Salvati F, Rasi G, Portalone L, Antilli A, Garaci E
VIII Divisione di Pneumologia, Ospedale C. Forlanini, Roma, Italia.
Anticancer Res. 1996 Mar-Apr;16(2):1001-4.
22 patients with advanced non-small-cell lung cancer were randomized to receive chemotherapy (ifosfamide) or chemotherapy followed by thymosin alpha1 + low-dose IFNalpha. Chemo-immunotherapy induced an enhanced response rate compared with chemotherapy alone (33% and 10% respectively). Although these differences were not significant, the difference in time to progression was (p=0.0059). CD4+, CD8+ and NK cell counts were significantly depressed after two cycles of chemotherapy, while no difference in cell count were seen in chemo-immunotherapy treated patients. Hematologic toxicity was reduced by the immunotherapy, with no grade 3/4 toxicity seen compared to 50% in patients treated with chemotherapy alone.
22例晚期非小细胞肺癌患者被随机分为两组,一组接受化疗(异环磷酰胺),另一组接受化疗后加用胸腺肽α1 + 低剂量干扰素α。与单纯化疗相比,化学免疫疗法诱导的缓解率有所提高(分别为33%和10%)。虽然这些差异不显著,但疾病进展时间的差异具有统计学意义(p = 0.0059)。化疗两个周期后,CD4 +、CD8 + 和NK细胞计数显著降低,而接受化学免疫疗法治疗的患者细胞计数无差异。免疫疗法降低了血液学毒性,与单纯化疗患者50%出现3/4级毒性相比,接受化学免疫疗法治疗的患者未出现3/4级毒性。