Lakhani Laila, Alasfar Sami, Bhalla Anshul, Aala Amtul, Rosenberg Avi, Ostrander Darin, Schollenberger Megan D, Brennan Daniel C, Lipson Evan J
Emory Transplant Center, Emory University School of Medicine, Atlanta, GA.
Johns Hopkins Medical Institute, Baltimore, MD.
Transplant Direct. 2021 Jan 15;7(2):e656. doi: 10.1097/TXD.0000000000001113. eCollection 2021 Feb.
Donor-derived cell-free DNA (dd-cfDNA) is a useful biomarker of rejection that originates from allograft cells undergoing injury. Plasma levels <1% in kidney transplant recipients have a high negative predictive value for active allograft rejection. The utility of this biomarker in kidney transplant recipients receiving immune checkpoint inhibitor therapy is unknown.
We describe a case in which serial dd-cfDNA monitoring facilitated the use of immune checkpoint inhibitor therapy, which is known to be associated with high rates of rejection, in a kidney transplant recipient with metastatic cancer.
A 72-y-old man with end-stage kidney disease secondary to autosomal dominant polycystic kidney disease underwent living unrelated kidney transplant in December 2010. His immunosuppression regimen included tacrolimus, mycophenolate, and prednisone. In July 2017, he presented with metastatic cutaneous squamous cell carcinoma. After his disease progressed through radiation therapy and cetuximab, he received pembrolizumab (antiprogrammed cell death protein 1). His dd-cfDNA level was undetectable at baseline, then increased during treatment but remained <1%. This trend, despite fluctuations in serum creatinine levels during therapy, allowed for continuation of pembrolizumab and successful treatment of his metastatic cancer without clinically evident allograft rejection. After discontinuation of pembrolizumab, dd-cfDNA levels fell below the level of detection. Genetic analysis of the cutaneous squamous cell carcinoma demonstrated a genetic profile distinct from the dd-cfDNA, indicating that tumor lysis did not impact increases in dd-cfDNA.
Serial dd-cfDNA measurements may provide a useful, noninvasive biomarker for detecting allograft injury that may facilitate the use of immunomodulatory therapies in organ transplant recipients with cancer.
供体来源的游离细胞DNA(dd-cfDNA)是一种有用的排斥反应生物标志物,其来源于发生损伤的同种异体移植细胞。肾移植受者血浆水平<1%对活动性同种异体移植排斥反应具有较高的阴性预测价值。这种生物标志物在接受免疫检查点抑制剂治疗的肾移植受者中的效用尚不清楚。
我们描述了一例通过连续监测dd-cfDNA促进免疫检查点抑制剂治疗的病例,该疗法已知与高排斥率相关,患者为一名患有转移性癌症的肾移植受者。
一名72岁男性,因常染色体显性遗传性多囊肾病导致终末期肾病,于2010年12月接受了非亲属活体肾移植。他的免疫抑制方案包括他克莫司、霉酚酸酯和泼尼松。2017年7月,他出现转移性皮肤鳞状细胞癌。在疾病经放射治疗和西妥昔单抗治疗进展后,他接受了帕博利珠单抗(抗程序性细胞死亡蛋白1)治疗。他的dd-cfDNA水平在基线时无法检测到,然后在治疗期间升高,但仍<1%。尽管治疗期间血清肌酐水平有波动,但这种趋势使得帕博利珠单抗得以继续使用,并且成功治疗了他的转移性癌症,而没有临床明显的同种异体移植排斥反应。停用帕博利珠单抗后,dd-cfDNA水平降至检测水平以下。对皮肤鳞状细胞癌的基因分析显示其基因谱与dd-cfDNA不同,表明肿瘤溶解并未影响dd-cfDNA的升高。
连续测量dd-cfDNA可能为检测同种异体移植损伤提供一种有用的非侵入性生物标志物,这可能有助于在患有癌症的器官移植受者中使用免疫调节疗法。