Hara Isao, Miyake Hideaki, Yamada Yuji, Takechi Yoshizumi, Hara Shoji, Gotoh Akinobu, Fujisawa Masato, Okada Hiroshi, Arakawa Soichi, Soejima Toshinori, Sugimura Kazuro, Kamidono Sadao
Department of Urology, Kobe University School of Medicine, Japan.
Int J Urol. 2002 Jun;9(6):322-8; discussion 328. doi: 10.1046/j.1442-2042.2002.00470_1.x.
It is unclear whether positive interactions between radiation and androgen withdrawal for patients with locally advanced prostate cancer is synergistic or additive. The present study aimed to clarify the significance of neoadjuvant androgen ablation prior to external radiotherapy in a human prostate LNCaP tumor model and in patients with locally advanced prostate cancer.
Comparisons were made between the effect of castration prior to radiation on the growth of subcutaneous LNCaP tumors implanted into male nude mice and their serum prostate-specific antigen (PSA) levels, and the results of castration or radiation alone. Twenty-nine patients with histologically proven and locally advanced adenocarcinoma of the prostate were treated with luteinizing hormone-releasing hormone analog at least 3 months before, during, and after external radiation therapy with a total dose of 70 Gy. The toxicity and response to this therapy were evaluated.
Treatment combining castration and radiation resulted in synergistic inhibition of LNCaP tumor growth and a significant delay in the emergence of androgen-independent recurrence as opposed to either treatment alone. The external radiotherapy was completed in 28 patients (96.6%), resulting in a reduction of serum PSA levels in all 28 patients to below 1.0 ng/mL. All patients were alive after a mean follow-up period of 34 months (range 11-53) with a 3-year PSA relapse-free survival rate of 83.7%. Among several factors examined, only the Gleason score was significantly associated with PSA relapse-free survival in univariate analysis, but not in multivariate analysis. Thirteen of 28 patients (46%) and 7 of 28 (25%) also showed at least one form of gastrointestinal or genitourinary toxicity, respectively. Of these patients, 8 with gastrointestinal toxicities, and 1 with genitourinary toxicity, experienced acute complications higher than grade 3.
The experimental findings objectively suggested the use of neoadjuvant androgen withdrawal prior to radiation therapy. Although our clinical experience is preliminary, combined androgen ablation and radiation therapy may also be effective in controlling locally advanced prostate cancer, with tolerable side-effects.
对于局部晚期前列腺癌患者,放疗与雄激素剥夺之间的正向相互作用是协同还是相加尚不清楚。本研究旨在阐明在人前列腺LNCaP肿瘤模型及局部晚期前列腺癌患者中,新辅助雄激素消融在体外放疗前的意义。
比较放疗前去势对植入雄性裸鼠的皮下LNCaP肿瘤生长及其血清前列腺特异性抗原(PSA)水平的影响,以及单纯去势或放疗的结果。29例经组织学证实的局部晚期前列腺腺癌患者在体外放疗(总剂量70 Gy)前、放疗期间及放疗后至少3个月接受促性腺激素释放激素类似物治疗。评估该治疗的毒性和反应。
与单独任何一种治疗相比,去势与放疗联合治疗导致LNCaP肿瘤生长受到协同抑制,且雄激素非依赖性复发的出现显著延迟。28例患者(96.6%)完成了体外放疗,所有28例患者的血清PSA水平均降至1.0 ng/mL以下。平均随访34个月(范围11 - 53个月)后所有患者均存活,3年PSA无复发生存率为83.7%。在检测的几个因素中,单因素分析中只有Gleason评分与PSA无复发生存显著相关,但多因素分析中并非如此。28例患者中有13例(46%)和7例(25%)分别至少出现一种形式的胃肠道或泌尿生殖系统毒性。在这些患者中,8例有胃肠道毒性,1例有泌尿生殖系统毒性,经历了高于3级的急性并发症。
实验结果客观地提示了放疗前使用新辅助雄激素剥夺。虽然我们的临床经验是初步的,但雄激素消融与放疗联合治疗在控制局部晚期前列腺癌方面可能也有效,且副作用可耐受。