First lymph node to receive drainage from a primary tumor
The sentinel lymph node is the hypothetical first lymph node or group of nodes draining a cancer. In case of established cancerous dissemination it is postulated that the sentinel lymph nodes are the target organs primarily reached by metastasizingcancercells from the tumor.
The sentinel node procedure (also termed sentinel lymph node biopsy or SLNB) is the identification, removal and analysis of the sentinel lymph nodes of a particular tumour.[1]
Physiology
The spread of some forms of cancer usually follows an orderly progression, spreading first to regional lymph nodes, then the next echelon of lymph nodes, and so on, since the flow of lymph is directional, meaning that some cancers spread in a predictable fashion from where the cancer started. In these cases, if the cancer spreads it will spread first to lymph nodes (lymph glands) close to the tumor before it spreads to other parts of the body. The concept of sentinel lymph node surgery is to determine if the cancer has spread to the very first draining lymph node (called the "sentinel lymph node") or not. If the sentinel lymph node does not contain cancer, then there is a high likelihood that the cancer has not spread to any other area of the body.[2]
Uses
The concept of the sentinel lymph node is important because of the advent of the sentinel lymph node biopsy technique, also known as a sentinel node procedure. This technique is used in the staging of certain types of cancer to see if they have spread to any lymph nodes, since lymph node metastasis is one of the most important prognostic signs. It can also guide the surgeon to the appropriate therapy.[3]
There are various procedures entailing the sentinel node detection:
Preoperative planar lymphoscintigraphy
Preoperative planar lymphoscintigraphy in conjunction with SPECT/CT [single photonemission CT (SPECT) with a low-dose CT][4][5]
Preoperative or intraoperative super paramagnetic iron oxide nanoparticles injection, detection by using Sentimag instrument[6][7]
Postoperative scintigraphy of main specimen with planar acquisition
In everyday clinical activity, entailing sentinel node detection and sentinel lymph node biopsy, it is not required to include all different techniques listed above. In skilled hands and in a center with sound routines, one, two or three of the listed methods can be considered sufficient.
To perform a sentinel lymph node biopsy, the physician performs a lymphoscintigraphy, wherein a low-activity radioactive substance is injected near the tumor. The injected substance, filtered sulfur colloid, is tagged with the radionuclide technetium-99m. The injection protocols differ by doctor but the most common is a 500 μCi dose divided among 5 tuberculin syringes with 1/2 inch, 24 gauge needles.[citation needed] In the UK 20 megabecquerels of nanocolloid is recommended.[8] The sulphur colloid is slightly acidic and causes minor stinging. A gentle massage of the injection sites spreads the sulphur colloid, relieving the pain and speeding up the lymph uptake. Scintigraphic imaging is usually started within 5 minutes of injection and the node appears from 5 min to 1 hour. This is usually done several hours before the actual biopsy. About 15 minutes before the biopsy the physician injects a blue dye in the same manner. Then, during the biopsy, the physician visually inspects the lymph nodes for staining and uses a gamma probe or a Geiger counter to assess which lymph nodes have taken up the radionuclide. One or several nodes may take up the dye and radioactive tracer, and these nodes are designated the sentinel lymph nodes. The surgeon then removes these lymph nodes and sends them to a pathologist for rapid examination under a microscope to look for the presence of cancer.
A frozen section procedure is commonly employed (which takes less than 20 minutes), so if neoplasia is detected in the lymph node a further lymph node dissection may be performed. With malignant melanoma, many pathologists eschew frozen sections for more accurate "permanent" specimen preparation due to the increased instances of false-negative with melanocytic staining.
As a bridge to translational medicine, various aspects of cancer dissemination can be studied using sentinel node detection and ensuing sentinel node biopsy. Tumor biology pertaining to metastatic capacity,[19] mechanisms of dissemination, the EMT-MET-process (epithelial–mesenchymal transition) and cancer immunology[20] are some subjects which can be more distinctly investigated.
Disadvantages
However, the technique is not without drawbacks, particularly when used for melanoma patients. This technique only has therapeutic value in patients with positive nodes.[21] Failure to detect cancer cells in the sentinel node can lead to a false negative result—there may still be cancerous cells in the lymph node basin. In addition, there is no compelling evidence that patients who have a full lymph node dissection as a result of a positive sentinel lymph node result have improved survival compared to those who do not have a full dissection until later in their disease, when the lymph nodes can be felt by a physician. Such patients may be having an unnecessary full dissection, with the attendant risk of lymphedema.[22]
History
The concept of a sentinel node was first described by Gould et al. 1960 in a
patient with cancer of the parotid gland[23] and was implemented clinically on a broad scale by Cabanas in penile cancer.[24]
The technique of sentinel node radiolocalization was co-founded by James C. Alex, MD, FACS and David N. Krag MD (University of Vermont Medical Center) and they were the first ones to pioneer this method for the use of cutaneous melanoma, breast cancer, head and neck cancer and Merkel cell carcinoma. Confirmative trials followed soon after.[25] Studies were also conducted at the Moffitt Cancer Center with Charles Cox, MD, Cristina Wofter, MD, Douglas Reintgen, MD and James Norman, MD.
Following validation of the sentinel node biopsy technique, a number of randomised controlled trials were initiated to establish whether the technique could safely be used to avoid unnecessary axillary dissection among women with early breast cancer. The first such trial, led by Umberto Veronesi at the European Institute of Oncology, showed that women with breast tumours of 2 cm or less could safely forgo axillary dissection if their sentinel lymph nodes were found to be cancer-free on biopsy.[26] The benefits included less pain, greater arm mobility and less swelling in the arm.[27]
See also
ALMANAC, Axillary Lymphatic Mapping Against Nodal Axillary Clearance trial
^Kumar V, Abbas AK, Fausto N, Aster JC, eds. (2009). Robbins & Cotran Pathologic Basis of Disease (8th ed.). Elsevier Health Sciences. p. 270. ISBN978-1-4377-2015-0.
^Sherif A, Garske U, de la Torre M, Thörn M (July 2006). "Hybrid SPECT-CT: an additional technique for sentinel node detection of patients with invasive bladder cancer". European Urology. 50 (1): 83–91. doi:10.1016/j.eururo.2006.03.002. PMID16632191.
^Tanis PJ, Boom RP, Koops HS, Faneyte IF, Peterse JL, Nieweg OE, Rutgers EJ, Tiebosch AT, Kroon BB (April 2001). "Frozen section investigation of the sentinel node in malignant melanoma and breast cancer". Annals of Surgical Oncology. 8 (3): 222–6. doi:10.1245/aso.2001.8.3.222. PMID11314938.
^Sherif A, De La Torre M, Malmström PU, Thörn M (September 2001). "Lymphatic mapping and detection of sentinel nodes in patients with bladder cancer". The Journal of Urology. 166 (3): 812–5. doi:10.1016/s0022-5347(05)65842-9. PMID11490224.
^Liedberg F, Chebil G, Davidsson T, Gudjonsson S, Månsson W (January 2006). "Intraoperative sentinel node detection improves nodal staging in invasive bladder cancer". The Journal of Urology. 175 (1): 84–8, discussion 88–9. doi:10.1016/S0022-5347(05)00066-2. PMID16406877. S2CID32329157.
^Wawroschek F, Vogt H, Weckermann D, Wagner T, Harzmann R (December 1999). "The sentinel lymph node concept in prostate cancer - first results of gamma probe-guided sentinel lymph node identification". European Urology. 36 (6): 595–600. doi:10.1159/000020054. PMID10559614. S2CID46760854.
^Jeschke S, Nambirajan T, Leeb K, Ziegerhofer J, Sega W, Janetschek G (June 2005). "Detection of early lymph node metastases in prostate cancer by laparoscopic radioisotope guided sentinel lymph node dissection". The Journal of Urology. 173 (6): 1943–6. doi:10.1097/01.ju.0000158159.16314.eb. PMID15879787.
^Ohyama C, Chiba Y, Yamazaki T, Endoh M, Hoshi S, Arai Y (October 2002). "Lymphatic mapping and gamma probe guided laparoscopic biopsy of sentinel lymph node in patients with clinical stage I testicular tumor". The Journal of Urology. 168 (4 Pt 1): 1390–5. doi:10.1016/S0022-5347(05)64456-4. PMID12352400.
^Bex A, Vermeeren L, de Windt G, Prevoo W, Horenblas S, Olmos RA (June 2010). "Feasibility of sentinel node detection in renal cell carcinoma: a pilot study". European Journal of Nuclear Medicine and Molecular Imaging. 37 (6): 1117–23. doi:10.1007/s00259-009-1359-7. PMID20111964. S2CID61891.
^Malmström PU, Ren ZP, Sherif A, de la Torre M, Wester K, Thörn M (November 2002). "Early metastatic progression of bladder carcinoma: molecular profile of primary tumor and sentinel lymph node". The Journal of Urology. 168 (5): 2240–4. doi:10.1016/S0022-5347(05)64363-7. PMID12394767.
^Marits P, Karlsson M, Sherif A, Garske U, Thörn M, Winqvist O (January 2006). "Detection of immune responses against urinary bladder cancer in sentinel lymph nodes". European Urology. 49 (1): 59–70. doi:10.1016/j.eururo.2005.09.010. PMID16321468.
^Veronesi, Umberto et al. (2006) Sentinel-lymph-node biopsy as a staging procedure in breast cancer: update of a randomised controlled study. Lancet Oncol 7:983‒990 doi:10.1016/S1470-2045(06)70947-0
^Veronesi, Umberto et al. (2003) A Randomized Comparison of Sentinel-Node Biopsy with Routine Axillary Dissection in Breast Cancer. N Engl J Med 349:546-553 DOI:10.1056/NEJMoa012782
Krag DN, Weaver DL, Alex JC, Fairbank JT (December 1993). "Surgical resection and radiolocalization of the sentinel lymph node in breast cancer using a gamma probe". Surgical Oncology. 2 (6): 335–9, discussion 340. doi:10.1016/0960-7404(93)90064-6. PMID8130940.
Krag DN, Meijer SJ, Weaver DL, Loggie BW, Harlow SP, Tanabe KK, Laughlin EH, Alex JC (June 1995). "Minimal-access surgery for staging of malignant melanoma". Archives of Surgery. 130 (6): 654–8, discussion 659–60. doi:10.1001/archsurg.1995.01430060092018. PMID7539252.
Alex JC, Krag DN (January 1996). "The gamma-probe-guided resection of radiolabeled primary lymph nodes". Surgical Oncology Clinics of North America. 5 (1): 33–41. doi:10.1016/S1055-3207(18)30403-4. PMID8789492.