Valeria Moreno, Ludovic Saba, Sara Tama-Shekan, Chakra P Chaulagain
{"title":"系统性 AL 淀粉样变性的现有和新兴免疫疗法。","authors":"Valeria Moreno, Ludovic Saba, Sara Tama-Shekan, Chakra P Chaulagain","doi":"10.24976/Discov.Med.202436188.162","DOIUrl":null,"url":null,"abstract":"<p><p>Systemic light-chain (AL) amyloidosis is a rare and complex clonal plasma cell neoplasm characterized by the production of misfolded and unstable immunoglobulin light-chains leading to multisystem amyloid deposition, which progresses to organ dysfunction and eventual failure. The importance and urgency of AL amyloidosis depends on its potential to induce significant organ impairment, progressive course, risk of life-threatening complications, and the limited treatment options available. Treatment options and prognosis depend on the number and severity of organ involvement at the time of diagnosis with cardiac involvement carrying the worst outcomes. The treatments aim to target eliminating the underlying clonal plasma cell neoplasm and prevent the production and deposition of amyloid precursor immunoglobulin light-chain protein in the affected vital organs. Strategies for treating systemic AL amyloidosis have incorporated anti-plasma cell therapies approved in the management of multiple myeloma due to their shared cellular derivation. Quadruplet therapy of cyclophosphamide, bortezomib, dexamethasone and daratumumab (DaraCyborD) is the currently approved first-line induction therapy for systemic AL amyloidosis. Some patients need upfront autologous hematopoietic stem cell transplantation (HSCT) after high-dose melphalan conditioning particularly if DaraCyborD is not able to achieve complete hematologic response (CHR). Additionally, a promising treatment option involves disassembling amyloid deposits from the vital organs using monoclonal antibodies such as CAEL 101 or Birtamimab with the expectation of restoring damaged tissues of the vital organs affected thereby improving or reversing patients' symptoms. Both CAEL 101 and Birtamimab are currently being tested in phase 3 clinical trials for systemic AL amyloidosis patients with advanced cardiac involvement. This comprehensive review provides an up-to-date overview of AL amyloidosis therapy, with a particular focus on recent advances and future directions of immunotherapeutic strategies.</p>","PeriodicalId":93980,"journal":{"name":"Discovery medicine","volume":"36 188","pages":"1761-1771"},"PeriodicalIF":0.0000,"publicationDate":"2024-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Current and Emerging Immunotherapies for Systemic AL Amyloidosis.\",\"authors\":\"Valeria Moreno, Ludovic Saba, Sara Tama-Shekan, Chakra P Chaulagain\",\"doi\":\"10.24976/Discov.Med.202436188.162\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Systemic light-chain (AL) amyloidosis is a rare and complex clonal plasma cell neoplasm characterized by the production of misfolded and unstable immunoglobulin light-chains leading to multisystem amyloid deposition, which progresses to organ dysfunction and eventual failure. 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Some patients need upfront autologous hematopoietic stem cell transplantation (HSCT) after high-dose melphalan conditioning particularly if DaraCyborD is not able to achieve complete hematologic response (CHR). Additionally, a promising treatment option involves disassembling amyloid deposits from the vital organs using monoclonal antibodies such as CAEL 101 or Birtamimab with the expectation of restoring damaged tissues of the vital organs affected thereby improving or reversing patients' symptoms. Both CAEL 101 and Birtamimab are currently being tested in phase 3 clinical trials for systemic AL amyloidosis patients with advanced cardiac involvement. 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引用次数: 0
摘要
全身性轻链(AL)淀粉样变性是一种罕见而复杂的克隆性浆细胞肿瘤,其特点是产生折叠错误和不稳定的免疫球蛋白轻链,导致多系统淀粉样沉积,进而发展为器官功能障碍并最终衰竭。谷丙转氨酶淀粉样变性的重要性和紧迫性取决于其诱发严重器官损害的可能性、进展性病程、危及生命的并发症风险以及有限的治疗方案。治疗方案和预后取决于诊断时受累器官的数量和严重程度,其中心脏受累的预后最差。治疗的目的是消除潜在的克隆性浆细胞肿瘤,防止淀粉样前体免疫球蛋白轻链蛋白在受累重要器官中产生和沉积。治疗全身性 AL 淀粉样变性的策略已纳入了在多发性骨髓瘤治疗中获得批准的抗浆细胞疗法,因为它们具有相同的细胞来源。环磷酰胺、硼替佐米、地塞米松和达拉单抗(DaraCyborD)四联疗法是目前获批的全身性AL淀粉样变性的一线诱导疗法。一些患者需要在大剂量美法仑治疗后进行前期自体造血干细胞移植(HSCT),尤其是在DaraCyborD无法获得完全血液学应答(CHR)的情况下。此外,一种很有前景的治疗方案是使用 CAEL 101 或 Birtamimab 等单克隆抗体分解重要器官中的淀粉样蛋白沉积物,期望恢复受影响重要器官的受损组织,从而改善或逆转患者的症状。目前,CAEL 101 和 Birtamimab 正在进行 3 期临床试验,用于治疗晚期心脏受累的全身性 AL 淀粉样变性患者。本综述全面概述了AL淀粉样变性治疗的最新进展,尤其关注免疫治疗策略的最新进展和未来方向。
Current and Emerging Immunotherapies for Systemic AL Amyloidosis.
Systemic light-chain (AL) amyloidosis is a rare and complex clonal plasma cell neoplasm characterized by the production of misfolded and unstable immunoglobulin light-chains leading to multisystem amyloid deposition, which progresses to organ dysfunction and eventual failure. The importance and urgency of AL amyloidosis depends on its potential to induce significant organ impairment, progressive course, risk of life-threatening complications, and the limited treatment options available. Treatment options and prognosis depend on the number and severity of organ involvement at the time of diagnosis with cardiac involvement carrying the worst outcomes. The treatments aim to target eliminating the underlying clonal plasma cell neoplasm and prevent the production and deposition of amyloid precursor immunoglobulin light-chain protein in the affected vital organs. Strategies for treating systemic AL amyloidosis have incorporated anti-plasma cell therapies approved in the management of multiple myeloma due to their shared cellular derivation. Quadruplet therapy of cyclophosphamide, bortezomib, dexamethasone and daratumumab (DaraCyborD) is the currently approved first-line induction therapy for systemic AL amyloidosis. Some patients need upfront autologous hematopoietic stem cell transplantation (HSCT) after high-dose melphalan conditioning particularly if DaraCyborD is not able to achieve complete hematologic response (CHR). Additionally, a promising treatment option involves disassembling amyloid deposits from the vital organs using monoclonal antibodies such as CAEL 101 or Birtamimab with the expectation of restoring damaged tissues of the vital organs affected thereby improving or reversing patients' symptoms. Both CAEL 101 and Birtamimab are currently being tested in phase 3 clinical trials for systemic AL amyloidosis patients with advanced cardiac involvement. This comprehensive review provides an up-to-date overview of AL amyloidosis therapy, with a particular focus on recent advances and future directions of immunotherapeutic strategies.