Tevlin R, Larkin J O, Hyland J M, O'Connell P R, Winter D C
Centre for Colorectal Disease, St. Vincent's University Hospital, Dublin, Ireland,
Ir J Med Sci. 2015 Sep;184(3):673-5. doi: 10.1007/s11845-015-1272-y. Epub 2015 Mar 24.
Brain metastases (BM) from colorectal cancer (CRC) are rare. As survival increases in patients with metastatic CRC, it is hypothesised that new metastatic patterns will emerge: for instance, as CRC with limited metastatic involvement of the liver and lung can now be successfully resected, we propose that sites, previously rarely involved in metastatic spread, will become more common. The objective of this study was to describe the experience with BM from CRC in a single cancer centre.
A prospectively compiled database (1988-2012) of patients with CRC treated in a tertiary referral hospital was retrospectively examined. Patients with a histological diagnosis of CRC and radiologically documented BM were included. Clinical information (including patient demographics, primary and metastatic disease factors) was obtained from medical records.
Eleven patients (0.3 % of 4219 patients) were identified (8 male, 3 female). The median age at CRC diagnosis was 70 years (range 55-80 years) while the median age at diagnosis of BM was 73 years (range 56-83 years). Three patients diagnosed with synchronous metastases underwent palliative treatment while eight patients had undergone surgical resection of the primary tumour with curative intent a median of 24 months (range 0-48 months) prior to diagnosis of BM. 10/11 patients were symptomatic at diagnosis of BM. All were diagnosed using computed tomography and managed palliatively. The cerebellum was most the frequently involved site. The median overall survival time following diagnosis of BM was 2.5 months (range 2-9 months). Notably, 8/11 patients were diagnosed in the latter 8 years of the study period (between 2004 and 2012).
With increased survival, improved systemic therapy and aggressive approaches to surgical management of "classical" metastases from CRC, it is likely that a changing pattern of metastases will emerge. As survival rates increase, we propose that metastatic sites, which were previously considered rare (e.g. brain), will now become more common and thus, surgeons must recognise pertinent symptomatology.
结直肠癌(CRC)脑转移(BM)较为罕见。随着转移性CRC患者生存率的提高,推测会出现新的转移模式:例如,由于肝脏和肺转移累及有限的CRC现在可以成功切除,我们认为以前很少发生转移扩散的部位将变得更加常见。本研究的目的是描述在单一癌症中心治疗CRC脑转移的经验。
回顾性研究一家三级转诊医院前瞻性编制的(1988 - 2012年)CRC患者数据库。纳入经组织学诊断为CRC且有放射学记录的BM患者。从病历中获取临床信息(包括患者人口统计学、原发性和转移性疾病因素)。
共识别出11例患者(占4219例患者的0.3%)(8例男性,3例女性)。CRC诊断时的中位年龄为70岁(范围55 - 80岁),而BM诊断时的中位年龄为73岁(范围56 - 83岁)。3例诊断为同步转移的患者接受了姑息治疗,8例患者在诊断BM前中位24个月(范围0 - 48个月)已接受了旨在治愈的原发性肿瘤手术切除。10/11例患者在BM诊断时有症状。所有患者均通过计算机断层扫描诊断并接受了姑息治疗。小脑是最常受累的部位。BM诊断后的中位总生存时间为2.5个月(范围2 - 9个月)。值得注意的是,11例患者中有8例在研究期的后8年(2004年至2012年)被诊断出。
随着生存率的提高、全身治疗的改善以及对CRC“经典”转移灶手术管理的积极方法,转移模式可能会发生变化。随着生存率的提高,我们认为以前被认为罕见的转移部位(如脑)现在将变得更加常见,因此,外科医生必须认识到相关症状。