Montpellier Academic Hospital, Service d'Oncologie Thoracique, Montpellier, France.
Lung Cancer. 2012 Feb;75(2):213-6. doi: 10.1016/j.lungcan.2011.07.012. Epub 2011 Aug 9.
In small cell lung cancer (SCLC), despite the high response rates induced by platinum-based first line chemotherapies, relapse happens in 85% of the first-line responding tumors. Since 1992 we used a combination of epirubicin and ifosfamide (EI) as a non-cross-resistant regimen in relapsed or refractory SCLC. With the topotecan approval in second line treatment, this combination has been moved from the second line to the third line setting.
Patients presenting with a relapsed or refractory, histologically proven, SCLC were considered for this combination associating ifosfamide 3 g/m(2) day 1-2 with uroprotection using mesna, and epirubicin 90 mg/m(2) day 1 given every four weeks until progression or unacceptable toxicity.
Seventy patients were accrued between September 1992 and August 2010 (seven women). Median age was 56 years. Performance Status was 0, 1, 2 and 3 for 16 (23%), 25 (35%), 20 (29%) and 9 (13%) patients respectively. Proportion of refractory, resistant and sensitive tumors was 20, 21 and 59% respectively. Median time from first line chemotherapy until progression was 90 days (range 5-1720 days). Forty-four patients were treated in second line setting whereas the 26 others have had received two lines at time of accrual. A total of 203 cycles were delivered (median 2 cycles, range: 1-6). Fifteen patients (21.4%) achieved an objective response (including one complete), and 10% had a stable disease. Median overall survival was 3.9 months (95% confidence interval: 3.3-5.1). Overall NCI-CTC grade 3 and 4 toxicity was mainly hematological: neutropenia (71% of the patients, febrile neutropenia 9.4% of the cycles), thrombocytopenia (23%), and anemia (22%). In univariate analysis, previous anthracyclines treatment was associated with a trend towards shorter survival (median overall survival 3.9 versus 4.6 months, p=0.12). In multivariate analysis, only a high serum NSE level and presence of brain metastases were independent prognostic variables.
The EI combination is an active regimen in relapsed or refractory SCLC. The trend towards a greater activity of this regimen in patients not pretreated using anthracyclines suggests that class of agents should be tested in SCLC relapsing after the etoposide-platinum standard regimen.
在小细胞肺癌(SCLC)中,尽管铂类一线化疗诱导的反应率很高,但 85%的一线应答肿瘤会复发。自 1992 年以来,我们使用表柔比星和异环磷酰胺(EI)联合方案作为复发或难治性 SCLC 的非交叉耐药方案。随着拓扑替康在二线治疗中的批准,该联合方案已从二线治疗转移到三线治疗。
对组织学证实的复发或难治性 SCLC 患者考虑使用该联合方案,即在异环磷酰胺 3g/m2(第 1-2 天)的同时使用美司钠进行尿路保护,表柔比星 90mg/m2(第 1 天),每四周一次,直到进展或不可接受的毒性。
1992 年 9 月至 2010 年 8 月期间共纳入 70 例患者(7 例女性)。中位年龄为 56 岁。体能状态为 0、1、2 和 3 的患者分别占 16%(23%)、25%(35%)、20%(29%)和 9%(13%)。难治性、耐药性和敏感性肿瘤的比例分别为 20%、21%和 59%。从一线化疗到进展的中位时间为 90 天(范围 5-1720 天)。44 例患者在二线治疗中接受治疗,而其余 26 例患者在入组时已接受了两线治疗。共进行了 203 个周期的治疗(中位数 2 个周期,范围:1-6)。15 例(21.4%)患者获得客观缓解(包括 1 例完全缓解),10%患者疾病稳定。中位总生存期为 3.9 个月(95%置信区间:3.3-5.1)。总体 NCI-CTC 3 级和 4 级毒性主要为血液学毒性:中性粒细胞减少症(71%的患者,发热性中性粒细胞减少症占周期的 9.4%)、血小板减少症(23%)和贫血(22%)。单因素分析显示,既往蒽环类药物治疗与生存时间缩短呈趋势相关(总生存期中位数分别为 3.9 个月和 4.6 个月,p=0.12)。多因素分析显示,只有高血清 NSE 水平和脑转移存在是独立的预后因素。
EI 联合方案是治疗复发或难治性 SCLC 的有效方案。该方案在未使用蒽环类药物预处理的患者中具有更大的活性趋势表明,此类药物应在依托泊苷-铂类标准方案治疗后复发的 SCLC 中进行测试。