免疫力低下患者的原发性中枢神经系统淋巴瘤需要特定的应答标准。

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC ACS Applied Electronic Materials Pub Date : 2024-08-01 Epub Date: 2024-06-12 DOI:10.1007/s11060-024-04694-3
Nina Schulz, Lucia Nichelli, Laurence Schenone, Renata Ursu, Julie Abraham, Marie Le Cann, Véronique Morel, Inès Boussen, Dario Herran, Delphine Leclercq, Marie Blonski, Bertrand Mathon, Khê Hoang-Xuan, Carole Soussain, Sylvain Choquet, Caroline Houillier
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引用次数: 0

摘要

目的:免疫抑制是原发性中枢神经系统淋巴瘤(PCNSL)的公认风险因素,在这种情况下,PCNSL具有不同的放射学特征。我们的目的是描述免疫功能低下患者经治疗后 PCNSL 的放射学演变,并提出适应的 MRI 反应标准:我们对来自法国 LOC、K-Virogref 和 CANCERVIH 网络数据库的患者进行了一项多中心回顾性研究,并招募了新确诊 PCNSL 的成年免疫受损患者:我们评估了31名患者(9名艾滋病毒携带者、16名实体器官移植患者和6名长期接受免疫抑制治疗的自身免疫性疾病患者)的基线、中期、治疗末期和随访磁共振成像数据。基线时,23/30(77%)名患者的坏死病灶呈环状强化,28%的病灶为出血性。在一线治疗结束时,12/28(43%)名患者无法根据 IPCG 标准进行分类。28例患者中有13例(46%)仍有造影剂增强,11/28(39%)例患者有持续性大面积坏死病灶,中位直径为15毫米。这些方面与严重后果无关,并且在随访期间逐渐减轻。有六名患者复发,但我们未能在治疗结束后的磁共振成像中发现任何神经影像风险因素:结论:在免疫功能低下的患者中,PCNSL在治疗结束后的磁共振成像中往往会出现令人担忧的特征,经常会观察到持续的造影剂增强病灶。然而,这些特征似乎与病变的坏死和出血性质有关,并不能预测恶性结果。因此,我们提出了这一人群的具体反应标准。
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Primary central nervous system lymphomas in immunocompromised patients require specific response criteria.

Purpose: Immunosuppression is a well-established risk factor for primary central nervous system lymphomas (PCNSLs), which present in this context distinct radiological characteristics. Our aim was to describe the radiological evolution of treated PCNSL in immunocompromised patients and suggest adapted MRI response criteria.

Methods: We conducted a multicenter retrospective study of patients from the French LOC, K-Virogref and CANCERVIH network databases and enrolled adult immunocompromised patients with newly diagnosed PCNSL.

Results: We evaluated the baseline, intermediate, end-of-treatment and follow-up MRI data of 31 patients (9 living with HIV, 16 with solid organ transplantation and 6 with an autoimmune disease under chronic immunosuppressive therapy). At baseline, 23/30 (77%) patients had necrotic lesions with ring enhancement and 28% of the lesions were hemorrhagic. At the end of the first-line treatment, 12/28 (43%) patients could not be classified according to the IPCG criteria. Thirteen of 28 (46%) patients still harbored contrast enhancement, and 11/28 (39%) patients had persistent large necrotic lesions with a median diameter of 15 mm. These aspects were not associated with a pejorative outcome and progressively diminished during follow-up. Six patients relapsed; however, we failed to identify any neuroimaging risk factors on the end-of-treatment MRI.

Conclusion: In immunocompromised patients, PCNSLs often harbor alarming features on end-of-treatment MRI, with persistent contrast-enhanced lesions frequently observed. However, these aspects seemed to be related to the necrotic and hemorrhagic nature of the lesions and were not predictive of a pejorative outcome. Specific response criteria for this population are thereby proposed.

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