References
- Hirvikoski PP, Kumpulainen EJ, Johansson RT. CNF combination as adjuvant treatment in breast cancer patients is well tolerated. Anti-Cancer Drugs 1997; 8: 376–8
- Hirvikoski PP, Kumpulainen EJ, Johansson RT. Hepatic toxicity caused by adjuvant CMF/CNF in breast cancer patients and reversal by tamoxifen. Breast Cancer Res Treat 1997; 44: 269–74
- Kumpulainen EJ, Hirvikoski PP, Pukkala E, Johansson RT. Cancer risk after adjuvant chemo- or chemohormonal therapy of breast cancer. Anti-Cancer Drugs 1998; 9: 131–4
- Bonadonna G, Valagussa P. Dose-response effect of adjuvant chemotherapy in breast cancer. N Engl J Med 1981; 304: 10–5
- Saarto T, Blomqvist C, Rissanen P, Auvinen A, Elomaa I. Haematological toxicity: A marker of adjuvant chemotherapy efficacy in stage II and III breast cancer. Br J Cancer 1997; 75: 301–5
- Poikonen P, Saarto T, Lundin J, Joensuu H, Blomqvist C. Leucocyte nadir as a marker for chemotherapy efficacy in node-positive breast cancer treated with adjuvant CMF. Br J Cancer 1999; 80: 1763–6
- Mayers C, Panzarella T, Tannock IF. Analysis of the prognostic effects of inclusion in a clinical trial and of myelosuppression on survival after adjuvant chemotherapy for breast carcinoma. Cancer 2001; 91: 2246–57
- Bergh J, Wiklund T, Erikstein B, Lidbrink E, Lindmar H, Malmström P, et al. Tailored fluorouracil, epirubicin, and cyclophosphamide compared with marrow-supported high-dose chemotherapy as adjuvant treatment for high-risk breast cancer: A randomised trial. Scandinavian Breast Group 9401 study. Lancet 2000; 356: 1384–91