Try Mélanie, Harel Stéphanie
Centre hospitalier universitaire de Bicêtre, assistance publique-hôpitaux de Paris (APHP), université Paris-Saclay, service de néphrologie, dialyse et transplantation, 94270 Le Kremlin-Bicêtre, France; Groupe de Recherche Interdisciplinaire Francophone en Onco-Néphrologie, Paris, France.
Centre hospitalier universitaire de Saint-Louis, assistance publique-hôpitaux de Paris (APHP), université Paris Cité, service d'immuno-hématologie, 75010 Paris, France.
Bull Cancer. 2024 Jul-Aug;111(7-8):733-740. doi: 10.1016/j.bulcan.2022.12.015. Epub 2023 Feb 8.
Renal impairment is common during multiple myeloma and persistent reduction in kidney function strongly affects prognosis. Cast nephropathy, by monoclonal free light chains precipitation with uromodulin in renal tubules, is the main cause of acute kidney injury in multiple myeloma. Kidney biopsy, although not necessary for diagnosis, allows assessment of renal prognosis according to the extent of cast formation, tubular atrophy and interstitial fibrosis. Prevention and early diagnosis of acute kidney injury are essential to optimize management and avoid progression to chronic kidney disease. Rehydration, interruption of nephrotoxic treatments, correction of precipitating factors, anti-plasma cell chemotherapy can rapidly reduce the free light chains nephrotoxicity. The association of the proteasome inhibitor Bortezomib and high dose Dexamethasone is the reference treatment in newly diagnosed patients with renal impairment. Adding Cyclophosphamide or the immunomodulator Lenalidomide may improve the hematological response, but with a poorer tolerance. Use of anti-CD38 monoclonal antibodies is being evaluated in this population. Hemodialysis with high-flux or high-cut-off membranes, combined to chemotherapy, may improve renal function recovery. Management of multiple myeloma have to be adapted in patients with chronic kidney disease, dialysis or kidney transplantation. Because of improvement in global survival, kidney transplantation remains an option to consider in selected patients. Collaboration between hematologists and nephrologists is essential throughout the course of the disease.
肾功能损害在多发性骨髓瘤中很常见,肾功能持续下降会严重影响预后。管型肾病是由于单克隆游离轻链与尿调节蛋白在肾小管中沉淀,是多发性骨髓瘤急性肾损伤的主要原因。肾活检虽然不是诊断所必需的,但可根据管型形成、肾小管萎缩和间质纤维化的程度评估肾脏预后。急性肾损伤的预防和早期诊断对于优化治疗和避免进展为慢性肾脏病至关重要。补液、中断肾毒性治疗、纠正诱发因素、抗浆细胞化疗可迅速降低游离轻链的肾毒性。蛋白酶体抑制剂硼替佐米和高剂量地塞米松联合使用是新诊断的肾功能损害患者的标准治疗方法。添加环磷酰胺或免疫调节剂来那度胺可能会改善血液学反应,但耐受性较差。抗CD38单克隆抗体在该人群中的应用正在评估中。采用高通量或高截留膜进行血液透析并联合化疗,可能会改善肾功能恢复。对于患有慢性肾脏病、透析或肾移植的患者,多发性骨髓瘤的治疗必须进行调整。由于总体生存率的提高,肾移植仍然是某些患者可考虑的选择。在疾病的整个过程中,血液科医生和肾内科医生之间的合作至关重要。