Gregor A, Cull A, Stephens R J, Kirkpatrick J A, Yarnold J R, Girling D J, Macbeth F R, Stout R, Machin D
Western General Hospital, Edinburgh, U.K.
Eur J Cancer. 1997 Oct;33(11):1752-8. doi: 10.1016/s0959-8049(97)00135-4.
Prophylactic cranial irradiation (PCI) reduces the risk of cranial metastasis in small cell lung cancer (SCLC), but the magnitude and value of this reduction, the risks of radiation morbidity and whether PCI influences survival are unclear. We conducted a randomised trial in patients with limited-stage SCLC who had had a complete response to induction therapy. Initially, patients were randomised equally to (1) PCI 36 Gy in 18 daily fractions, (2) PCI 24 Gy in 12 fractions and (3) no PCI; subsequently, to increase the rate of accrual, randomisation was to clinicians' choice of PCI regimen versus no PCI (at a 3:2 ratio). The endpoints were appearance of brain metastases, survival, cognitive function, and quality of life (QoL). Three hundred and fourteen patients (194 PCI, 120 No PCI) were randomised. In the revised design, the most commonly used PCI regimens were 30 Gy in 10 fractions and 8 Gy in a single dose. With PCI, there was a large and highly significant reduction in brain metastases (HR = 0.44, 95% CI 0.29-0.67), a significant advantage in brain-metastasis-free survival (HR = 0.75, 95% CI 0.58-0.96) and a non-significant overall survival advantage (HR = 0.86, 95% CI 0.66-1.12). In both groups, there was impairment of cognitive function and QoL before PCI and additional impairment at 6 months and 1 year, but no consistent difference between the two groups and thus no evidence over 1 year of major impairment attributable to PCI. PCI can safely reduce the risk of brain metastases. Further research is needed to define optimal dose and fractionation and to clarify the effect on survival. Patients with SCLC achieving a complete response to induction therapy should be offered PCI.
预防性颅脑照射(PCI)可降低小细胞肺癌(SCLC)发生颅脑转移的风险,但这种降低的幅度和价值、放射性损伤风险以及PCI是否影响生存尚不清楚。我们对局限期SCLC且诱导治疗完全缓解的患者进行了一项随机试验。最初,患者被等比例随机分为三组:(1)PCI 36 Gy,分18次每日照射;(2)PCI 24 Gy,分12次照射;(3)不进行PCI;随后,为提高入组率,随机分组改为临床医生选择PCI方案与不进行PCI(比例为3:2)。终点指标为脑转移的出现、生存、认知功能和生活质量(QoL)。共314例患者(194例接受PCI,120例未接受PCI)被随机分组。在修订后的设计中,最常用的PCI方案是30 Gy分10次照射和单次8 Gy照射。接受PCI治疗后,脑转移显著且大幅减少(HR = 0.44,95%CI 0.29 - 0.67),无脑转移生存期有显著优势(HR = 0.75,95%CI 0.58 - 0.96),总生存期有非显著优势(HR = 0.86,95%CI 0.66 - 1.12)。两组在PCI治疗前认知功能和QoL均有损害,在6个月和1年时进一步受损,但两组间无一致差异,因此无证据表明1年内PCI会导致严重损害。PCI可安全降低脑转移风险。需要进一步研究来确定最佳剂量和分割方式,并阐明对生存的影响。对诱导治疗取得完全缓解的SCLC患者应给予PCI治疗。