Krumholtz Jason S, Carvalhal Gustavo F, Ramos Christian G, Smith Deborah S, Thorson Phataraporn, Yan Yan, Humphrey Peter A, Roehl Kimberly A, Catalona William J
Division of Urologic Surgery, Washington University School of Medicine, St. Louis, Missouri 63110, USA.
Urology. 2002 Sep;60(3):469-73; discussion 473-4. doi: 10.1016/s0090-4295(02)01875-7.
To evaluate the pathologic characteristics of clinical Stage T1c (nonpalpable, prostate-specific antigen [PSA]-detected) prostate cancers detected in the 2.6 to 4.0-ng/mL PSA range and compare them with Stage T1c cancers concurrently detected in the 4.1 to 10.0-ng/mL PSA range. All cancers were detected in a prostate cancer screening study.
We studied 94 patients with clinical Stage T1c prostate cancer diagnosed by four or six-sector ultrasound-guided needle biopsy who underwent radical prostatectomy between June 1995 and December 1996. We included all men whose prostatectomy specimens were processed with complete embedding of all prostatic tissue. Of these, 42 had a PSA level of 2.6 to 4.0 ng/mL and 52 a PSA level 4.1 to 10.0 ng/mL at the time of cancer detection. We determined the tumor volume by complete embedding and grid morphometry, pathologic stage, Gleason sum, and surgical margin status and compared the cancer volume and pathologic tumor stages for each group.
Men with cancer detected at the 2.6 to 4.0 ng/mL PSA range had significantly smaller cancer volumes (1.1 +/- 1.1 cm(3) versus 1.8 +/- 1.5 cm(3), P = 0.02); however, no difference was found in the proportion (11.9% versus 11.5%, P = 0.9, and 23.8% versus 26.9%, P = 0.7, respectively) of tumors that met previously published criteria of "clinically insignificant" (organ confined, less than 0.2 cm(3) tumor volume, Gleason sum 6 or less) or "clinically unimportant" (organ confined, less than 0.5 cm(3) tumor volume, and Gleason sum 6 or less) tumors. Using the lower PSA cutoff point resulted in the detection of a significantly higher percentage of organ-confined tumors (88% versus 63%, P = 0.01).
The use of a 2.6-ng/mL PSA threshold for screening resulted in the more frequent detection of small, organ-confined tumors without overdetecting possibly clinically insignificant ones.
评估在前列腺特异性抗原(PSA)水平为2.6至4.0 ng/mL范围内检测到的临床T1c期(不可触及,PSA检测到)前列腺癌的病理特征,并将其与同时在PSA水平为4.1至10.0 ng/mL范围内检测到的T1c期癌症进行比较。所有癌症均在一项前列腺癌筛查研究中被检测到。
我们研究了94例经四分区或六分区超声引导下穿刺活检诊断为临床T1c期前列腺癌且在1995年6月至1996年12月期间接受根治性前列腺切除术的患者。我们纳入了所有前列腺切除标本对所有前列腺组织进行完整包埋处理的男性。其中,42例在癌症检测时PSA水平为2.6至4.0 ng/mL,52例PSA水平为4.1至10.0 ng/mL。我们通过完整包埋和网格形态计量学确定肿瘤体积、病理分期、Gleason评分以及手术切缘状态,并比较每组的癌体积和病理肿瘤分期。
在PSA水平为2.6至4.0 ng/mL范围内检测到癌症的男性,其癌体积明显较小(1.1±1.1 cm³对1.8±1.5 cm³,P = 0.02);然而,在符合先前公布的“临床意义不显著”(器官局限,肿瘤体积小于0.2 cm³,Gleason评分6分或更低)或“临床不重要”(器官局限,肿瘤体积小于0.5 cm³,Gleason评分6分或更低)标准的肿瘤比例方面(分别为11.9%对11.5%,P = 0.9,以及23.8%对26.9%,P = 0.7)未发现差异。使用较低的PSA临界值导致器官局限性肿瘤的检出率显著更高(88%对63%,P = 0.01)。
使用2.6 ng/mL的PSA阈值进行筛查可更频繁地检测到小的、器官局限的肿瘤,且不会过度检测可能临床意义不显著的肿瘤。