Des Guetz Gaetan, Landre Thierry, Westeel Virginie, Milleron Bernard, Vaylet Fabien, Urban Thierry, Barlesi Fabrice, Souquet Pierre-Jean, Debieuvre Didier, Braun Denis, Fraboulet Gislaine, Monnet Isabelle, Uzzan Bernard, Molinier Olivier, Morin Franck, Moro-Sibilot Denis, Morère Jean Francois
Intergroupe Francophone de Cancérologie Thoracique (IFCT), Paris, France; Unité de Coordination Onco - Gériatrique (UCOG 93), HUPSSD - APHP, France.
Intergroupe Francophone de Cancérologie Thoracique (IFCT), Paris, France; Unité de Coordination Onco - Gériatrique (UCOG 93), HUPSSD - APHP, France.
J Geriatr Oncol. 2015 May;6(3):233-40. doi: 10.1016/j.jgo.2015.02.002. Epub 2015 Feb 16.
We evaluated the impact of age in a randomized phase II trial that compared three first-line drugs in elderly patients with advanced non-small cell lung cancer (NSCLC) and a poor performance status (PS).
Patients with advanced NSCLC with a PS of 2 or 3 were enrolled into a multicenter randomized trial: arm A, gefitinib; arm B, gemcitabine; and arm C, docetaxel. We performed subgroup analyses according to age.
Between December 2004 and June 2007, 127 patients were enrolled. Analyses were performed between the two subgroups aged <70years (younger, n=56) and ≥70years (older, n=71). Patients mainly had adenocarcinoma (46% young vs. 51%: elderly), of which 62% vs. 75% had a PS of 2, respectively. Significantly more elderly patients were women and non-smokers, and there was a non-significant trend towards more PS-2 among the elderly. Progression-free survival (PFS) was 1.4months (95% CI: 1.1-1.9) for younger compared to 2.3months (95% CI: 2.1-2.9) for elderly patients. Overall survival (OS) was 2.0months (95% CI: 1.5-2.4) and 3.7months (95% CI: 2.4-4.8), respectively. Toxicity did not differ between younger and older patients. NSCLC was better controlled in elderly patients after three cycles of monotherapy compared to younger patients (p=0.034). When adjusted for stratification criteria, age was the main prognostic factor for PFS. Adjusted HRs for PFS was 0.57 (95% CI: 0.38-0.85) for the elderly compared to patients aged <70years (p=0.004).
Older patients had a decreased risk of progression/death compared to younger patients. Single-agent chemotherapy can be considered for patients aged ≥70years with a PS of 2.
在一项随机II期试验中,我们评估了年龄对老年晚期非小细胞肺癌(NSCLC)且体能状态(PS)较差患者使用三种一线药物的影响。
PS为2或3的晚期NSCLC患者被纳入一项多中心随机试验:A组,吉非替尼;B组,吉西他滨;C组,多西他赛。我们根据年龄进行了亚组分析。
2004年12月至2007年6月期间,共入组127例患者。对年龄<70岁(较年轻组,n = 56)和≥70岁(老年组,n = 71)的两个亚组进行了分析。患者主要为腺癌(较年轻组46% vs.老年组51%),其中PS为2的分别占62%和75%。老年女性和非吸烟者明显更多,且老年患者中PS为2的有增多趋势但无统计学意义。较年轻患者的无进展生存期(PFS)为1.4个月(95%CI:1.1 - 1.9),而老年患者为2.3个月(95%CI:2.1 - 2.9)。总生存期(OS)分别为2.0个月(95%CI:1.5 - 2.4)和3.7个月(95%CI:2.4 - 4.8)。较年轻和老年患者的毒性无差异。与较年轻患者相比,老年患者在三个周期单药治疗后NSCLC得到更好控制(p = 0.034)。调整分层标准后,年龄是PFS的主要预后因素。与<70岁患者相比,老年患者PFS的调整后风险比为0.57(95%CI:0.38 - 0.85)(p = 0.004)。
与较年轻患者相比,老年患者进展/死亡风险降低。对于PS为2的≥70岁患者可考虑单药化疗。