Relapsed and refractory primary CNS lymphoma: treatment approaches in routine practice.

Prakash Ambady, Nancy D Doolittle, Christopher P Fox
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Abstract

Despite recent therapeutic progress and improved survival for many patients with primary central nervous system lymphoma (PCNSL), up to 50% of patients will experience refractory or relapsed disease following first-line treatment with high dose methotrexate (HD-MTX) based regimens. The majority of such events occur within 2 years of diagnosis although, unlike their systemic counterpart, the risk of PCNSL relapse remains, even for patients in radiologic complete response at 10 years following diagnosis. Currently, there are no approved therapies, and no widely accepted 'standard-of-care' approaches for the treatment of refractory or recurrent primary central nervous system lymphoma (rrPCNSL). Re-treatment with HD-MTX based regimens, use of non-cross resistant chemotherapy regimens, high-dose chemotherapy and autologous stem cell transplantation (HDT-ASCT), and brain irradiation all remain important therapeutic approaches for rrPCNSL. However, the survival outcomes for patients with rrPCNSL remain extremely poor and the vast majority of patients will die of their disease. Increasingly, novel treatment approaches are being investigated in early phase clinical studies. Importantly, such therapies need to be evaluated in the context of both refractory and relapsed disease; in older patients and those with co-morbid conditions; and those with neurocognitive dysfunction. A deeper understanding of the molecular genetic mechanisms underpinning rrPCNSL and its unique tumor microenvironment is urgently needed to inform biologically rational and effective therapies. rrPCNSL remains a clear unmet clinical need and a high priority area for clinical research that will require national and international collaborative studies with embedded translational science in order to improve outcomes for patients.

复发和难治性原发性中枢神经系统淋巴瘤:常规治疗方法。
尽管原发性中枢神经系统淋巴瘤(PCNSL)的治疗取得了最新进展,许多患者的生存率也得到了改善,但仍有多达 50% 的患者在接受以大剂量甲氨蝶呤(HD-MTX)为基础的一线治疗后出现难治或复发。尽管与全身性治疗不同,PCNSL复发的风险仍然存在,即使患者在确诊后10年仍处于放射学完全反应状态,但大多数此类事件发生在确诊后2年内。目前,治疗难治性或复发性原发性中枢神经系统淋巴瘤(rrPCNSL)的疗法尚未获得批准,也没有被广泛接受的 "标准疗法"。以HD-MTX为基础的再治疗方案、使用无交叉耐药性化疗方案、大剂量化疗和自体干细胞移植(HDT-ASCT)以及脑部照射仍是治疗rrPCNSL的重要方法。然而,rrPCNSL 患者的生存率仍然极低,绝大多数患者将死于疾病。越来越多的新型治疗方法正在早期临床研究中接受调查。重要的是,此类疗法需要在难治性和复发性疾病、老年患者、合并症患者以及神经认知功能障碍患者中进行评估。rrPCNSL显然仍是一个未得到满足的临床需求,也是临床研究的一个高度优先领域,需要开展包含转化科学的国内和国际合作研究,以改善患者的预后。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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