Shipley W U, Verhey L J, Munzenrider J E, Suit H D, Urie M M, McManus P L, Young R H, Shipley J W, Zietman A L, Biggs P J
Department of Radiation Oncology, Harvard Medical School, Boston, MA 02114, USA.
Int J Radiat Oncol Biol Phys. 1995 Apr 30;32(1):3-12. doi: 10.1016/0360-3016(95)00063-5.
Following a thorough Phase I/II study, we evaluated by a Phase III trial high versus conventional dose external beam irradiation as mono-therapy for patients with Stage T3-T4 prostate cancer. Patient outcome following standard dose radiotherapy or following a 12.5% increase in total dose to 75.6 Cobalt Gray Equivalent (CGE) using a conformal perineal proton boost was compared for local tumor control, disease-free survival, and overall survival.
Stage T3-T4, Nx, N0-2, M0 patients received 50.4 Gy by four-field photons and were randomized to receive either an additional 25.2 CGE by conformal protons (arm 1--the high dose arm, 103 patients, total dose 75.6 CGE) or an additional 16.8 Gy by photons (arm 2--the conventional dose arm, 99 patients, total dose 67.2 Gy). Actuarial overall survival (OS), disease-specific survival (DSS), total recurrence-free survival (TRFS), (clinically free, prostate specific antigen (PSA) less than 4ng/ml and a negative prostate rebiopsy, done in 38 patients without evidence of disease) and local control (digital rectal exam and rebiopsy negative) were evaluated.
The protocol completion rate was 90% for arm 1 and 97% for arm 2. With a median follow-up of 61 months (range 3 to 139 months) 135 patients are alive and 67 have died, 20 from causes other than prostate cancer. We found no significant differences in OS, DSS, TRFS or local control between the two arms. Among those completing randomized treatment (93 in arm 1 and 96 in arm 2), the local control at 5 and 8 years for arm 1 is 92% and 77%, respectively and is 80% and 60%, respectively for arm 2 (p = .089) and there are no significant differences in OS, DSS, and TRFS. The local control for the 57 patients with poorly differentiated (Gleason 4 or 5 of 5) tumors at 5 and 8 years for arm 1 is 94% and 84% and is 64% and 19% on arm 2 (p = 0.0014). In patients whose digital rectal exam had normalized following treatment and underwent prostate rebiopsy there was a lower positive rebiopsy rate for arm 1 versus arm 2 patients (28 vs. 45%) and also for those with well and moderately differentiated tumors versus poorly differentiated tumors (32 and 50%). These differences were not statistically significant. Grade 1 and 2 rectal bleeding is higher (32 vs. 12%, p = 0.002) as may be urethral stricture (19 vs. 8%, p = 0.07) in the arm 1 versus arm 2.
An increase in prostate tumor dose by external beam of 12.5% to 75.6 CGE by a conformal proton boost compared to a conventional dose of 67.2 Gy by a photon boost significantly improved local control only in patients with poorly differentiated tumors. It has increased late radiation sequelae, and as yet, has not increased overall survival, disease-specific survival, or total recurrence-free survival in any subgroup. These results have led us to test by a subsequent Phase III trial the potential beneficial effect on local control and disease-specific survival of a 12.5% increase in total dose relative to conventional dose in patients with T1, T2a, and T2b tumors.
在完成全面的I/II期研究后,我们通过III期试验评估了高剂量与传统剂量外照射作为T3 - T4期前列腺癌患者单一疗法的疗效。比较了标准剂量放疗后或使用适形会阴质子增强将总剂量提高12.5%至75.6钴灰当量(CGE)后的患者结局,包括局部肿瘤控制、无病生存期和总生存期。
T3 - T4、Nx、N0 - 2、M0期患者接受四野光子束照射50.4 Gy,并随机分为两组,一组接受适形质子额外照射25.2 CGE(组1——高剂量组,103例患者,总剂量75.6 CGE),另一组接受光子额外照射16.8 Gy(组2——传统剂量组,99例患者,总剂量67.2 Gy)。评估精算总生存期(OS)、疾病特异性生存期(DSS)、总无复发生存期(TRFS)(临床无病、前列腺特异性抗原(PSA)小于4 ng/ml且前列腺再次活检阴性,38例无疾病证据的患者进行了此项检查)以及局部控制情况(直肠指检和再次活检阴性)。
组1的方案完成率为90%,组2为97%。中位随访61个月(范围3至139个月),135例患者存活,67例死亡,20例死于前列腺癌以外的原因。我们发现两组在OS、DSS、TRFS或局部控制方面无显著差异。在完成随机治疗的患者中(组1 93例,组2 96例),组1在5年和8年时的局部控制率分别为92%和77%,组2分别为80%和60%(p = 0.089),在OS、DSS和TRFS方面无显著差异。组1中57例低分化(Gleason评分4或5分)肿瘤患者在5年和8年时的局部控制率分别为94%和84%,组2分别为64%和19%(p = 0.0014)。在治疗后直肠指检恢复正常并接受前列腺再次活检的患者中,组1患者的再次活检阳性率低于组2患者(28%对45%),高分化和中分化肿瘤患者的再次活检阳性率也低于低分化肿瘤患者(32%和50%)。这些差异无统计学意义。组1的1级和2级直肠出血发生率较高(32%对12%,p = 0.002),尿道狭窄发生率也较高(19%对8%,p = 0.07)。
与光子增强的传统剂量67.2 Gy相比,通过适形质子增强将前列腺肿瘤外照射剂量提高12.5%至75.6 CGE,仅在低分化肿瘤患者中显著改善了局部控制。它增加了晚期放射后遗症,并且尚未提高任何亚组的总生存期、疾病特异性生存期或总无复发生存期。这些结果促使我们通过后续的III期试验来测试相对于传统剂量将总剂量提高12.5%对T1、T2a和T2b期肿瘤患者的局部控制和疾病特异性生存期的潜在有益影响。