Interaction of Age and Comorbidities and Their Impacts on Hematopoietic Cell Transplantation (HCT) Outcomes

Interaction of Age and Comorbidities and Their Impacts on Hematopoietic Cell Transplantation (HCT) Outcomes
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年龄和合并症的相互作用及其对造血细胞移植 (HCT) 结果的影响

DOI:
10.1182/blood.v118.21.665.665
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发表时间:
2011
期刊:
影响因子:
20.3
通讯作者:
M. Sorror
M. Sorror
中科院分区:
医学1区
文献类型:
--
作者:
F. Ostronoff;B. Storer;R. Storb;S. Bhatia;R. Maziarz;M. Pulsipher;M. Maris;H. Deeg;P. Martin;F. Appelbaum;D. Maloney;B. Sandmaier;M. Sorror

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从历史上看,年龄一直是同种异体HCT的主要患者(pt)特异性决策因素。HCT合并症指数(CI)被开发用于捕获移植前合并症。该指数预测非复发死亡率(NRM),并彻底改变了同种异体HCT的结果分析。日历年龄是否在结果预测中为HCT-CI增加了额外的信息水平尚不清楚。在这里,我们研究了1)HCT-CI预测不同年龄组结果的效果如何,2)年龄是否可以纳入HCT-CI。在2000年1月至2006年12月期间,来自5个合作机构的3033名连续接受同种异体HCT治疗的患者的数据来自hla匹配的相关或非相关供体。所有数据均由一名研究者收集,该研究者对患者的最终结果不知情,以确保合并症编码的一致性。中位年龄为45岁(范围0.1-74.5)。总体而言,年龄增加与HCT-CI评分增加之间存在弱相关性(r=0.26)。患者随机分为训练组(n=1853)和验证组(n=1180)。在训练集中,HCT-CI预测NRM的累积发病率增加和总生存率(OS)的恶化在5个不同年龄组中一致(表1)。51%的患者未进行肺功能检查p使用比例风险模型来估计NRM和OS与不同年龄间隔和其他协变量(包括HCT-CI评分)相关的风险比(hr)(表2)。在该模型中,不同年龄组HCT-CI评分1-2和≥3的hr同质性检验均未被NRM(分别为p= 0.66和p= 0.86)或OS(分别为p= 0.76和p= 0.24)拒绝。与其他协变量相比,HCT-CI评分的增加与NRM的最高hr相关。40 - 50岁、50-60岁和60岁年龄组的患者NRM的hr范围为1.48-1.84,而40岁年龄组的患者HCT-CI评分为1分。在验证集中,尽管我们继续观察到NRM的hr随着年龄的增加而增加,但当年龄加入到HCT-CI时,NRM的c-统计数据只有轻微的改善(0.66对0.68)。这些结果表明,HCT- ci对所有年龄组的预后预测都是有效的,在考虑合共病的模型中,年龄本身对HCT预后预测的影响相对较小。年龄bb0 - 40岁的影响相当于单一合并症,权重为1,因此在使用HCT-CI/年龄综合指数时应给予1分。披露:无相关利益冲突需要申报。
Abstract 665 Historically, age has been the main patient (pt)-specific decision-making factor for allogeneic HCT. The HCT comorbidity index (CI) was developed to capture pretransplant comorbidities. The index predicts non-relapse mortality (NRM) and has revolutionized outcome analysis for allogeneic HCT. Whether calendar age adds additional level of information to the HCT-CI in outcome prediction is unknown. Here, we investigated 1) how well the HCT-CI predicts outcomes across different age groups and 2) whether age could be incorporated into the HCT-CI. Data from 3033 consecutive pts treated with allogeneic HCT between January 2000 and December 2006 from HLA-matched related or unrelated donors at five collaborating institutions were used for this study. All data were collected by a single investigator, who was blinded from the final outcomes of pts, to ensure consistent comorbidity coding. Median age was 45 (range 0.1–74.5) years. Overall, there was a weak correlation between increasing age and increasing HCT-CI scores (r=0.26). Pts were randomly divided into training (n=1853) and validation (n=1180) sets. In the training set, the HCT-CI predicted increased cumulative incidence rates of NRM and worsening of overall survival (OS) rates consistently in the 5 separate age groups (Table 1). Pulmonary function tests were not performed in 51% of pts p A proportional hazards model was used to estimate the hazard ratios (HRs) for NRM and OS associated with different age intervals and other covariates, including the HCT-CI scores (Table 2). In this model, tests of homogeneity of HRs associated with HCT-CI scores of 1–2 and ≥3 across age groups were not rejected for either NRM ( p =0.66 and p =0.86, respectively) or OS ( p= 0.76 and p =0.24, respectively). Increasing HCT-CI scores were associated with the highest HRs for NRM compared to other covariates. Pts in age groups 40–50, 50–60, and >60 years had HRs for NRM ranging between 1.48–1.84 compared to pts 40 years was assigned a score of 1 to be added to the HCT-CI scores. In the validation set, although we continued to observe increases in HRs for NRM with increasing age, only minor improvement in c-statistics for NRM (0.66 versus 0.68) was detected when age was added to the HCT-CI. These results indicate that the HCT-CI is valid for outcome prediction across all age groups and that age per se has a relatively minor impact on HCT outcome prediction in models that account for comorbidities. Age >40 years had an impact equivalent to a single comorbidity with a weight of 1, and therefore should be assigned a score of 1 when using the HCT-CI/Age composite index. Disclosures: No relevant conflicts of interest to declare.