首页> 外文期刊>Cancer radiotherapie: journal de la Soci閠?fran鏰ise de radiotherapie oncologique >Conformal radiotherapy to 76Gy in localized prostate cancer. Therapeutic modalities and preliminary results.
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Conformal radiotherapy to 76Gy in localized prostate cancer. Therapeutic modalities and preliminary results.

机译:局部前列腺癌的保形放疗为76Gy。治疗方式和初步结果。

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PURPOSE: To describe therapeutic modalities for localized prostate cancer treated by conformal radiation to 76Gy with or without androgen ablation. To evaluate the preliminary results in terms of survival, biological control and toxicity. PATIENTS AND METHOD: Between January 1998 and June 2001, 321 patients with localized prostate cancer were irradiated at institut Curie. Tumors were stratified into the three Memorial Sloan-Kettering Cancer Center prognostic groups (1998) for analysis: favorable risk group (FG) 23%, intermediate risk group (IG) 36.5%, unfavorable risk group (UG) 40.5%. Androgen deprivation, mainly neoadjuvant, less or equal to one year was prescribed to 93.8% of patients (72.6% less or equal to six months). Planning target volume prescription doses were: prostate: 76Gy, seminal vesicles: 56 to 76Gy, and pelvic lymph nodes: 44Gy to 16.8% of patients. RESULTS: The five-year actuarial overall survival was 94% (95% IC: 90-97%). The median post-therapeutic follow-up was 36 months (nine to 60 months). The 48-month actuarial rates of biochemical control for the three prognostic groups were statistically different according to both the American Society for Therapeutic Radiology and Oncology consensus (ASTRO 1997) and the Fox Chase Cancer Center definitions of biochemical failure (FCCC 2000) with respectively 87 and 94% for FG, 78 and 84% for IG, 54 and 58% for UG (P<10(-6) and P<10(-8)). At time of our analysis, late post-treatment rectal and bladder bleedings were 17,4 and 13,6%, respectively. According to a 1-4 scale adapted from M.D. Anderson Cancer Center criteria: rectal bleedings were grade 1 (9.6%), grade 2 (6.2%) and grade 3 (1.6%). Bladder bleedings were grade 2 (13%) and grade 3 (0.6%). Analysis of rectal bleeding risk factors showed significant correlations with pelvic lymph nodes irradiation for grade 2 and 3, (P=0.02), and for all grades, a correlation with smaller rectal wall volumes (P=0.03), and greater percentages of rectal wall irradiated to higher doses: 65, 70, 72 and 75Gy (P=0.02, P=0.01, P=0.0007 and P=0.003, respectively). CONCLUSIONS: These results are comparable to those previously reported with the same follow-up. Impact of dose escalation with short androgen deprivation on local control, survival and complications needs longer follow-up and further analysis.
机译:目的:描述通过对76Gy进行保形放射治疗,伴或不伴雄激素消融的局部前列腺癌的治疗方式。在生存,生物控制和毒性方面评估初步结果。患者与方法:1998年1月至2001年6月,居里研究所对321例局限性前列腺癌患者进行了照射。将肿瘤分为斯隆-凯特琳纪念中心的三个预后组(1998年)进行分析:有利风险组(FG)23%,中风险组(IG)36.5%,不利风险组(UG)40.5%。 93.8%(72.6%小于或等于六个月)的患者开具了少于或等于一年的雄激素剥夺(主要是新辅助)。计划的目标体积处方剂量为:前列腺癌:76Gy,精囊:56至76Gy,骨盆淋巴结:44Gy,占16.8%。结果:五年精算总生存率为94%(95%IC:90-97%)。治疗后的中位随访时间为36个月(9到60个月)。根据美国放射治疗和肿瘤学会共识(ASTRO 1997)和福克斯·蔡斯癌症中心对生化衰竭的定义(FCCC 2000),三个预后组生化控制的48个月精算率在统计学上不同。 FG为94%,IG为78%和84%,UG为54%和58%(P <10(-6)和P <10(-8))。在我们进行分析时,治疗后晚期直肠和膀胱出血分别为17.4和13.6%。根据M.D. Anderson癌症中心的1-4评分标准:直肠出血为1级(9.6%),2级(6.2%)和3级(1.6%)。膀胱出血为2级(13%)和3级(0.6%)。直肠出血危险因素分析显示,对于2级和3级,与盆腔淋巴结照射密切相关(P = 0.02),对于所有等级,与较小的直肠壁体积(P = 0.03)和较大的直肠壁百分比相关辐照至更高剂量:65、70、72和75Gy(分别为P = 0.02,P = 0.01,P = 0.0007和P = 0.003)。结论:这些结果与先前报道的相同随访结果相当。雄激素缺乏的剂量增加对局部控制,生存和并发症的影响需要更长的随访和进一步分析。

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