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钯-103前列腺近距离放射治疗中20 Gy与44 Gy补充束辐射的比较:一项前瞻性随机多中心试验的初步生化结果

20 Gy versus 44 Gy supplemental beam radiation with Pd-103 prostate brachytherapy: preliminary biochemical outcomes from a prospective randomized multi-center trial.

作者信息

Wallner Kent, Merrick Gregory, True Lawrence, Sherertz Tracey, Sutlief Steven, Cavanagh William, Butler Wayne

机构信息

Department of Veterans Affairs, Radiation Oncology, Puget Sound Health Care System, Seattle, WA 98108-1597, USA.

出版信息

Radiother Oncol. 2005 Jun;75(3):307-10. doi: 10.1016/j.radonc.2005.03.019.

Abstract

BACKGROUND AND PURPOSE

While favorable results are achieved with combined modality irradiation, there has never been a rigorous study of the need for supplemental beam. The study reported here compares clinical outcomes with substantially different external beam radiation doses. Similar to classic randomized Wilm's tumor studies from the 1980s, the intention of the trial design was to decrementally test the need for beam radiation.

PATIENTS AND METHODS

As of June 2000, 165 of a planned 600 patients with 1997 AJC clinical stage T1c-T2a prostatic carcinoma, Gleason grade 7-10 and/or PSA 10-20 ng/ml, were treated on a randomized protocol comparing 44 versus 20 Gy pre-implant supplemental beam radiation, combined with Pd-103, 90 versus 115 Gy, respectively (NIST-1999). Freedom from biochemical failure was defined as a serum PSA</=0.5 ng/ml at last follow-up. Patients were censored at last follow-up if their serum PSA was still decreasing. Patients whose serum PSA nadired at a value >0.5 ng/ml were scored as failures at the time at which their PSA nadired. The follow-up period for non-failing patients ranged from 0.5 to 4.9 years (median: 2.9 years). Accrual of 566 patients was achieved in October 2004. The study was closed at that time because of slowing accrual, due in part to the findings reported here.

RESULTS

The overall actuarial freedom from biochemical progression at 3 years is 85%, with 59 patients followed beyond 3 years. A total of 21 patients have developed biochemical failure, 12 treated with 20 Gy and nine treated with 44 Gy. There were no clinically evident local failures. The actuarial biochemical freedom-from-failure rate at 3 years was 83% for 20 Gy patients versus 88% for 44 Gy patients (P=0.64). For 112 patients with a pre-treatment PSA<10 ng/ml, the 3-year freedom from progression was 84% in patients receiving 20 Gy beam radiation versus 94% in those who received 44 Gy beam (P=0.16). For 47 patients with a pre-treatment PSA>10 ng/ml, the 3-year freedom from progression was 82% in patients receiving 20 Gy beam radiation versus 72% in those who received 44 Gy beam (P=0.38).

CONCLUSIONS

The randomized data presented here suggests that the likelihood of biochemical cure is similar with standard (44 Gy) or lower dose (20 Gy) supplemental beam radiation. Since the biological effect of 20 Gy external beam radiation is likely to be small, we interpret these preliminary results to suggest that supplemental beam radiation is unnecessary, in the setting of a high degree of prostate coverage by the brachytherapy prescription dose. With closure of this study, we have begun treating intermediate and high risk patients on a prospective randomized comparison of Pd-103 with 20 versus 0 Gy supplemental beam radiation.

摘要

背景与目的

虽然联合放疗取得了良好效果,但对于补充照射的必要性从未有过严格研究。本文报告的研究比较了显著不同的外照射剂量下的临床结果。与20世纪80年代经典的随机肾母细胞瘤研究类似,试验设计的目的是逐步检验照射的必要性。

患者与方法

截至2000年6月,计划纳入的600例1997年美国癌症联合委员会(AJC)临床分期为T1c - T2a前列腺癌、Gleason分级为7 - 10级和/或前列腺特异性抗原(PSA)为10 - 20 ng/ml的患者中,165例按照随机方案接受治疗,该方案比较植入前补充照射44 Gy与20 Gy,分别联合103钯,剂量为90 Gy与115 Gy(NIST - 1999)。生化无进展定义为末次随访时血清PSA≤0.5 ng/ml。如果患者血清PSA仍在下降,则在末次随访时进行截尾。血清PSA最低点>0.5 ng/ml的患者在其PSA达到最低点时计为失败。未失败患者的随访期为0.5至4.9年(中位数:2.9年)。2004年10月共纳入566例患者。由于入组速度减慢,该研究于彼时结束,部分原因是本文报告的研究结果。

结果

3年时总体精算生化无进展率为85%,59例患者随访超过3年。共有21例患者出现生化失败,12例接受20 Gy照射,9例接受44 Gy照射。无临床明显的局部失败。20 Gy组患者3年精算生化无失败率为83%,44 Gy组为88%(P = 0.64)。对于112例治疗前PSA<10 ng/ml的患者,接受20 Gy照射的患者3年无进展率为84%,接受44 Gy照射的患者为94%(P = 0.16)。对于47例治疗前PSA>10 ng/ml的患者,接受20 Gy照射的患者3年无进展率为82%,接受44 Gy照射的患者为72%(P = 0.38)。

结论

本文给出的随机数据表明,标准(44 Gy)或低剂量(20 Gy)补充照射实现生化治愈的可能性相似。由于20 Gy外照射的生物学效应可能较小,我们将这些初步结果解释为表明在近距离治疗处方剂量对前列腺高度覆盖的情况下,补充照射是不必要的。随着该研究结束,我们已开始对中高危患者进行前瞻性随机比较,比较103钯联合20 Gy与0 Gy补充照射的效果。

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