Skip to main content
Log in

Preoperative chemotherapy of continuous infusion of 5-fluorouracil, epirubicin or pirarubicin and cyclophosphamine in operable primary breast cancer

  • Articles
  • Published:
Chinese Journal of Cancer Research

Abstract

Objective: To evaluate the feasibility and activity of continuous-infusion of fluorouracil in association with epirubicin or pirarubicin and cyclophosphamine as neoadjuvant regimen in patients with primary breast cancer. Methods: A total of 111 (including 114 breasts) were entered into the study. Chemotherapy consisted of two to six cycles of epirubicin 50 mg/(m2·d) and cyclophosphamide 500 mg/(m2·d) on day 1 and 8, and continuous intravenous administration of 5-fluorouracil 200 mg/(m2·d) from day 1 to 28 with a microinfusional elastomer (CEFci) or pirarubicin 35 mg/(m2·d) on day 1 and 8 instead of epirubicin (CTFci). Results: The overall response rate was 87.7%. Forty-five patients (39.5%) attained a complete clinical response and 27 (23.7%) attained a pathological complete response. CTFci regimen was superior to CEFci regimen in response rate, the pathological complete response rate (pCR) of former regimen was significantly higher than that of latter regimen (34.8% vs. 16.2%) (P=0.022). The pCR rate in ER/PgR negative tumor was significantly higher than that of ER/PgR positive tumor, achieving 33.3% and 7.5% respectively (P=0.001, x 2=11.043). There was no relationship between HER-2 expression and tumor response. The toxicity of two regimens was well tolerated. Alopecia was mild in CTFci regimen comparing with CEFci regimen but neutropenia in CTFci regimen was higher than CEFci regimen. Conclusion: Continuous-infusion of fluorouracil in association with epirubicin or pirarubicin and cyclophosphamine is effective regimens as neoadjuvant chemotherapy for primary breast cancer and the toxicity is well tolerated. Pirarubicin regimen was superior to epirubicin regimen in response rate.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  1. Fisher B, Brown A, Mamounas E, et al. Effect of preoperative chemotherapy on local-regional disease in women with operable breast cancer: Findings from National Surgical Adjuvant Breast and Bowel Project B-18 [J]. J Clin Oncol 1997; 15:2483–93.

    PubMed  CAS  Google Scholar 

  2. Powles TJ, Hickish TF, Makris A, et al. Randomized trial of chemoendocrine therapy started before or after surgery for treatment of primary breast cancer [J]. J Clin Oncol 1995; 13:547–52.

    PubMed  CAS  Google Scholar 

  3. Mauriac L, MacGrogan G, Avril A, et al. Neoadjuvant chemotherapy for operable breast carcinoma larger than 3 cm: a unicentre randomized trial with a 124-month median follow-up. Institute Bergonie Bordeaux Groupe Sein (IBBGS). Ann Oncol 1999; 10:47–52.

    Article  PubMed  CAS  Google Scholar 

  4. Scholl SM, Fourquet A, Asselain B, et al. Neoadjuvant versus adjuvant chemotherapy in premenopausal patients with tumors considered too large for breast conserving surgery: preliminary results of a randomized trial: S6 [J]. Eur J Cancer 1994; 30A:645–52.

    Article  PubMed  CAS  Google Scholar 

  5. Makris A, Powles TJ, Ashley SE, et al. A reduction in the requirements for mastectomy in a randomized trial of neoadjuvant chemoendocrine therapy in primary breast cancer [J]. Ann Oncol 1998; 9:1179–84.

    Article  PubMed  CAS  Google Scholar 

  6. Fisher B, Bryant J, Wolmark N, et al. Effects of preoperative chemotherapy on the outcome of women with operable breast cancer [J]. J Clin Oncol 1998; 16:2672–85.

    PubMed  CAS  Google Scholar 

  7. Green S, Weiss GR. Southwest Oncology Group standard response criteria, endpoint definitions and toxicity criteria [J]. Invest New Drugs 1992; 10:239–53.

    Article  PubMed  CAS  Google Scholar 

  8. Hayward JL, Carbone PP, Heusen JC, et al. Assessment of response to therapy in advanced breast cancer [J]. Br J Cancer 1977; 35:292–8.

    PubMed  CAS  Google Scholar 

  9. Clahsen PC, van de Velde CJH, Julien JP, et al. Improved local control and disease-free survival after perioperative chemotherapy for early-stage breast cancer [J]. J Clin Oncol 1996; 14:745–53.

    PubMed  CAS  Google Scholar 

  10. Mauriac L, Durand M, Avril A, et al. Effects on primary chemotherapy in conservative treatment of breast cancer patients with operable tumor larger than 3 cm [J]. Ann Oncol 1991; 2:347–54.

    PubMed  CAS  Google Scholar 

  11. Scholl SM, Pierga JY, Asselain B, et al. Breast tumor response to primary chemotherapy predicts local and distant control as well as survival [J]. Eur J Cancer 1995; 31A:1969–75.

    Article  PubMed  CAS  Google Scholar 

  12. van der Hage JA, van de Velde CJ, Julien JP, et al. Preoperative chemotherapy in primary operable breast cancer: Results from the European Organization for Research and Treatment of Cancer Trial 10902 [J]. J Clin Oncol 2001; 19:4224–37.

    PubMed  Google Scholar 

  13. National Institutes of Health Consensus Development Panel. National Institutes of Health Consensus Development Conference Statement: Adjuvant therapy for breast cancer, November 1–3, 2000. J Natl Cancer Inst Monogr 2001; 30:5–15.

    Google Scholar 

  14. Mamounas EP. NSABP protocol B-27: preoperative doxorubicin plus cyclophosphamide followed by preoperative or postoperative docetaxel [J]. Oncology 1997; 6:37–40.

    Google Scholar 

  15. Dhingra K, Frye D, Newman RA, et al. Phase II clinical and pharmacological study of pirarubicin in combination with 5-fluorouracil and cyclophosphamide in metastatic breast cancer [J]. Clin Cancer Res 1995; 1:691–7.

    PubMed  CAS  Google Scholar 

  16. Spielamn M, Kerbrat P, Delozier T, et al. Pirarubicin in advanced breast cancer: a French cooperative phase II study [J]. Eur J Cancer 1990; 26:821–3.

    Article  Google Scholar 

  17. Ansfield FJ, Ramirez G, Mackman S, et al. A 10-year study of 5-fluorouracil in disseminated breast cancer with clinical results and survival times [J]. Cancer Res 1969; 29:1062–6.

    PubMed  CAS  Google Scholar 

  18. Carter SK. Integration of chemotherapy into combined modality treatment of solid tumors [J]. Cancer Treat Rev 1976; 3:141–74.

    Article  PubMed  CAS  Google Scholar 

  19. Jones RB, Shpall EJ, Shogan J, et al. The Duke AFM program: intensive induction chemotherapy for metastatic breast cancer [J]. Cancer 1990; 66:431–6.

    Article  PubMed  CAS  Google Scholar 

  20. Lemon HM. Reduction of 5-fluorouracil toxicity in man with retention of anticancer effects by prolonged intravenous administration in 5% dextrose [J]. Cancer Chemther Rep 1960; 8:97–101.

    CAS  Google Scholar 

  21. Fraile RJ, Baker LH, Buroker TR, et al. Pharmacokinetics of 5-fluorouracil administered orally by rapid intravenous and by slow infusion [J]. Cancer Res 1980; 40:2223–8.

    PubMed  CAS  Google Scholar 

  22. Regazzoni S, Pesce G, Marini G, et al. Low-dose continuous intravenous infusion of 5-fluorouracil for metastatic breast cancer [J]. Ann Oncol 1996; 7:807–13.

    PubMed  CAS  Google Scholar 

  23. Cameron DA, Gabra H, Leonard NC. Continuous 5-fluorouracil in the treatment of breast cancer [J]. Br J Cancer 1994; 70:120–4.

    PubMed  CAS  Google Scholar 

  24. Hansen R, Quebbeman E, Beatty P, et al. Continuous 5-fluorouracil infusion in refractory carcinoma of the breast [J]. Breast Cancer Res Treat 1987; 10:145–9.

    Article  PubMed  CAS  Google Scholar 

  25. Lokich JJ, Ahlgren JD, Gullo JJ, et al. A prospective randomized comparison of continuous infusion fluorouracil with a conventional bolus schedule in metastatic colorectal carcinoma: a Mid-Atlantic Oncology Program Study [J]. J Clin Oncol 1989; 7:425–32.

    PubMed  CAS  Google Scholar 

  26. Collichio FA, Amamoo MA, Fogleman J, et al. Phase II study of low-dose infusional 5-fluorouracil and paclitaxel (Taxol) given every 2 weeks in metastatic breast cancer [J]. Am J Clin Oncol 2002; 25:194–7.

    Article  PubMed  Google Scholar 

  27. Nole F, Munzone E, Mandala M, et al. Vinorelbine, cisplatin and continuous infusion of 5-fluorouracil (ViFuP) in metastatic breast cancer patients: a phase II study [J]. Ann Oncol 2001; 12:95–100.

    Article  PubMed  CAS  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Li Jin-feng.

Additional information

Foundation item: This work was supported by a grant from the Key project of Beijing Science & Technology Committee.

Biography: LI Jin-feng (1965–), male, associate professor, doctor of medicine, Peking University School of Oncology, majors in surgical oncology.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Li, Jf., Ou, YT., Wang, Tf. et al. Preoperative chemotherapy of continuous infusion of 5-fluorouracil, epirubicin or pirarubicin and cyclophosphamine in operable primary breast cancer. Chin. J. Cancer Res. 16, 197–202 (2004). https://doi.org/10.1007/s11670-004-0026-6

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s11670-004-0026-6

Key words

CLC number

Navigation