(technetium Tc 99m tilmanocept) Injection for Subcutaneous, Intradermal, Subareolar, or Peritumoral Use
The active ingredient in Lymphoseek, a radioactive diagnostic agent, is technetium Tc 99m tilmanocept. Technetium Tc 99m binds to the diethylenetriaminepentaacetic acid (DTPA) moieties of the tilmanocept molecule.
- Chemically, technetium Tc 99m tilmanocept consists of technetium Tc 99m, dextran 3-[(2- aminoethyl)thio]propyl 17-carboxy-10,13,16-tris(carboxymethyl)-8-oxo-4-thia-7,10,13,16- tetraazaheptadec-1-yl 3-[[2-[[1-imino-2-(D-mannopyranosylthio)ethyl]amino]ethyl]thio]propyl ether complexes.
- The molecular formula of technetium Tc 99m tilmanocept is [C6H10O5]n .(C19H28N4O9S99m Tc)b .(C13H24N2O5S2)c .(C5H11NS)a . It contains 3-8 conjugated DTPA (diethylenetriaminepentaacetic acid) molecules (b); 12-20 conjugated mannose molecules (c) with 0-17 amine side chains (a) remaining free.
- The calculated average molecular weight of tilmanocept ranges from 15,281 to 23,454 g/mol.
- Technetium Tc 99m tilmanocept has the following structural formula:
Lymphoseek (technetium Tc 99m tilmanocept) injection is supplied as a Kit which contains five Tilmanocept Powder vials. Each Tilmanocept Powder vial contains the non-radioactive ingredients needed to produce technetium Tc 99m tilmanocept. The vial contains a sterile, non-pyrogenic, white to off-white lyophilized powder (under nitrogen) that consists of a mixture of 250 mcg tilmanocept, 20 mg trehalose dihydrate, 0.5 mg glycine, 0.5 mg sodium ascorbate, and 0.075 mg stannous chloride dihydrate.
The DILUENT for Lymphoseek contains 4.5 mL sterile buffered saline consisting of 0.04% (w/v) potassium phosphate, 0.11% (w/v) sodium phosphate (heptahydrate), 0.5% (w/v) sodium chloride, and 0.4% (w/v) phenol.
Technetium Tc 99m decays by isomeric transition with a physical half-life of approximately 6 hours. The principal photon that is useful for detection and imaging studies is listed in Table 4.
Table 4. Principal Radiation Emission Data
|Radiation||Mean % Disintegration||Mean Energy (keV)|
The linear mass energy absorption attenuation coefficient for Tc 99m is 18.9 cm-1 . The first half-value layer is 0.037 cm of lead (Pb). The use of a 0.25 cm thick standard radiation lead shield will attenuate the radiation emitted by millicurie amounts of technetium Tc 99m by a factor of about 100. A range of values for the relative attenuation of the radiation of technetium Tc 99m that results with various thicknesses of lead shielding are displayed in Table 5.
Table 5. Radiation Attenuation by Lead Shielding
|Shield Thickness , cm of
|Coefficient of Attenuation|
To correct for physical decay of the radionuclide, the fractions that remain at selected intervals after the time of calibration are shown in Table 6.
Table 6. Physical Decay Chart; Tc 99m, Half-Life of
approximately 6 Hours
Lymphoseek is a radioactive diagnostic agent indicated with or without scintigraphic imaging for:
- Lymphatic mapping using a handheld gamma counter to locate lymph nodes draining a primary tumor site in patients with solid tumors for which this procedure is a component of intraoperative management.
- Guiding sentinel lymph node biopsy using a handheld gamma counter in patients with clinically node negative squamous cell carcinoma of the oral cavity, breast cancer or melanoma.
DOSAGE AND ADMINISTRATION
Radiation Safety – Drug Handling
Lymphoseek is a radioactive drug and should be handled with appropriate safety measures to minimize radiation exposure [see WARNINGS AND PRECAUTIONS]. Use waterproof gloves, effective radiation shielding, and appropriate safety measures when preparing and handling Lymphoseek.
Radiopharmaceuticals should be used by or under the control of physicians who are qualified by specific training and experience in the safe use and handling of radionuclides, and whose experience and training have been approved by the appropriate governmental agency authorized to license the use of radionuclides.
The recommended dose of Lymphoseek is 18.5 MBq (0.5 mCi) as a radioactivity dose and 50 mcg as a mass dose. Administer Lymphoseek at least 15 minutes prior to initiating intraoperative lymphatic mapping and sentinel node biopsy; complete these procedures within 15 hours after Lymphoseek injection.
Route Of Administration And Injection Method
The route of administration depends on the tumor location and the planned injection technique and includes: subcutaneous, intradermal, subareolar, or peritumoral injection.
Lymphoseek may be administered to a patient as a single injection or as multiple injections. The recommended total injection volume for each patient (Table 1) is 0.1 mL administered in a single syringe; 0.5 mL administered in a single syringe or in multiple syringes (0.1 mL to 0.25 mL each); or 1 mL administered in multiple syringes (0.2 mL to 0.5 mL each).
The lymphatic system architecture and function may be changed by prior surgery, radiation, edema, inflammation or metastatic disease, and may result in changes to lymph node localization by a radiopharmaceutical or other tracers, including colorimetric agents. Avoid injections into biopsy wound areas that show evidence of edema or inflammation.
In animal studies, locally injected anesthetics have been reported to reduce lymphatic flow. Concomitant administration of local anesthetics with Lymphoseek is not recommended and may impair the lymph nodal mapping.
- Kit for the preparation of Lymphoseek contains five
Tilmanocept Powder vials, each containing 250 mcg of tilmanocept from which 50
mcg is intended for administration to a patient.
- The Kit for the preparation of Lymphoseek is packaged either with or without five DILUENT for Lymphoseek vials each containing 4.5 mL of sterile buffered saline with phenol.
- The Kit for the preparation of Lymphoseek may also be diluted with pharmacy-available sterile 0.9% sodium chloride injection.
- A diluent is used to dilute Lymphoseek after the radiolabeling procedure. The amount of diluent used varies, depending on the total injection volume and the number of syringes used for each patient.
- The vial components of the Kit for the preparation of Lymphoseek are intended solely for use in the preparation of Lymphoseek. Do not administer the unprepared vial components of the Kit directly to a patient.
- Follow aseptic procedures during preparation and administration.
Drug Preparation Instructions
Prior to preparation of Lymphoseek, determine the planned injection technique and the number of injections that will be used for a given patient. For each injection prepare a separate syringe. Based on the planned number of injection syringes and the planned total injection volume per patient, determine (from Table 1 below) the Reconstituted Vial Volume of radiolabeled Lymphoseek.
Table 1: Preparation of Lymphoseek for Administration
|Planned Number of Injections for a Patient||Total Injection Volume Per Patient||Reconstituted Vial Volume of Radiolabeled Lymphoseek|
|1 syringe x 0.1 mL||0.1 mL||0.5 mL|
|5 syringes x 0.1 mL or 2 syringes x 0.25 mL or 1 syringe x 0.5 mL||0.5 mL||2.5 mL|
|5 syringes x 0.2 mL or 4 syringes x 0.25 mL or 2 syringes x 0.5 mL||1 mL||5 mL|
Once the Reconstituted Vial Volume is established, use the following steps to prepare radiolabeled Lymphoseek:
- Inspect the Tilmanocept Powder vial for any damage. Do not use if vial integrity appears compromised. Do not vent the Tilmanocept Powder vial prior to or during radiolabeling.
- Use Technetium Tc 99m pertechnetate, sodium injection solution from a technetium Tc 99m generator within 8 hours of its elution.
- Using a sterile syringe, aseptically draw approximately 92.5 MBq (2.5 mCi) of Technetium Tc 99m pertechnetate sodium injection solution in either about 0.35 mL volume (for 0.5 mL Reconstituted Vial Volume) or about 0.7 mL volume (for 2.5 mL or 5 mL Reconstituted Vial Volume). Assay the syringe for technetium Tc 99m activity in a dose calibrator.
- Write the radioactivity amount, the Reconstituted Vial Volume, date and time, expiration time and lot number in the space provided on the radioactive product vial label and affix it to the Tilmanocept Powder vial. Place the vial in a radiation shield and sanitize the septum with alcohol wipe.
- Aseptically add Technetium Tc 99m pertechnetate, sodium injection solution to the Tilmanocept Powder vial. Without withdrawing the needle, remove an equal volume of headspace gas. Do not vent.
- Remove the needle, gently shake the vial to mix the contents, and then let it stand at room temperature for at least 15 minutes.
- Aseptically add the supplied DILUENT for Lymphoseek or pharmacy-available sterile 0.9% sodium chloride injection to the radiolabeled product in the Tilmanocept Powder vial to bring the volume to the Reconstituted Vial Volume of 0.5 mL, 2.5 mL, or 5 mL prior to filling the patient dose in syringe(s). To normalize pressure, withdraw an equal volume of headspace gas.
- Each Lymphoseek vial, once radiolabeled and reconstituted, would contain sufficient amount to provide doses for up to four patients when prepared according to the instructions.
- Assay the reconstituted vial for total radioactivity using a dose calibrator. Write the technetium Tc 99m activity concentration, total volume, assay time and date, expiration time, and lot number on the shield label supplied with the Kit. Affix the label to the shield.
- Determine the radiochemical purity of the radiolabeled product [see Determination of Radiochemical Purity of Radiolabeled Lymphoseek]. Do not use if the radiochemical purity is less than 90%.
- Withdraw the required volume of the radiolabeled product into the required number of syringes. Assay the syringe(s) in a dose calibrator. Write the radioactivity amount, date and time of assay, volume, and expiration time (this is not to exceed 6 hours from preparation time) on the supplied syringe label and affix it to the syringe(s).
- Store the radiolabeled Lymphoseek in radiation shielding at room temperature.
- Use the radiolabeled Lymphoseek within 6 hours of preparation. Discard the unused radiolabeled Lymphoseek.
Quality Control Of Radiolabeled Solution
Duration Of Use And Storage Of Radiolabeled Solution
Determination Of Radiochemical Purity Of Radiolabeled Lymphoseek
Determine radiochemical purity of the reconstituted radiolabeled Lymphoseek by Instant Thin Layer Chromatography (ITLC) using either Whatman Grade 1, 3MM, 31ET Chr or Biodex 150-001 Red Strips (cellulose chromatography paper) using the following method:
- Mark the chromatographic strip for origin, mid and solvent front lines with a pencil as shown below:
- Apply a small drop (3 -10 microliters) of the reconstituted product at the center of the origin line chromatography strip. Let the product spot dry.
- Place the strip into a chromatography chamber containing 1 mL of acetone as the developing solvent. Allow the solvent to migrate to the solvent front line (5 cm from the bottom of the Whatman strips and 3.5 cm for the Biodex strip). Remove the strip from the chamber, let it dry and cut it in half. Count each half of the strip with a suitable radioactivity counting apparatus (dose calibrator or multichannel analyzer).
- Calculate the percent radiochemical purity (% RCP) as
% RCP = Counts (activity) in bottom half
Counts (activity) in bottom half + Counts (activity) in top half
- Do not use the reconstituted Lymphoseek if the radiochemical purity is less than 90%.
Lymphatic Mapping And Sentinel Lymph Node Biopsy Following Injection Of Lymphoseek
- Lymphoscintigraphy may be used to assist in planning the lymph node mapping procedures. In clinical studies, preoperative scintigraphic imaging was performed using planar imaging techniques and/or SPECT/CT to establish a map of nodal basins and to facilitate intraoperative identification of lymph nodes. Imaging was performed as early as immediately after injection and up to 21 hours [see Clinical Studies].
- Use a handheld gamma counter to identify nodes that concentrated the injected radioactivity.
- For intraoperative lymphatic mapping, first measure the background radioactivity counts from tissue at least 20 centimeters distal to the injection site. The three sigma threshold (background radioactivity counts plus three times the square root of the mean background count) may be used as an estimate of the threshold for positive localization of Lymphoseek, as exemplified in Table 2.
Table 2: Examples of Three Sigma Threshold Values
|Background Counta (cpm)||Threshold Value (cpm)|
|a Average of three 2-second counts or one 10-second count|
- Lymphoseek is intended to supplement palpation, visual inspection, and other procedures important to lymph node mapping and sentinel node biopsy. Intraoperative lymphatic mapping and sentinel node biopsy using gamma detection of Lymphoseek within lymph nodes should be initiated no sooner than 15 minutes following injection. In clinical studies of breast cancer and melanoma, patients also received a concomitant blue dye tracer for comparative detection of lymph nodes. While most lymph nodes were detected with Lymphoseek, some were detected only with the blue dye tracer or only with palpation [see Clinical Studies].
The radiation doses to organs and tissues of a patient weighing 70 kg given 18.5 MBq (0.5 mCi) of Lymphoseek are shown in Table 3.
Table 3: Estimated Absorbed
Radiation Dose from 18.5 MBq (0.5 mCi) Lymphoseek in Patients with Breast
Cancer and Melanoma
|Target Organ||Breast Cancera mGy (rad)||Melanomab mGy (rad)|
|brain||0.003 (0.0003)||0.0927 (0.0093)|
|breast (injection site)||1.659 (0.1659)||0.7903 (0.079)|
|gall bladder wall||0.0349 (0.0035)||0.0712 (0.0071)|
|lower large intestine wall||0.0123 (0.0012)||0.057 (0.0057)|
|small intestine||0.0101 (0.001)||0.0594 (0.0059)|
|stomach||0.0184 (0.0018)||0.0562 (0.0056)|
|upper large intestine wall||0.0125 (0.0012)||0.0582 (0.0058)|
|kidney||0.1863 (0.0186)||0.278 (0.0278)|
|liver||0.0324 (0.0032)||0.0929 (0.0093)|
|lungs||0.0374 (0.0037)||0.0599 (0.006)|
|muscle||0.0092 (0.0009)||0.0451 (0.0045)|
|ovaries||0.187 (0.0187)||0.2991 (0.0299)|
|red marrow||0.0127 (0.0013)||0.0507 (0.0051)|
|bone||0.0177 (0.0018)||0.0878 (0.0088)|
|spleen||0.0285 (0.0029)||0.0598 (0.006)|
|testes||0.0501 (0.005)||0.1043 (0.0104)|
|thymus||0.1168 (0.0117)||0.0577 (0.0058)|
|thyroid||0.088 (0.0088)||0.0464 (0.0046)|
|urinary bladder||0.0586 (0.0059)||0.1401 (0.014)|
|total body||0.0195 (0.0019)||0.0547 (0.0055)|
|Effective Dose Equivalent||microSv||microSv|
|a Calculated from data of 18 patients with
breast cancer who received four peritumoral injections of 4 mcg, 20 mcg, and
100 mcg doses of Lymphoseek.
b Calculated from data of 18 patients with melanoma who received four intradermal injections of 20 mcg, 100 mcg, and 200 mcg doses of Lymphoseek. Due to the differences in injection sites among patients with melanoma, the injection site was assumed to be the breast for the purposes of this calculation, as it represents the nearest anatomical construct for the skin from the anatomical sites appropriately included in the estimates.
Dosage Forms And Strengths
The Kit for preparation of Lymphoseek (technetium Tc 99m tilmanocept) injection is supplied as five Tilmanocept Powder vials each containing 250 mcg tilmanocept, and is packaged either with or without five DILUENT for Lymphoseek vials each containing 4.5 mL of sterile buffered saline with phenol. After radiolabeling with technetium Tc 99m, Lymphoseek contains approximately 92.5 MBq (2.5 mCi) and 250 mcg technetium Tc 99m tilmanocept in 0.5 mL to 5 mL total volume.
Storage And Handling
The Kit for the preparation of Lymphoseek (technetium Tc 99m tilmanocept) injection (NDC 65857-42505) includes:
Five vials of Tilmanocept Powder, 250 mcg (NDC 65857-400-01)
- Prescribing information
- Five labels for shields
- Twenty-five labels for product vials and individual syringes
The Kit for the preparation of Lymphoseek (technetium Tc 99m tilmanocept) injection (NDC 65857-45005) includes:
Five vials of Tilmanocept Powder, 250 mcg (NDC 65857-400-01)
Five vials of DILUENT for Lymphoseek (NDC 65857-401-45)
- Prescribing information
- Five labels for shields
- Twenty-five labels for product vials and individual syringes
Store Kit for the preparation of Lymphoseek (technetium Tc 99m tilmanocept) injection in the original packaging at USP controlled room temperature 20°C -25°C (68°F -77°F), excursions permitted to 15°C to 30°C (59°F to 86°F). Store radiolabeled Lymphoseek in radiation shielding at room temperature.
Use radiolabeled Lymphoseek within 6 hours of preparation.
This Kit for the preparation of Lymphoseek (technetium Tc 99m tilmanocept) injection is approved for distribution to persons licensed by the U.S. Nuclear Regulatory Commission to use by product material identified in 10 CFR 35.200 or under an equivalent license issued by an Agreement State.
Distributed by: Cardinal Health 414, LLC Dublin, OH 43017. Revised: Jun 2019
Clinical Trials Experience
Because clinical trials are conducted under widely varying conditions, adverse reaction rates observed in the clinical trials of a drug cannot be directly compared to rates in the clinical trials of another drug and may not reflect the rates observed in practice.
In open label, single arm clinical trials, 553 patients with either breast cancer, melanoma, or squamous cell carcinoma of the oral cavity, skin, and lip received Lymphoseek. No patients experienced serious adverse reactions. Injection site irritation (4 patients; 0.7%) and pain (1 patient; 0.2%) were reported.
No Information provided
Included as part of the PRECAUTIONS section.
Lymphoseek may pose a risk of hypersensitivity reactions due to its chemical similarity to dextran [see DESCRIPTION]. Serious hypersensitivity reactions have been associated with dextran and modified forms of dextran (such as iron dextran drugs).
Before administering Lymphoseek, ask patients about prior hypersensitivity reactions to drugs, especially to dextran and modified forms of dextran. Have resuscitation equipment and trained personnel immediately available at the time of Lymphoseek administration.
Any radiation-emitting product may increase the risk for cancer, especially in pediatric patients. Adhere to the dose recommendations and ensure safe handling to minimize the risk for excessive radiation exposure to either patients or health care workers.
Carcinogenesis, Mutagenesis, Impairment Of Fertility
Studies to assess the carcinogenicity potential of tilmanocept have not been conducted. Tilmanocept was not mutagenic in vitro in the Ames bacterial mutation assay and in the in vitro mouse lymphoma test, and was negative in the in vivo micronucleus test in mice.
Studies on reproductive fertility have not been conducted.
Use In Specific Populations
There are no available data on Lymphoseek use in pregnant women. Additionally, animal reproduction studies have not been conducted with technetium Tc 99m tilmanocept. However, all radiopharmaceuticals, including Lymphoseek, have a potential to cause fetal harm depending on the fetal stage of development and the magnitude of the radiation dose. If considering Lymphoseek administration to a pregnant woman, inform the patient about the potential for adverse pregnancy outcomes based on the radiation dose from the drug and the gestational timing of exposure.
The estimated background risk of major birth defects and miscarriage for the indicated population is unknown. All pregnancies have a background risk of birth defect, loss, or other adverse outcomes. In the U.S. general population, the estimated background risks of major birth defects and miscarriage in clinically recognized pregnancies are 2 to 4% and 15 to 20%, respectively, regardless of drug exposure.
No data are available regarding the presence of technetium Tc 99m tilmanocept in human milk, the effects of the drug on the breastfed child, or the effects of the drug on milk production. Exposure of Lymphoseek to a breastfed infant can be minimized by temporary discontinuation of breastfeeding [see Clinical Considerations]. The developmental and health benefits of breastfeeding should be considered along with the mother's clinical need for Lymphoseek and any potential adverse effects on the breastfed child from Lymphoseek or from the underlying maternal condition.
To decrease radiation exposure to the breastfed infant, advise a lactating woman to pump and discard breast milk after the administration of Lymphoseek for 24 hours, in order to minimize radiation to a breastfed child.
Safety and effectiveness of Lymphoseek in patients less than 18 years of age have not been established.
Of the 553 patients enrolled in clinical studies of breast cancer, melanoma, and squamous cell carcinoma (SCC) of oral cavity, skin, and lip, 179 (32%) were aged 65 or older. Review of the clinical data, including evaluation of the frequency of adverse reactions, has not identified differences in safety or efficacy between elderly patients (65 to 90 years of age) and younger patients (18 to 65 years of age).
Mechanism Of Action
Lymphoseek (technetium Tc 99m tilmanocept) is a radioactive diagnostic agent. It accumulates in lymphatic tissue and selectively binds to mannose binding receptors (CD206) located on the surface of macrophages and dendritic cells. Technetium Tc 99m tilmanocept is a macromolecule consisting of multiple units of diethylenetriaminepentaacetic acid (DTPA) and mannose, each covalently attached to a 10 kDa dextran backbone. The mannose acts as a ligand for the receptor, and the DTPA serves as a chelating agent for labeling with technetium Tc 99m.
In in vitro studies, technetium Tc 99m tilmanocept exhibited binding to human mannose binding receptors with a primary binding site affinity of Kd = 2.76 x 10-11 M.
In clinical studies, technetium Tc 99m tilmanocept has been detectable in lymph nodes within 10 minutes and up to 30 hours after injection.
In dose-ranging clinical studies, injection site clearance rates were similar across all Lymphoseek doses (4 to 200 mcg) with a mean elimination rate constant in the range of 0.222 to 0.396/hr, resulting in a drug half-life at the injection site of 1.8 to 3.1 hours.
The amount of the accumulated radioactive dose in the liver, kidney, and bladder reached a maximum 1 hour post administration of Lymphoseek and was approximately 1% to 2% of the injected dose in each tissue.
Overview Of Clinical Studies
The efficacy and safety of Lymphoseek were assessed in three open-label, multicenter, single arm trials of patients with melanoma, breast cancer, or squamous cell carcinoma (SCC) of the oral cavity, skin, and lip (Studies 1, 2, and 3). Prior to the lymph node mapping and sentinel lymph node biopsy procedures, patients had no known regional nodal or metastatic disease by standard clinical staging criteria.
- In Studies 1 and 2, Lymphoseek was evaluated in patients
with breast cancer and melanoma. Diagnostic efficacy for lymphatic mapping was
determined by the number of histology-confirmed lymph nodes detected by
Lymphoseek and/or the blue dye comparator. Lymphoseek was injected into
patients at least 15 minutes prior to initiating lymphatic mapping procedures,
and preoperative scintigraphic imaging was performed in 91% of patients.
Separately, blue dye was injected shortly prior to initiation of the surgery.
Lymphatic mapping was performed intraoperatively using a handheld gamma
detection probe followed by excision of lymph nodes identified by Lymphoseek,
blue dye, or the surgeon's visual and palpation examination. The resected lymph
nodes were evaluated by histopathology. Lymphoseek localization rate in
pathology-positive lymph nodes was also determined.
- In Study 1, of 179 patients who received Lymphoseek, 94 (53%) had known or suspected breast cancer and 85 (47%) had known or suspected melanoma. The median age was 59 years (range 20 to 90 years) and most (72%) were women.
- In Study 2, of 153 patients who received Lymphoseek, 77 (50%) had known or suspected breast cancer and 76 (50%) had known or suspected melanoma. The median age was 61 years (range 26 to 88 years) and most (68%) were women.
- In Study 3, Lymphoseek was evaluated primarily in patients with SCC of the oral cavity (T1-T4a, N0, M0). Diagnostic efficacy was determined by the patient level false negative rate of sentinel lymph node detection by Lymphoseek as confirmed by pathologic assessment of all lymph nodes removed during planned elective neck dissection (END). Lymphoseek was administered at least 15 minutes prior to the scheduled surgery, and preoperative scintigraphic imaging was performed in all patients. Lymphatic mapping was performed intraoperatively using a handheld gamma counter followed by excision of sentinel lymph nodes identified by Lymphoseek. Additional lymph nodes were removed during the END based upon tumor location and surgical practice. All resected lymph nodes (sentinel and non-sentinel) were evaluated for histopathology at the local site. Lymphoseek-identified nodes determined negative for cancer were further evaluated by a central pathology laboratory using additional step sectioning and cytokeratin staining.
An analysis of the three studies was performed to evaluate the agreement in location of lymph nodes identified by scintigraphic imaging and the handheld gamma counter. At least one scintigraphic “hot spot” was identified in 95% of patients imaged; the percentages were similar across tumor types. Overall, there was 84% agreement on a nodal level (when considering all missing observations as disagreement, as worst case scenario) between the location of preoperative scintigraphic imaging hot spots and the intraoperative lymph node findings (Table 7). Missing observations took the following form: 43 hot spots without corresponding hot nodes and 31 hot nodes without corresponding hot spots.
Table 7: Location Agreement between Scintigraphic
Imaging and Gamma Counter Findings
|Melanoma||Breast Cancer||Head and Neck Cancer||Overall Results|
|Agreement of Hot||182/206;||116/147;||95/115;||393/468;|
|Spot and Hot Node Location *||88% (83%, 93%)**||79% (70%, 88%)**||83% (76%, 90%)**||84% (81%, 87%)**|
|* Denominator equals total
number of hot spots and/or hot nodes. Numerator equals the numbers where hot
spots and hot nodes agreed in location.
** 95% Confidence Intervals.
In Studies 1 and 2 in melanoma and breast cancer, efficacy analyses were based upon comparisons of the number and proportion of resected lymph nodes that contained a lymph node tracer (Lymphoseek and/or blue dye) or neither tracer. Evaluable lymph nodes were resected from 176 Study 1 patients and 152 Study 2 patients who received Lymphoseek at the dose of 0.5 to 2 mCi in 50 mcg administered 15 minutes to 30 hours prior to surgery. Table 8 shows the distribution of resected lymph nodes by the presence or absence of a tracer. Most of the resected lymph nodes were identified by either Lymphoseek (LS) or blue dye (BD) or both. Significantly more resected lymph nodes were identified by Lymphoseek in comparison to blue dye.
Table 8: Resected Lymph Nodes and Content of
Lymphoseek (LS) and/or Blue Dye (BD) from Studies in Breast Cancer and Melanoma
|Study||Tumor||Nodes n||BD Present % (95% CI)||LS Present % (95% CI)||Only BD Present % (95% CI)||Only LS Present % (95% CI)||Neither BD nor LS Present % (95% CI)|
|One||Melanoma||187||65% (57% , 72%)||93% (88% , 96%)||2% (0 , 5%)||29% (23% , 37%)||6% (3% , 10%)|
|Breast Cancer||192||70% (63% , 77%)||89% (83% , 93%)||7% (4% , 12%)||26% (20% , 32%)||4% (2 , 8%)|
|Two||Melanoma||198||59% (51% , 66%)||99% (97% , 100%)||0 (0 , 2%)||41% (34% , 48%)||1% (0 , 3%)|
|Breast Cancer||181||62% (55% , 70%)||100% (98% , 100%)||0 (0 , 2%)||38% (30% , 45%)||0 (0 , 2%)|
|The percentages may not add to
100% due to rounding.
95% Confidence Intervals (CI) are based on Exact Binomial and represent the spread in the individual estimates.
In Studies 1 and 2 lymphatic mapping was performed in 328 patients with melanoma or breast cancer. The overall rate of lymph node detection by Lymphoseek at the patient level was 97% (319/328). The average number of lymph nodes detected by Lymphoseek was approximately 2 per patient.
In Study 3 lymphatic mapping was performed in 83 patients with SCC of the oral cavity. The rate of lymph node detection by Lymphoseek at the patient level was 98% (81/83) with a 95% confidence interval of 92% to 100%. The average number of lymph nodes identified was 4 per patient.
Guiding Sentinel Lymph Node Biopsy
In Study 3 in patients with SCC of the oral cavity (n=79), skin (n=5), and lip (n=1), pathology findings for Lymphoseek-identified nodes (sentinel lymph nodes) were compared to the pathology findings of all other lymph nodes removed during the scheduled elective node dissection to determine the false negative rate of Lymphoseek. Thirty-nine patients were determined to have pathology-positive regional lymph nodes. In these patients, the Lymphoseek false negative rate for detecting patients with cancer-positive nodes was 2.6% (95% CI: 0.06% to 13.5%). In this study the pathology-positive nodes were all found in patients with SCC of the oral cavity.
Supportive analyses were conducted in Studies 1 and 2 in patients with breast cancer or melanoma. The presence or absence of Lymphoseek in nodes resected from patients determined by pathology staging to have lymphatic spread of cancer (n=64) was evaluated. The overall patient level rate for identifying at least one cancer-positive node in these pathology-positive patients (both cancers combined) was 97%. Lymphoseek identified 27 out of 29 node positive breast cancer patients and all of the 35 node positive melanoma patients.
Advise patients to seek medical attention for reactions following injection of Lymphoseek such as difficulty breathing, skin rash, or other allergy manifestations.
Inform nursing women to pump and discard breast milk for at least 24 hours following administration of Lymphoseek injection [see Use In Specific Populations].
Report Problems to the Food and Drug Administration
You are encouraged to report negative side effects of prescription drugs to the FDA. Visit the FDA MedWatch website or call 1-800-FDA-1088.
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