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原发性中枢神经系统淋巴瘤患者的第二原发恶性肿瘤。

Second malignancies in patients with primary central nervous system lymphoma.

作者信息

Wang Jun, Pulido Jose S, O'Neill Brian Patrick, Johnston Patrick B

机构信息

Department of Hematology, First People's Hospital of Changde, Changde, China (J.W.); Department of Ophthalmology, Mayo Clinic, Rochester, Minnesota (J.S.P.); Department of Neurology, Mayo Clinic, Rochester, Minnesota (B.P.O.); Division of Hematology, Mayo Clinic, Rochester, Minnesota (P.B.J.).

出版信息

Neuro Oncol. 2015 Jan;17(1):129-35. doi: 10.1093/neuonc/nou105. Epub 2014 Jun 19.

Abstract

BACKGROUND

Primary central nervous system lymphoma (PCNSL) is a rare extranodal lymphoma with distinctive biological behaviors. The evolving treatment of PCNSL has greatly improved the outcome for patients with this disease and has stimulated interest in second malignancies (SMs) in patients diagnosed with PCNSL.

METHODS

The records of 129 cases of PCNSL at Mayo Clinic, diagnosed between January 1, 1988, and November 26, 2012, were reviewed. Data on clinical characteristics, laboratory parameters, treatments, outcomes, and SMs were collected. The mean follow-up time was 44.8 months (range, 0.5-240 months; median, 28.0 months).

RESULTS

Altogether, 28 cases with 30 (23.26%) SMs were identified. Twenty (15.50%) patients had prior or synchronous SM. Ten (7.76%) patients developed a subsequent primary cancer after PCNSL. The most common sites of prior or synchronous SMs were prostate (4/20), skin (4/20), and gastrointestinal (3/20). The most common site of the subsequent SM was skin (4/10). Two cases were identified with both prior SM and subsequent SM.

CONCLUSIONS

Second malignancies in cases with PCNSL were not uncommon and occurred in nearly a quarter of our cohort. Nonmelanoma skin cancers were frequently seen. Therefore, screening for SMs should also be considered in long-term follow-up of patients with PCNSL. In addition, the high incidence of subsequent cancer, synchronous cancer, and frequently seen nonmelanoma skin cancers may all indicate an immunosuppressed state in patients with PCNSL.

摘要

背景

原发性中枢神经系统淋巴瘤(PCNSL)是一种罕见的结外淋巴瘤,具有独特的生物学行为。PCNSL治疗方法的不断发展极大地改善了该病患者的预后,并引发了对诊断为PCNSL患者发生第二原发性恶性肿瘤(SMs)的关注。

方法

回顾了梅奥诊所1988年1月1日至2012年11月26日期间诊断的129例PCNSL病例记录。收集了临床特征、实验室参数、治疗、结局和SMs的数据。平均随访时间为44.8个月(范围0.5 - 240个月;中位数28.0个月)。

结果

共识别出28例患者发生了30例(23.26%)SMs。20例(15.50%)患者有先前或同步发生的SM。10例(7.76%)患者在PCNSL后发生了后续原发性癌症。先前或同步SMs最常见的部位是前列腺(4/20)、皮肤(4/20)和胃肠道(3/20)。后续SM最常见的部位是皮肤(4/10)。2例患者同时有先前SM和后续SM。

结论

PCNSL病例中的第二原发性恶性肿瘤并不罕见,在我们的队列中近四分之一的患者发生。非黑色素瘤皮肤癌很常见。因此,在PCNSL患者的长期随访中也应考虑筛查SMs。此外,后续癌症、同步癌症的高发生率以及常见的非黑色素瘤皮肤癌可能都表明PCNSL患者处于免疫抑制状态。

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