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环磷酰胺、阿霉素、5-氟尿嘧啶及大剂量托瑞米芬用于晚期/复发性乳腺癌患者。日本托瑞米芬合作研究组。

Cyclophosphamide, adriamycin, 5-fluorouracil and high-dose toremifene for patients with advanced/recurrent breast cancer. The Japan Toremifene Cooperative Study Group.

作者信息

Tominaga T, Nomura Y, Uchino J, Hirata K, Kimura M, Yoshida M, Aoyama H, Kinoshita H, Koyama H, Monden Y, Takashima S, Ogawa M

机构信息

Department of Surgery, Tokyo Metropolitan Komagome Hospital, Japan.

出版信息

Jpn J Clin Oncol. 1998 Apr;28(4):250-4. doi: 10.1093/jjco/28.4.250.

DOI:10.1093/jjco/28.4.250
PMID:9657010
Abstract

BACKGROUND

Multi-combination chemotherapy consisting of anthracyclines has been effective but has not invariably prolonged the survival period in advanced/recurrent breast cancer. The possibility has been discussed that chemoendocrine therapy combined with endocrine agents is more effective.

METHODS

In order to evaluate the toxicity and efficacy of a new endocrine therapy for advanced/recurrent breast cancer, we ran a pilot study during the period from July 1994 to July 1996.

RESULTS

Twenty-two patients with advanced/recurrent breast cancer were treated with chemoendocrine therapy consisting of cyclophosphamide (100 mg/body) p.o. daily for 14 days, with adriamycin (40 mg/m2) i.v. and 5-fluorouracil (500 mg/body) i.v. on day 1 (repeated every 3 weeks for 9 weeks) (CAF therapy), and high-dose toremifene (120 mg/body) p.o. daily. Of 20 evaluable patients, two showed complete response (10%), eight partial response (40%), six no change (30%) and four progressive disease (20%). The overall response rate was 50%, and the median duration of response was 69.5 days (28-133+ days). The major toxicities were drug-induced alopecia, gastrointestinal toxicity and hematological toxicity, but these were clinically well tolerated. No serious cardiac, liver or renal symptom was seen.

CONCLUSIONS

Based on these results, we consider the addition of high-dose toremifene to the CAF therapy to be useful in the treatment of advanced and recurrent breast cancer.

摘要

背景

由蒽环类药物组成的多药联合化疗虽有疗效,但在晚期/复发性乳腺癌中并不能始终延长生存期。已讨论过化疗内分泌治疗联合内分泌药物可能更有效。

方法

为评估一种用于晚期/复发性乳腺癌的新内分泌治疗的毒性和疗效,我们在1994年7月至1996年7月期间进行了一项试点研究。

结果

22例晚期/复发性乳腺癌患者接受了化疗内分泌治疗,包括口服环磷酰胺(100mg/体),每日1次,共14天,第1天静脉注射阿霉素(40mg/m²)和5-氟尿嘧啶(500mg/体)(每3周重复1次,共9周)(CAF治疗),以及口服高剂量托瑞米芬(120mg/体),每日1次。在20例可评估患者中,2例完全缓解(10%),8例部分缓解(40%),6例病情稳定(30%),4例病情进展(20%)。总缓解率为50%,中位缓解持续时间为69.5天(28 - 133 +天)。主要毒性为药物性脱发、胃肠道毒性和血液学毒性,但临床耐受性良好。未观察到严重的心脏、肝脏或肾脏症状。

结论

基于这些结果,我们认为在CAF治疗中添加高剂量托瑞米芬对晚期和复发性乳腺癌的治疗有用。

相似文献

1
Cyclophosphamide, adriamycin, 5-fluorouracil and high-dose toremifene for patients with advanced/recurrent breast cancer. The Japan Toremifene Cooperative Study Group.环磷酰胺、阿霉素、5-氟尿嘧啶及大剂量托瑞米芬用于晚期/复发性乳腺癌患者。日本托瑞米芬合作研究组。
Jpn J Clin Oncol. 1998 Apr;28(4):250-4. doi: 10.1093/jjco/28.4.250.
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[Combined chemoendocrine therapy using adriamycin, cyclophosphamide and high dose toremifene in patients with recurrent breast cancer].[在复发性乳腺癌患者中使用阿霉素、环磷酰胺和高剂量托瑞米芬进行联合化疗内分泌治疗]
Gan To Kagaku Ryoho. 2002 Nov;29(11):1935-42.
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[A case of breast cancer patient of CAF (cyclophosphamide, adriamycin, 5-fluorouracil) resistant lung metastasis with remarkable response to reverse drug-resistance by toremifene].[一例对环磷酰胺、阿霉素、5-氟尿嘧啶(CAF)耐药的乳腺癌肺转移患者对托瑞米芬逆转耐药反应显著]
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[Adriamycin, cyclophosphamide, ftorafur and tamoxifen (ACFT) in patients with advanced breast cancer].
Gan To Kagaku Ryoho. 1988 Jan;15(1):121-6.
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[Results of clinical trials with a CMitF (cyclophosphamide, mitoxantrone, and 5-fluorouracil) regimen versus a CAF (cyclophosphamide, adriamycin, and 5-fluorouracil) regimen in advanced/relapsed breast cancer].[环磷酰胺、米托蒽醌和5-氟尿嘧啶(CMitF)方案与环磷酰胺、阿霉素和5-氟尿嘧啶(CAF)方案治疗晚期/复发性乳腺癌的临床试验结果]
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[Clinical evaluation of adriamycin in advanced and recurrent breast cancer (No. 4)--Joint study by 30 institutes on the duration of remission using various maintenance therapies in patients treated with CAF. Clinical Study Group of Adriamycin for Breast Cancer in Japan].阿霉素治疗晚期及复发性乳腺癌的临床评估(第4号)——日本30家机构关于CAF方案治疗患者采用不同维持疗法的缓解期联合研究。日本乳腺癌阿霉素临床研究组
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