Evaluation of the Effects of Letrozole in Combination with Neoadjuvant Chemotherapy on Clinical Response Rate of Breast Cancer

Zahra, Mozahheb, Abolghasem, Alahyari, Seyyedeh, Fatemeh, Seyyedi, Khabbaz, A. Fattahi, Mohsen Najafi
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Abstract

AbstractThis randomized clinical trial was aimed to assess the efficacy of neoadjuvant letrozole in combination with standard neoadjuvant chemotherapy regimen on clinical response rate of hormone receptor positive locally advanced breast cancer.In this randomized clinical study, 42 female patients, ≥ 18 years, with clinical stage IIB-IIIC (T1-4, N0-3, M0), pathologically proven hormone receptor positive and HER2 negative, invasive ductal carcinoma of breast, were randomly assigned to receive standard neoadjuvant chemotherapy alone (control group) or letrozole 2.5 mg/d (in association with goserlin in premenopausal patients) concurrent with standard neoadjuvant chemotherapy (study group). Standard neoadjuvant chemotherapy regimen has consisted of 4 cycles of doxorubicin (60mg/m2) and cyclophodphamide (600mg/m2), followed by 4 cycles of paclitaxel (175mg/m2) every two weeks.At the beginning of the study all patients underwent thorough exmination of breast mass and axillary lymph nudes by palpation and ultrasonography. At the end of the study response rates were also evaluated by palpation and ultrasonography and subsequently patients were referred for surgury. Pathologic response rates were also evaluated on surgical specimens. All of the clinical, ultrasonographic and pathologic examinations during the trial were performed by a single specialist. Finally all the data were analysed statistically.Overall clinical response rates in breast were 95.2%, in both study and control group. Overall clinical response rates in axilla were 80.9% and 76.2% in study and control group respectively. Similarly, overall radiologic complete response rates in breast and axilla were 95.2% and 76.2% respectively in both study and control group. Totally, the comparison of overall clinical and radiologic response rates in th breast and axilla, showed no significant difference between control and study group (p>0.05).The addition of letrozol to standard neoadjuvant chemotherapy regimen was not associated with higher clinical and radiologic response rates in patients with locally advanced hormon receptor positive breast cancer.Keywords: Neoadjuvant chemotherapy, Letrozole, Locally advanced breast cancer
来曲唑联合新辅助化疗对乳腺癌临床反应率的影响
摘要本随机临床试验旨在评价新辅助来曲唑联合标准新辅助化疗方案对激素受体阳性局部晚期乳腺癌临床反应率的影响。在这项随机临床研究中,42例年龄≥18岁,临床分期为IIB-IIIC (T1-4, N0-3, M0),病理证实激素受体阳性,HER2阴性的浸润性乳腺导管癌女性患者,随机分为单独接受标准新辅助化疗(对照组)或来曲唑2.5 mg/d(绝经前患者与戈舍林联合)同时接受标准新辅助化疗(研究组)。标准的新辅助化疗方案为阿霉素(60mg/m2)和环磷酰胺(600mg/m2) 4个周期,随后每两周使用紫杉醇(175mg/m2) 4个周期。在研究开始时,所有患者都通过触诊和超声检查彻底检查乳房肿块和腋窝淋巴结。在研究结束时,还通过触诊和超声检查评估反应率,随后患者转介手术。手术标本的病理反应率也进行了评估。试验期间所有临床、超声和病理检查均由一名专家完成。最后对所有数据进行统计分析。研究组和对照组乳腺癌患者的临床总有效率均为95.2%。研究组和对照组腋窝总有效率分别为80.9%和76.2%。同样,研究组和对照组乳腺和腋窝的放射学完全缓解率分别为95.2%和76.2%。总的来说,乳房和腋窝的临床和放射学总有效率与对照组比较,差异无统计学意义(p < 0.05)。在标准新辅助化疗方案中加入来曲唑与局部晚期激素受体阳性乳腺癌患者更高的临床和放射学反应率无关。关键词:新辅助化疗来曲唑局部晚期乳腺癌
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