Ploner F, Jakesz R, Hausmaninger H, Kolb R, Stierer M, Fridrik M, Steindorfer P, Gnant M, Haider K, Mlineritsch B, Tschurtschenthaler G, Steger G, Seifert M, Kubista E, Samonigg H
Klinische Abteilung für Onkologie, Medizinische Universitätsklinik, Karl-Franzens-Universität Graz.
Onkologie. 2003 Apr;26(2):115-9. doi: 10.1159/000069831.
A randomised, controlled clinical trial was initiated in 1984 to test whether 1 cycle of anthracycline-containing adjuvant chemotherapy improves the outcome of breast cancer patients presenting with stage II disease and negative oestrogen and progesterone receptors (ER, PgR), as compared with 6 cycles of dose-reduced CMF.
Within 7 years 263 women with stage II breast cancer were randomised either to receive 1 cycle of doxorubicin, vinblastine, cyclophosphamide, methotrexate and 5- fluorouracil (AV-CMF) or to receive 6 cycles of cyclophosphamide, methotrexate and 5-fluorouracil (CMF). Patients were stratified for tumour stage, nodal stage, menopausal status, type of surgery and participating centre.
After a median follow-up of 100 months, neither disease-free (DFS) nor overall survival (OS) differed significantly between the two groups.
Compared to 6 cycles of a non-standard low-dose CMF regimen 1 cycle of anthracycline- containing adjuvant chemotherapy failed to improve the outcome in women with stage II receptor-negative breast cancer in terms of DFS and OS.
1984年开展了一项随机对照临床试验,以检验与6个周期的剂量减少的CMF方案相比,1个周期含蒽环类药物的辅助化疗是否能改善II期疾病且雌激素和孕激素受体(ER、PgR)阴性的乳腺癌患者的预后。
7年内,263例II期乳腺癌女性患者被随机分为两组,一组接受1个周期的阿霉素、长春碱、环磷酰胺、甲氨蝶呤和5-氟尿嘧啶(AV-CMF),另一组接受6个周期的环磷酰胺、甲氨蝶呤和5-氟尿嘧啶(CMF)。患者按肿瘤分期、淋巴结分期、绝经状态、手术类型和参与中心进行分层。
中位随访100个月后,两组的无病生存期(DFS)和总生存期(OS)均无显著差异。
与6个周期的非标准低剂量CMF方案相比,1个周期含蒽环类药物的辅助化疗在DFS和OS方面未能改善II期受体阴性乳腺癌女性患者的预后。