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一项比较血液恶性肿瘤患者接受造血细胞移植时使用和不使用培非格司亭的长期结局的前瞻性队列研究。

A Prospective Cohort Study Comparing Long-Term Outcomes with and without Palifermin in Patients Receiving Hematopoietic Cell Transplantation for Hematologic Malignancies.

机构信息

Center for International Blood and Marrow Transplant Research, Department of Medicine, Medical College of Wisconsin, Milwaukee, Wisconsin.

Center for International Blood and Marrow Transplant Research, Department of Medicine, Medical College of Wisconsin, Milwaukee, Wisconsin.

出版信息

Transplant Cell Ther. 2021 Oct;27(10):837.e1-837.e10. doi: 10.1016/j.jtct.2021.06.028. Epub 2021 Jul 2.

DOI:10.1016/j.jtct.2021.06.028
PMID:34224914
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8606163/
Abstract

The incidence of debilitating oral mucositis (OM) can be as high as 99% after myeloablative conditioning regimens preparing patients with hematologic malignancies for hematopoietic cell transplantation (HCT). Palifermin (KGF) is a recombinant human keratinocyte growth factor that reduces the incidence and duration of severe OM. The long-term safety of KGF has not been well established, however. In this long-term prospective matched-cohort study, patients who received KGF (cases) and underwent autologous or allogeneic HCT for hematologic malignancies between 2006 and 2013 were matched 1:1 to patients who did not receive KGF (controls). The primary outcome was overall survival (OS). Other outcomes were disease relapse, new malignancies, pancreatitis, renal failure requiring dialysis, pulmonary complications, cataract surgery, and acute and chronic graft-versus-host disease (GVHD). The analysis population comprised 2191 matched pairs with a wide range of diseases and donor types that received diverse conditioning and GVHD preventive regimens, representing contemporary practice patterns. The median duration of follow-up was 8 years (range, 1 to 12.5 years). In multivariate analyses, the probabilities of OS (relative risk [RR], 1.01; 95% confidence interval [CI], 0.91 to 1.12), relapse (RR, 1.06; 95% CI, 0.94 to 1.18), new malignancies (RR, 0.89; 95% CI, 0.67 to 1.18), and cataract surgery (RR, 1.05; 95% CI, 0.74 to 1.50) were not statistically significantly different between cases and controls. In univariate analyses, no increased risks were observed for renal failure requiring dialysis, pancreatitis, acute GVHD, chronic GVHD, interstitial pneumonitis/acute respiratory distress syndrome/idiopathic pneumonia syndrome, or bronchiolitis obliterans/cryptogenic organizing pneumonia/bronchiolitis obliterans organizing pneumonia among cases compared with controls. This long-term prospective safety cohort study demonstrates that the KGF group had no increased risk of overall mortality, relapse, new malignancies, or any other key outcome. The broad inclusion criteria allow the results to be generalized to contemporary practice for patients with a wide range of diseases and receiving a wide range of HCT conditioning regimens and graft sources from diverse donor types.

摘要

骨髓清除性预处理方案可使 99%以上血液系统恶性肿瘤患者发生严重的口腔黏膜炎(OM)。Palifermin(KGF)是一种重组人角质细胞生长因子,可降低 OM 的发生率和严重程度。然而,KGF 的长期安全性尚未得到很好的证实。在这项长期前瞻性匹配队列研究中,2006 年至 2013 年间接受 KGF(病例组)治疗并接受自体或同种异体造血细胞移植(HCT)治疗血液系统恶性肿瘤的患者与未接受 KGF 治疗的患者(对照组)按 1:1 匹配。主要结局是总生存(OS)。其他结局包括疾病复发、新发恶性肿瘤、胰腺炎、需要透析的肾衰竭、肺部并发症、白内障手术以及急性和慢性移植物抗宿主病(GVHD)。分析人群包括 2191 对匹配对,涵盖了广泛的疾病和供者类型,接受了不同的预处理和 GVHD 预防方案,代表了当代的实践模式。中位随访时间为 8 年(范围 1 至 12.5 年)。多变量分析显示,OS(相对风险 [RR],1.01;95%置信区间 [CI],0.91 至 1.12)、复发(RR,1.06;95%CI,0.94 至 1.18)、新发恶性肿瘤(RR,0.89;95%CI,0.67 至 1.18)和白内障手术(RR,1.05;95%CI,0.74 至 1.50)的概率在病例组和对照组之间无统计学差异。单变量分析显示,与对照组相比,病例组并未增加透析需要的肾衰竭、胰腺炎、急性 GVHD、慢性 GVHD、间质性肺炎/急性呼吸窘迫综合征/特发性肺炎综合征或细支气管炎闭塞性/隐源性机化性肺炎/细支气管炎闭塞性机化性肺炎的风险。这项长期前瞻性安全性队列研究表明,KGF 组的总死亡率、复发率、新发恶性肿瘤率或任何其他关键结局均无升高风险。广泛的纳入标准允许将结果推广到广泛疾病患者的当代实践中,并接受来自不同供者类型的广泛的 HCT 预处理方案和移植物来源。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/01dd/8606163/a3ee31c691af/nihms-1733777-f0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/01dd/8606163/b5bc4ef6990a/nihms-1733777-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/01dd/8606163/6e521475a9f5/nihms-1733777-f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/01dd/8606163/a3ee31c691af/nihms-1733777-f0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/01dd/8606163/b5bc4ef6990a/nihms-1733777-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/01dd/8606163/6e521475a9f5/nihms-1733777-f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/01dd/8606163/a3ee31c691af/nihms-1733777-f0004.jpg

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