Isokangas O P, Joensuu H, Halme M, Jekunen A, Mattson K
Department of Oncology, Helsinki University Central Hospital, Finland.
Lung Cancer. 1998 May;20(2):127-33. doi: 10.1016/s0169-5002(98)00025-7.
We assessed the efficacy and toxicity of low-dose paclitaxel (Taxol) given combined with carboplatin before radiotherapy, and with cisplatin concomitantly with radiotherapy, in 27 patients with previously untreated inoperable stage IIA/IIIB non-small cell lung cancer. The induction chemotherapy consisted of paclitaxel 135 mg/m2 given over 1 h on day 1 and carboplatin 200 mg/m2 on day 2 repeated every 3 weeks for three cycles. Patients free of progression after induction chemotherapy received megavoltage radiation (56 Gy, 2 Gy/fraction) along with paclitaxel (30 mg/m2/1 h) and cisplatin (30 mg/m2/1 h) given 2-4 h before irradiation on days, 1, 2, 3, 22, 23 and 24. A combination of antero-posterior and oblique treatment fields was used to limit the dose to the spinal cord and to the left side of the heart to 36 Gy. The overall response rate was 78% (complete response, 19%). With a median follow-up of 19 months the median survival is 12 months, the estimated 2-year survival rate is 36%, and all patients with a complete response survived for at least 12 months after starting treatment. A total of 17 deaths occurred with metastases predominantly in the brain. Major acute toxicities (> grade 3) during induction chemotherapy included leuko-/neutropenia (n = 5/27, 19%), and during chemoradiotherapy leuko-/neutropenia (n = 10/23, 43%), thrombocytopenia (n = 1, 4%), oesophagitis (n = 3, 13%) and pneumonitis (n = 7, 30%). No toxic deaths occurred. Marked renal toxicity was not observed. We conclude that this chemoradiotherapy regimen is effective and well-tolerated, and should be further evaluated in a randomised phase III trial.
我们评估了低剂量紫杉醇(泰素)联合卡铂在放疗前给药,以及与顺铂在放疗期间同步给药,对27例先前未经治疗的无法手术的IIA/IIIB期非小细胞肺癌患者的疗效和毒性。诱导化疗方案为第1天静脉滴注紫杉醇135mg/m²,持续1小时,第2天静脉滴注卡铂200mg/m²,每3周重复1次,共3个周期。诱导化疗后病情无进展的患者接受兆伏级放疗(56Gy,每次2Gy),并在放疗日第1、2、3、22、23和24天,于放疗前2 - 4小时静脉滴注紫杉醇(30mg/m²/1小时)和顺铂(30mg/m²/1小时)。采用前后野和斜野相结合的方式,将脊髓和心脏左侧的剂量限制在36Gy。总缓解率为78%(完全缓解率为19%)。中位随访19个月,中位生存期为12个月,预计2年生存率为36%,所有完全缓解的患者在开始治疗后至少存活了12个月。共有17例患者死亡,主要死于脑转移。诱导化疗期间主要的急性毒性反应(>3级)包括白细胞/中性粒细胞减少(n = 5/27,19%),放化疗期间白细胞/中性粒细胞减少(n = 10/23,43%)、血小板减少(n = 1,4%)、食管炎(n = 3,13%)和肺炎(n = 7,30%)。未发生因毒性反应导致的死亡。未观察到明显的肾毒性。我们得出结论,这种放化疗方案有效且耐受性良好,应在随机III期试验中进一步评估。