Joint Program in Nuclear Medicine
Lymphoscintigraphy and Melanoma : "Expected Drainage"
Pritinder K. Thind, MD
Kevin J. Donohoe, MD
January 4, 2000
Presentation
A 40 year old male presented with superficial spreading malignant melanoma of the left upper back, Clarke stage 4 and Breslow depth of 3.9 mm.
Imaging Findings
On the dynamic images (posterior projection), there is tracer uptake inferior and lateral to the melanoma site. The intense focus is activity at the injection sites around the melanoma. Static images were performed in the anterior projection; the image on the left includes activity from a transmission source which helps to outline the body. There are 3 discrete foci of tracer uptake (shown by arrows) anterior, inferior and lateral to the injection sites (shown by arrowhead). The skin was marked anteriorly. Micrometatses were found in one of the marked lesions.
A lateral static image from another patient who had a left cheek melanoma (arrowhead shows sites of injection) demonstrates tracer uptake in the submandibular and posterior cervical lymph nodes
(shown by arrows).
Discussion
History
Lymphoscintigraphy was introduced in 1950s. During the 1970s, it was used clinically in evaluating the internal mammary lymph node chain in breast cancer to help plan the radiation port sites. In the1990s, the sentinel node concept resurged. There are 2 major criteria for identifying the sentinel node:
- first node to receive drainage from the tumour
- visualization of an afferent lymphatic vessel from the tumour site to the node
Implications of the sentinel node in malignant melanoma:
The presence of regional nodal involvement lowers the 5 year survival rate to ~ 50% (Yudd et al). The sentinel node is the best tissue to sample for histopathologic examination.
Characteristic of ideal imaging agents:
- rapid clearance from the interstitial space into the lymphatic channels
- produce high quality images
- deliver low radiation dose to the patient
- good tracer retention in the lymph nodes to insure gamma probe localization at surgery
Types of radiopharmaceuticals that have been used:
- gold-198: first agent (45 years ago), small size, long half-life (2.7 days), beta emission, 412 keV gamma emission
- Tc-99m antimony trisulfide colloid: favourable energy, uniform size, moderate retention
- Tc-99m human serum albumin: 4.5 nm in diameter, poor retention
Currently In The United States, Filtered Tc Sulfur Colloid Is Used.
Procedure and imaging (Alazraki et al):
- inject 400 uCi of Tc-sc (0.1ml each) intradermally at four points around the tumour site
- early dynamic images: 10 seconds per frame for 10 minutes
- static images every 5 minutes for 30 to 40 minutes
- late imaging at up to 2 hours
- transmission images-cobalt 57 flood source: improves localization of channels and nodes relative to body contour and skin surfaces
Melanoma technique (Yudd et al):
- intradermal injection of 0.1 ml of filtered tc sc at 4 to 8 points around the lesion/scar
- prior to injection, remove air from the syringe to avoid aerosolization of the tracer and surface contamination
- 30 sets of dynamic images are acquired at 30 seconds/frame
- 2 to 3 sets of dynamic images are obtained
- at ~ 30 minutes, localize lymph nodes with respect to anatomic landmarks
- static images of 3-5 minute duration are obatined with cobalt 57 source transmission images
- final set of images at 1.5-2 hours
Following imaging:
- cobalt 57 source is used to assist in marking the skin surface
- in the or, the gamma probe is placed over the marked skin surface for 10 seconds to obtain a reading
- after the incision, the probe is placed over the node for 10 seconds
- following excision, count readings of the lymph node bed and excised node are obtained
Comments about the technique:
- reproducibility: 85-88%
- causes of non-reproducibility
- particle size
- label efficiency tecniques
- injection dose and volume
- location of tumour
- camera acquisition and display parameters
- timing of imaging
- lymphatic disruption due to prior biopsy
Malignant melanoma classification/staging:
- Breslow classification: 4 groups based on tumour depth of invasion [<. 75mm, .76-1.5 mm, 1.51-2.25 mm, 2.26-3.0 mm, >3 mm]
- Clarke scheme: 5 levels on the basis of dermal invasion
- american joint committee on cancer (1988): tumour thickness, level of dermal invasion, +/- regional or distant metastases
Difficulties in evaluation:
- variability of drainage basins: frequently occurs with trunk melanoma
- reproducibility in 2 series varied from 85-88%
- Yudd et al: 17% discrepency between the scintigraphic demonstration of sentinal nodes and the number of sentinel nodes found during gamma probe and blue dye-assisted surgery
Variable drainage patterns:
- extremities: inguinal and axillary regions
- head, neck and trunk: drainage to more than 1 adjacent predictable group varies from 40-75%
- Berman et al: 135 patients with melanoma of the head, neck, shoulder and trunk
- 41% discordancy rate between expected drainage and imaging
- discordancy rate highest for head (64%) and neck (73%)
- altered surgical management in 33%
Effects On Elective Lymph Node Dissection:
- intermediate thickness and/or stage i/ii melanoma: no evidence of tumour spread
- 80% don’t have nodal metastases by elnd
- of the 20% with metastases, elnd can offer more accurate staging
- with the sentinel node concept, invasive surgery can be avoided in 80%
- in the remaining 20%, sln biopsies and lymphatic mapping can direct the lymphatic dissection
Results For Melanoma
- >95% sensitivity for localizing sentinal lymph nodes and lymph node basins (yudd et al)
- berger et al: primary axial cutaneous melanoma- scintigraphy predicted >98% of basins with positive metastases
- 209 patients with high risk melanoma of the trunk: 94% sensitivity in detecting metastases
References
Alazraki N, Eshima D, Herda S, Et Al: Lymphoscintigraphy, the sentinel node concept, and the intraoperative gamma probe in melanoma, breast cancer, and other potential cancers. Seminars in Nuclear Medicine 27 (1): 55-67, 1997
Bonges V, Borel Rinkes H, Barneveld P, et al: Towards quality assurance of the sentinel node procedure in malignant melanoma patients: a single institution evaluation and a european survey. European Journal of Nuclear Medicine 26 (2): 84-90, 1999.
Valdes Olmos R, Hoefnagel C, Nieweg O, et al: Lymphoscintigraphy in oncology: a rediscovered challenge. European Journal of Nuclear Medicine 26 (4), Suppl.: S2-s10, 1999.
Wilhelm A, Mijnhout G, Fransenn E: Radiopharmaceuticals in sentinel lymph-node detection- an overview. European Journal of Nuclear Medicine 26 (4), Suppl.: S36-s42, 1999.
Yudd A, Kempf J, Goydos J, et al: Use of sentinel node lymphoscintigraphy in malignant melanoma. Radiographics 19: 343-353, 1999.
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J. Anthony Parker, MD PhD, Tony_Parker@CareGroup.Harvard.edu