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논문 기본 정보

자료유형
학술저널
저자정보
Bou Zerdan Maroun (Department of Hematology-Oncology Myeloma and Amyloidosis Program Maroone Cancer Center Cleveland C) Sabine Allam (Faculty of Medicine University of Balamand Beirut Lebanon) Chakra P. Chaulagain (Department of Hematology-Oncology Myeloma and Amyloidosis Program Maroone Cancer Center Cleveland C)
저널정보
대한혈액학회 Blood Research Blood Research Vol.57 No.2
발행연도
2022.6
수록면
106 - 116 (11page)
DOI
10.5045/br.2022.2021227

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The immunoglobulin light-chain amyloidosis is a multisystemic disease which manifests by damage to the vital organs by light chain-derived amyloid fibril. Traditionally, the treatment has been directed to the underlying plasma cell clone with or without high dose chemotherapy followed by autologous stem cell transplantation using melphalan based conditioning. Now with the approval of highly tolerable anti-CD38 monoclonal antibody daratumumab based anti-plasma cell therapy in 2021, high rates of hematologic complete responses are possible even in patients who are otherwise deemed not a candidate for autologous stem cell transplantation. However, despite the progress, there remains a limitation in the strategies to improve symptoms particularly in patients with advanced cardiac involvement, those with nephrotic syndrome and autonomic dysfunction due to underlying systemic AL amyloidosis. The symptoms can be an ordeal for the patients and their caregivers and effective strategies are urgently needed to address them. The supportive care is aimed to counteract the symptoms of the disease and the effects of the treatment on involved organs’ function and preserve patients’ quality of life. Here we discuss multidisciplinary approach in a system-based fashion to address the symptom management in this dreadful disease. In addition to achieving excellent anti-plasma cell disease control, using treatment directed to remove amyloid from the vital organs can theoretically hasten recovery of the involved organs thereby improving symptoms at a faster pace. Ongoing phase III clinical trials of CAEL-101 and Birtamimab will address this question.

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