Wechalekar Ashutosh D, Cibeira M Teresa, Gibbs Simon D, Jaccard Arnaud, Kumar Shaji, Merlini Giampaolo, Palladini Giovanni, Sanchorawala Vaishali, Schönland Stefan, Venner Christopher, Boccadoro Mario, Kastritis Efstathios
National Amyloidosis Centre, University College London (Royal Free Campus), London, UK.
Amyloidosis and Myeloma Unit, Hospital Clinic of Barcelona, IDIBAPS, Barcelona, Spain.
Amyloid. 2023 Mar;30(1):3-17. doi: 10.1080/13506129.2022.2093635. Epub 2022 Jul 15.
This guideline has been developed jointly by the European Society of Haematology and International Society of Amyloidosis recommending non-transplant chemotherapy treatment for patients with AL amyloidosis.
A review of literature and grading of evidence as well as expert recommendations by the ESH and ISA guideline committees.
The recommendations of this committee suggest that treatment follows the clinical presentation which determines treatment tolerance tempered by potential side effects to select and modify use of drugs in AL amyloidosis. All patients with AL amyloidosis should be considered for clinical trials where available. Daratumumab-VCD is recommended from most untreated patients (VCD or VMDex if daratumumab is unavailable). At relapse, the two guiding principles are the depth and duration of initial response, use of a class of agents not previously exposed as well as the limitation imposed by patients' fitness/frailty and end organ damage. Targeted agents like venetoclax need urgent prospective evaluation. Future prospective trials should include advanced stage patients to allow for evidence-based treatment decisions. Therapies targeting amyloid fibrils or those reducing the proteotoxicity of amyloidogenic light chains/oligomers are urgently needed.
本指南由欧洲血液学学会和国际淀粉样变性病学会联合制定,推荐对轻链(AL)淀粉样变性病患者进行非移植化疗治疗。
对文献进行综述、证据分级,并参考欧洲血液学学会(ESH)和国际淀粉样变性病学会(ISA)指南委员会的专家建议。
该委员会的建议表明,治疗应根据临床表现进行,同时考虑潜在副作用对治疗耐受性的影响,以选择和调整AL淀粉样变性病的用药。所有AL淀粉样变性病患者均应考虑参加可用的临床试验。对于大多数未治疗的患者,推荐使用达雷妥尤单抗 - VCD方案(如果无法使用达雷妥尤单抗,则使用VCD或VMDex方案)。复发时,两个指导原则是初始缓解的深度和持续时间、使用一类未曾用过的药物以及患者身体状况/虚弱程度和终末器官损伤所带来的限制。像维奈克拉这样的靶向药物需要进行紧急前瞻性评估。未来的前瞻性试验应纳入晚期患者,以便做出基于证据的治疗决策。迫切需要针对淀粉样纤维的疗法或那些降低淀粉样轻链/寡聚体蛋白毒性的疗法。