Pathological characteristics and prognosis of nonpalpable and palpable prostate cancers with a Hybritech prostate specific antigen of 4 to 10 ng./ml
- PMID: 8709306
Pathological characteristics and prognosis of nonpalpable and palpable prostate cancers with a Hybritech prostate specific antigen of 4 to 10 ng./ml
Abstract
Purpose: We compared the surgical pathological findings and postoperative course of patients with palpable and nonpalpable prostate cancers.
Materials and methods: All patients with untreated prostate specific antigen (PSA) 4 to 10 ng./ml. who underwent radical prostatectomy between December 1984 and December 1993 were reviewed to select 61 with clinical stage T1c (nonpalpable) with stages T2a to c (palpable) disease.
Results: Nonpalpable cancers were smaller (2.99 versus 4.42 cc for palpable tumors), had smaller volumes of Gleason grade 4 to 5 cancer (0.66 versus 1.32 cc, respectively) and were less likely to have positive surgical margins (13 versus 22%, respectively) or significant (1 cm. or more) capsular penetration (10 versus 26%, respectively). Nonpalpable and palpable cancers had similar rates of seminal vesicle invasion (3.3 versus 4.3%, respectively) and positive lymph nodes (1.6 versus 0%, respectively). More than 90% of patients with nonpalpable cancer were biochemically cancer-free postoperatively, and the remainder were alive with disease after a mean followup of 25.1 months, compared to 69% disease-fee, 28% alive with disease and 2.5% dead of prostate cancer after mean followup of 43.8 months among those with palpable disease.
Conclusions: We conclude that nonpalpable prostate cancers are pathologically more favorable than palpable prostate cancers with PSA 4 to 10 ng./ml. Our preliminary results also indicate that nonpalpable cancers are less likely to recur postoperatively than palpable cancers with a similar PSA range.
Comment in
-
Significant versus insignificant prostate cancer--can we identify the tigers from the pussy cats?J Urol. 1996 Sep;156(3):1069-70. doi: 10.1016/s0022-5347(01)65704-5. J Urol. 1996. PMID: 8709309 No abstract available.
Similar articles
-
Improved clinical staging system combining biopsy laterality and TNM stage for men with T1c and T2 prostate cancer: results from the SEARCH database.J Urol. 2003 Jun;169(6):2129-35. doi: 10.1097/01.ju.0000065763.21602.14. J Urol. 2003. PMID: 12771734
-
Clinical and pathological characteristics, and recurrence rates of stage T1c versus T2a or T2b prostate cancer.J Urol. 1999 May;161(5):1525-9. J Urol. 1999. PMID: 10210388
-
Standard versus age-specific prostate specific antigen reference ranges among men with clinically localized prostate cancer: A pathological analysis.J Urol. 1996 Apr;155(4):1336-9. J Urol. 1996. PMID: 8632568
-
The use of percent free prostate specific antigen for staging clinically localized prostate cancer.J Urol. 1998 Apr;159(4):1238-42. J Urol. 1998. PMID: 9507844 Review.
-
Stage T1c prostate cancer: perspectives on clinical management.Semin Urol Oncol. 1995 Aug;13(3):238-44. Semin Urol Oncol. 1995. PMID: 8521137 Review.
Cited by
-
Comparison of pathologic characteristics of T1c and non-T1c cancers detected in a population-based screening study, the European Randomized Study of Screening for Prostate Cancer.World J Urol. 1997;15(6):339-45. doi: 10.1007/BF01300181. World J Urol. 1997. PMID: 9436283 Clinical Trial.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical
Research Materials
Miscellaneous