eMedicine Specialties > Urology > Surgery
Laparoscopic Pelvic Lymph Node Dissection
Updated: Jan 29, 2007
Introduction
History of the Procedure
The introduction of prostate-specific antigen (PSA) as a screening test for prostate cancer created a dramatic shift or stage migration, which led to the diagnosis of prostate cancer in earlier stages of the disease. As a result, more patients are now undergoing treatment for prostate cancer, exercising many different treatment options, which include radical prostatectomy (open, laparoscopic, robotic), brachytherapy, external beam radiation therapy, intensity-modulated radiation therapy (IMRT), cryosurgery, microwave thermotherapy, and high-frequency ultrasound therapy.
Despite refinements in surgical technique of all the treatment options, radical prostatectomy remains an operative procedure that is associated with significant morbidity. Complications that result from these different treatment options, including urinary incontinence, impotence, and fecal incontinence, dictate a conservative approach in patients shown to have metastatic disease. In addition, decisions concerning nonsurgical treatment of prostate cancer using external beam radiation, brachytherapy, or adjuvant hormonal therapy may be altered in cases with microscopic metastatic disease. Thus, the goal of laparoscopic pelvic lymph node dissection (LPLND) is to exclude high-risk patients from noncurative therapy.
Since the establishment of LPLND as a staging procedure in patients with prostate cancer, indications have been expanded to include the staging of bladder, penile, and urethral malignancies. In these other types of genitourinary cancers, the presence of metastatic disease also has a tremendous impact on therapeutic choices.
Indications
Noninvasive imaging technologies including computed tomography (CT), magnetic resonance imaging (MRI), and positron emission tomography (PET) scan can be useful in the diagnosis of metastatic disease in a number of malignancies. However, these imaging modalities are inadequate to reliably diagnose pelvic lymph node involvement in most patients with prostate cancer and can have false-positive findings due to infection or inflammation of the prostate after biopsy.
The utility of capromab pendetide (ProstaScint) imaging in the management and staging of prostate cancer continues to be explored but has not yet been fully determined. The appropriate techniques for obtaining images, the clinical indications, and its use in clinical staging of pelvic spread of prostate cancer still are being optimized. Once additional information is gathered through careful clinical trials, capromab pendetide scans may be a complementary diagnostic tool to PSA, Gleason score determined by prostate biopsy findings, and digital rectal examination.
Pelvic lymphadenectomy remains the criterion standard for detecting metastatic spread to the pelvic lymph nodes. The indications for staging pelvic lymphadenectomy prior to prostatectomy include (1) prebiopsy serum PSA greater than 20; (2) Gleason sum greater than or equal to 8; (3) 5 or more positive systematic sextant biopsies or total linear involvement of 28% or more; (4) palpably advanced local disease, clinical stages T3 and T4; (5) positive seminal vesicle biopsy; and (6) enlargement of pelvic lymph nodes as seen by pelvic imaging. Using standard nomograms, such as the Partin tables below, we can predict that 24-51% of patients with PSA greater than 20 and a Gleason sum of 8-10 will have nodal disease and would not be candidates for curative resection.
Table 1. Multivariate Logistic Regression Analysis for Prediction of Pathologic Stage Using Prostate-Specific Antigen, Gleason Score, and Clinical Stage (TNM): Prediction of Organ-Confined Disease (percent)
Open table in new window
Table
| Prostate-Specific Antigen Level (ng/mL) | ||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Score | 0-4 Clinical Stage | 4.1-10 Clinical Stage | ||||||||||||
| T1a | T1b | T1c | T2a | T2b | T2c | T3a | T1a | T1b | T1c | T2a | T2b | T2c | T3a | |
| 2-4 | 100 | 85 | 92 | 88 | 76 | 82 | — | 100 | 78 | 82 | 83 | 67 | 71 | — |
| 5 | 100 | 78 | 81 | 81 | 67 | 73 | — | 100 | 70 | 71 | 73 | 56 | 64 | 43 |
| 6 | 100 | 68 | 69 | 72 | 54 | 60 | 42 | 100 | 53 | 59 | 62 | 44 | 48 | 33 |
| 7 | — | 54 | 55 | 61 | 41 | 46 | — | 100 | 39 | 43 | 51 | 32 | 37 | 26 |
| 8-10 | — | — | — | 48 | 31 | — | — | — | 32 | 31 | 39 | 22 | 25 | 12 |
| Prostate-Specific Antigen Level (ng/mL) | ||||||||||||||
| Score | 10.1-20 Clinical Stage | >20 Clinical Stage | ||||||||||||
| T1a | T1b | T1c | T2a | T2b | T2c | T3a | T1a | T1b | T1c | T2a | T2b | T2c | T3a | |
| 2-4 | 100 | — | — | 61 | 52 | — | — | — | — | 33 | 20 | 7 | — | — |
| 5 | 100 | 49 | 55 | 58 | 43 | 37 | 26 | — | — | 24 | 32 | — | 3 | — |
| 6 | — | 36 | 41 | 44 | 28 | 37 | 19 | — | — | 22 | 14 | 1 | 4 | 5 |
| 7 | — | 24 | 24 | 36 | 19 | 24 | 14 | — | — | 7 | 18 | 4 | 5 | 3 |
| 8-10 | — | 11 | — | 29 | 14 | 15 | 9 | — | — | 3 | 3 | — | 2 | 2 |
| Prostate-Specific Antigen Level (ng/mL) | ||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Score | 0-4 Clinical Stage | 4.1-10 Clinical Stage | ||||||||||||
| T1a | T1b | T1c | T2a | T2b | T2c | T3a | T1a | T1b | T1c | T2a | T2b | T2c | T3a | |
| 2-4 | 100 | 85 | 92 | 88 | 76 | 82 | — | 100 | 78 | 82 | 83 | 67 | 71 | — |
| 5 | 100 | 78 | 81 | 81 | 67 | 73 | — | 100 | 70 | 71 | 73 | 56 | 64 | 43 |
| 6 | 100 | 68 | 69 | 72 | 54 | 60 | 42 | 100 | 53 | 59 | 62 | 44 | 48 | 33 |
| 7 | — | 54 | 55 | 61 | 41 | 46 | — | 100 | 39 | 43 | 51 | 32 | 37 | 26 |
| 8-10 | — | — | — | 48 | 31 | — | — | — | 32 | 31 | 39 | 22 | 25 | 12 |
| Prostate-Specific Antigen Level (ng/mL) | ||||||||||||||
| Score | 10.1-20 Clinical Stage | >20 Clinical Stage | ||||||||||||
| T1a | T1b | T1c | T2a | T2b | T2c | T3a | T1a | T1b | T1c | T2a | T2b | T2c | T3a | |
| 2-4 | 100 | — | — | 61 | 52 | — | — | — | — | 33 | 20 | 7 | — | — |
| 5 | 100 | 49 | 55 | 58 | 43 | 37 | 26 | — | — | 24 | 32 | — | 3 | — |
| 6 | — | 36 | 41 | 44 | 28 | 37 | 19 | — | — | 22 | 14 | 1 | 4 | 5 |
| 7 | — | 24 | 24 | 36 | 19 | 24 | 14 | — | — | 7 | 18 | 4 | 5 | 3 |
| 8-10 | — | 11 | — | 29 | 14 | 15 | 9 | — | — | 3 | 3 | — | 2 | 2 |
Table 2. Multivariate Logistic Regression Analysis for Prediction of Pathologic Stage Using Prostate-Specific Antigen, Gleason Score, and Clinical Stage (TNM): Prediction of Lymph Nodal Status (percent)
Open table in new window
Table
| Prostate-Specific Antigen Level (ng/mL) | ||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Score | 0-4 Clinical Stage | 4.1-10 Clinical Stage | ||||||||||||
| T1a | T1b | T1c | T2a | T2b | T2c | T3a | T1a | T1b | T1c | T2a | T2b | T2c | T3a | |
| 2-4 | 0 | 2 | <1 | 1 | 2 | 4 | — | 0 | 2 | 1 | 1 | 2 | 5 | — |
| 5 | 0 | 4 | 1 | 2 | 4 | 8 | — | 0 | 4 | 1 | 2 | 5 | 10 | 8 |
| 6 | 0 | 8 | 2 | 3 | 9 | 17 | 15 | 0 | 9 | 2 | 4 | 11 | 19 | 16 |
| 7 | — | 15 | 2 | 7 | 18 | 31 | — | 0 | 18 | 3 | 8 | 20 | 34 | 28 |
| 8-10 | — | — | — | 13 | 32 | — | — | — | 30 | 5 | 15 | 35 | 53 | 50 |
| Prostate-Specific Antigen Level (ng/mL) | ||||||||||||||
| Score | 10.1-20 Clinical Stage | >20 Clinical Stage | ||||||||||||
| T1a | T1b | T1c | T2a | T2b | T2c | T3a | T1a | T1b | T1c | T2a | T2b | T2c | T3a | |
| 2-4 | 0 | — | — | 1 | 3 | — | — | — | — | 6 | 2 | 7 | — | — |
| 5 | 0 | 5 | 3 | 2 | 6 | 13 | 11 | — | — | 9 | 3 | — | 29 | — |
| 6 | — | 11 | 4 | 5 | 13 | 22 | 20 | — | — | 8 | 9 | 18 | 53 | 31 |
| 7 | — | 21 | 7 | 9 | 24 | 39 | 35 | — | — | 24 | 11 | 44 | 62 | 55 |
| 8-10 | — | 41 | — | 17 | 40 | 59 | 54 | — | — | 41 | 35 | 76 | 73 | 65 |
| Prostate-Specific Antigen Level (ng/mL) | ||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Score | 0-4 Clinical Stage | 4.1-10 Clinical Stage | ||||||||||||
| T1a | T1b | T1c | T2a | T2b | T2c | T3a | T1a | T1b | T1c | T2a | T2b | T2c | T3a | |
| 2-4 | 0 | 2 | <1 | 1 | 2 | 4 | — | 0 | 2 | 1 | 1 | 2 | 5 | — |
| 5 | 0 | 4 | 1 | 2 | 4 | 8 | — | 0 | 4 | 1 | 2 | 5 | 10 | 8 |
| 6 | 0 | 8 | 2 | 3 | 9 | 17 | 15 | 0 | 9 | 2 | 4 | 11 | 19 | 16 |
| 7 | — | 15 | 2 | 7 | 18 | 31 | — | 0 | 18 | 3 | 8 | 20 | 34 | 28 |
| 8-10 | — | — | — | 13 | 32 | — | — | — | 30 | 5 | 15 | 35 | 53 | 50 |
| Prostate-Specific Antigen Level (ng/mL) | ||||||||||||||
| Score | 10.1-20 Clinical Stage | >20 Clinical Stage | ||||||||||||
| T1a | T1b | T1c | T2a | T2b | T2c | T3a | T1a | T1b | T1c | T2a | T2b | T2c | T3a | |
| 2-4 | 0 | — | — | 1 | 3 | — | — | — | — | 6 | 2 | 7 | — | — |
| 5 | 0 | 5 | 3 | 2 | 6 | 13 | 11 | — | — | 9 | 3 | — | 29 | — |
| 6 | — | 11 | 4 | 5 | 13 | 22 | 20 | — | — | 8 | 9 | 18 | 53 | 31 |
| 7 | — | 21 | 7 | 9 | 24 | 39 | 35 | — | — | 24 | 11 | 44 | 62 | 55 |
| 8-10 | — | 41 | — | 17 | 40 | 59 | 54 | — | — | 41 | 35 | 76 | 73 | 65 |
Numbers represent the percent predictive probability (95% confidence interval) of the patient having a given final pathological stage based on a multinomial log-liner regression of all 3 variables (Partin, 1997).
Other genitourinary malignancies requiring pelvic lymphadenectomy often need a more extensive nodal dissection that includes removing the common iliac, external iliac, and obturator lymph nodes. Transitional cell carcinoma of the bladder with lymphatic spread often has an aggressive clinical course. Like prostate cancer, noninvasive techniques to determine nodal status are inadequate, and pelvic lymphadenectomy is the most accurate way to definitively establish the presence of metastatic disease in the lymph nodes.
Given the poor survival rate of patients with aggressive bladder cancer, those with enlarged lymph nodes on pelvic imaging studies may be candidates for laparoscopic staging prior to radical cystoprostatectomy. Patients who choose bladder-sparing treatment with chemotherapy, radiation therapy, or partial cystectomy and those who desire orthotopic neobladder construction also may benefit from staging laparoscopic pelvic lymph node dissection (LPLND).
Carcinoma of the penis has a characteristic pattern of nodal spread depending on the location and depth of the primary lesion. Laparoscopic extended pelvic lymphadenectomy may be used in the initial staging of penile cancer.
Laparoscopic pelvic lymph node dissection in the staging of urethral cancer has been recommended for patients meeting the following criteria: (1) radiologic evidence of pelvic lymphadenopathy not accessible to fine-needle aspiration biopsy, (2) preceding exenterative surgery in tumors of the proximal urethra, and (3) patients with locally invasive distal urethral lesions. The use of laparoscopic pelvic node dissection for bladder cancer, urethral cancer, and penile cancer continues to develop, and further study is necessary to establish definitive indications.
Contraindications
Contraindications for laparoscopic pelvic lymph node dissection (LPLND) include severe cardiopulmonary disease, bowel obstruction, active infection, and uncorrected coagulopathy. Morbid obesity, prior abdominal surgery, hiatal hernia, history of pelvic fractures, hip replacement, or large pelvic or intra-abdominal masses may be considered as relative contraindications. Relative contraindications are related to the surgeon's experience with laparoscopic surgery and LPLND.
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References
Baldwin DD, Desai PJ. Laparoscopic pelvic lymph node dissection. In: Bishoff JT, Kavoussi LR, eds. Atlas of Laparoscopic Urologic Surgery. Elseiver;2007:Ch. 20.
Bishoff JT, Motley G, Optenberg SA, et al. Incidence of fecal and urinary incontinence following radical perineal and retropubic prostatectomy in a national population. J Urol. Aug 1998;160(2):454-8. [Medline].
Brendler CB, Cleeve LK, Anderson EE, Paulson DF. Staging pelvic lymphadenectomy for carcinoma of the prostate risk versus benefit. J Urol. Dec 1980;124(6):849-50. [Medline].
Catalona WJ. Urothelial tumors of the urinary tract. In: Walsh PC, Retik AB, Stamey TA, eds. Campbell's Urology. 6th ed. Philadelphia, Pa: WB Saunders;. 1992:1094-158.
Catalona WJ, Stein AJ. Accuracy of frozen section detection of lymph node metastases in prostatic carcinoma. J Urol. Mar 1982;127(3):460-1. [Medline].
Corvin S, Schilling D, Eichhorn K, et al. Laparoscopic sentinel lymph node dissection - a novel technique for the staging of prostate cancer. Eur Urol. Feb 2006;49(2):280-5. [Medline].
Glascock MJ, Winfield HN. Lymphadenectomy. In: Sosa RE, ed. Textbook of Endourology. Philadelphia, Pa: WB Saunders;. 1997:494-505.
Herrell SD, Trachtenberg J, Theodorescu D. Staging pelvic lymphadenectomy for localized carcinoma of the prostate: a comparison of 3 surgical techniques. J Urol. Apr 1997;157(4):1337-9. [Medline].
Hricak H. Noninvasive imaging for staging of prostate cancer: magnetic resonance imaging, computed tomography, and ultrasound. NCI Monogr. 1988;31-5. [Medline].
Hu JC, Nelson RA, Wilson TG, et al. Perioperative complications of laparoscopic and robotic assisted laparoscopic radical prostatectomy. J Urol. Feb 2006;175(2):541-6; discussion 546. [Medline].
Kavoussi LR, Sosa E, Chandhoke P, et al. Complications of laparoscopic pelvic lymph node dissection. J Urol. Feb 1993;149(2):322-5. [Medline].
Moore RG, Kavoussi LR. Laparoscopic lymphadenectomy in genitourinary malignancies. Surg Oncol. 1993;2 Suppl 1:51-66. [Medline].
Mukamel E, deKernion JB. Early versus delayed lymph-node dissection versus no lymph-node dissection in carcinoma of the penis. Urol Clin North Am. Nov 1987;14(4):707-11. [Medline].
Mukamel E, Hannah J, Barbaric Z, deKernion JB. The value of computerized tomography scan and magnetic resonance imaging in staging prostatic carcinoma: comparison with the clinical and histological staging. J Urol. Dec 1986;136(6):1231-3. [Medline].
O''Dowd GJ, Veltri RW, Orozco R, et al. Update on the appropriate staging evaluation for newly diagnosed prostate cancer. J Urol. Sep 1997;158(3 Pt 1):687-98. [Medline].
Partin AW, Kattan MW, Subong EN, et al. Combination of prostate-specific antigen, clinical stage, and Gleason score to predict pathological stage of localized prostate cancer. A multi-institutional update. JAMA. May 14 1997;277(18):1445-51. [Medline].
Paul DB, Loening SA, Narayana AS, Culp DA. Morbidity from pelvic lymphadenectomy in staging carcinoma of the prostate. J Urol. Jun 1983;129(6):1141-4. [Medline].
Raboy A, Adler H, Albert P. Extraperitoneal endoscopic pelvic lymph node dissection: a review of 125 patients. J Urol. Dec 1997;158(6):2202-4; discussion 2204-5. [Medline].
Schellhammer PF, Jordan GH, Schlossberg SM. Tumors of the penis. In: Walsh PC, Retik AB, Stamey TA, eds. Campbell's Urology. 6th ed. Philadelphia, Pa: WB Saunders;. 1992:1094-158.
Stone NN, Stock RG, Unger P. Laparoscopic pelvic lymph node dissection for prostate cancer: comparison of the extended and modified techniques. J Urol. Nov 1997;158(5):1891-4. [Medline].
Thompson IM. Sophisticated imaging techniques in prostate cancer screening. Controversies in the management of prostate cancer: Part 7. 1991;12-19.
Wyler SF, Sulser T, Seifert HH, et al. Laparoscopic extended pelvic lymph node dissection for high-risk prostate cancer. Urology. Oct 2006;68(4):883-7.
Further Reading
Keywords
laparoscopic pelvic lymph node dissection, pelvic lymph node dissection, LPLND, Partin's tables, Partin tables, prostate cancer, PSA, prostate-specific antigen, Partin nomogram, radical prostatectomy
Overview: Laparoscopic Pelvic Lymph Node Dissection