program, Minneapolis, Minnesota.
National Marrow Donor Program, Minneapolis, Minnesota.
Biol Blood Marrow Transplant. 2015 Jan;21(1):142-50. doi: 10.1016/j.bbmt.2014.10.001. Epub 2014 Oct 15.
Patients and physicians may defer unrelated donor hematopoietic cell transplantation (HCT) as curative therapy because of the mortality risk associated with the procedure. Therefore, it is important for physicians to know the current outcomes data when counseling potential candidates. To provide this information, we evaluated 15,059 unrelated donor hematopoietic cell transplant recipients between 2000 and 2009. We compared outcomes before and after 2005 for 4 cohorts: age <18 years with malignant diseases (n = 1920), ages 18 to 59 years with malignant diseases (n = 9575), ages ≥ 60 years with malignant diseases (n = 2194), and nonmalignant diseases (n = 1370). Three-year overall survival in 2005 to 2009 was significantly better in all 4 cohorts (<18 years: 55% versus 45%, 18 to 59 years: 42% versus 35%, ≥ 60 years: 35% versus 25%, nonmalignant diseases: 69% versus 60%; P < .001 for all comparisons). Multivariate analyses in leukemia patients receiving HLA 7/8 to 8/8-matched transplants showed significant reduction in overall and nonrelapse mortality in the first year after HCT among patients who underwent transplantation in 2005 to 2009; however, risks for relapse did not change over time. Significant survival improvements after unrelated donor HCT have occurred over the recent decade and can be partly explained by better patient selection (eg, HCT earlier in the disease course and lower disease risk), improved donor selection (eg, more precise allele-level matched unrelated donors) and changes in transplantation practices.
由于与该手术相关的死亡风险,患者和医生可能会推迟将无关供体造血细胞移植(HCT)作为根治性治疗方法。因此,医生在为潜在候选者提供咨询时了解当前的预后数据非常重要。为了提供这些信息,我们评估了2000年至2009年间15059例无关供体造血细胞移植受者。我们比较了2005年前后4个队列的预后:年龄<18岁的恶性疾病患者(n = 1920)、年龄18至59岁的恶性疾病患者(n = 9575)、年龄≥60岁的恶性疾病患者(n = 2194)和非恶性疾病患者(n = 1370)。在所有4个队列中,2005年至2009年的3年总生存率均显著提高(<18岁:55%对45%,18至59岁:42%对35%,≥60岁:35%对25%,非恶性疾病:69%对60%;所有比较P <.001)。对接受HLA 7/8至8/8匹配移植的白血病患者进行的多变量分析显示,2005年至2009年接受移植的患者在HCT后第一年的总死亡率和非复发死亡率显著降低;然而,复发风险并未随时间变化。在最近十年中,无关供体HCT后的生存率有显著提高,部分原因可以解释为更好的患者选择(例如,在疾病病程早期进行HCT和较低的疾病风险)、改进的供体选择(例如,更精确的等位基因水平匹配无关供体)以及移植实践的变化。