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一项针对局部晚期非小细胞肺癌老年患者的诱导化疗后序贯同步放化疗的II期研究。

A phase II study of induction chemotherapy followed by concurrent chemoradiotherapy in elderly patients with locally advanced non-small-cell lung cancer.

作者信息

Giorgio Carmelo G, Pappalardo Alessandro, Russo Antonio, Santini Daniele, Di Rosa Carlo, Di Salvo Carmela, Castorina Sergio, Marletta Franco, Bellissima Giuseppe, Palermo Nuccio, Scuderi Concetto, Bordonaro Roberto

机构信息

Gravina Hospital, Oncology Unit, Caltagirone, Italy.

出版信息

Anticancer Drugs. 2007 Jul;18(6):713-9. doi: 10.1097/CAD.0b013e328082558a.

Abstract

The optimal management of unresectable locally advanced non-small-cell lung cancer in older patients has not been defined to date. The present phase II study was planned to evaluate the activity and safety of platinum-based induction chemotherapy followed by concurrent chemoradiotherapy in elderly patients with locally advanced non-small-cell lung cancer. Patients received two cycles of paclitaxel (175 mg/m) and carboplatin (area under the curve: 5) day 1, every 3 weeks. Chemoradiotherapy (thoracic radiation therapy) was initiated on day 42 and consisted of 1.8 Gy daily, five times per week over 5 weeks (45.0 Gy target dose) followed by 10 2.0 Gy daily fractions. Concomitant chemotherapy was weekly paclitaxel 50 mg/mq followed by weekly carboplatin at an area under the curve of 2. The eligibility for patients: age 70 or older and histologically documented untreated non-small-cell lung cancer, locally advanced, unresectable, stage III A N2 bulky or III B. Thirty consecutive patients were enrolled onto the study. The median age was 73 (range 70-76). According to the intention-to-treat analysis, 1 month after the end of combined chemoradiotherapy, we observed complete and partial responses in one and 19 of the 30 patients, respectively, for an overall response rate of 66% (95% confidence interval, 45-76%). Median progression-free survival was 8.7 months (95% confidence interval, 3.4-37.8) and median survival was 15 months (95% confidence interval, 4.2-52.1). During the treatment, 12 patients (40.0%) experienced grade 3-4 neutropenia, two patients neutropenic fever, and three patients grade 3 anaemia and grade 3 thrombocytopenia, respectively. Grade 3 oesophagitis, during concomitant radiotherapy, was observed in six patients (20.0%). No treatment-related mortality was reported. The investigated sequential approach including induction chemotherapy followed by concurrent chemoradiotherapy appears safe and seems a reasonable chance for the treatment of locally advanced non-small-cell lung cancer in the elderly population.

摘要

老年患者不可切除的局部晚期非小细胞肺癌的最佳治疗方案迄今尚未明确。本II期研究旨在评估铂类诱导化疗联合同步放化疗在老年局部晚期非小细胞肺癌患者中的有效性和安全性。患者在第1天接受两周期的紫杉醇(175mg/m²)和卡铂(曲线下面积:5),每3周一次。放化疗(胸部放疗)在第42天开始,包括每日1.8Gy,每周5次,共5周(靶剂量45.0Gy),随后每日2.0Gy分10次照射。同步化疗为每周紫杉醇50mg/m²,随后每周卡铂曲线下面积为2。患者入选标准:年龄70岁及以上,组织学确诊为未经治疗的非小细胞肺癌,局部晚期、不可切除,IIIA期N2肿大或IIIB期。连续30例患者入组本研究。中位年龄为73岁(范围70 - 76岁)。根据意向性分析,在联合放化疗结束1个月后,我们分别观察到30例患者中有1例完全缓解和19例部分缓解,总缓解率为66%(95%置信区间,45 - 76%)。中位无进展生存期为8.7个月(95%置信区间,3.4 - 37.8),中位生存期为15个月(95%置信区间,4.2 - 52.1)。治疗期间,12例患者(40.0%)出现3 - 4级中性粒细胞减少,2例患者出现中性粒细胞减少性发热,3例患者分别出现3级贫血和3级血小板减少。同步放疗期间,6例患者(20.0%)出现3级食管炎。未报告与治疗相关的死亡病例。所研究的包括诱导化疗联合同步放化疗的序贯治疗方法似乎是安全的,并且对于老年局部晚期非小细胞肺癌患者的治疗似乎是一个合理的选择。

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