Lu Bei, Sun Lixin, Yan Xi, Ai Zhenzhong, Xu Jinzhi
Department of Thoracic Surgery, The Fourth Affiliated Hospital of Harbin Medical University, No. 37, Yi Yuan Street, Nan Gang District, Harbin, 150001, Heilongjiang Province, China.
Med Oncol. 2015 Jan;32(1):345. doi: 10.1007/s12032-014-0345-5. Epub 2014 Nov 28.
The aim of the study was to evaluate the efficacy and safety of intratumoral chemotherapy with paclitaxel liposome combined with systemic chemotherapy as induction therapy in clinical stage III unresectable non-small cell lung cancer (NSCLC). Between January 2011 and July 2014, 48 patients, stage III, performance status 0-1, with unresectable clinical stage IIIA or IIIB NSCLC suitable for definitive radiation treatment, were included in the study. Patients with T3N1M0 and T4 (ipsilateral lung nodules) N0-1M0 were not included. Patients were given 3 cycles of chemotherapy every 3 weeks. Carboplatin (AUC5 by i.v. on day 1) and gemcitabine (i.v. 1,000 mg/m(2) on days 1 and 8) were administered. Paclitaxel liposome was injected at 1-3 mg/ml concentration into the tumor lesion by computed tomography-guided percutaneous fine-needle intratumoral injection and proven malignant lymph nodes according to pretreatment histological/cytological results by endobronchial ultrasound drug delivery with a needle on day 1 and day 8. Toxicity was assessed on days 8 and 22 in each cycle. Overall response rate (ORR) evaluation was performed at the end of cycle 3. Out of the 48 enrolled patients, 28 were males and 20 females, 19 patients had stage IIIA and 29 stage IIIB NSCLC. Thirty-six partial responses and two complete responses were observed, for an ORR of 81 %. The most frequent G3-G4 toxicity included neutropenia (in 15 % of cases), hypertransaminasemia (6 %), and diarrhea (4 %). A median PFS of 16.5 months (95 % CI 13.7-19.2) and median OS of 23.2 months (95 % CI 20.0-26.3) were observed. Eleven stage IIIA patients underwent surgery, for a resection rate of 58 %. Intratumoral chemotherapy with paclitaxel liposome combined with systemic chemotherapy demonstrated a considerable disease response and resection rate, with acceptable toxicity.
本研究的目的是评估紫杉醇脂质体瘤内化疗联合全身化疗作为诱导治疗在临床 III 期不可切除非小细胞肺癌(NSCLC)中的疗效和安全性。2011 年 1 月至 2014 年 7 月期间,48 例 III 期、体能状态为 0 - 1、临床 IIIA 期或 IIIB 期不可切除且适合确定性放疗的 NSCLC 患者纳入本研究。T3N1M0 和 T4(同侧肺结节)N0 - 1M0 的患者未纳入。患者每 3 周接受 3 个周期的化疗。给予卡铂(第 1 天静脉注射,AUC5)和吉西他滨(第 1 天和第 8 天静脉注射,1000 mg/m²)。根据治疗前组织学/细胞学结果,在第 1 天和第 8 天通过支气管内超声引导下针吸药物递送,将浓度为 1 - 3 mg/ml 的紫杉醇脂质体经计算机断层扫描引导下经皮细针瘤内注射到肿瘤病灶及已证实的恶性淋巴结中。在每个周期的第 8 天和第 22 天评估毒性。在第 3 周期结束时进行总体缓解率(ORR)评估。在纳入的 48 例患者中,男性 28 例,女性 20 例,19 例患者为 IIIA 期 NSCLC,29 例为 IIIB 期 NSCLC。观察到 36 例部分缓解和 2 例完全缓解,ORR 为 81%。最常见的 3 - 4 级毒性包括中性粒细胞减少(15%的病例)、高转氨酶血症(6%)和腹泻(4%)。观察到中位无进展生存期(PFS)为 16.5 个月(95%CI 13.7 - 19.2),中位总生存期(OS)为 23.2 个月(95%CI 20.0 - 26.3)。11 例 IIIA 期患者接受了手术,切除率为 58%。紫杉醇脂质体瘤内化疗联合全身化疗显示出相当可观的疾病缓解率和切除率,且毒性可接受。