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多原发肿瘤背景下成人恶性胶质瘤患者的管理和生存趋势:一项基于人群的分析。

Management and survival trends for adult patients with malignant gliomas in the setting of multiple primary tumors: a population based analysis.

机构信息

Department of Neurosurgery, Medical College of Wisconsin, Milwaukee, WI, USA.

California Institute of Neuroscience, Thousand Oaks, CA, USA.

出版信息

J Neurooncol. 2019 Jan;141(1):213-221. doi: 10.1007/s11060-018-03028-4. Epub 2018 Nov 5.

Abstract

INTRODUCTION

The impact of multiple primary tumors, in the setting of malignant glioma (MG), has not been heavily explored.

METHODS

We extracted demographics and clinical data from the SEER-18 registry for adult patients with MGs. The cases were separated based on the sequence of MG diagnosis relative to the other primary tumors: Group (A) One primary only or first primary of multiple primaries and Group (B) second primary or subsequent primary tumor. Incidences, frequencies, and glioma-related survivals were analyzed.

RESULTS

Group B constituted 12.8% of new MG. The incidences of group B, relative to those of all new MG, range from 0.14 to 0.18. Compared to group A, group B exhibited an older age. Moreover, group B exhibited a higher proportion of females, Caucasians, smaller tumors, non-operative cases, and those receiving radiation (p < 0.05); the proportion with GTR remained comparable. Multiple groupings (oral cavity, digestive system, respiratory system, skin, breast, genital systems, urinary system, lymphoma) exhibited lower glioma-related observed survival (p < 0.05) compared to Group A. An active diagnosis of "leukemia" appears to confer longer glioma-related survival while a history of "breast" or "digestive system" malignancies portends a shorter glioma-related survival.

CONCLUSION

For newly diagnosed MG, a high proportion does have history of extra-CNS primary tumors. Generally, these patients appear to have worse glioma-related observed survival compare to those with malignant glioma as the only primary or the first of multiple primary tumors. Knowledge regarding epidemiology, clinical factors, and observed survival can help guide clinical management/consultation for this subset of patients.

摘要

简介

在恶性胶质瘤(MG)的背景下,多发原发性肿瘤的影响尚未得到深入探讨。

方法

我们从 SEER-18 注册中心提取了成人 MG 患者的人口统计学和临床数据。根据 MG 诊断相对于其他原发性肿瘤的先后顺序,将病例分为两组:A 组为单一原发性或多发性原发性的首发原发性肿瘤,B 组为第二原发性或后续原发性肿瘤。分析发病率、频率和与胶质瘤相关的生存率。

结果

B 组构成了新 MG 的 12.8%。B 组的发病率相对于所有新 MG 的发病率在 0.14 到 0.18 之间。与 A 组相比,B 组年龄较大。此外,B 组女性、白种人、肿瘤较小、非手术病例和接受放疗的比例较高(p<0.05);全切比例仍相当。多个分组(口腔、消化系统、呼吸系统、皮肤、乳腺、生殖系统、泌尿系统、淋巴瘤)与 A 组相比,胶质瘤相关观察生存率较低(p<0.05)。积极诊断“白血病”似乎能延长与胶质瘤相关的生存时间,而“乳腺”或“消化系统”恶性肿瘤病史则预示着与胶质瘤相关的生存时间较短。

结论

对于新诊断的 MG,很大一部分患者有中枢神经系统外原发性肿瘤的病史。一般来说,与恶性胶质瘤作为唯一原发性或多发性原发性肿瘤的患者相比,这些患者的胶质瘤相关观察生存率较差。了解流行病学、临床因素和观察生存率有助于指导这部分患者的临床管理/咨询。

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