Department of Research and Innovation, Haugesund Hospital, Helse Fonna Hospital Trust, Haugesund, Norway.
Fondazione Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS) Ca' Granda Ospedale Maggiore Policlinico, Milan, Italy.
Blood. 2020 Jul 23;136(4):480-488. doi: 10.1182/blood.2020005674.
We retrospectively studied 232 patients with cold agglutinin disease (CAD) at 24 centers in 5 countries. In Norway and a northern region of Italy, the study was close to being population-based. For the first time, we demonstrate fourfold differences between cold and warmer climates regarding prevalence (20 vs 5 cases/million) and incidence (1.9 vs 0.48 cases/million per year). Mean baseline hemoglobin level was 9.3 g/dL, but 27% had hemoglobin <8 g/dL. Identification of typical features of CAD-associated lymphoproliferative disorder in the bone marrow was greatly increased by centralized biopsy assessment. CAD seems to be associated with a slightly increased risk of venous thrombosis. This work includes a follow-up study of therapies, focusing on the long-term outcomes of the rituximab plus bendamustine and rituximab plus fludarabine regimens. Rituximab plus bendamustine therapy resulted in responses in 35 (78%) of 45 patients; 24 (53%) achieved complete response. Interestingly, these rates were still higher than observed in the original (2017) prospective trial, and we also found a shift toward deeper responses with time. This is explained by the prolonged time to response seen in many patients, probably related to long-lived plasma cells. In patients responding to rituximab-bendamustine, median response duration was not reached after 88 months, and estimated 5-year sustained remission was 77%. The regimen appeared safe regarding late-occurring malignancies. Rituximab plus fludarabine therapy seems to carry a higher risk of long-term adverse effects.
我们回顾性研究了 232 例冷凝集素病(CAD)患者,这些患者来自于 5 个国家的 24 个中心。在挪威和意大利北部,这项研究接近基于人群的研究。我们首次证明,在寒冷和温暖气候之间,CAD 的患病率(20 例/百万与 5 例/百万)和发病率(每年 1.9 例/百万与 0.48 例/百万)存在四倍差异。平均基线血红蛋白水平为 9.3 g/dL,但 27%的患者血红蛋白<8 g/dL。通过集中评估骨髓活检,大大提高了对与 CAD 相关的淋巴增生性疾病的典型特征的识别。CAD 似乎与静脉血栓形成的风险略有增加相关。这项工作包括对治疗的随访研究,重点关注利妥昔单抗加苯达莫司汀和利妥昔单抗加氟达拉滨方案的长期结果。利妥昔单抗加苯达莫司汀治疗在 45 例患者中的 35 例(78%)中产生了应答;24 例(53%)获得完全缓解。有趣的是,这些比率仍然高于原始(2017 年)前瞻性试验中的观察结果,我们还发现随着时间的推移,反应深度有所增加。这是由于许多患者的反应时间延长所致,可能与长寿浆细胞有关。在对利妥昔单抗-苯达莫司汀有反应的患者中,中位缓解持续时间在 88 个月后未达到,估计 5 年持续缓解率为 77%。该方案在晚期发生恶性肿瘤方面似乎是安全的。利妥昔单抗加氟达拉滨治疗似乎具有更高的长期不良事件风险。