Department of Neurological Surgery, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania, USA.
J Neurosurg. 2011 Mar;114(3):769-79. doi: 10.3171/2010.5.JNS1014. Epub 2010 Jun 4.
To evaluate the role of stereotactic radiosurgery (SRS) in the management of brain metastases from melanoma, the authors assessed clinical outcomes and prognostic factors for survival and tumor control.
The authors reviewed 333 consecutive patients with melanoma who underwent SRS for 1570 brain metastases from cutaneous and mucosal/acral melanoma. The patient population consisted of 109 female and 224 male patients with a median age of 53 years. Two hundred eleven patients (63%) had multiple metastases. One hundred eighteen patients (35%) underwent whole-brain radiation therapy (WBRT). The target volume ranged from 0.1 cm(3) to 37.2 cm(3). The median marginal dose was 18 Gy.
Actuarial survival rates were 70% at 3 months, 47% at 6 months, 25% at 12 months, and 10% at 24 months after radiosurgery. Factors associated with longer survival included controlled extracranial disease, better Karnofsky Performance Scale score, fewer brain metastases, no prior WBRT, no prior chemotherapy, administration of immunotherapy, and no intratumoral hemorrhage before radiosurgery. The median survival for patients with a solitary brain metastasis, controlled extracranial disease, and administration of immunotherapy after radiosurgery was 22 months. Sustained local tumor control was achieved in 73% of the patients. Sixty-four (25%) of 259 patients who had follow-up imaging after SRS had evidence of delayed intratumoral hemorrhage. Sixteen patients underwent a craniotomy due to intratumoral hemorrhage. Seventeen patients (6%) had asymptomatic and 21 patients (7%) had symptomatic radiation effects. Patients with ≤ 8 brain metastases, no prior WBRT, and the recursive partitioning analysis Class I had extended survivals (median 54.3 months).
Stereotactic radiosurgery is an especially valuable option for patients with controlled systemic disease even if they have multiple metastatic brain tumors.
评估立体定向放射外科(SRS)在治疗黑素瘤脑转移中的作用,作者评估了生存和肿瘤控制的临床结果和预后因素。
作者回顾了 333 例连续接受 SRS 治疗的黑素瘤患者,这些患者共接受了 1570 个来自皮肤和粘膜/肢端黑素瘤的脑转移灶治疗。患者人群包括 109 名女性和 224 名男性,中位年龄为 53 岁。211 例(63%)有多发性转移灶。118 例(35%)接受了全脑放疗(WBRT)。靶体积范围为 0.1 cm³至 37.2 cm³。边缘剂量中位数为 18 Gy。
放射外科治疗后 3 个月、6 个月、12 个月和 24 个月的生存率分别为 70%、47%、25%和 10%。与生存时间较长相关的因素包括:控制的颅外疾病、较好的 Karnofsky 表现评分、较少的脑转移灶、无既往 WBRT、无既往化疗、免疫治疗以及放射外科治疗前无肿瘤内出血。对于接受 SRS 治疗后有单发脑转移灶、控制的颅外疾病和免疫治疗的患者,中位生存期为 22 个月。73%的患者获得了持续的局部肿瘤控制。在 SRS 后进行随访成像的 259 例患者中,有 64 例(25%)出现了迟发性肿瘤内出血证据。16 例患者因肿瘤内出血而行开颅手术。17 例(6%)患者无症状,21 例(7%)患者有症状性放射效应。对于脑转移灶数量≤8 个、无既往 WBRT 和递归分区分析 I 级的患者,生存时间延长(中位 54.3 个月)。
即使患者有多发性脑转移瘤,立体定向放射外科对系统疾病得到控制的患者来说也是一种特别有价值的选择。