Sentinel lymph node

Image illustrating sentinel lymph nodes. The axillary lymph nodes drain 75% of the lymph from the breasts((uncited)) and so may be the first lymph nodes affected in breast cancer.

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 node/s is/are the target organs primarily reached by metastasizing cancer cells from the tumor.

The sentinel node procedure is the identification, removal and analysis of the sentinel lymph nodes of a particular tumour.

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.[1]

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.[2]

A blue stained sentinel lymph node in the axilla.
A micrograph showing an adenocarcinoma of the breast (dark pink) in a lymph node (purple) and extending into the surrounding fat (white, chicken-wire appearance). H&E stain.

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][3][4]
  • Intraoperative visual blue dye detection
  • Intraoperative fluorescence detection (fluorescence image-guided surgery)
  • Intraoperative gamma probe/Geiger meter-detection
  • Preoperative or intraoperative super paramagnetic iron oxide nanoparticles injection, detection by using Sentimag instrument[5][6]
  • 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. In the UK 20 megabecquerels of nanocolloid is recommended.[7] 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.

Clinical advantages

There are various advantages to the sentinel node procedure. First and foremost, it decreases lymph node dissections where unnecessary, thereby reducing the risk of lymphedema, a common complication of this procedure. Increased attention on the node(s) identified to most likely contain metastasis is also more likely to detect micro-metastasis and result in staging and treatment changes. Its main uses are in breast cancer and malignant melanoma surgery, although it has been used in other tumor types (colon cancer) with a degree of success.[8] Other cancers which have been investigated with this technique are penile cancer, urinary bladder cancer,[9][10] prostate cancer,[11][12][13] testicular cancer[14][15] and renal cell cancer.[16][17]

Research advantages

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,[18] mechanisms of dissemination, the EMT-MET-process (epithelial–mesenchymal transition) and cancer immunology[19] 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.[20] 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.[21]

History

The concept of a sentinel node was first described by Gould et al. 1960 in a patient with cancer of the parotid gland[22] and was implemented clinically on a broad scale by Cabanas in penile cancer.[23] 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.[24] 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.[25] The benefits included less pain, greater arm mobility and less swelling in the arm.[26]

See also

  • ALMANAC, Axillary Lymphatic Mapping Against Nodal Axillary Clearance trial

References

  1. ↑ Wang, Xiao-juan; Fang, Fang; Li, Ye-fei (2014-11-28). "Sentinel-lymph-node procedures in early stage cervical cancer: a systematic review and meta-analysis". Medical Oncology. 32 (1): 385. doi:10.1007/s12032-014-0385-x. ISSN 1559-131X. PMC 4246132. PMID 25429838.
  2. ↑ Kumar V, Abbas AK, Fausto N, Aster JC, eds. (2009). Robbins & Cotran Pathologic Basis of Disease (8th ed.). Elsevier Health Sciences. p. 270. ISBN 978-1-4377-2015-0.
  3. ↑ 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. PMID 16632191.
  4. ↑ Leijte JA, Valdés Olmos RA, Nieweg OE, Horenblas S (October 2008). "Anatomical mapping of lymphatic drainage in penile carcinoma with SPECT-CT: implications for the extent of inguinal lymph node dissection". European Urology. 54 (4): 885–90. doi:10.1016/j.eururo.2008.04.094. PMID 18502024.
  5. ↑ Karakatsanis A, Christiansen PM, Fischer L, Hedin C, Pistioli L, Sund M, Rasmussen NR, Jørnsgård H, Tegnelius D, Eriksson S, Daskalakis K, Wärnberg F, Markopoulos CJ, Bergkvist L (June 2016). "The Nordic SentiMag trial: a comparison of super paramagnetic iron oxide (SPIO) nanoparticles versus Tc(99) and patent blue in the detection of sentinel node (SN) in patients with breast cancer and a meta-analysis of earlier studies". Breast Cancer Research and Treatment. 157 (2): 281–294. doi:10.1007/s10549-016-3809-9. PMC 4875068. PMID 27117158.
  6. ↑ "Sentimag". Endomag. Retrieved 2019-03-09.
  7. ↑ BNMS (August 2011). "Lymphoscintigraphy Clinical Guidelines" (PDF). Retrieved 3 January 2017.
  8. ↑ 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. PMID 11314938.
  9. ↑ 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. PMID 11490224.
  10. ↑ 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. PMID 16406877.
  11. ↑ 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. PMID 10559614. S2CID 46760854.
  12. ↑ Ganswindt U, Paulsen F, Corvin S, Eichhorn K, Glocker S, Hundt I, Birkner M, Alber M, Anastasiadis A, Stenzl A, Bares R, Budach W, Bamberg M, Belka C (July 2005). "Intensity modulated radiotherapy for high risk prostate cancer based on sentinel node SPECT imaging for target volume definition". BMC Cancer. 5: 91. doi:10.1186/1471-2407-5-91. PMC 1190164. PMID 16048656.
  13. ↑ 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. PMID 15879787.
  14. ↑ 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. PMID 12352400.
  15. ↑ Brouwer OR, Valdés Olmos RA, Vermeeren L, Hoefnagel CA, Nieweg OE, Horenblas S (April 2011). "SPECT/CT and a portable gamma-camera for image-guided laparoscopic sentinel node biopsy in testicular cancer". Journal of Nuclear Medicine. 52 (4): 551–4. doi:10.2967/jnumed.110.086660. PMID 21421720.
  16. ↑ 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. PMID 20111964. S2CID 61891.
  17. ↑ Sherif AM, Eriksson E, Thörn M, Vasko J, Riklund K, Ohberg L, Ljungberg BJ (April 2012). "Sentinel node detection in renal cell carcinoma. A feasibility study for detection of tumour-draining lymph nodes". BJU International. 109 (8): 1134–9. doi:10.1111/j.1464-410X.2011.10444.x. PMID 21883833.
  18. ↑ 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. PMID 12394767.
  19. ↑ 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. PMID 16321468.
  20. ↑ Wagman LD. "Principles of Surgical Oncology" in Pazdur R, Wagman LD, Camphausen KA, Hoskins WJ (Eds) Cancer Management: A Multidisciplinary Approach. 11 ed. 2008.
  21. ↑ Thomas JM (January 2008). "Prognostic false-positivity of the sentinel node in melanoma". Nature Clinical Practice. Oncology. 5 (1): 18–23. doi:10.1038/ncponc1014. PMID 18097453. S2CID 7068382.
  22. ↑ Gould EA, Winship T, Philbin PH, Kerr HH (1960). "Observations on a "sentinel node" in cancer of the parotid". Cancer. 13: 77–8. doi:10.1002/1097-0142(196001/02)13:1<77::aid-cncr2820130114>3.0.co;2-d. PMID 13828575.
  23. ↑ Cabanas RM (February 1977). "An approach for the treatment of penile carcinoma". Cancer. 39 (2): 456–66. doi:10.1002/1097-0142(197702)39:2<456::aid-cncr2820390214>3.0.co;2-i. PMID 837331.
  24. ↑ Tanis PJ, Nieweg OE, Valdés Olmos RA, Th Rutgers EJ, Kroon BB (2001). "History of sentinel node and validation of the technique". Breast Cancer Research. 3 (2): 109–12. doi:10.1186/bcr281. PMC 139441. PMID 11250756.
  25. ↑ 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
  26. ↑ 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

Further reading

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