Preview

Cancer Urology

Advanced search

Salvage lymph node dissection in nodal oligorecurrent prostate cancer: literature review and our experience

https://doi.org/10.17650/1726-9776-2024-20-1-52-59

Abstract

Background. Despite improved surgical techniques in treatment of prostate cancer, biochemical recurrence after surgery (increase in prostate-specific antigen level (PSA) by 0.2 mg/mL or higher in 2 consecutive measurements) develops in 20–40 % of patients depending on disease stage and tumor aggressiveness. To diagnose the source of biochemical recurrence, patients undergo positron emission tomography/computed tomography (PET/CT) with 18F- or 68Ga-labeled prostate-specific membrane antigen (PSMA). Both tracers showed comparable results in phase III trials with positive prognostic values between 84 and 92 % at PSA level ≥1 ng/mL. A number of articles has been published demonstrating the effectiveness of salvage lymph node dissection (SLND) after local treatment of carefully selected patients in the long-term. According to the results of these publications, drug therapy in patients with oligometastatic progression can be delayed by years and potentially increse overall survival.

Aim. To analyze the literature and our own experience of SLND in treatment of nodal oligorecurrent prostate cancer.

Materials and methods. At the Clinic of the Moscow City Oncological Hospital No. 62 between 2012 and 2023 in the frame-work of the clinical protocol, 32 patients with nodal oligorecurrent prostate cancer underwent SLND after radical prostatectomy: 12.5 % (4 of 32) of patients through open access, 87.5 % (28 of 32) through laparoscopic access.

Results. Two groups were identified: 1st group (n = 20) of patients without androgen deprivation therapy (ADT) and/or external beam radiotherapy after SLND; 2nd group (n = 12) of patients receiving immediate ADT and/or external beam radiotherapy after SLND.

In the 1st group, an additional criterion of SLND effectiveness was introduced, namely, PSA response: complete, partial PSA response, or its absence. In patients with partial PSA response (n = 4), its depth was evaluated; it varied between 16 and 83 %. PSA response depth did not correlate with duration of response.

Complete PSA response was achieved in 60 % (n = 12) of patients. Duration of response varied between 3 and 133 months without additional treatment.

In the 1st group, median follow-up was 6 months and progression-free survival was 18 months; in the 2nd group, median follow-up was 31 months and median progression-free survival was 41.9 months (p = 0.84456).

Conclusion. The standard of treatment for patients with metastatic hormone-sensitive prostate cancer is ADT in combination with 2nd generation antiandrogens. Improvement and availability of PET/CT with PSMA allowed to identify patients with nodal oligorecurrent prostate cancer in which SLND without ADT allows to achieve complete PSA response in 60 % of cases and delay ADT associated with a number of adverse events. SLND is characterized by low number of postoperative complications, short hospital stay.

About the Authors

V. I. Shirokorad
Moscow City Oncology Hospital No. 62, Moscow Healthcare Department
Russian Federation

27 Istra, Moscow Region 143515


Competing Interests:

None



A. A. Izmailov
Moscow City Oncology Hospital No. 62, Moscow Healthcare Department
Russian Federation

Albert A. Izmailov.

27 Istra, Moscow Region 143515


Competing Interests:

None



D. G. Lupashko
Moscow City Oncology Hospital No. 62, Moscow Healthcare Department
Russian Federation

27 Istra, Moscow Region 143515


Competing Interests:

None



References

1. Malignant tumors in Russia in 2021 (morbidity and mortality). Eds.: А.D. Kaprin, V.V. Starinskiy, A.O. Shakhzadova. Moscow: MNIOI im. P.A. Gertsena – filial FGBU “NMITS radiologii” Minzdrava Rossii, 2022. 252 p. (In Russ.).

2. Suardi N., Porter C.R., Reuther A.M. et al. A nomogram predicting long-term biochemical recurrence after radical prostatectomy. Cancer;112(6):1254–63. DOI: 10.1002/cncr.23293

3. Morris M.J., Rowe S.P., Gorin M.A. et al. Diagnostic performance of 18F-DCFPyL-PET/CT in men with biochemically recurrent prostate cancer: results from the CONDOR phase III, multicenter study. Clin Cancer Res 2021;27(13):3674–82. DOI: 10.1158/1078-0432.CCR-20-4573

4. Fendler W.P., Calais J., Eiber M. et al. Assessment of 68Ga-PSMA-11 PET accuracy in localizing recurrent prostate cancer: a prospective single-arm clinical trial. JAMA Oncol 2019;5(6):856–63. DOI: 10.1001/jamaoncol.2019.0096

5. Trock B.J., Han M., Freedland S.J. et al. Prostate cancer-specific survival following salvage radiotherapy vs observation in men with biochemical recurrence after radical prostatectomy. JAMA 2008;299(23):2760–9. DOI: 10.1001/jama.299.23.2760

6. Tendulkar R.D., Agrawal S., Gao T. et al. Contemporary update of a multi-institutional predictive nomogram for salvage radiotherapy after radical prostatectomy. J Clin Oncol 2016;34(30):3648–54. DOI: 10.1200/JCO.2016.67.9647

7. Pollack A., Karrison T., Balogh A. et al. Short term androgen deprivation therapy without or with pelvic lymph node treatment added to prostate bed only salvage radiotherapy: the NRG Oncology/RTOG 0534 SPPORT trial. Int J Radiat Oncol Biol Phys 2018;102(5):1605. DOI: 10.1016/j.ijrobp.2018.08.052

8. Suardi N., Gallina A., Lista G. et al. Impact of adjuvant radiation therapy on urinary continence recovery after radical prostatectomy. Eur Urol 2014;65(3):546–51. DOI: 10.1016/j.eururo.2013.01.027

9. Fossati N., Karnes R.J., Boorjian S.A. et al. Long-term impact of adjuvant versus early salvage radiation therapy in pT3N0 prostate cancer patients treated with radical prostatectomy: results from a multi-institutional series. Eur Urol 2017;71(6):886–93. DOI: 10.1016/j.eururo.2016.07.028

10. Nguyen P.L., Alibhai S.M., Basaria S. et al. Adverse effects of androgen deprivation therapy and strategies to mitigate them. Eur Urol 2015;67(5):825–36. DOI: 10.1016/j.eururo.2014.07.010

11. Ploussard G., Gandaglia G., Borgmann H. et al. Salvage lymph node dissection for nodal recurrent prostate cancer: a systematic review. Eur Urol 2019;76(4):493–504. DOI: 10.1016/j.eururo.2018.10.041

12. Sivaraman A., Benfante N., Touijer K. et al. Can pelvic node dissection at radical prostatectomy influence the nodal recurrence at salvage lymphadenectomy for prostate cancer? Investig Clin Urol 2018;59(2):83–90. DOI: 10.4111/icu.2018.59.2.83

13. Nyushko K.M., Krasheninnikov A.A., Sergienko S.A. et al. Results of salvage lymphadenectomy in patients with prostate cancer after radical treatment. Issledovaniya i praktika v meditsine = Research and Practice in Medicine 2017;4(S1):87. (In Russ.).

14. Brassetti A., Proietti F., Pansadoro V. Oligometastatic prostate cancer and salvage lymph node dissection: systematic review. Minerva Chir 2019;74(1):97–106. DOI: 10.23736/S0026-4733.18.07796-9

15. Izmailov A.A., Shkurnikov M.Yu., Alekseev B.Ya. Molecular genetic methods in detecting lymph node metastases in patients with prostatic cancer. Onkologiya. Zhurnal im. P.A. Gertsena = P.A. Herzen Journal of Oncology 2023;12(4):74–7. (In Russ.). DOI: 10.17116/onkolog20231204174


Review

For citations:


Shirokorad V.I., Izmailov A.A., Lupashko D.G. Salvage lymph node dissection in nodal oligorecurrent prostate cancer: literature review and our experience. Cancer Urology. 2024;20(1):52-59. (In Russ.) https://doi.org/10.17650/1726-9776-2024-20-1-52-59

Views: 337


Creative Commons License
This work is licensed under a Creative Commons Attribution 4.0 License.


ISSN 1726-9776 (Print)
ISSN 1996-1812 (Online)
X