Vargas Carlos, Kestin Larry L, Weed Dan W, Krauss Daniel, Vicini Frank A, Martinez Alvaro A
Department of Radiation Oncology, William Beaumont Hospital, 3601 W. Thirteen Mile Road, Royal Oak, MI 48073, USA.
Int J Radiat Oncol Biol Phys. 2005 Mar 1;61(3):714-24. doi: 10.1016/j.ijrobp.2004.06.018.
The indications for adjuvant external beam radiotherapy (EBRT) after radical prostatectomy (RP) are poorly defined. We performed a retrospective comparison of our institution's experience treating prostate cancer with RP vs. RP followed by adjuvant EBRT.
Between 1987 and 1998, 617 patients with clinical Stage T1-T2N0M0 prostate cancer underwent RP. Patients who underwent preoperative androgen deprivation and those with positive lymph nodes were excluded. Of the 617 patients, 34 (5.5%) with an undetectable postoperative prostate-specific antigen (PSA) level underwent adjuvant prostatic fossa RT at a median of 0.25 year (range, 0.1-0.6) postoperatively because of poor pathologic features. The median total dose was 59.4 Gy (range, 50.4-66.6 Gy) in 1.8-2.0-Gy fractions. These 34 RP+RT patients were compared with the remaining 583 RP patients. Biochemical failure was defined as any postoperative PSA level > or =0.1 ng/mL and any postoperative PSA level > or =0.3 ng/mL (at least 30 days after surgery). Administration of androgen deprivation was also scored as biochemical failure when applying either definition. The median clinical follow-up was 8.2 years (range, 0.1-11.2 years) for RP and 8.4 years (range, 0.3-13.8 years) for RP+RT.
Radical prostatectomy + radiation therapy patients had a greater pathologic Gleason score (mean, 7.3 vs. 6.5; p < 0.01) and pathologic T stage (median, T3a vs. T2c; p < 0.01). Age (median, 65.7 years) and pretreatment PSA level (median, 7.9 ng/mL) were similar between the treatment groups. Extracapsular extension was present in 72% of RP+RT patients vs. 27% of RP patients (p < 0.01). The RP+RT patients were more likely to have seminal vesicle invasion (29% vs. 9%, p < 0.01) and positive margins (73% vs. 36%, p < 0.01). Despite these poor pathologic features, the 5-year biochemical control (BC) rate (PSA <0.1 ng/mL) was 57% for RP+RT and 47% for RP (p = 0.28). For patients with extracapsular extension, the 5-year BC rate was 52% for RP+RT vs. 30% for RP (p < 0.01). The 5-year BC rate for patients with seminal vesicle invasion was 60% for RP+RT vs. 18% for RP (p < 0.01). For those with positive margins, the 5-year BC rate was 64% for RP+RT vs. 27% for RP (p < 0.01). The use of adjuvant RT remained statistically significant on multivariate analysis when applying either biochemical failure definition. Adjuvant RT also remained statistically significant when including the postoperative PSA level (>30 days after surgery) in the multivariate analyses. In addition, 99 (17%) of the 583 RP patients required salvage prostatic fossa RT (median dose, 59.4 Gy) at a median interval of 1.3 years after surgery (range, 0.1-8.4) for a palpable recurrence (n = 10) or a detectable/rising postoperative PSA level (n = 89). The median PSA level before salvage RT was 0.8 ng/mL (mean, 3.2 ng/mL). The 5-year and 8-year BC rate, using the PSA <0.1 ng/mL definition, from the date of salvage RT was 41% and 35%, respectively. The 5-year and 8-year BC rate, using the PSA <0.3 ng/mL definition, was 46% and 36%, respectively. The 8-year local recurrence rate after salvage RT was 4%.
Adjuvant RT demonstrated improved efficacy against prostate cancer. For patients with poor pathologic features (extracapsular extension, seminal vesicle invasion, positive margins), adjuvant RT improved the biochemical outcome independent of other prognostic factors.
根治性前列腺切除术后辅助性体外照射放疗(EBRT)的适应证尚不明确。我们对本机构采用根治性前列腺切除术(RP)与采用RP联合辅助性EBRT治疗前列腺癌的经验进行了回顾性比较。
1987年至1998年间,617例临床分期为T1-T2N0M0的前列腺癌患者接受了RP。排除接受术前雄激素剥夺治疗的患者以及淋巴结阳性的患者。在这617例患者中,34例(5.5%)术后前列腺特异性抗原(PSA)水平检测不到,因病理特征较差,于术后中位时间0.25年(范围0.1 - 0.6年)接受了前列腺窝辅助放疗。总剂量中位数为59.4 Gy(范围为50.4 - 66.6 Gy),分1.8 - 2.0 Gy分次给予。将这34例RP + RT患者与其余583例RP患者进行比较。生化失败定义为术后任何PSA水平≥0.1 ng/mL以及术后任何PSA水平≥0.3 ng/mL(术后至少30天)。应用任何一种定义时,雄激素剥夺治疗的使用也计为生化失败。RP组的中位临床随访时间为8.2年(范围0.1 - 11.2年),RP + RT组为8.4年(范围0.3 - 13.8年)。
根治性前列腺切除术 + 放疗患者的病理Gleason评分更高(平均7.3对6.5;p < 0.01),病理T分期更高(中位T3a对T分期更高(中位T3a对T2c;p < 0.01)。治疗组之间的年龄(中位65.7岁)和治疗前PSA水平(中位7.9 ng/mL)相似。72%的RP + RT患者存在包膜外侵犯,而RP患者为27%(p < 0.01)。RP + RT患者更易发生精囊侵犯(29%对9%,p < 0.01)和切缘阳性(73%对36%,p < 0.01)。尽管有这些较差的病理特征,但RP + RT组的5年生化控制(BC)率(PSA < 0.1 ng/mL)为57%,RP组为47%(p = 0.28)。对于有包膜外侵犯的患者,RP + RT组的5年BC率为52%,RP组为30%(p < 0.01)。有精囊侵犯的患者,RP + RT组的5年BC率为60%,RP组为18%(p < 0.01)。对于切缘阳性的患者,RP + RT组的5年BC率为64%,RP组为27%(p < 0.01)。应用任何一种生化失败定义时,在多因素分析中辅助放疗的使用仍具有统计学意义。在多因素分析中纳入术后PSA水平(术后>30天)时,辅助放疗也仍具有统计学意义。此外,583例RP患者中有99例(17%)因可触及的复发(n = 10)或术后可检测到/升高的PSA水平(n = 89),在术后中位时间1.3年(范围0.1 - 8.4年)需要进行挽救性前列腺窝放疗(中位剂量59.4 Gy)。挽救性放疗前的PSA水平中位数为0.8 ng/mL(平均3.2 ng/mL)。从挽救性放疗日期起,采用PSA < 0.1 ng/mL定义的5年和8年BC率分别为41%和35%。采用PSA < 0.3 ng/mL定义的5年和8年BC率分别为46%和36%。挽救性放疗后的8年局部复发率为4%。
辅助放疗显示出对前列腺癌更好的疗效。对于病理特征较差(包膜外侵犯、精囊侵犯、切缘阳性)的患者,辅助放疗可改善生化结局,且独立于其他预后因素。