Abstract
Background
The development process of recurrence in prostate cancer patients with pathologically organ-confined (pT2) disease and negative surgical margins is unclear. The aim of the present study was to determine factors associated with the development of biochemical recurrence following robot-assisted radical prostatectomy among those prostate cancer patients.
Methods
We retrospectively reviewed the data of patients who underwent robot-assisted radical prostatectomy without neoadjuvant endocrine therapy. We evaluated prognostic factors in 1096 prostate cancer patients with pT2 disease and negative surgical margins. Univariate and multivariate Cox proportional hazards regression analyses were used to identify independent predictors for biochemical recurrence.
Results
Of the 1096 patients, 55 experienced biochemical recurrence during the follow-up period. The 5-year biochemical recurrence-free survival rate for patients with pT2 and negative surgical margins was 91.8%. On univariate analysis, clinical stage, biopsy Gleason score, percent of positive core, pathological Gleason score, and the presence of micro-lymphatic invasion were significantly associated with biochemical recurrence. On a multivariate analysis, the presence of micro-lymphatic invasion and a pathological Gleason score ≥ 4 + 3 were significant prognostic factors for biochemical recurrence. Based on these factors, we developed a risk stratification model. The biochemical recurrence-free survival rate differed significantly among the risk groups.
Conclusions
The prognosis of prostate cancer patients with pT2 disease and negative surgical margins is favorable. However, patients with the presence of micro-lymphatic invasion and a pathological Gleason score ≥ 4 + 3 tend to experience biochemical recurrence more often after surgery. Therefore, careful follow-up might be necessary for those patients.
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References
Heidenreich A, Bellmunt J, Bolla M et al (2011) EAU guidelines on prostate cancer. Part 1: screening, diagnosis, and treatment of clinically localised disease. Eur Urol 59:61–71
Bill-Axelson A, Holmberg L, Ruutu M et al (2005) Scandinavian Prostate Cancer Group Study No. 4. Radical prostatectomy versus watchful waiting in early prostate cancer. N Engl J Med 352:1977–1984
Yossepowitch O, Briganti A, Eastham JA et al (2014) Positive surgical margins after radical prostatectomy: a systematic review and contemporary update. Eur Urol 65:303–313
Liesenfeld L, Kron M, Gschwend JE et al (2017) Prognostic factors for biochemical recurrence more than 10 years after radical prostatectomy. J Urol 197:143–148
Mitsuzuka K, Narita S, Koie T et al (2015) Lymphovascular invasion is significantly associated with biochemical relapse after radical prostatectomy even in patients with pT2N0 negative resection margin. Prostate Cancer Prostatic Dis 18:25–30
Aoun F, Albisinni S, Henriet B et al (2017) Predictive factors associated with biochemical recurrence following radical prostatectomy for pathological T2 prostate cancer with negative surgical margins. Scand J Urol 51:20–26
The Japanese Urological Association, The Japanese Society of Pathology, Japan Radiological Society (2010) General Rule for Clinical and Pathological Studies on prostate cancer, 4th edn, in Japanese, Kanehara & Co., LTD. Tokyo
Eble JN, Sauter G, Epstein JI et al (2004) World Health Organization classification of tumours: pathology and genetics of tumours of the urinary system and male genital organs. IARC Press, Lyon
Soga H, Takenaka A, Murakami G et al (2011) Distribution of the lymphatic vessels in the prostatic fascia. Prostate 71:1294–1298
Suzuki A, Togashi K, Nokubi M et al (2009) Evaluation of venous invasion by Elastica van Gieson stain and tumor budding predicts local and distant metastases in patients with T1 stage colorectal cancer. Am J Surg Pathol 33:1601–1607
Atzpodien J, Royston P, Wandert T et al (2003) Metastatic renal cell carcinoma comprehensive prognostic system. Br J Cancer 88:348–353
Bill-Axelson A, Holmberg L, Garmo H et al (2014) Radical prostatectomy or watchful waiting in early prostate cancer. N Engl J Med 370:932–942
Wilt TJ, Brawer MK, Jones KM et al (2012) Radical prostatectomy versus observation for localized prostate cancer. N Engl J Med 367:203–213
Budaus L, Isbarn H, Eichelberg C et al (2010) Biochemical recurrence after radical prostatectomy: multiplicative interaction between surgical margin status and pathological stage. J Urol 184:1341–1346
Wilczak W, Wittmer C, Clauditz T et al (2018) Marked prognostic impact of minimal lymphatic tumor spread in prostate cancer. Eur Urol. 74:376–386
Hashimoto T, Yoshioka K, Nagao G et al (2015) Prediction of biochemical recurrence after robot-assisted radical prostatectomy: analysis of 784 Japanese patients. Int J Urol 22:188–193
Sooriakumaran P, Haendler L, Nyberg T et al (2012) Biochemical recurrence after robot-assisted radical prostatectomy in a European single-centre cohort with a minimum follow-up time of 5 years. Eur Urol 62:768–774
Liss MA, Lusch A, Morales B et al (2012) Robot-assisted radical prostatectomy: 5-year oncological and biochemical outcomes. J Urol 188:2205–2211
Yee DS, Shariat SF, Lowrance WT et al (2011) Prognostic significance of lymphovascular invasion in radical prostatectomy specimens. BJU Int 108:502–507
Saeter T, Vlatkovic L, Waaler G et al (2016) Combining lymphovascular invasion with reactive stromal grade predicts prostate cancer mortality. Prostate 76:1088–1094
von Rundstedt FC, Mata DA, Groshen S et al (2015) Significance of lymphovascular invasion in organ-confined, node-negative urothelial cancer of the bladder: data from the prospective p53-MVAC trial. BJU Int 116:44–49
Fajkovic H, Mathieu R, Lucca I et al (2016) Validation of lymphovascular invasion is an independent prognostic factor for biochemical recurrence after radical prostatectomy. Urol Oncol 34:233.e1–6
Ito K, Nakashima J, Mukai M et al (2003) Prognostic implication of microvascular invasion in biochemical failure in patients treated with radical prostatectomy. Urol Int 70:297–302
Shariat SF, Khoddami SM, Saboorian H et al (2004) Lymphovascular invasion is a pathological feature of biologically aggressive disease in patients treated with radical prostatectomy. J Urol 171:1122–1127
Herman CM, Wilcox GE, Kattan MW et al (2000) Lymphovascular invasion as a predictor of disease progression in prostate cancer. Am J Surg Pathol 24:859–863
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Hashimoto, T., Nakashima, J., Inoue, R. et al. The significance of micro-lymphatic invasion and pathological Gleason score in prostate cancer patients with pathologically organ-confined disease and negative surgical margins after robot-assisted radical prostatectomy. Int J Clin Oncol 25, 377–383 (2020). https://doi.org/10.1007/s10147-019-01561-4
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DOI: https://doi.org/10.1007/s10147-019-01561-4