Johnson D H, Turrisi A T, Chang A Y, Blum R, Bonomi P, Ettinger D, Wagner H
Vanderbilt University, Nashville, TN.
J Clin Oncol. 1993 May;11(5):879-84. doi: 10.1200/JCO.1993.11.5.879.
This pilot study was undertaken to determine the efficacy and feasibility of alternating cisplatin and etoposide with multiple daily fractions of thoracic radiotherapy (TRT) in patients with limited-stage small-cell lung cancer (SCLC).
Thirty-four SCLC patients received four courses of cisplatin (30 mg/m2/d x 3) plus etoposide (120 mg/m2/d x 3) (PE) every 3 weeks. TRT was administered twice daily (1.5 Gy per fraction) for 5 consecutive days in the week after cycles 1, 2, and 3 of chemotherapy (total TRT dose, 45 Gy). Patients who achieved a complete response (CR) received one course of late-intensification (LI) treatment consisting of cyclophosphamide (4 g/m2) and etoposide (900 mg/m2). Prophylactic cranial irradiation (PCI) was optional.
Nineteen of 32 assessable patients achieved a CR (59%) and 12 had a partial response (38%), for an overall response rate of 97% (95% confidence interval [CI], 84% to 99%). Median survival was 18 months, while 2-year progression-free survival was 47%. Leukopenia < or = 1,000/microL occurred in 12% of induction treatment cycles. Severe esophagitis was uncommon. Pulmonary fibrosis that was asymptomatic or minimally symptomatic was observed in eight patients (25%). There was one episode of adult respiratory distress syndrome (ARDS) during LI chemotherapy. Life-threatening neutropenia (< or = 500/microL) developed in all patients who underwent LI chemotherapy, with a median duration of 10 days (range, 8 to 19). Two patients died of sepsis during LI chemotherapy.
Alternating PE and TRT as performed in this trial is an effective brief induction regimen for limited-stage SCLC. However, this particular regimen did not appear to be substantially different in terms of efficacy or toxicity compared with regimens using concurrent chemotherapy and standard-fraction TRT. LI chemotherapy was associated with unacceptable toxicity and did not appear to have a favorable impact on survival.
开展这项初步研究以确定顺铂和依托泊苷交替使用并联合胸部放疗(TRT)每日多次分割剂量治疗局限期小细胞肺癌(SCLC)患者的疗效和可行性。
34例SCLC患者每3周接受4个疗程的顺铂(30mg/m²/d×3)加依托泊苷(120mg/m²/d×3)(PE)治疗。在化疗第1、2和3周期后的那周,TRT每天给药2次(每次1.5Gy),连续5天(TRT总剂量45Gy)。达到完全缓解(CR)的患者接受1个疗程的强化治疗(LI),包括环磷酰胺(4g/m²)和依托泊苷(900mg/m²)。预防性颅脑照射(PCI)为可选方案。
32例可评估患者中,19例达到CR(59%),12例部分缓解(38%),总缓解率为97%(95%置信区间[CI],84%至99%)。中位生存期为18个月,2年无进展生存率为47%。12%的诱导治疗周期出现白细胞减少≤1000/μL。严重食管炎不常见。8例患者(25%)观察到无症状或症状轻微的肺纤维化。LI化疗期间发生1例成人呼吸窘迫综合征(ARDS)。所有接受LI化疗的患者均出现危及生命的中性粒细胞减少(≤500/μL),中位持续时间为10天(范围8至19天)。2例患者在LI化疗期间死于败血症。
本试验中所采用的PE与TRT交替方案是局限期SCLC一种有效的短期诱导方案。然而,与使用同步化疗和标准分割TRT的方案相比,该特定方案在疗效或毒性方面似乎没有实质性差异。LI化疗毒性不可接受,且似乎对生存没有有利影响。