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首页> 外文期刊>BMC Cancer >A phase II study of cisplatin with intravenous and oral vinorelbine as induction chemotherapy followed by concomitant chemoradiotherapy with oral vinorelbine and cisplatin for locally advanced non-small cell lung cancer
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A phase II study of cisplatin with intravenous and oral vinorelbine as induction chemotherapy followed by concomitant chemoradiotherapy with oral vinorelbine and cisplatin for locally advanced non-small cell lung cancer

机译:顺铂静脉和口服长春瑞滨作为诱导化疗,然后伴随长春瑞滨和顺铂口服放化疗联合治疗局部晚期非小细胞肺癌的II期研究

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Background Concomitant platinum-based chemotherapy and radiotherapy (CT-RT) is the recommended treatment for unresectable locally advanced stage III non-small cell lung cancer (NSCLC). We conducted a phase II study to evaluate the efficacy and safety of fractionated oral vinorelbine with cisplatin as induction CT followed by CT-RT. Methods Patients with stage III NSCLC received 2 induction cycles of intravenous vinorelbine 25?mg/m2 and cisplatin 80?mg/m2 on day 1 and oral vinorelbine 60?mg/m2 on day 8. Responding patients received 2 more cycles of cisplatin 80?mg/m2 on day 1 and oral vinorelbine 20?mg on days 1, 3 and 5 concomitantly with radiotherapy 2?Gy daily, 5?days/week for a total of 66?Gy. Results Seventy patients, median age 61?years, were enrolled. Overall response rate (ORR) was 50.0%; Disease Control Rate was 81.42%. Median PFS was 14.58?months [95% CI, 10.97-18.75]. Median OS was 17.08?months [95% CI, 13.57-29.57]. One-year and 2-year survival rates were 68.6% [95% CI, 57.7-79.4] and 37%. One patient had a grade 3 pulmonary radiation injury and 26.5% had graded 1/2 esophagitis. Conclusion In non-operable IIIA-IIIB NSCLC, the combination oral vinorelbine (fractionated fixed dose) plus cisplatin, during concomitant CT-RT, could offer a well-tolerated option, with comparable activity to I.V. vinorelbine-based chemoradiotherapy regimens. Trial registration ClinicalTrials.gov, NCT01839032
机译:背景技术铂类化学疗法和放射疗法(CT-RT)伴有不可切除的局部晚期III期非小细胞肺癌(NSCLC)的推荐治疗方法。我们进行了一项II期研究,以评估口服长春瑞滨联合顺铂先导CT再行CT-RT的有效性和安全性。方法III期NSCLC患者在第1天接受2个静脉内长春瑞滨25?mg / m 2 和顺铂80?mg / m 2 的诱导周期,并口服长春瑞滨60?mg / m 2 在第8天。有反应的患者在第1天再接受2个周期的顺铂80?mg / m 2 的周期,在第1、3和3天口服长春瑞滨20 mg 5例与放疗同时进行,每天2?Gy,每周5?天,总共66?Gy。结果共纳入70例患者,中位年龄61岁。整体回应率(ORR)为50.0%;疾病控制率为81.42%。 PFS中位数为14.58个月[95%CI,10.97-18.75]。 OS中位数为17.08个月[95%CI,13.57-29.57]。一年和两年生存率分别为68.6%[95%CI,57.7-79.4]和37%。一名患者遭受了3级肺部放射损伤,而26.5%的患者患有1/2级食管炎。结论在不可手术的IIIA-IIIB NSCLC中,在伴随CT-RT的同时口服长春瑞滨(固定剂量)加顺铂可提供良好的耐受性,其活性可与I.V媲美。基于长春瑞滨的放化疗方案。试用注册ClinicalTrials.gov,NCT01839032

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