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Published in: International Journal of Clinical Oncology 2/2020

01-02-2020 | Prostate Cancer | Original Article

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

Authors: Takeshi Hashimoto, Jun Nakashima, Rie Inoue, Osamu Komori, Yuri Yamaguchi, Takeshi Kashima, Naoya Satake, Yoshihiro Nakagami, Kazunori Namiki, Toshitaka Nagao, Yoshio Ohno

Published in: International Journal of Clinical Oncology | Issue 2/2020

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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.
Literature
1.
go back to reference 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 59:61–71CrossRef 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 59:61–71CrossRef
2.
go back to reference 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 352:1977–1984CrossRef 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 352:1977–1984CrossRef
3.
go back to reference Yossepowitch O, Briganti A, Eastham JA et al (2014) Positive surgical margins after radical prostatectomy: a systematic review and contemporary update. Eur Urol 65:303–313CrossRef Yossepowitch O, Briganti A, Eastham JA et al (2014) Positive surgical margins after radical prostatectomy: a systematic review and contemporary update. Eur Urol 65:303–313CrossRef
4.
go back to reference Liesenfeld L, Kron M, Gschwend JE et al (2017) Prognostic factors for biochemical recurrence more than 10 years after radical prostatectomy. J Urol 197:143–148CrossRef Liesenfeld L, Kron M, Gschwend JE et al (2017) Prognostic factors for biochemical recurrence more than 10 years after radical prostatectomy. J Urol 197:143–148CrossRef
5.
go back to reference 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 18:25–30CrossRef 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 18:25–30CrossRef
6.
go back to reference 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 51:20–26CrossRef 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 51:20–26CrossRef
7.
go back to reference 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 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
8.
go back to reference 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 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
9.
go back to reference Soga H, Takenaka A, Murakami G et al (2011) Distribution of the lymphatic vessels in the prostatic fascia. Prostate 71:1294–1298PubMed Soga H, Takenaka A, Murakami G et al (2011) Distribution of the lymphatic vessels in the prostatic fascia. Prostate 71:1294–1298PubMed
10.
go back to reference 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 33:1601–1607CrossRef 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 33:1601–1607CrossRef
11.
go back to reference Atzpodien J, Royston P, Wandert T et al (2003) Metastatic renal cell carcinoma comprehensive prognostic system. Br J Cancer 88:348–353CrossRef Atzpodien J, Royston P, Wandert T et al (2003) Metastatic renal cell carcinoma comprehensive prognostic system. Br J Cancer 88:348–353CrossRef
12.
go back to reference Bill-Axelson A, Holmberg L, Garmo H et al (2014) Radical prostatectomy or watchful waiting in early prostate cancer. N Engl J Med 370:932–942CrossRef Bill-Axelson A, Holmberg L, Garmo H et al (2014) Radical prostatectomy or watchful waiting in early prostate cancer. N Engl J Med 370:932–942CrossRef
13.
go back to reference Wilt TJ, Brawer MK, Jones KM et al (2012) Radical prostatectomy versus observation for localized prostate cancer. N Engl J Med 367:203–213CrossRef Wilt TJ, Brawer MK, Jones KM et al (2012) Radical prostatectomy versus observation for localized prostate cancer. N Engl J Med 367:203–213CrossRef
14.
go back to reference 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 184:1341–1346CrossRef 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 184:1341–1346CrossRef
15.
go back to reference Wilczak W, Wittmer C, Clauditz T et al (2018) Marked prognostic impact of minimal lymphatic tumor spread in prostate cancer. Eur Urol. 74:376–386CrossRef Wilczak W, Wittmer C, Clauditz T et al (2018) Marked prognostic impact of minimal lymphatic tumor spread in prostate cancer. Eur Urol. 74:376–386CrossRef
16.
go back to reference 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 22:188–193CrossRef 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 22:188–193CrossRef
17.
go back to reference 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 62:768–774CrossRef 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 62:768–774CrossRef
18.
go back to reference Liss MA, Lusch A, Morales B et al (2012) Robot-assisted radical prostatectomy: 5-year oncological and biochemical outcomes. J Urol 188:2205–2211CrossRef Liss MA, Lusch A, Morales B et al (2012) Robot-assisted radical prostatectomy: 5-year oncological and biochemical outcomes. J Urol 188:2205–2211CrossRef
19.
go back to reference Yee DS, Shariat SF, Lowrance WT et al (2011) Prognostic significance of lymphovascular invasion in radical prostatectomy specimens. BJU Int 108:502–507CrossRef Yee DS, Shariat SF, Lowrance WT et al (2011) Prognostic significance of lymphovascular invasion in radical prostatectomy specimens. BJU Int 108:502–507CrossRef
20.
go back to reference Saeter T, Vlatkovic L, Waaler G et al (2016) Combining lymphovascular invasion with reactive stromal grade predicts prostate cancer mortality. Prostate 76:1088–1094CrossRef Saeter T, Vlatkovic L, Waaler G et al (2016) Combining lymphovascular invasion with reactive stromal grade predicts prostate cancer mortality. Prostate 76:1088–1094CrossRef
21.
go back to reference 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 116:44–49CrossRef 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 116:44–49CrossRef
22.
go back to reference 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.e1–6CrossRef 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.e1–6CrossRef
23.
go back to reference 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 70:297–302CrossRef 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 70:297–302CrossRef
24.
go back to reference 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 171:1122–1127CrossRef 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 171:1122–1127CrossRef
25.
go back to reference Herman CM, Wilcox GE, Kattan MW et al (2000) Lymphovascular invasion as a predictor of disease progression in prostate cancer. Am J Surg Pathol 24:859–863CrossRef Herman CM, Wilcox GE, Kattan MW et al (2000) Lymphovascular invasion as a predictor of disease progression in prostate cancer. Am J Surg Pathol 24:859–863CrossRef
Metadata
Title
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
Authors
Takeshi Hashimoto
Jun Nakashima
Rie Inoue
Osamu Komori
Yuri Yamaguchi
Takeshi Kashima
Naoya Satake
Yoshihiro Nakagami
Kazunori Namiki
Toshitaka Nagao
Yoshio Ohno
Publication date
01-02-2020
Publisher
Springer Singapore
Published in
International Journal of Clinical Oncology / Issue 2/2020
Print ISSN: 1341-9625
Electronic ISSN: 1437-7772
DOI
https://doi.org/10.1007/s10147-019-01561-4

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