Cohen M H, Chretien P B, Ihde D C, Fossieck B E, Makuch R, Bunn P A, Johnston A V, Shackney S E, Matthews M J, Lipson S D, Kenady D E, Minna J D
JAMA. 1979 Apr 27;241(17):1813-5. doi: 10.1001/jama.241.17.1813.
Patients with small-cell bronchogenic carcinoma who received intensive remission-induction chemotherapy randomly received either thymosin fraction V, 60 mg/sq m or 20 mg/sq m twice weekly, or no thymosin treatment during the initial six weeks of chemotherapy. Chemotherapy was then continued for two years. Thymosin administration did not increase the complete response rate. Patients receiving thymosin, 60 mg/sq m, had significantly prolonged survival times relative to the other treatment groups. This benefit was due to prolonged relapse-free survival in complete responders to treatment. The mechanism by which thymosin increased survival duration is unclear but may relate to restoration of immune deficits due to disease or treatment.
患有小细胞支气管癌且接受强化缓解诱导化疗的患者在化疗的最初六周内被随机分为三组,分别接受胸腺肽Ⅴ治疗(60mg/平方米,每周两次)、胸腺肽Ⅴ治疗(20mg/平方米,每周两次)或不接受胸腺肽治疗。之后化疗持续两年。胸腺肽治疗并未提高完全缓解率。接受60mg/平方米胸腺肽治疗的患者相对于其他治疗组的生存期显著延长。这种益处归因于完全缓解的患者无复发生存期延长。胸腺肽延长生存期的机制尚不清楚,但可能与恢复因疾病或治疗导致的免疫缺陷有关。