首页> 外文期刊>Clinical breast cancer >Phase II trial of combination of pegylated liposomal doxorubicin, cisplatin, and infusional 5-fluorouracil (CCF) plus trastuzumab as preoperative treatment for locally advanced and inflammatory breast cancer.
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Phase II trial of combination of pegylated liposomal doxorubicin, cisplatin, and infusional 5-fluorouracil (CCF) plus trastuzumab as preoperative treatment for locally advanced and inflammatory breast cancer.

机译:聚乙二醇化脂质体阿霉素,顺铂和5-氟尿嘧啶(CCF)输注加曲妥珠单抗联合治疗局部晚期和炎症性乳腺癌的II期试验。

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BACKGROUND: Pegylated liposomal doxorubicin (PLD) was shown as active but less toxic compared to doxorubicin in advanced breast cancer. Given its low cardiotoxicity, the combination of PLD and trastuzumab appears most attractive in the treatment of human epidermal factor receptor 2 (HER2)-positive breast cancer. PATIENTS AND METHODS: We investigated the activity of 8 courses of PLD in combination with cisplatin and infusional 5-fluorouracil (CCF) plus 3-week trastuzumab in patients with primary or recurrent cT2-T4 a-d, N0-3, M0 any estrogen receptor (ER), HER2-positive breast cancer. Patients with ER and/or progesterone receptor (PgR) >/= 10% tumors received also letrozole (plus triptorelin if premenopausal). The principal endpoint was clinical response rate; secondary endpoints were the pathologic complete response rate (pCR) and the cardiac safety of the combination. RESULTs: Thirty-two patients were enrolled in the study and all are evaluable for response and toxicity. Fifteen patients (47%) had ER-positive tumors, 15 patients and 2 patients had ER absent and ER poor tumors, respectively. Thirteen patients (41%) had inflammatory breast cancer (IBC) and 84% of patients had clinically positive nodes. A clinical response rate of 94% (95% CI, 79%-99%) and a pCR rate of 41% (95% CI, 24%-59%) were observed. Fifty-four percent of patients with IBC obtained a pCR. Eleven patients discontinued treatment before completing 8 courses as planned. No patient developed relevant cardiac toxicity. CONCLUSION: In this series of very locally advanced breast cancer, the combination of CCF and trastuzumab was very active obtaining an impressive rate of pCR, particularly in IBC, which merits further investigation in larger series.
机译:背景:与阿霉素相比,聚乙二醇脂质体阿霉素(PLD)在晚期乳腺癌中具有活性,但毒性较低。鉴于其低的心脏毒性,PLD和曲妥珠单抗的组合在治疗人类表皮因子受体2(HER2)阳性乳腺癌中似乎最有吸引力。病人和方法:我们调查了原发性或复发性cT2-T4 ad,N0-3,M0任何雌激素受体(8疗程)的PLD联合顺铂和5-氟尿嘧啶(CCF)和3周曲妥珠单抗输注的活性。 ER),HER2阳性乳腺癌。 ER和/或孕激素受体(PgR)> / = 10%肿瘤的患者也接受来曲唑(如果绝经前加曲普瑞林)。主要终点为临床缓解率;次要终点是组合的病理完全缓解率(pCR)和心脏安全性。结果:32名患者入选了该研究,所有患者的反应和毒性均得到评估。 15例(47%)患有ER阳性肿瘤,15例患者和2例患有ER缺失和ER较差的肿瘤。 13名患者(41%)患有炎症性乳腺癌(IBC),84%的患者患有临床阳性淋巴结。观察到临床反应率为94%(95%CI,79%-99%)和pCR率为41%(95%CI,24%-59%)。有54%的IBC患者获得了pCR。 11名患者在按计划完成8个疗程之前中断了治疗。没有患者出现相关的心脏毒性。结论:在这一系列非常局部晚期的乳腺癌中,CCF和曲妥珠单抗的组合非常有效,获得了令人印象深刻的pCR率,尤其是在IBC中,这值得在更大系列中进行进一步的研究。

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