Clinical study of neoadjuvant chemotherapy of pirarubicin in stage III primary breast carcinoma
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R 737.9; R 979.1

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    Abstract:

    Abstract:Objective:To investigate the shortterm effect of anthracycline(pirarubicin)based combination regimen as neoadjuvant chemotherapy for stage III primary breast cancer. Methods:For 138 patients with stage III primary breast cancer , one to four cycles of anthracyclinebased combination chemotherapy as CTF regimen were given. The clinical results, the feasibility rate of conservative breast surgery and toxic and side reaction were observed. Results:The overall response rate was 75.4%(104/138), including one case with clinical complete response(cCR), and 102 cases with clinial partial response(cPR),no change rate 23.2%, and progressive disease rate(PD) 1.4%(2/138). Seven cases received conservative breast surgery(5.1%,7/138). The cardiotoxicity was light without congestive heart failure, and the incidence of premature ventricular extrasystole(PVE) was 1.4%. The regimen resulted in mild alopecia and serious myelosuppression. The incidence of grade II myelosuppression was 27.5%, grade III 21.0%, and grade IV 7.2%.Conclusions:the shortterm effect of anthracyclinebased combination neoadjuvant chemotherapy as CTF regimen for primary breast cancer was satisfactory with little cardiotoxic effects.

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HAI Jian, MAO Jie, TANG Lili, SHEN Zhengtang.Clinical study of neoadjuvant chemotherapy of pirarubicin in stage III primary breast carcinoma [J]. Chin J Gen Surg,2006,15(10):2-727.
DOI:10.7659/j. issn.1005-6947.2006.10.002

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History
  • Received:January 01,1900
  • Revised:January 01,1900
  • Adopted:
  • Online: October 25,2006
  • Published: