Sengupta Shomik, Davis Brian J, Mynderse Lance A, Sebo Thomas J, Cheville John C, Lohse Christine M, Hillman David W, Haddock Michael G, Wilson Torrence M
Department of Urology, Mayo Clinic and Mayo Foundation, Rochester, Minnesota 55905, USA.
Urology. 2006 Oct;68(4):810-4. doi: 10.1016/j.urology.2006.04.039.
To assess the impact of clinical selection criteria on pathologic features among patients treated by radical retropubic prostatectomy and to evaluate the implications of broadening eligibility for permanent prostate brachytherapy monotherapy.
A consecutive series of 423 patients with prostate cancer, who underwent diagnostic biopsy and subsequent radical retropubic prostatectomy, were selected for this study. Four subgroups were defined using the American Brachytherapy Society selection criteria, including prostate size limits (group 1), no prostate size limits (group 2A), a modified set of criteria (group 2B), and clinical Stage T1-T2 (group 3). The rates of extraprostatic extension, seminal vesicle invasion, and lymph node involvement were compared.
Adverse pathologic features at radical retropubic prostatectomy were noted in 8 (9.3%) of 86 patients in group 1, 11 (5.6%) of 195 patients in group 2A, 35 (12.0%) of 292 patients in group 2B, and 90 (21.8%) of 413 patients in group 3. The rates of extraprostatic extension, seminal vesicle invasion, and lymph node involvement appeared comparable among groups 1 (5.8%, 3.5%, and 0.0%, respectively), 2A (3.6%, 2.1%, and 0.0%, respectively), and 2B (6.9%, 3.8%, and 1.4%, respectively), but were greater in group 3 (9.7%, 7.8%, and 4.4%, respectively).
Judicious broadening of the clinical selection criteria may allow a greater number of patients to be eligible for permanent prostate brachytherapy monotherapy by including patients whose risk of having adverse pathologic features is comparable to that of patients currently deemed suitable for permanent prostate brachytherapy monotherapy. Prospective assessment of oncologic outcomes of such an approach is required.
评估临床选择标准对耻骨后根治性前列腺切除术患者病理特征的影响,并评估扩大永久性前列腺近距离放射治疗单一疗法适用范围的意义。
本研究选取了连续的423例前列腺癌患者,这些患者均接受了诊断性活检及随后的耻骨后根治性前列腺切除术。使用美国近距离放射治疗学会的选择标准定义了四个亚组,包括前列腺大小限制(第1组)、无前列腺大小限制(第2A组)、一组修改后的标准(第2B组)以及临床分期T1 - T2(第3组)。比较了前列腺外扩展、精囊侵犯和淋巴结受累的发生率。
第1组86例患者中有8例(9.3%)在耻骨后根治性前列腺切除术中出现不良病理特征,第2A组195例患者中有11例(5.6%),第2B组292例患者中有35例(12.0%),第3组413例患者中有90例(21.8%)。前列腺外扩展、精囊侵犯和淋巴结受累的发生率在第1组(分别为5.8%、3.5%和0.0%)、第2A组(分别为3.6%、2.1%和0.0%)和第2B组(分别为6.9%、3.8%和1.4%)中似乎相当,但在第3组(分别为9.7%、7.8%和4.4%)中更高。
明智地放宽临床选择标准可能会使更多患者有资格接受永久性前列腺近距离放射治疗单一疗法,纳入那些出现不良病理特征风险与目前被认为适合永久性前列腺近距离放射治疗单一疗法的患者相当的患者。需要对这种方法的肿瘤学结局进行前瞻性评估。