我们还应该用卡米塔的重度再生障碍性贫血标准吗?

The Korean Journal of Hematology Pub Date : 2012-06-01 Epub Date: 2012-06-26 DOI:10.5045/kjh.2012.47.2.126
Hyun Hwa Yoon, Seok Jae Huh, Ji Hyun Lee, Suee Lee, Sung-Hyun Kim, Hyuk Chan Kwon, Hyo-Jin Kim
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引用次数: 5

摘要

背景:Camitta诊断重度再生障碍性贫血(SAA)的标准自1976年开始使用。然而,没有人试图验证Camitta的标准,SAA患者的生存可能因绝对中性粒细胞计数(ANC)、血小板计数(PLT)和校正网织红细胞计数(CRC)而异,这是Camitta标准的组成部分。方法:对117例经Camitta诊断为SAA的患者进行回顾性分析。采用单因素和多因素分析评估影响总生存期(OS)的因素。结果:免疫抑制治疗(IST)或干细胞移植(SCT)对OS有显著影响(P=0.001)。因此,我们排除了治疗应答者进行分析。最后对92例SAA患者进行单因素和多因素分析,包括IST或SCT治疗无反应组和保守治疗组。分析患者的中位年龄为54.5岁。男女比例为1:1。中位随访时间为74.23个月(54.71 ~ 93.74个月)。中位ANC、PLT和CRC分别为394/µL、12000 /µL和0.39%。在多变量分析中,ANC结论:ANC可能是诊断SAA的必要标准,而不是可选标准。这项研究提出了修改Camitta标准的可能性。需要大规模的研究来改变Camitta的标准。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Should we still use Camitta's criteria for severe aplastic anemia?

Should we still use Camitta's criteria for severe aplastic anemia?

Should we still use Camitta's criteria for severe aplastic anemia?

Should we still use Camitta's criteria for severe aplastic anemia?

Background: The criteria by Camitta for diagnosis in severe aplastic anemia (SAA) has been used since 1976. However, there has been no attempt to verify the Camitta's criteria, that the survival in patients with SAA may differ by absolute neutrophil count (ANC), platelet count (PLT), and corrected reticulocyte count (CRC), which are components of the Camitta's criteria.

Methods: 117 SAA patients diagnosed by the Camitta's criteria were analyzed, retrospectively. Univariate and multivariate analyses were used to evaluate the factors affecting overall survival (OS).

Results: Response by immunosuppressive therapy (IST) or stem cell transplantation (SCT) significantly affected OS (P=0.001). Therefore, we excluded treatment responders for analysis. Finally, 92 SAA patients including treatment non-responders by IST or SCT and conservative care group were analyzed by using univariate and multivariate analyses. The median age of analyzed patients was 54.5 years. Male to female ratio was 1:1. The median follow-up duration was 74.23 months (range, 54.71-93.74 months). The median ANC, PLT, and CRC were 394/µL, 12,000/µL, and 0.39%, respectively. In multivariate analyses, ANC <500/µL or ≥500/µL (P=0.015, HR 2.694, 95% CI: 1.20-6.01) and age (P=0.015, HR 1.022, 95% CI: 1.00-1.04) were the significant factors for OS.

Conclusion: ANC could be an essential, not an optional criterion for diagnosing SAA. This study suggests the possibility that the Camitta's criteria be modified. Studies in large cohorts are needed to transform the Camitta's criteria.

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