Immunology and Rheumatology Department, Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán, Mexico City, Mexico.
Primary Healthcare Transversal Research Group, IDIBAPS.
Rheumatology (Oxford). 2022 Dec 23;62(1):243-255. doi: 10.1093/rheumatology/keac205.
To characterize 414 patients with primary SS who developed haematological malignancies and to analyse how the main SS- and lymphoma-related features can modify the presentation patterns and outcomes.
By January 2021, the Big Data Sjögren Project Consortium database included 11 966 patients fulfilling the 2002/2016 classification criteria. Haematological malignancies diagnosed according to the World Health Organization (WHO) classification were retrospectively identified.
There were 414 patients (355 women, mean age 57 years) with haematological malignancies (in 43, malignancy preceded at least one year the SS diagnosis). A total of 376 (91%) patients had mature B-cell malignancy, nearly half had extranodal marginal zone lymphoma (MZL) of mucosa-associated lymphoid tissue (MALT lymphoma) (n = 197), followed by diffuse large B-cell lymphoma (DLBCL) (n = 67), nodal MZL lymphoma (n = 29), chronic lymphocytic leukemia/small lymphocytic lymphoma (CLL/SLL) (n = 19) and follicular lymphoma (FL) (n = 17). Rates of complete response, relapses and death were 80%, 34% and 13%, respectively, with a 5-year survival rate of 86.5% after a mean follow-up of 8 years. There were significant differences in age at diagnosis (younger in MALT, older in CLL/SLL), predominant clinical presentation (glandular enlargement in MALT lymphoma, peripheral lymphadenopathy in nodal MZL and FL, constitutional symptoms in DLBCL, incidental diagnosis in CLL/SLL), therapeutic response (higher in MALT lymphoma, lower in DLBCL) and survival (better in MALT, nodal MZL and FL, worse in DLBCL).
In the largest reported study of haematological malignancies complicating primary SS, we confirm the overwhelming predominance of B-cell lymphomas, especially MALT, with the salivary glands being the primary site of involvement. This highly-specific histopathological scenario is linked with the overall good prognosis with a 5-year survival rate of nearly 90%.
描述 414 例原发性干燥综合征(SS)并发血液系统恶性肿瘤患者的特征,并分析主要 SS 和淋巴瘤相关特征如何改变其表现模式和结局。
截至 2021 年 1 月,大数据干燥综合征项目联盟数据库纳入了 11966 例符合 2002/2016 分类标准的患者。根据世界卫生组织(WHO)分类,回顾性识别血液系统恶性肿瘤。
共有 414 例(355 例女性,平均年龄 57 岁)患者患有血液系统恶性肿瘤(43 例患者中,恶性肿瘤至少先于 SS 诊断一年)。总共 376 例(91%)患者患有成熟 B 细胞恶性肿瘤,近一半患者患有黏膜相关淋巴组织(MALT)结外边缘区淋巴瘤(MALT 淋巴瘤)(n=197),其次是弥漫性大 B 细胞淋巴瘤(DLBCL)(n=67)、结内边缘区淋巴瘤(n=29)、慢性淋巴细胞白血病/小淋巴细胞淋巴瘤(CLL/SLL)(n=19)和滤泡性淋巴瘤(FL)(n=17)。完全缓解率、复发率和死亡率分别为 80%、34%和 13%,中位随访 8 年后 5 年生存率为 86.5%。诊断时的年龄(MALT 淋巴瘤中较年轻,CLL/SLL 中较年长)、主要临床表现(MALT 淋巴瘤为腺体肿大,结内边缘区淋巴瘤和 FL 为外周淋巴结病,DLBCL 为全身症状,CLL/SLL 为偶然诊断)、治疗反应(MALT 淋巴瘤较高,DLBCL 较低)和生存(MALT、结内边缘区淋巴瘤和 FL 较好,DLBCL 较差)存在显著差异。
在最大的原发性干燥综合征并发血液系统恶性肿瘤报告研究中,我们确认了 B 细胞淋巴瘤,尤其是 MALT 的压倒性优势,唾液腺是主要受累部位。这种高度特异性的组织病理学特征与总体良好的预后相关,5 年生存率接近 90%。