Istituto Scientifico Romagnolo per lo Studio e la Cura dei Tumori (IRST) IRCCS, Meldola, Italy.
Istituto Scientifico Romagnolo per lo Studio e la Cura dei Tumori (IRST) IRCCS, Meldola, Italy.
Lung Cancer. 2019 Mar;129:35-40. doi: 10.1016/j.lungcan.2018.12.025. Epub 2019 Jan 15.
Brain metastases are common among patients with non-squamous non-small-cell lung cancer (NSCLC) and result in a poor prognosis. Consequently, such patients are often excluded from clinical trials. In Italy an expanded access program (EAP) was used to evaluate nivolumab efficacy and safety in this subpopulation outside a clinical trial.
In this EAP, nivolumab was available for patients with non-squamous NSCLC in progression after at least one systemic treatment for stage IIIB/IV disease. Nivolumab 3 mg/kg was administered intravenously every 2 weeks. Patients with brain metastases could be included if they were asymptomatic, neurologically stable and either off corticosteroids or on a stable or decreasing dose of ≤10 mg/day prednisone.
409 out of 1588 patients included had asymptomatic or controlled brain metastases. A median of 7 doses (range 1-45) were delivered. Median follow-up was 6.1 months (range 0.1-21.9). The disease control rate was 39%: 4 patients had a complete response, 64 a partial response and 96 showed stable disease. At baseline, 118 patients were on corticosteroids and 74 were undergoing concomitant radiotherapy. The median overall survival in this subpopulation was 8.6 months (95% CI: 6.4-10.8). 337 discontinued treatment for various reasons, 23 (7%) of whom due to adverse events, in line with that observed in the overall population and in previous studies.
Our results confirm that nivolumab is active in non-squamous NSCLC patients with brain metastases, despite their poor prognosis. Its safety profile is also concordant with results in the EAP overall population and in patients with other malignancies.
脑转移是常见的非鳞状非小细胞肺癌(NSCLC)患者,并导致预后不良。因此,这些患者往往被排除在临床试验之外。在意大利,一个扩大准入计划(EAP)被用于评估纳武单抗在临床试验之外的这一亚人群中的疗效和安全性。
在这个 EAP 中,纳武单抗可用于至少接受过一次针对 IIIB/IV 期疾病的全身治疗后进展的非鳞状 NSCLC 患者。纳武单抗 3mg/kg 每 2 周静脉输注一次。如果患者无脑转移相关症状,神经状态稳定,且停用或正在使用≤10mg/天泼尼松的稳定或剂量递减的皮质类固醇,则可纳入脑转移患者。
在 1588 名患者中,有 409 名患者有无症状或可控制的脑转移。中位给药 7 剂(范围 1-45)。中位随访时间为 6.1 个月(范围 0.1-21.9)。疾病控制率为 39%:4 名患者完全缓解,64 名部分缓解,96 名患者疾病稳定。基线时有 118 名患者接受皮质类固醇治疗,74 名患者同时接受放射治疗。该亚组的中位总生存期为 8.6 个月(95%CI:6.4-10.8)。337 名患者因各种原因停药,其中 23 名(7%)因不良反应停药,与总体人群和先前研究中的观察结果一致。
我们的结果证实,纳武单抗在有脑转移的非鳞状 NSCLC 患者中具有活性,尽管他们的预后较差。其安全性特征也与 EAP 总体人群和其他恶性肿瘤患者的结果一致。