Ajlouni M, Chapman R, Kim J H
Department of Radiation Oncology, Henry Ford Hospital, Detroit, Michigan 48202, USA.
Cancer J Sci Am. 1996 Nov-Dec;2(6):314-20.
To evaluate the efficacy of multidrug chemotherapy combined with accelerated radiation therapy in the treatment of localized but unresectable non-small cell lung cancer.
Between September 1990 and February 1993, 35 patients with Stage III (15 IIIA & 20 IIIB) non-small cell lung cancer were entered on a protocol using combined accelerated radiation therapy and chemotherapy. Radiation therapy consisted of 55.6 Gy in 30 fractions (1.8 Gy bid for 5 consecutive days given in 3 weeks [total of 15 days], every other week). Chemotherapy consisted of cisplatin (10 mg/m2), vinblastine (4 mg/m2), 6-thioguanine (40 mg bid), and 5-fluorouracil (400 mg/m2 as continuous infusion) given concomitantly with radiation therapy. Approximately 3 weeks following completion of radiation therapy, two cycles of consolidation chemotherapy were given, consisting of two doses of cisplatin (120 mg/m2) 4 weeks apart and six doses of vinblastine (4 mg/m2) given on two consecutive days every other week for 3 weeks.
Six patients were still alive at last follow-up; for them the median follow-up time is 47 months (range, 39-55.8). The median survival time is 17.5 months. The 1-, 2-, 3- and 4.5-year survival rates are 69%, 37%, 20% and 17%, respectively. Overall response rate is 63%, with 51.5% partial response and 11.5% complete response rates. Esophagitis occurred as follows: Grade 4 = 0, Grade 3 = 1, Grade 2 = 6, and Grade 1 = 13. No patient developed Grade 3 or 4 acute respiratory toxicity. Significant hematologic toxicity occurred as follows: 37% Grade 3 and 31% Grade 4 leukopenia. Radiation pneumonitis occurred in two patients.
The regimen tested in this protocol appears to be very well tolerated with minimal pulmonary or esophageal toxicity. This, coupled with the shortened course of radiation therapy and the ability to deliver the combined radiation and chemotherapy portion of the treatment on an outpatient basis most of the time, has made multi-modality treatment for this malignancy much easier and more convenient for patients. In addition, the favorable survival in this group of patients with locally advanced disease is very encouraging and warrants further study.
评估多药化疗联合加速放疗在治疗局限性但不可切除的非小细胞肺癌中的疗效。
1990年9月至1993年2月,35例Ⅲ期(15例ⅢA期和20例ⅢB期)非小细胞肺癌患者进入一项使用联合加速放疗和化疗的方案。放疗包括30次分割给予55.6 Gy(3周内每周连续5天每天给予1.8 Gy,共15天,每隔一周重复)。化疗包括顺铂(10 mg/m²)、长春碱(4 mg/m²)、6-硫鸟嘌呤(40 mg bid)和5-氟尿嘧啶(400 mg/m²持续输注),与放疗同时进行。放疗完成后约3周,给予两个周期的巩固化疗,包括相隔4周的两剂顺铂(120 mg/m²)以及每隔一周连续两天给予六剂长春碱(4 mg/m²),共3周。
最后一次随访时有6例患者仍存活;他们的中位随访时间为47个月(范围39 - 55.8个月)。中位生存时间为17.5个月。1年、2年、3年和4.5年生存率分别为69%、37%、20%和17%。总缓解率为63%,部分缓解率为51.5%,完全缓解率为11.5%。食管炎发生情况如下:4级 = 0例,3级 = 1例,2级 = 6例,1级 = 13例。无患者发生3级或4级急性呼吸毒性。显著的血液学毒性发生情况如下:37%为3级白细胞减少,31%为4级白细胞减少。两名患者发生放射性肺炎。
本方案中测试 的治疗方案耐受性良好,肺部或食管毒性极小。这一点,再加上放疗疗程缩短以及大部分时间能够在门诊进行放疗和化疗联合治疗部分,使得针对这种恶性肿瘤的多模式治疗对患者来说更加容易和方便。此外,这组局部晚期疾病患者良好的生存率非常令人鼓舞,值得进一步研究。