Zhao Xinmin, Yu Hui, Zhao Jing, Wu Xianghua, Sun Si, Luo Zhiguo, Wang Huijie, Qiao Jie, Chang Jianhua, Wang Jialei
Department of Medical Oncology, Fudan University Shanghai Cancer Center, Department of Oncology, Shanghai Medical College, Fudan University, Shanghai 200032, China.
Department of Medical Oncology, Shanghai Pulmonary Hospital Affiliated to Tongji University, Tongji University Medical School Cancer Institute, Shanghai 200433, China.
Oncotarget. 2017 Sep 23;8(49):86384-86394. doi: 10.18632/oncotarget.21186. eCollection 2017 Oct 17.
Chemotherapy with pemetrexed plus carboplatin followed by pemetrexed maintenance therapy is a first-line regimen for patients with advanced non-squamous non-small-cell lung cancer. This phase II clinical study investigated the efficacy and safety of this regimen in older patients (aged ≥65 years) with advanced non-squamous non-small-cell lung cancer. All patients received 4 courses of induction therapy with pemetrexed (500 mg/m) combined with carboplatin once every 3 weeks. If patients had stable disease or achieved a complete or partial tumor response after 4 courses of pemetrexed + carboplatin therapy, maintenance treatment with pemetrexed monotherapy was administered until either disease progression or intolerable toxicity occurred. The primary endpoint was progression-free survival, while secondary endpoints were the objective response rate, overall survival, and tolerability. A total of 105 elderly patients (median age, 71 years) with advanced lung adenocarcinoma were enrolled in the trial. The ORR with induction therapy was 36.2% and the disease control rate was 70.5%. Sixty-two patients (59.0%) subsequently received pemetrexed maintenance therapy. The median progression-free survival for all patients was 8.23 months (95% CI 5.85-10.62 months) and the median overall survival was 22.6 months (95% CI 20.09-25.11 months). Grade 3 or greater toxicities included neutropenia (15.3%), thrombocytopenia (9.5%), anemia (8.6%), leukopenia (4.8%), nausea (1.0%), vomiting (1.0%), and fatigue (1.0%). No treatment-related deaths occurred. These results indicate that pemetrexed combined with carboplatin therapy maintained by single-agent pemetrexed treatment of elderly patients with advanced non-squamous non-small-cell lung cancer was effective and tolerable. ClinicalTrials.gov identifier: NCT01860508.
培美曲塞联合卡铂化疗后序贯培美曲塞维持治疗是晚期非鳞状非小细胞肺癌患者的一线治疗方案。这项II期临床研究调查了该方案在老年(年龄≥65岁)晚期非鳞状非小细胞肺癌患者中的疗效和安全性。所有患者接受4个疗程的诱导治疗,培美曲塞(500mg/m²)联合卡铂,每3周1次。如果患者在4个疗程的培美曲塞+卡铂治疗后病情稳定或达到完全或部分肿瘤缓解,则给予培美曲塞单药维持治疗,直至疾病进展或出现无法耐受的毒性。主要终点是无进展生存期,次要终点是客观缓解率、总生存期和耐受性。共有105例老年(中位年龄71岁)晚期肺腺癌患者入组该试验。诱导治疗的客观缓解率为36.2%,疾病控制率为70.5%。62例患者(59.0%)随后接受了培美曲塞维持治疗。所有患者的中位无进展生存期为8.23个月(95%CI 5.85-10.62个月),中位总生存期为22.6个月(95%CI 20.09-25.11个月)。3级或以上毒性包括中性粒细胞减少(15.3%)、血小板减少(9.5%)、贫血(8.6%)、白细胞减少(4.8%)、恶心(1.0%)、呕吐(1.0%)和疲劳(1.0%)。未发生与治疗相关的死亡。这些结果表明,培美曲塞联合卡铂治疗后序贯培美曲塞单药维持治疗老年晚期非鳞状非小细胞肺癌患者有效且耐受性良好。ClinicalTrials.gov标识符:NCT01860508。