University of Chicago, Chicago, IL.
Bing Center for Waldenström Macroglobulinemia, Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA.
Am Soc Clin Oncol Educ Book. 2022 Apr;42:1-10. doi: 10.1200/EDBK_349643.
Our knowledge of monoclonal gammopathies is continuously evolving. Once accepted as a possible precursor condition to multiple myeloma, monoclonal gammopathies as an entity are now associated with many renal, neurologic, and dermatologic disorders of clinical significance. This change has created a challenge for patients and clinicians, as a monoclonal gammopathy may be a harbinger not of multiple myeloma but of other lymphoproliferative disorders such as light-chain amyloidosis and Waldenström macroglobulinemia. Early recognition of monoclonal gammopathies along with a careful workup are essential in determining the next steps in the care of a given patient. Recognition has become all the more important as we understand how to triage the 4% to 9% of patients with monoclonal gammopathies depending on age, with the goal of limiting overdiagnosis and misdiagnosis. In this review, we focus on treatment strategies for patients with monoclonal gammopathies that are not multiple myeloma, including smoldering multiple myeloma, light-chain amyloidosis, and Waldenström macroglobulinemia.
我们对单克隆丙种球蛋白病的认识在不断发展。单克隆丙种球蛋白病曾被认为是多发性骨髓瘤的可能前驱病症,而现在,作为一种实体疾病,它与许多具有临床意义的肾脏、神经和皮肤疾病有关。这种变化给患者和临床医生带来了挑战,因为单克隆丙种球蛋白病可能不是多发性骨髓瘤的先兆,而是其他淋巴增殖性疾病的先兆,如轻链淀粉样变性和华氏巨球蛋白血症。早期识别单克隆丙种球蛋白病并进行仔细的检查对于确定特定患者的治疗下一步至关重要。随着我们了解如何根据年龄对 4%至 9%的单克隆丙种球蛋白病患者进行分类(目标是限制过度诊断和误诊),识别变得更加重要。在这篇综述中,我们重点讨论了非多发性骨髓瘤的单克隆丙种球蛋白病患者的治疗策略,包括冒烟型多发性骨髓瘤、轻链淀粉样变性和华氏巨球蛋白血症。