Department of Oncology, Binzhou Medical University Hospital, Binzhou, Shandong, People's Republic of China.
Department of Orthopedics, Binzhou Medical University Hospital, Binzhou, Shandong, People's Republic of China.
Cancer Med. 2024 Jun;13(11):e7349. doi: 10.1002/cam4.7349.
Patients with Eastern Cooperative Oncology Group performance status (ECOG PS) 2 probably cannot tolerate chemotherapy or other antitumor therapies. Some studies have reported that immunotherapy combined with antiangiogenic therapy is well-tolerated and shows good antitumor activity. However, the efficacy of this combination as a later-line therapy in patients with ECOG PS 2 is unclear. This study evaluated the effectiveness and safety of this combination strategy as third- or further-line therapy in stage IV non-small cell lung cancer (NSCLC) patients with ECOG PS 2.
In this retrospective study, patients treated with camrelizumab plus antiangiogenic therapy (bevacizumab, anlotinib, or recombinant human endostatin) were included. Objective response rate (ORR), disease control rate (DCR), progression-free survival (PFS), overall survival (OS), quality of life (QOL) assessed by ECOG PS, and safety were analyzed.
Between January 10, 2019, and February 28, 2024, a total of 59 patients were included. The ORR was 35.6% (21/59) and the DCR was 86.4%. With a median follow-up of 10.5 months (range: 0.7-23.7), the median PFS was 5.5 months (95% confidence interval [CI]: 3.8-7.3) and the median OS was 10.5 months (95% CI: 11.2-13.6). QOL was improved (≥1 reduction in ECOG PS) in 39 patients (66.1%). The most common Grade 3-4 treatment-related adverse events were hepatic dysfunction (6 [10%]), hypertension (5 [8%]), and hypothyroidism (3 [5%]). There were no treatment-related deaths.
Third- or further-line immunotherapy combined with antiangiogenic therapy is well-tolerated and shows good antitumor activity in stage IV NSCLC patients with ECOG PS 2. Future large-scale prospective studies are required to confirm the clinical benefits of this combination therapy.
东部肿瘤协作组体能状态(ECOG PS)为 2 的患者可能无法耐受化疗或其他抗肿瘤治疗。一些研究报告称,免疫治疗联合抗血管生成治疗具有良好的耐受性和抗肿瘤活性。然而,ECOG PS 为 2 的患者作为三线或更后线治疗的疗效尚不清楚。本研究评估了 ECOG PS 为 2 的 IV 期非小细胞肺癌(NSCLC)患者三线或更后线使用该联合方案的疗效和安全性。
在这项回顾性研究中,纳入了接受卡瑞利珠单抗联合抗血管生成治疗(贝伐珠单抗、安罗替尼或重组人血管内皮抑制素)的患者。分析了客观缓解率(ORR)、疾病控制率(DCR)、无进展生存期(PFS)、总生存期(OS)、ECOG PS 评估的生活质量(QOL)和安全性。
2019 年 1 月 10 日至 2024 年 2 月 28 日,共纳入 59 例患者。ORR 为 35.6%(21/59),DCR 为 86.4%。中位随访 10.5 个月(范围:0.7-23.7),中位 PFS 为 5.5 个月(95%CI:3.8-7.3),中位 OS 为 10.5 个月(95%CI:11.2-13.6)。39 例患者(66.1%)的 QOL 得到改善(ECOG PS 至少降低 1 分)。最常见的 3-4 级治疗相关不良事件是肝功能障碍(6 例[10%])、高血压(5 例[8%])和甲状腺功能减退(3 例[5%])。无治疗相关死亡。
ECOG PS 为 2 的 IV 期 NSCLC 患者三线或更后线免疫治疗联合抗血管生成治疗具有良好的耐受性和抗肿瘤活性。需要进一步开展大规模前瞻性研究来证实该联合治疗的临床获益。