Kakolyris S, Agelidou A, Androulakis N, Tsaroucha E, Kouroussis Ch, Agelidou M, Karvounis N, Veslemes M, Christophylakis Ch, Argyraki A, Geroyianni A, Georgoulias V
Department of Medical Oncology, University General Hospital of Alexandroupolis, Alexandroupolis, Greece.
Lung Cancer. 2006 Jul;53(1):59-65. doi: 10.1016/j.lungcan.2006.03.011. Epub 2006 May 23.
To evaluate the efficacy and tolerance of a cisplatin plus etoposide regimen followed by thoracic radiotherapy (TRT) and paclitaxel plus cisplatin consolidation chemotherapy in patients with limited stage small cell lung cancer (SCLC).
Thirty-nine patients with limited SCLC were enrolled onto this study. Patients received three courses of cisplatin 75 mg/m2 i.v., day 1 and etoposide 100 mg/m2 i.v., days 1-3 (EP regimen), followed by TRT (45-56 Gy administered in 15 fractions), and three courses of paclitaxel 175 mg/m2 i.v., day 1 and cisplatin, as previously, on day 2 (PP regimen); cycles were repeated every 21 days.
All patients were evaluable for toxicity and 34 for response. The overall response rate was 67% (CR: 26%; PR: 41%; intention-to-treat analysis) (95% CI: 53.0-84.2%). After a median follow-up period of 15 months, the median survival time was 15 months, the median time to tumor progression 8.3 months and the 1-year survival rate 53.8%. Grade 3/4 neutropenia occurred in 39% and 36% of patients receiving EP and PP regimens, respectively. The incidence of febrile neutropenia was 5% and 3% for EP and PP regimens, respectively. Other hematologic and non-hematologic toxicities were mild, with the exception of esophagitis occurring in 36% of patients during and/or immediately after radiotherapy.
Consolidation therapy with PP after sequential EP and thoracic radiotherapy is feasible and well-tolerated; however, the efficacy results are comparable with those previously obtained in the same patients' population using a combination of EP and TRT.
评估顺铂联合依托泊苷方案序贯胸部放疗(TRT)以及紫杉醇联合顺铂巩固化疗在局限期小细胞肺癌(SCLC)患者中的疗效和耐受性。
39例局限期SCLC患者入组本研究。患者接受3个疗程的顺铂75mg/m²静脉滴注,第1天给药,依托泊苷100mg/m²静脉滴注,第1 - 3天给药(EP方案),随后进行TRT(45 - 56Gy分15次给予),以及3个疗程的紫杉醇175mg/m²静脉滴注,第1天给药,顺铂同前,第2天给药(PP方案);每21天重复1个周期。
所有患者均可评估毒性,34例可评估疗效。总缓解率为67%(完全缓解:26%;部分缓解:41%;意向性分析)(95%可信区间:53.0 - 84.2%)。中位随访期15个月后,中位生存时间为15个月,中位肿瘤进展时间为8.3个月,1年生存率为53.8%。接受EP方案和PP方案的患者中,3/4级中性粒细胞减少的发生率分别为39%和36%。发热性中性粒细胞减少的发生率,EP方案和PP方案分别为5%和3%。其他血液学和非血液学毒性均较轻,但36%的患者在放疗期间和/或放疗后立即发生食管炎。
序贯EP方案和胸部放疗后采用PP方案巩固治疗可行且耐受性良好;然而,疗效结果与之前在同一患者群体中使用EP方案联合TRT所获得的结果相当。