Hematology Department, Hospital Británico & Hospital de Clinicas, Montevideo, Uruguay.
Hospital Universitario CEMIC, Buenos Aires, Argentina.
JCO Glob Oncol. 2022 Aug;8:e2100380. doi: 10.1200/GO.21.00380.
Waldenstrom Macroglobulinemia (WM) is a rare lymphoma with distinct clinical features, and data from Latin American patients are lacking. Therefore, we aim to investigate the clinical, therapy, and outcome patterns of WM in Latin America.
We retrospectively analyzed patients with WM diagnosed between 1991 and 2019 from 24 centers in seven Latin American countries. The study outcomes were overall survival (OS) and progression-free survival (PFS).
We identified 159 cases (median age 67 years, male 62%). Most patients (95%) were symptomatic at diagnosis. The International Prognostic Scoring System for WM (IPSSWM) at diagnosis was available in 141 (89%) patients (high-risk 40%, intermediate-risk 37%, and low-risk 23%). Twenty-seven (17%) patients were tested for MYD88, with 89% (n = 24 of 27) carrying the mutation. First-line and second-line therapies were administered to 142 (89%) and 53 (33%) patients, respectively. Chemoimmunotherapy was the most commonly used first-line (66%) and second-line (45%) approach; only 18 (11%) patients received ibrutinib. With a median follow-up of 69 months, the 5-year OS rate was 81%. In treated patients, the 5-year OS and PFS rates were 78% and 59%, respectively. High-risk IPSSWM at treatment initiation was an independent risk factor for OS (adjusted hazard ratio: 4.73, 95% CI, 1.67 to 13.41, = .003) and PFS (adjusted hazard ratio: 2.43, 95% CI, 1.31 to 4.50, = .005).
In Latin America, the management of WM is heterogeneous, with limited access to molecular testing and novel agents. However, outcomes were similar to those reported internationally. We validated the IPSSWM score as a prognostic factor for OS and PFS. There is an unmet need to improve access to recommended diagnostic approaches and therapies in Latin America.
华氏巨球蛋白血症(WM)是一种罕见的淋巴瘤,具有独特的临床特征,且拉丁美洲患者的数据尚缺乏。因此,我们旨在研究拉丁美洲 WM 的临床、治疗和预后模式。
我们回顾性分析了 1991 年至 2019 年间,来自七个拉丁美洲国家的 24 个中心的 159 例 WM 患者。研究结果为总生存期(OS)和无进展生存期(PFS)。
我们共发现 159 例患者(中位年龄 67 岁,男性占 62%),大多数患者(95%)在诊断时存在症状。141 例(89%)患者有国际 WM 预后评分系统(IPSSWM)诊断数据(高危占 40%,中危占 37%,低危占 23%)。27 例(17%)患者进行了 MYD88 检测,89%(n=24/27)携带突变。142 例(89%)患者接受了一线治疗,53 例(33%)患者接受了二线治疗。化疗免疫治疗是最常用的一线(66%)和二线(45%)治疗方法;仅有 18 例(11%)患者接受了伊布替尼治疗。中位随访 69 个月时,5 年 OS 率为 81%。在接受治疗的患者中,5 年 OS 和 PFS 率分别为 78%和 59%。治疗开始时高风险的 IPSSWM 是 OS(调整后的危险比:4.73,95%CI,1.67 至 13.41, =.003)和 PFS(调整后的危险比:2.43,95%CI,1.31 至 4.50, =.005)的独立危险因素。
在拉丁美洲,WM 的管理具有异质性,对分子检测和新型药物的获取有限。然而,结果与国际报道相似。我们验证了 IPSSWM 评分是 OS 和 PFS 的预后因素。拉丁美洲在获得推荐的诊断方法和治疗方面存在未满足的需求。