首页> 美国卫生研究院文献>American Journal of Cancer Research >Randomized phase II study of pemetrexed-cisplatin or docetaxel-cisplatin plus thoracic intensity-modulated radiation therapy in patients with stage IV lung adenocarcinoma
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Randomized phase II study of pemetrexed-cisplatin or docetaxel-cisplatin plus thoracic intensity-modulated radiation therapy in patients with stage IV lung adenocarcinoma

机译:培美曲塞-顺铂或多西他赛-顺铂联合胸腔调强放疗对IV期肺腺癌患者的II期随机研究

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摘要

Systemic chemotherapy is the standard treatment modality for stage IV lung adenocarcinoma patients with EGFR wild-type or unknown mutation status. Recent years, there is increasing evidence showed that selected patients with stage IV disease could benefit from aggressive thoracic radiotherapy. Either pemetrexed or docetaxel, combined with cisplatin, can be used for patients with stage IV lung adenocarcinoma. However, no prospective trials have confirmed that Pem-Cis was superior to Doc-Cis in lung adenocarcinoma. In this randomized phase 2 trial, we evaluated survival outcomes, and toxicity of Pemetrexed-Cisplatin (arm A) or Docetaxel-Cisplatin (arm B) with concurrent IMRT to the primary tumor for stage IV lung adenocarcinoma patients with EGFR wild-type or unknown mutation status. Totally, 101 patients were randomly assigned (50 in arm A and 51 in arm B). Using an intention-to-treat analysis, one-year survival rates were 72.0% and 52.9%, respectively (P=0.020). Progression-free survival was also significantly improved in the arm A (median, 12.6 v 7.5 months, P=0.013). The incidence and severity of acute pneumonitis and esophagitis was similar between two arms. Although more of grade 3 or 4 anemia and thrombocytopenia in arm A, and higher rates grade 3 or 4 neutropenia, and leukopenia were observed in arm B. Pem-Cis first-line chemotherapy with concurrent radiation therapy for stage IV lung adenocarcinoma patients with EGFR wild-type or unknown mutation status represents a potential treatment option with acceptable toxicity and high overall survival rates.
机译:对于EGFR野生型或突变状态未知的IV期肺腺癌患者,全身化疗是标准治疗方式。近年来,越来越多的证据表明,某些患有IV期疾病的患者可以从积极的胸腔放疗中受益。培美曲塞或多西他赛联合顺铂均可用于IV期肺腺癌患者。然而,尚无前瞻性试验证实Pem-Cis在肺腺癌中优于Doc-Cis。在这项随机的2期临床试验中,我们评估了伴有IMRT的培美曲塞-顺铂(A组)或多西他赛-顺铂(B组)对患有EGFR野生型或未知EGFR的IV期肺腺癌患者的原发性肿瘤的生存结果和毒性突变状态。总共101例患者被随机分配(A组50例,B组51例)。使用意向性治疗分析,一年生存率分别为72.0%和52.9%(P = 0.020)。 A组的无进展生存期也得到了显着改善(中位数,12.6 v 7.5个月,P = 0.013)。两组之间的急性肺炎和食管炎的发生率和严重程度相似。尽管在A组中观察到3级或4级贫血和血小板减少的发生率更高,在B组中观察到3级或4级中性粒细胞减少和白细胞减少症的发生率更高。Pem-Cis一线化疗并发放射疗法治疗EGFR期IV肺腺癌患者野生型或未知突变状态代表了潜在的治疗选择,具有可接受的毒性和较高的总生存率。

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