Tracers and corresponding detection devices: technetium colloids, blue dyes & NIR fluorescence
Review Article

Tracers and corresponding detection devices: technetium colloids, blue dyes & NIR fluorescence

Agnieszka Rychlik1, Kamil Zalewski2

1Maria Skłodowska-Curie National Research Institute of Oncology in Warsaw, Warsaw, Poland; 2Holy Cross Cancer Centre in Kielce, Kielce, Poland

Contributions: (I) Conception and design: All authors; (II) Administrative support: None; (III) Provision of study materials or patients: None; (IV) Collection and assembly of data: None; (V) Data analysis and interpretation: None; (VI) Manuscript writing: All authors; (VII) Final approval of manuscript: All authors.

Correspondence to: Agnieszka Rychlik. Maria Skłodowska-Curie National Research Institute of Oncology in Warsaw, Warsaw, Poland. Email: agarychlik@gmail.com.

Abstract: Tracers and corresponding detection devices for the mapping of sentinel lymph nodes have been evolving since the first use of lymphangiogram methods in 1977 in penile carcinoma. Nowadays a variety of dyes and radiotracers have been validated for use in breast, vulvar and cervical cancer as well as melanoma. Each tumor site with its anatomical conditions requires different mapping protocol. While the combination of radiotracer and blue dye or radiotracer alone is an established method for breast surgery, vulvar cancer and melanoma, in pelvic sentinel lymph node mapping indocyanine green is currently gaining popularity. Near infrared fluorescence imaging is an emerging technique that enables a real-time image-guided procedure and is currently approved by the Food and Drug Administration as a sentinel lymph node mapping substance with standard of care. New tracers and devices are constantly under investigation to better understand the pathway of lymphatic drainage and increase the sensibility and sensitivity of the method. In the present review the evolution of available tracers and detection devices is discussed. An exhaustive review of current clinical indications of each method, its particularities and adverse effects is made. Finally, an update on ongoing clinical studies in sentinel lymph node mapping methods is presented.

Keywords: Sentinel lymph node; technetium colloids; blue dyes; NIR fluorescence


Submitted Dec 16, 2020. Accepted for publication Apr 05, 2021.

doi: 10.21037/cco-20-252


Introduction

A selection of a correct tracer and detection method is crucial for effective sentinel lymph node mapping. The story begins in 1977 when Cabanas used lymphangiograms method with a radiocontrast agent to successfully map Sentinel Lymph Node (SLN) in penile carcinoma in 100 patients (1). One year later a group from UCLA School of Medicine studied the use of colloidal gold radionucleotide 198Au to show the direction of regional lymphatic drainage in patients with primary malignant melanoma (2). In 1992 Morton and collaborators demonstrated the accuracy of intraoperative lymphatic mapping and selective sentinel lymphadenectomy in patients with primary cutaneous malignant melanoma, using isosulfan and patent blue-v (3). Krag and collaborators first investigated the use of radioisotopes for SLN identification in breast cancer (4). Later, Albertini identified the SLN using a combined technique of blue dye and radioisotope (5).

While the combination of radiotracer and blue dye or radiotracer is an established method for breast surgery, vulvar cancer and melanoma, in pelvic lymph node mapping indocyanine green is currently gaining popularity

New tracers and devices are constantly under investigation to better understand the biology of lymphatic drainage and increase the sensibility and sensitivity of the method. The evolution of available tracers and detection methods and new lines of investigation in sentinel lymph node mapping will be discussed in this review.


Vital dyes in SLN mapping

The colometric technique is simple, relatively cheap and does not require additional detection equipment.

Currently used vital dyes have first been tested on animal models. In pilot studies Cyalume® (visible light fluorescent dye), methylene blue and isosulfan blue were used (6). Cyalume® has not been found useful as it stained surrounding tissues together with lymphatics. Methylene blue was not satisfactory in animal models due to insufficient lymphatic intake. In contrast, isosulfan has been found to be the most promising dye with selective avidity for lymphatic circulation (7).

At present several blue dyes are used in clinical practice. Isosulfan blue is an isomer of the sodium salt-based patent blue V, and is also called lymphazurin. After injection, this dye binds to albumins and is absorbed by the lymphatics, which allows delineation of the lymphatic drainage.

Isosulfan blue for identification of lymphatic vessels has first experimentally been studied in 1980 in rat models with excellent results. The investigators found a sensibility of 97.4% for identification of lymphatic vessels (7).

This dye has been used in pilot studies by Morton and collaborators to map sentinel lymph nodes in more than five hundred patients with malignant melanoma. The authors demonstrated the accuracy of intraoperative lymphatic mapping and selective sentinel lymphadenectomy to identify lymph node metastasis and reported a less than 1% false-negative rate (3).

A few years later Giuliano used isosulfan blue to successfully map sentinel lymph nodes in breast carcinoma with a 2.8% false negative rate. In his study sentinel nodes were identified in 114 of 174 (65.5%) procedures and accurately predicted axillary nodal status in 109 of 114 (95.6%) cases (8).

Methylthioninium chloride or Methylene Blue is an organic chloride salt. This commonly used dye is an oxidation-reduction agent and is approved by Food and Drug Administration (FDA) for the treatment of methemoglobinemia. In past, methylene blue was widely used in treatment of malaria, or as an antiseptic drug. Currently its properties are being investigated in management of patients with Alzheimer disease. It can cause acute haemolysis in patients with G6PD deficiency. When administered in the lymphatic bed of the tumor, methylene blue stains sentinel lymph nodes and is used for mapping purpose. The molecule is smaller in size than isosulfan blue. However, the specificity remains the same as for other blue dyes used for SLN mapping.

Methylene blue is less expensive than isosulfan blue or patent blue and more accessible in developing countries. The first reports about methylene blue as an alternative to isosulfan blue for sentinel lymph node biopsy in breast cancer were published by Simmons (9). The detection rate of methylene blue with radiotracer is equivalent to that reported for isosulfan and radiocolloid.

Patent blue V is structurally similar to isosulfan blue. The mechanism of action and biology are analogous. Both tracers are indistinctly used for Sentinel Lymph Node mapping. In some countries, like United Kingdome patent blue V is the most recommended blue dye in breast SLN mapping.

Indigocarmine is a blue dye used in pilot studies in Japan with promising results (10). However, more detailed data are not available on a security profile and accuracy of this method.

Adverse effects of blue dyes

Isosulfan and patent blue have been associated with anaphylactic reactions such as allergic urticaria or anaphylaxis. In the ASCOSOG Z00010 trial showed 0.1% risk of anaphylaxis using isosulfan blue alone or in combination with radiocolloid (11). Other series showed up to 1% of anaphylactic reaction. In addition, the administration of a blue dye may result in oxygen saturation decrease. This event is so called pseudo desaturation with oxygen levels remaining normal. Consequently, anaesthetic team should always be informed prior to blue dye administration.

Methylene blue has been less associated with anaphylactic reaction with only a few cases reported in the literature (12,13). It can also interfere with oxygen saturation (pseudo-desaturation) but less severely that isosulfan blue (14). Methylene blue causes, however, skin reactions and ulcerations. It should not be used subcutaneously due to possible skin necrosis.

Intravenous injection of blue dyes may cause causes a bluish skin discoloration. In addition, blue dyes can transitionally change the urine colour into green.

Blue dyes are contraindicated in pregnant women due to anaphylactic reaction risk.

Current indications of blue dyes

Blue dyes are generally injected immediately before the surgery. The coloured lymph nodes are visible 5 minutes after the injection and stay up to 45 minutes. However, surprisingly some authors described injections 90 minutes prior to the surgery with positive results (15). Massage of the injection site has been described to improve the detection rate in breast cancer SLN mapping (16).

In breast cancer there is enough evidence that the combined use of blue dye and radioisotopes is significantly better than blue dye alone for SLN identification (17-19). In gynaecological cancer (endometrial, cervical and vulvar cancer) the evidence is similar. Blue dyes used alone are associated with the poorest detection rates, around 70% for endometrial cancer (50% for bilateral detection). In vulvar cancer the sensitivity of the blue dye technique in detecting the sentinel node is only 56-88% and the combined method with radiotracer significantly improves the SLN detection rate to approximately 100%.

Therefore, currently the use of blue dye alone is not recommended for SLN mapping.


Indocyanine green

Indocyanine green (ICG) is a cyanine fluorescent molecule used for diagnostic purpose in ophthalmology, neurosurgery, cardiology and hepatology. ICG has attractive characteristics due to its safety and high absorbance in a wavelength range of 600 to 900 nm. When injected intravenously or interstitially, and excited by a laser ICG emits a wavelength in the near infrared range between 750 and 950 nm, that can be detected by a near-infrared imaging devices. ICG is currently widely used as a sentinel lymph node tracer as after interstitial injection the drug diffuses into lymphatic pathways and lymph nodes similarly to vital dyes.

The ICG in lymph node mapping has first been used for skin cancer patients (20). Simultaneously, intraoperative near-infrared fluorescence was tested in breast cancer surgery (21-23). These first clinical trials showed similar detection rate to conventional combined technique. In 2010 ICG was first described as a feasible tracer for use in SLN mapping in gynaecologic cancers, initially cervical cancer, and then for endometrial cancer by the group of Rossi (24,25).

Recent prospective study by Frumovitz et al. proved that ICG is superior to the blue dye in detecting SLN in endometrial cancer. The authors concluded that interstitial injection of ICG appears to be safe as there were no adverse events related to the compound (26). ICG was also compared to the combined method (blue dye and radiotracer) in an international European retrospective study. The authors found significantly higher bilateral detection rate in ICG group (27). Similar studies have been performed for cervical cancer, founding better detection rate for ICG when compared to standard technique using radioisotope technetium 99m radiocolloid radiotracer with or without blue dye (28). ICG is found to be the most accurate detection method for obese patients in endometrial cancer SLN mapping (29,30).

The main advantage of this method is that it is a one-step technique and is fully performed during the surgical procedure what considerably impacts patient’s satisfaction. ICG is associated with minimal risk of adverse effects. Although, its use is contraindicated in patients with hepatic insufficiency and those allergic to iodine components.

Clinical use of ICG

ICG may be prepared with distilled water or saline solution. However, the dosage and injection site are not standardised. Some studies used the dilution of 1.25 mg/mL, using a total dosage of 5 mg, others used up to 10 mg.

An interesting experimental study used a porcine model to compare various dosages of ICG to determine the optimal dosage needed to accurately differentiate the sentinel node from surrounding tissue. The tracers have been injected into porcine uterine cervix and detected with robotic instrumentation. The authors suggest that the optimal ICG dose ranges from 250 to 500 μg/mL, both of which cause a large difference in the intensity signal between the sentinel node and the surrounding tissues.

The authors found that smaller dose of ICG migrated faster to the SLN. However, these finding have not been confirmed in different studies and the authors suggested that timing seems to be unrelated to the dosage of ICG (31).


Radiotracers

Since the development of scintigraphy and gamma camera in 1950s, radioactivity found another application in medicine. The most widely used radiation sources for medical purposes are gamma (γ) emitting radioisotopes, of hundreds of radioisotopes available today, technetium (99Tc) and particularly its metastable isotope (99mTc) found application in nuclear medicine. Technetium emits high-energy γ radiation and has a short half-life (6.01 hours), practical for clinical applications (32).

For lymph node imaging, 99mTc is bound to a colloid playing a role of a carrier, to form a radiocolloid. The schematic pharmacokinetics of the tracer is shown in the Figure 1 (33).

Figure 1 Schematic pharmacokinetics of the radiotracers.

Physical and chemical properties of colloid particle impact its kinetics and play an important role in the distribution of the radiocolloid in the lymphatic vessels. The idea size of the colloidal particle used for SLN mapping ranges beteween 80 and 200 nm. Smaller particles moves faster and reach immediately the SLN. In contrast, large particles may remain at the injection site, block lymphatic channels and not reach the SLN within a clinically acceptable time (34). It is estimated that 60 minutes after a subcutaneous administration of the 99m Tc albumin, around 3-5% of the applied activity will be detected in th LNs (35).

There are currently over ten colloidal products used in lymphoscintigraphy following 99mTc labeling.

Characteristics of different 99mTc-labelled colloids used for the SLN mapping are presented in Table 1.

Table 1
Table 1 Characteristics of selected 99mTc-labelled radiopharmaceuticals used for the SLN procedure (36)
Full table

Radiotracers, current indications

Different protocols are used for different tumor sites. In cervical cancer, the most frequently used activity is about 110 MBq in a total volume of 2 mL (0.5 mL per depot) (36). However, there are at least three protocols with different doses and different timing of injection. Long protocol consists of injection of high doses of radiotracer 24 hours before surgery. The doses range between 2 and 4 mCi, 74–148 MBq. In short protocols, 0.2 and 1mCi (7.4–37 MBq) of Technetium isotope is injected 2 to 4 hours prior surgery. In ultrashort protocols the application of the is made in the operating theatre under general anaesthesia and the dose is 0.4–0.55 mCi (14.8–20 MBq) (37).

The endometrial approach is more complex and several techniques have been described. Thus, the total dose injected may vary from 40 to 185 MBq and the volume injected from 0.5 to 8 mL (38,39).

For vulvar cancer two to four injections of radiotracer are performed with a total dose ranging from 20 to 150 MBq in an approximate volume of 0.4–0.5 mL (0.1 mL per injection) (40-42). The maximum activity of 99mTc should be loaded onto the smallest number of particles. Labelling at higher specific activity has been demonstrated to result in higher nodal count rates for the same administered activity (43).

Following application of a radiocolloid, lymph nodes can be localized either by planar scintigraphy or SPECT-CT. Imaging is advised to enable the preoperative identification, location and number of sentinel lymph nodes, including those outside the defined regional lymph flow. In long protocols, preoperative imaging is performed 1–3 hours after injection, whereas in short protocols the images are obtained 20–30 minutes after the injection. SPECT gamma camera and integrated CT scanner (SPECT/CT) appears to offer a significant improvement in sentinel node detection and anatomic localization when compared with lymphoscintigraphy. SPECT/CT fuses tomographic lymphoscintigrams with anatomical data. SPECT/CT systems consist of a dual-head variable-angle gamma camera equipped with low-energy high-resolution collimators and a low-intensity CT scanner. Patient stays in the same position during imaging and the two images are easily fused. SPECT/CT provides a three-dimensional image with better contrast and spatial resolution than planar imaging and has the possibility to correct for attenuation and scatter. This combination of imaging properties results in precise localization of the SLN (44,45).

SPECT CT has found to be particularly useful in detection of parametrial SLN in Cervical cancer (46,47). However, there is still a lack of data on the use of SPECT/CT in endometrial cancer. For other tumors such as vulvar cancer SPECT/CT is not widely used because deep drainage is less frequent.

Intraoperative detection of nodes with high gamma activity (hot nodes) requires a use of a gamma-probe that acquires the radioactive signal. The hot nodes are identified in comparison with background radioactivity. The ratio of radioactive counts depends on the dose, time elapsed and the type radiotracer used and type of gamma-probe applied. All hot nodes must be removed. Additionally, nodes that presents more than 20% of SLN count rate should be resected.

The quality of gamma-probe is essential for a successful mapping. The following criteria were used to describe the quality of a probe: Spatial selectivity at 30 cm (the width of the measurement cone), spatial resolution at 1 cm distance (determines the minimal distance needed between two lymph nodes for them to be detected separately, Sensitivity, Sensitivity at probe housing, energy discrimination, shape of probe (48).

Safety of radiotracers

The use of a radioactive tracer involves exposure to ionizing radiation not only for the patient but also for the medical personnel. However, operating room staff is exposed to a radiation dose reported as minimal (below 1 µSv per operation) with the highest occupational dose to the surgeons performing SLN biopsy and this is below 2 µSv per operation (49,50). The hand dose to the surgeons has been calculated as 5–94 µSv per operation. Thus, radiological safety must be secured by adherence to strict guidelines and safety rules at all stages of handling, applying and disposal of radioactive tracers

As there is limited data regarding safety of radiotracer based SLN mapping in pregnant women it is often listed as contraindication for the procedure (51). Others argue that taking into account fact that fetus exposure to radioactivity is negligible, SLN procedure is justified as is relatively related to less risks of complications than traditional axillary lymph node dissection (52).


Combined methods

The combinations of the radiotracer, ICG and blue dyes were tasted for several tumor sites in randomised trials.

In breast cancer dual detection of SLN using ICG and radioisotope was found reliable and sensitive but was not superior to isotope alone in successfully locating SLN in pilot randomized trial. Randomized comparison between indocyanine green fluorescence plus 99mtechnetium and 99mtechnetium alone methods for sentinel lymph node biopsy in breast cancer (53).

In another prospective trial, How et al. combined the 3 tracers blue ICG and Tc99 in endometrial cancer patients. Authors observed a 76% bilateral detection rate using this combination, similar to single-agent ICG detection rate described in different studies (54).

The comparison of available tracers and their combination have been analysed in systematic reviews and metanalyses.


New tracers

Some authors tried to use ICG-99m Tc nanocolloid as a hybrid tracer that combined the fluorescent and radioactive signatures in one compound. These traces have been preliminary tested in melanoma, cervical and breast cancer patients (55).

Novel techniques with iron oxide tracer (Sienna+®), have been evaluated in vulvar cancer to compare with promising results (56).

Other authors tested the fluorescence tracer with receptor targeted agents - Rituximab (a chimeric human/murine monoclonal antibody targeting the CD20 antigen on the surface of lymphocyte for SLN mapping in breast cancer (57).


Comparizon of tracers in different tumor sites

Breast cancer and melanoma

An exhaustive meta-analysis on optimal tracer for SLN mapping in breast cancer and melanoma provided data in favor of the use of radiocolloid alone or radiocolloid combined with a blue dye. Authors of this metanalysis recommend radiocolloid alone as a method of choice for experienced surgeons (58).

Vulvar cancer

The combination of radiotracer and blue dye has for long been gold standard in SLN mapping in vulvar cancer. This opinion was based on a result of a meta-analysis which demonstrated that the SLN detection rates were 94.0% (95% CI, 90–96%) for technetium Tc 99 m alone, 68.7% (95% CI, 63–74%) for blue dye alone, and 97.7% (95% CI, 96–98%) for 99mTc plus blue dye (59).

At present florescence guided SLN mapping is gaining importance also in vulvar cancer. Its feasibility was described in two promising studies (60,61).

Gynecological cancer

According to data from a recent metanalysis, ICG or the combined technique of blue dye with Tc99 seems to have the highest detection rates, generally greater than 90% overall detection and greater than 80% bilateral detection (62).


Conclusions

The SLN procedures requires an implication of four different medical specialities including surgery, pathology, nuclear medicine and radiology. The choice of the best tracer is a result of its safety, accuracy and cost-efficacy of the method. Currently ICG is found to be the most accurate in pelvic SLN mapping both for endometrial and cervical cancer. However, its use requires availability of costly near-infrared optical system device.

The decision of a used protocol should be made according to local availabilities and in consensus with a multidisciplinary team.


Acknowledgments

Funding: none


Footnote

Provenance and Peer Review: This article was commissioned by the Guest Editors (Denis Querleu and Cherif Akladios) for the series “Sentinel Lymph Node Biopsy in Gynecologic Cancer” published in Chinese Clinical Oncology. The article has undergone external peer review.

Conflicts of Interest: Both authors have completed the ICMJE uniform disclosure form (available at http://dx.doi.org/10.21037/cco-20-252). The series “Sentinel Lymph Node Biopsy in Gynecologic Cancer” was commissioned by the editorial office without any funding or sponsorship. The authors have no other conflicts of interest to declare.

Ethical Statement: the authors are accountable for all aspects of the work in ensuring that questions related to the accuracy or integrity of any part of the work are appropriately investigated and resolved.

Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0/.


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Cite this article as: Rychlik A, Zalewski K. Tracers and corresponding detection devices: technetium colloids, blue dyes & NIR fluorescence. Chin Clin Oncol 2021;10(2):16. doi: 10.21037/cco-20-252