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首页> 外文期刊>Cancer: A Journal of the American Cancer Society >Phase II trial of neoadjuvant docetaxel and gefitinib followed by radical prostatectomy in patients with high-risk, locally advanced prostate cancer.
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Phase II trial of neoadjuvant docetaxel and gefitinib followed by radical prostatectomy in patients with high-risk, locally advanced prostate cancer.

机译:在高危,局部晚期前列腺癌患者中,新辅助多西他赛和吉非替尼联合根治性前列腺切除术的II期试验。

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BACKGROUND:: Prostate cancer trials investigating neoadjuvant hormonal therapy, followed by surgery, have demonstrated that elimination of all tumor cells from the primary site is rare. The authors report a phase 2 trial assessing the efficacy and toxicity of docetaxel and gefitinib in patients with high-risk localized prostate cancer as neoadjuvant therapy before radical prostatectomy (RP). METHODS:: Thirty-one patients with high-risk prostate cancer were treated with docetaxel and gefitinib for 2 months before RP. All patients met the criteria of clinical stage T2b-3 or serum prostate-specific antigen (PSA) level >20 ng/mL, or Gleason score of 8 to 10. The primary endpoint was pathologic complete response. Secondary objectives included clinical response. When available, endorectal coil magnetic resonance imaging (eMRI) was performed as part of clinical response evaluation. Immunohistochemical staining of epidermal growth factor receptor and HER-2eu was performed on prechemotherapy and postchemotherapy prostate tissue. RESULTS:: The median age of the patients was 60 years, the median pretreatment PSA level was 7.43 ng/mL, and the median Gleason score was 8. Clinical staging prior to treatment consisted of: T1 in 4 patients, T2 in 17 patients, and T3 in 10 patients. One patient with enlarged pelvic adenopathy and T4 disease did not undergo RP. Thirty patients received all scheduled therapies including RP. Grade 3 toxicities included asymptomatic liver function test elevation in 4 (13%) patients, diarrhea in 1 (3%) patient, and fatigue in 1 (3%) patient. One patient experienced grade 4 toxicity with elevated alanine aminotransferase. RP specimen pathology demonstrated residual carcinoma in all cases. Twenty-nine (94%) patients achieved a clinical partial response, including 35% of patients who demonstrated radiographic improvement on eMRI. CONCLUSIONS:: No pathologic complete response was noted in 31 patients treated with docetaxel and gefitinib. This combination was well tolerated, and did not result in increased surgical morbidity. Cancer 2009. (c) 2009 American Cancer Society.
机译:背景:研究新辅助激素治疗并进行手术的前列腺癌试验已表明,从原发部位清除所有肿瘤细胞的情况很少见。作者报告了一项2期试验,评估多西他赛和吉非替尼在高危局限性前列腺癌患者中作为根治性前列腺切除术(RP)之前的新辅助治疗的疗效和毒性。方法:31例高危前列腺癌患者在RP之前接受多西他赛和吉非替尼治疗2个月。所有患者均符合临床T2b-3分期或血清前列腺特异性抗原(PSA)水平> 20 ng / mL或格里森评分8至10的标准。主要终点是病理完全缓解。次要目标包括临床反应。如果可行,作为临床反应评估的一部分,进行直肠内线圈磁共振成像(eMRI)。在化疗前和化疗后的前列腺组织上进行了表皮生长因子受体和HER-2 / neu的免疫组织化学染色。结果:患者的中位年龄为60岁,中位治疗前PSA水平为7.43 ng / mL,中位格里森评分为8。治疗前的临床分期包括:4例患者为T1,17例患者为T2, T3在10例患者中。一名盆腔淋巴结肿大和T4病患者未进行RP。 30名患者接受了包括RP在内的所有预定疗法。 3级毒性反应包括4例(13%)患者的无症状肝功能检查升高,1例(3%)的腹泻和1例(3%)的疲劳。一名患者因丙氨酸转氨酶升高而经历了4级毒性反应。 RP标本病理显示所有病例均残留癌。 29名(94%)患者达到了临床部分缓解,其中35%的患者在eMRI上表现出放射学上的改善。结论:在多西紫杉醇和吉非替尼治疗的31例患者中未发现病理完全缓解。这种组合耐受性良好,并且没有导致手术发病率增加。癌症,2009年。(c)2009美国癌症协会。

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