Department of Blood and Marrow Transplantation and Cellular Immunotherapy, H. Lee Moffitt Cancer Center and Research Institute, Tampa, Florida.
The Emmes Company, Rockville, Maryland.
JAMA Oncol. 2020 Jan 1;6(1):e192974. doi: 10.1001/jamaoncol.2019.2974. Epub 2020 Jan 9.
Immune suppression discontinuation is routinely attempted after allogeneic hematopoietic cell transplantation (HCT) and under current practices may lead to graft-vs-host disease (GVHD)-associated morbidity and death. However, the likelihood and predictive factors associated with successful immune suppression discontinuation after HCT are poorly understood.
To examine factors associated with successful immune suppression discontinuation and risk for immune suppression discontinuation failure under conventional HCT approaches and develop a practical tool to estimate successful immune suppression discontinuation likelihood at the clinical point of care.
DESIGN, SETTING, AND PARTICIPANTS: Using long-term follow-up data from 2 national Blood and Marrow Transplant Clinical Trial Network studies (N = 827), a multistate model was developed to investigate the probability and variables associated with immune suppression discontinuation success. The study began in July 2015, and analyses were completed in August 2019.
Immune suppression discontinuation and immune suppression discontinuation failure.
Of the 827 patients included in the analysis, 456 were men (55.1%). Median age at transplant was 44 (range, <1-67) years. With median follow-up of 72 (range, 11-124) months, 20.0% of the patients were alive and not receiving immune suppression at 5 years. Older recipient age (adjusted odds ratio [aOR] of >50 vs <30 years, 0.27, 99% CI, 0.14-0.50; P < .001), mismatched unrelated donor (aOR, mismatched unrelated vs matched related, 0.37; 99% CI, 0.14-0.97; P = .008), peripheral blood graft (aOR of peripheral blood graft vs bone marrow, 0.46; 99% CI, 0.26-0.82; P < .001), and advanced stage disease (aOR of advanced vs early disease, 0.45; 99% CI, 0.23-0.86, P = 0.002), were significantly associated with decreased odds of immune suppression discontinuation. Failed attempts at immune suppression discontinuation (127 patients [37.1% of total immune suppression discontinuation events]) resulting in GVHD were significantly associated with use of peripheral blood stem cells (HR, 2.62; 99% CI, 1.30-5.29; P < .001), prior GVHD, and earlier immune suppression discontinuation attempts. Earlier immune suppression discontinuation was not associated with protection from cancer relapse after HCT (adjusted hazard ratio for discontinuation vs not, 1.95; 99% CI, 0.88-4.31; P = .03).Dynamic prediction models were developed to provide future immune suppression discontinuation probability according to individual patient characteristics.
Successful immune suppression discontinuation is uncommon in the setting of peripheral blood stem cell grafts. The data suggest earlier attempts at ISD conferred no long-term benefit, given frequent ISD failure, limited subsequent success after initial failed ISD attempt, and no evidence of relapse reduction. Using a risk model-based clinical application, physicians may be able to identify individual patients' probability of successful immune suppression discontinuation.
在异基因造血细胞移植(HCT)后,通常会尝试停止免疫抑制,但根据目前的做法,这可能会导致移植物抗宿主病(GVHD)相关的发病率和死亡率。然而,对于 HCT 后成功停止免疫抑制的可能性及其相关预测因素,人们了解甚少。
研究与成功停止免疫抑制相关的因素,以及在传统 HCT 方法下免疫抑制停止失败的风险,并开发一种实用的工具,以便在临床护理点估计成功停止免疫抑制的可能性。
设计、地点和参与者:利用来自 2 项国家血液和骨髓移植临床研究网络研究(N=827)的长期随访数据,开发了一个多状态模型来研究与免疫抑制停止成功相关的概率和变量。该研究于 2015 年 7 月开始,分析于 2019 年 8 月完成。
免疫抑制停止和免疫抑制停止失败。
在纳入分析的 827 名患者中,有 456 名男性(55.1%)。移植时的中位年龄为 44 岁(范围,<1-67 岁)。中位随访时间为 72 个月(范围,11-124 个月),5 年后有 20.0%的患者存活且未接受免疫抑制治疗。受体年龄较大(调整后的优势比(OR)>50 岁与<30 岁,0.27,99%置信区间(CI),0.14-0.50;P<0.001)、非匹配无关供体(OR,非匹配无关与匹配相关,0.37;99%CI,0.14-0.97;P=0.008)、外周血移植物(OR,外周血移植物与骨髓,0.46;99%CI,0.26-0.82;P<0.001)和晚期疾病(OR,晚期与早期疾病,0.45;99%CI,0.23-0.86,P=0.002)与免疫抑制停止的可能性降低显著相关。免疫抑制停止失败(127 例患者[总免疫抑制停止事件的 37.1%])导致 GVHD 的患者,与使用外周血干细胞(HR,2.62;99%CI,1.30-5.29;P<0.001)、既往 GVHD 和更早的免疫抑制停止尝试显著相关。更早的免疫抑制停止与 HCT 后癌症复发的保护无关(停止与不停用的调整后的危险比,1.95;99%CI,0.88-4.31;P=0.03)。
在外周血干细胞移植的情况下,成功停止免疫抑制并不常见。数据表明,早期尝试 ISD 并没有带来长期益处,因为 ISD 失败频繁,初始 ISD 失败后随后成功的机会有限,并且没有证据表明复发减少。使用基于风险模型的临床应用,医生可以识别个别患者成功停止免疫抑制的可能性。