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一项评估西妥昔单抗联合放疗用于老年和/或体能状态不佳的局部晚期非小细胞肺癌患者(N0422)的Ⅱ期临床研究。

A phase II study of cetuximab and radiation in elderly and/or poor performance status patients with locally advanced non-small-cell lung cancer (N0422).

机构信息

Mayo Clinic Rochester, Rochester, MN.

Mayo Clinic Arizona, Scottsdale, AZ.

出版信息

Ann Oncol. 2010 Oct;21(10):2040-2044. doi: 10.1093/annonc/mdq075. Epub 2010 Jun 21.

Abstract

BACKGROUND

Non-small-cell lung cancer (NSCLC) is a disease of the elderly. Seeking a tolerable but effective regimen, we tested cetuximab + radiation in elderly and/or poor performance status patients with locally advanced NSCLC.

PATIENTS AND METHODS

Older patients [≥ 65 years with an Eastern Cooperative Oncology Group (ECOG) performance status of 0, 1, or 2] or younger patients (performance status of 2) received cetuximab 400 mg/m(2) i.v. on day 1 followed by weekly cetuximab 250 mg/m(2) i.v. with concomitant radiation of 6000 cGy in 30 fractions. The primary end point was the percentage who lived 11+ months.

RESULTS

This 57-patient cohort had a median age (range) of 77 years (60-87), and 12 (21%) had a performance status of 2. Forty of 57 (70%) lived 11+ months, thus exceeding the anticipated survival rate of 50%. The median survival was 15.1 months [95% confidence interval (CI) 13.1-19.3 months], and the median time to cancer progression was 7.2 months (95% CI 5.8-8.6 months). No treatment-related deaths occurred, but 31 patients experienced grade 3+ adverse events, most commonly fatigue, anorexia, dyspnea, rash, and dysphagia, each of which occurred in <10% of patients.

CONCLUSION

This combination merits further study in this group of patients.

摘要

背景

非小细胞肺癌(NSCLC)是一种老年病。为了寻求一种可耐受且有效的方案,我们对局部晚期 NSCLC 老年和/或体能状态较差的患者进行了西妥昔单抗+放疗的试验。

患者和方法

老年患者(≥ 65 岁,ECOG 体能状态 0、1 或 2)或年轻患者(体能状态 2)接受西妥昔单抗 400 mg/m2 静脉输注,第 1 天,随后每周静脉输注西妥昔单抗 250 mg/m2,同时给予 6000 cGy 30 次分割放疗。主要终点是 11+ 个月生存的患者比例。

结果

57 例患者队列的中位年龄(范围)为 77 岁(60-87 岁),12 例(21%)体能状态为 2。57 例患者中有 40 例(70%)存活 11+ 个月,超过了预期的 50%生存率。中位生存时间为 15.1 个月(95%CI 13.1-19.3 个月),中位癌症进展时间为 7.2 个月(95%CI 5.8-8.6 个月)。无治疗相关死亡,但 31 例患者出现 3+级不良事件,最常见的是疲劳、厌食、呼吸困难、皮疹和吞咽困难,这些不良事件均发生在<10%的患者中。

结论

这种联合治疗方案在这组患者中值得进一步研究。

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