Abstract
Osteosarcoma patients with overt metastases at primary diagnosis have a 5-year survival rate of less than 20%. TP-3 is a murine IgG2b monoclonal antibody with high affinity for an epitope residing on the p80 osteosarcoma cell surface membrane antigen. The tumor-associated antigen p80 is overexpressed in osteosarcomas, and has very low normal tissue expression. We propose a novel dual alpha targeting solution containing two radionuclides from the same decay chain, including the bone-seeking 224Ra, and cancer cell-surface seeking 212Pb-TCMC-TP-3 for the treatment of osteoblastic bone cancers, circulating cancer cells and micrometastases. In this in vitro study, the cytotoxic effects of 212Pb-TCMC-TP-3 (single alpha solution) and 224Ra/212Pb-TCMC-TP-3 (dual alpha solution) were investigated in a multicellular spheroid model mimicking micrometastatic disease in osteosarcoma. OHS spheroids with diameters of 253 ± 98 μm treated with 4.5, 2.7, and 3.3 kBq/ml of 212Pb-TCMC-TP-3 for 1, 4, and 24 h, respectively, were disintegrated within 3 weeks. The 212Pb-TCMC-TP-3 induced a 7-fold delay in spheroid doubling time compared to a 28-times higher dose with the non-specific 212Pb-TCMC-rituximab. The 224Ra/212Pb-TCMC-TP-3 completely disintegrated spheroids with diameters of 218–476 μm within 3 and 2 weeks after 4 and 24 h incubation with 5 kBq/ml, respectively. Treatment with 1 kBq/ml of 224Ra/212Pb-TCMC-TP-3 for 24 h caused an 11.4-fold reduction in spheroid viability compared with unconjugated 224Ra/212Pb. The single and dual alpha solutions with TP-3 showed cytotoxicity in spheroids of clinically relevant size, which warrant further testing of the dual alpha solution using in vivo osteosarcoma models.
Introduction
Osteosarcoma (OS) is the second most common bone cancer after chondrosarcoma, and the most common bone malignancy in adolescents and young adults (, ). The 5-year survival rate is <20% for patients with metastatic OS at primary diagnosis, and the median survival after multiple recurrences is only 1 year (–). Few new treatment options have been developed for metastatic OS during the past three decades, underscoring the need for novel therapies.
Immunotherapy using monoclonal antibodies (mAbs) specific for overexpressed cancer-related antigens is a promising treatment strategy for micrometastases and circulating tumor cells (–). Clinical trials have evaluated the efficacy of mAbs in OS, including trastuzumab targeting the human epidermal growth factor receptor 2 (HER2) (), glembatumumab targeting glycoprotein nonmetastatic B (), cixutumumab targeting insulin-like growth factor 1 (, ), and pembrolizumab, nivolumab and camrelizumab targeting PD-1 (–). Unfortunately, sufficient antitumor response was not demonstrated for OS patients receiving these immune-based therapies, possibly due to low expression of the tumor antigens and internal resistance mechanisms (, ). The murine IgG2b TP-3 mAb binds to an 80 kDa sarcoma-associated cell surface membrane antigen (p80) on an alkaline phosphatase isoform (, ). TP-3 is directly related to osteoblastic differentiation and has previously shown to bind to the vast majority of OS metastases in patients (, ). Moreover, an immunomagnetic isolation procedure using the TP-3 mAb detected single OS cells in bone marrow aspirates from OS patients that was shown to have prognostic information (, ). Because of the nonreactive activity of TP-3 on healthy human tissues, it is well suited for targeted therapy (, ).
Osteosarcoma is clinically regarded as a radioresistant cancer, and external beam radiotherapy is usually not effective for OS (–). Unfortunately, the mechanisms of action related to the radioresistance are not well investigated and remain unresolved (). Targeted therapies using mAbs labeled with the beta emitting 188Re or 177Lu, and the alpha emitting 211At or 213Bi have been studied for OS in vitro and in vivo (–). However, beta particles have low linear energy transfer (LET, ∼ 0.2 keV/μm), making them less effective for treating radioresistant tumor cells (). In contrast, alpha particles have a high LET (∼ 100 keV/μm) and short range in tissue (50–100 μm) compared to beta particles (0.5–12 mm), resulting in high cytotoxic potency via DNA double stranded breaks (). Therefore, alpha particles should be preferred over beta particles to overcome radiation resistance in OS.
The alpha emitting 223Ra (t1/2 ≈ 11.4 d) is a calcium-mimetic radiopharmaceutical with naturally bone-seeking properties (, ). Its accumulation in osteoblastic lesions resulted in improved overall survival and approval for the treatment of castration-resistant prostate cancer patients with symptomatic bone metastases (). Thus, 223Ra can also be efficient for OS patients due to the osteoblastic phenotype of this cancer (–). In 2021, a phase I escalation trial with 50, 75, and 100 kBq/kg of 223Ra was completed in 18 OS patients with progressive, locally recurrent or metastatic disease (). The radiopharmaceutical was well tolerated and a recommended phase II dose was set to 100 kBq/kg — a twice as high dose as approved for prostate cancer, due to the high radiation tolerance (). Unfortunately, the majority of patients developed extra-skeletal metastases (). Since 223Ra cannot be stably chelated to a targeting moiety, it must be combined with other agents that can target extra-skeletal disease in these patient groups ().
Similar to 223Ra, 224Ra (t1/2 ≈ 3.6 d) has the same bone-seeking properties, four alpha emissions in the decay chain and a relevant half-life for radiopharmaceutical production and shipment (). An important difference is that 224Ra decays into 212Pb (t1/2 ≈ 10.6 h), which, compared to 211Pb (t1/2 ≈ 36.1 min) in the 223Ra-series, has a convenient half-life for conjugation to targeting molecules (–). Lead-212 is itself a beta emitter, but serves as an in vivo generator of alpha particles via its decay to 212Bi (t1/2 ≈ 60.6 min) and 212Po (t1/2 ≈ 0.3 μs). With the bifunctional 1,4,7,10-tetraaza-1,4,7,10-tetra(2-carbamoylmethyl)cyclododecane (TCMC) chelator for 212Pb, several radioconjugates have been produced and tested in preclinical and clinical studies (–). The dual alpha technology utilizes the osteoblastic stroma-seeking properties of 224Ra that can treat primary bone cancer or bone metastases, while extra-skeletal and skeletal metastases can be targeted by a cancer specific moiety labeled with 212Pb (). In a preclinical prostate cancer study employing this technology, the biodistribution data showed high uptake of 224Ra in the femur and skull while a 212Pb-conjugate had high prostate tumor uptake (). The technology also showed promising potential in a breast cancer study, where the 224Ra solution with bone targeting 212Pb-EDTMP [ethylenediamine tetra (methylenephosphonic acid)] prolonged survival and lowered the incidence of bone metastases in mice ().
Representative in vitro models are essential to mimic tumor micrometastases. Three-dimensional (3D) multicellular spheroids have been utilized in preclinical cancer therapy studies since they exhibit physiologically relevant cell–cell and cell–matrix interactions, heterogeneity and structural complexity which better reflect cancer metastases that are found in patients (–). The cell–cell interactions allow contribution by the bystander and cross-fire effects to the cytotoxicity of targeted radionuclide therapy to be considered. Spheroids have a necrotic core surrounded by a viable rim of proliferating cells (), where steep gradients can exist for cellular oxygen levels, proliferation, pH and glucose concentration (, ), leading to development of cell subpopulations that may be resistant to treatment, similar to tumor cells in vivo (). Therefore, spheroids are advantageous in vitro models because overcoming these factors could not be considered in 2D monolayer models (, ).
In this work, the cytotoxic effect of a single alpha solution comprising 212Pb conjugated to the OS cell targeting mAb TP-3 and a dual alpha solution containing 224Ra in equilibrium with 212Pb-TCMC-TP-3 were evaluated using an in vitro 3D multicellular spheroid model.
Materials and methods
Cell line
The human OS cell line OHS (established at the Norwegian Radium Hospital) was used in this study (). The OHS cell line used in the present study was obtained from a repository at the Norwegian Radium Hospital, Oslo University Hospital. The cell line was cultured in RPMI 1640 medium (Sigma-Aldrich Norway AS, Oslo) supplemented with 10% heat inactivated fetal bovine serum (FBS, GE Healthcare Life Sciences, Chicago, IL), 100 units/ml penicillin and 100 μg/ml streptomycin (Sigma-Aldrich) at 37°C with 5% CO2.
Antibodies
The anti-p80 IgG2b murine mAb TP-3 was produced and purified as described by Bruland et al. (). TP-3 (PAK-732 batch), was used in all experiments (, ). The chimeric anti-CD20 IgG1 mAb rituximab (RTX, MabThera, Roche, Basel) and the humanized anti-HER2 IgG1 mAb trastuzumab (TRA, Herceptin, Roche) were used as antigen negative controls.
Flow cytometry
The expression of p80 on OHS cells was verified by flow cytometry using TP-3. The primary mAbs (TP-3 or RTX) were added to 5 × 105 OHS cells in 100 μl flow buffer [Dulbecco’s PBS with 0.5% bovine serum albumin (BSA) and 0.1% NaN3] at a concentration of 10 μg/ml and incubated at 4°C with gentle shaking for 60 min, followed by three washes with 2 ml flow buffer. FITC-conjugated anti-mouse IgG F(ab’)2 fragment (Thermo Fisher Scientific, Waltham, MA) was used as a secondary Ab and added at a concentration of 10 μg/ml, incubated at 4°C with gentle shaking for 30 min in the dark and washed as in the previous step. All wash steps were performed by centrifugation at 260 × g for 5 min. Washed cell pellets were resuspended in 200 μl flow buffer and analyzed by a Cytoflex S flow cytometer (Beckman Coulter, Inc., Brea, CA) using the CytExpert 2.0 software (Beckman Coulter, Inc.) for data acquisition. The FlowJo software (FlowJo, LLC, Ashland, OR) was used for data analysis.
Preparation of radionuclides and activity measurements
Radium-224 was extracted from a generator column containing DIPEX® actinidine resin (Eichrom Technologies, Lisle, IL) with immobilized 228Th (Eckert & Ziegler, Braunschweig) by elution with 1 M HCl. The details of the 224Ra generator setup have previously been described by Westrøm et al. and Stenberg et al. (, ). Lead-212 was produced and extracted from a 228Th generator, via emanation of 220Rn in a simplified single-chamber generator system, described by Li et al. (). Lead-212 was extracted from the flask using 0.1 M HCl, with a 228Th breakthrough ≤0.005%. The collector flask was replaced 2–3 days prior to the experiments to prevent accumulation of 208Pb. A Capintec CRC-25R radioisotope dose calibrator (Capintec Inc., Ramsey, NJ) was used to quantify the 224Ra and 212Pb activities ().
A Hidex automatic gamma counter (Hidex Oy, Turku) or Cobra gamma counter (Packard Instrument Company, Downer Grove, IL) with the 50–120 keV counting window was used to determine 212Pb activities. The counting window mainly measures 212Pb activity (34.9% relative to the 224Ra mother nuclide) with only small contribution from other radionuclides (1.2% relative to 224Ra) in the 224Ra series (, , , ). All samples were measured at least 2 h after 212Pb extraction to ensure transient equilibrium with daughters. The activity of 224Ra was determined by measurements performed 4–5 days after the experiment, when 212Pb had decayed and equilibrium between 224Ra and the newly formed 212Pb was reached.
Radiolabeling of antibodies
The mAbs were conjugated to a TCMC chelator (Macrocyclics Inc., Dallas, TX), to allow radiolabeling with 212Pb. The original buffer of the mAbs was first exchanged with carbonate buffer (0.1 M NaHCO3 and 5 mM Na2CO3 in metal free water) by washing the mAb solution through a centrifugal concentrator (30 kDa, Amicon Ultra-15 Centrifugal Filter Unit, Millipore, Sigma-Aldrich) three times at 1620 × g for 15–25 min. A TCMC solution in 5 mM HCl was added to the Abs in a 5:1 molar ratio, and the mixture were allowed to react for 2 h with gentle shaking (250 min–1) at room temperature. Then, unconjugated TCMC was removed from TCMC-mAb conjugates by exchanging the carbonate buffer to 0.9% NaCl by washing the mAb solution through the centrifugal concentrator as described above. The concentration of the mAbs was quantified by Nanodrop (Nanodrop 1000 Spectrophotometer, V3.8, Thermo Fisher Scientific), using the standard absorbance value of IgG at 280 nm and 10 mm path length.
The mAbs were labeled with 212Pb using 224Ra or 212Pb solutions (pH adjusted to 5–6 by 0.5 M C2H7NO2 or C2H3NaO2) in equilibrium with daughters. TCMC-TP-3, TCMC-RTX, or TCMC-TRA was added to a final concentration of 0.1–1 mg/ml. The solutions were mixed on a Thermomixer (Eppendorf, Hamburg) for 45 min at 37°C and 450–750 rpm. Radiochemical purity of the samples was determined by instant thin layer chromatography (Tec-control, Biodex, Medical Systems, Shirley, NY), and only products with purities ≥95% were used in the experiments. The final solution consisting of 212Pb-TCMC-mAb is referred to as the “single alpha solution” while 212Pb-labeled mAbs in the presence of 224Ra is called the “dual alpha solution.”
Saturation binding studies
OHS cells were detached from a cell culture flask using TrypLE Express (Sigma-Aldrich). Saturation binding studies of 212Pb-TCMC-TP-3 to OHS cells were performed by collecting 106 of the cells and incubating them as cell suspension in 0.2 ml of PBS including 0.5% BSA (Sigma-Aldrich) with 6 different concentrations (0.03–10 μg/ml) of the radioimmunoconjugate (in duplicates) for 1 h at 37°C and 150 min–1. Non-specific binding was measured by pre-incubating cells with unlabeled TP-3 (5–20 μg/ml) for 15 min before addition of 212Pb-TCMC-TP-3. Activities were measured in a gamma counter before (added activity) and after incubated cells were washed 3 times with PBS containing 0.5% BSA (cell bound activity). Specific cell bound activity was estimated as percentage of added activity minus non-specific binding (activity on blocked cells). The number of specifically bound ligands per cell was plotted against ligand concentration and the equilibrium dissociation constant (KD) and the number of specific binding sites (Bmax), were determined by nonlinear regression (Sigmaplot version 14.5, Systat Software, Inc., San Jose, CA, USA).
Spheroid formation and treatment
Multicellular tumor spheroids were generated using the liquid-overlay technique (, ). Spheroids were formed by seeding 500 OHS cells in 100 μl of culture medium per well in a 96-well flat-bottom plate coated with 50 μl of 1.5% agarose (weight/volume, Sigma-Aldrich) solution in PBS (Sigma Aldrich). The plates were centrifuged at 470–1000 × g for 15 min, and maintained at 37°C with 5% CO2.
For the single alpha solution studies, spheroids were treated 4–5 days after formation (day 0) with 0.3–100 kBq/ml of 212Pb-TCMC-TP-3 (specific activities of 7.3–15.4 MBq/mg) or 212Pb-TCMC-RTX (specific activities of 7.5–9.9 MBq/mg). For the dual alpha solution studies, 0.3–10 kBq/ml of 224Ra/212Pb, 224Ra/212Pb-TCMC-TP-3 (specific activities of 2.3–9 MBq/mg), or 224Ra/212Pb-TCMC-RTX/TRA (specific activities of 3.7–9 MBq/mg) were added 3 or 14 days after spheroids were formed. One experiment with TP-3 alone (0.25 μg per spheroid 2.1 μg/ml) was performed in OHS spheroids to investigate the cytotoxicity of the mAb itself. The spheroids were incubated with the mAb alone or with radioconjugates at 37°C for 1, 4, or 24 h before they were carefully washed 6 times with medium and further incubated for 3 weeks. Replacement of culture medium was performed 2–3 times per week. The spheroid diameter (d) was measured weekly using an inverted Axiovert 200M microscope (Carl Zeiss AG, Jena, Germany). Volumes of each spheroid were calculated using the formula, where r = d/2. The spheroid volumes were normalized by dividing the volumes at different activities by the volume at 0 kBq/ml at each time point (activity vs. normalized volume), and by dividing the volumes of the treated spheroids at each week by the volume of spheroids at day 0 for each activity concentration (time vs. normalized volume).
A CellTiter-Glo®3D cell viability assay (Promega Corporation, Madison, WI, USA), was performed 48 h, 72 h and 12 days after spheroids were administered with 224Ra/212Pb, 224Ra/212Pb-TCMC-TP-3 and 224Ra/212Pb-TCMC-TRA for 24 h according to the manufacture’s protocol.
Live and dead cells in the spheroids were determined by a fluorescence-based staining assay using fluorescein diacetate (FDA, 5 mg/ml, Sigma-Aldrich) and propidium iodide (PI, 2 mg/ml, Sigma-Aldrich), respectively. Fluorescent images of spheroids were taken by an inverted Axiovert 200M microscope (Carl Zeiss AG) and analyzed with the AxioVision Rel. 4.8 software (Carl Zeiss AG). The experiment was performed with 3–12 spheroids per treatment condition. The relative viability was calculated by dividing the viability of the treated spheroid by the viability of the control spheroid (0 kBq/ml) at different activity concentrations.
Complete growth inhibition of a spheroid was considered when no live cells were detected in the spheroid, or when the spheroid diameter was reduced or remained unchanged, or when the spheroid was disintegrated/fell apart.
Statistical analyses
SigmaPlot 14.5 (Systat Software) was used for the statistical analyses. Nonlinear regression with one-site saturation ligand binding was used to estimate the number of specific binding sites (Bmax) and the equilibrium dissociation constant (KD) for 212Pb-TCMC-TP-3 on the OHS cells:
where B is the number of antigens per cell and [Ab] is the Ab concentration. Exponential decay fitting was used to plot the correlation between the radioactivity and spheroid volume.
The spheroid volumes and viabilities were analyzed for significance using a one-way ANOVA with multiple comparisons and a pairwise t-test, respectively, using SigmaPlot 14.5 (Systat Software). A p-value of < 0.05 was considered statistically significant.
Results
Binding of TP-3
A high expression of p80 was confirmed by a well-defined histogram shape of TP-3, which demonstrated binding to 99.7% of the OHS cells with no overlap and clear separation from the histograms representing the control samples (Figure 1A). Negligible non-specific binding was detected (< 0.06%) as the histogram of RTX was identical as the unstained cells and the secondary Ab control.
FIGURE 1
The OHS cells showed an average of 2.7 ± 0.3 × 105 binding sites per cell (Bmax). The 212Pb-TCMC-TP-3 demonstrated increased binding to OHS cells at 0.03–1 μg/ml after 1 h with a KD of 0.49 ± 0.05 μg/ml (Figure 1B). Similar levels of 212Pb-TCMC-TP-3 were bound to the OHS cells at 4 h (Supplementary Figure 1). From 1 to 10 μg/ml, the percentage of specific bound 212Pb-TCMC-TP-3 was reduced due to saturated binding sites (Figure 1C). Of total added radioimmunoconjugate, 5.7–12.2% was internalized to the cells after 1 h (Supplementary Figure 1).
Cytotoxicity of the 212Pb-TCMC-TP-3 single alpha solution
The spheroids had a diameter of 253 ± 98 μm and a volume of 8.5 ± 0.5 × 106 μm3 at day 0 (treatment day). The majority of OHS cells in these spheroids were viable at this time point (Supplementary Figure 6). The volume of spheroids decreased with increasing 212Pb-TCMC-TP-3 activity (Figure 2A and Supplementary Figure 2). At 3 weeks, 1 and 4 h incubation with 2.7–9 kBq/ml of 212Pb-TCMC-TP-3 significantly inhibited the spheroid growth and reduced the number of live cells compared to the control (p < 0.005, Figures 2B,C, Supplementary Figures 3, 4, and Supplementary Table 3). The doubling time was 7-fold longer for the spheroids treated with 2.7 kBq/ml of 212Pb-TCMC-TP-3 for 4 h compared to the control, while 6.3-fold longer than for the spheroids treated with 75 kBq/ml of 212Pb-TCMC-RTX (Supplementary Table 1). After 3 weeks, no live cells or spheroid growth were detected in the spheroids treated with ≥ 2.7 kBq/ml of 212Pb-TCMC-TP-3 for 4 and 24 h (Figure 2C and Supplementary Figures 4, 5). The non-specific 212Pb-TCMC-RTX was only able to completely inhibit spheroid growth after 3 weeks when treated with the high activity dose of 72.8 kBq/ml for 24 h (Supplementary Figure 5).
FIGURE 2
Cytotoxicity of the 224Ra/212Pb-TCMC-TP-3 dual alpha solution
The cytotoxicity of the dual alpha solutions was investigated in small (diameter of 222 ± 14.0 μm and volume of 5.8 ± 1.0 × 106 μm3 at day 0) and large (diameter of 474 ± 2 μm and volume of 60 ± 5.0 × 106 μm3 at day 0) spheroids. The majority of OHS cells in the small spheroids were viable, while the large spheroids developed central necrosis with a 20–30 μm rim of viable cells (Supplementary Figure 6). All spheroid volumes were reduced at increasing activities, and the growth of spheroids treated for 4 or 24 h with ≥ 5 kBq/ml of 224Ra/212Pb-TCMC-TP-3 was completely inhibited (Figure 3 and Supplementary Figure 7).
FIGURE 3
Over time, the volume of spheroids treated with 1 kBq/ml of 224Ra/212Pb or 224Ra/212Pb-TCMC-RTX for 4 h increased, whereas this activity concentration of 224Ra/212Pb-TCMC-TP3 inhibited spheroid growth (Supplementary Figure 7). The doubling time of spheroids treated with 10 kBq/ml of 224Ra/212Pb-TCMC-TP-3 for 1 h was 101 days, while it was 15 and 22 days for spheroids treated with 224Ra/212Pb and 224Ra/212Pb-TCMC-RTX, respectively (Supplementary Table 2).
A viability assay was performed for spheroids treated with the dual alpha solutions for 24 h. At 72 h, a significant reduction in viability was seen in the spheroids treated with 5 kBq/ml of 224Ra/212Pb-TCMC-TP-3 versus 224Ra/212Pb or 224Ra/212Pb-TCMC-TRA (p < 0.05, Supplementary Table 4). Twelve days after treatment, the relative viabilities of the spheroids treated with 1 kBq/ml of the 224Ra/212Pb-TCMC-TP-3,224Ra/212Pb and 224Ra/212Pb-TCMC-TRA dual alpha solutions were 11.6 ± 2.7, 56.2 ± 6.6 and 47.2 ± 6, respectively (Figure 4A).
FIGURE 4
Complete disintegration was observed for all spheroids incubated for 24 h with 10 kBq/ml of any dual alpha solution. However, only spheroids treated with the 224Ra/212Pb-TCMC-TP-3 dual alpha solution were disintegrated 12 days after incubation with 5 kBq/ml (Figure 4B), while the relative viability of spheroids treated with 224Ra/212Pb and 224Ra/212Pb-TCMC-TRA were 8.0 ± 3.4 and 7.4 ± 2.4 at this time point, respectively.
Discussion
The treatment options for advanced OS after standard regimen are limited due to chemotherapeutic resistance (–). Micrometastases are found in the majority of patients with advanced and/or recurrent OS (, ). Patients with micrometastases in the bone marrow or peripheral blood, also from other forms of cancer than OS, have shown statistically poorer survival compared to patients without micrometastases (, , –). The size of spheroids used in the present study was chosen based on a previous study by Däster et al. (). In agreement with the study, the small spheroids herein consisted almost entirely of viable cells, while the large spheroids had a necrotic core surrounded by a rim of viable cells (Supplementary Figure 6). The single and dual alpha solutions containing TP-3 were able to disintegrate spheroids with diameters ranging from 210 to 480 μm, which is similar to the diameter of micrometastatic clusters found in patients (250–750 μm) (, , ). As already mentioned, TP-3 has previously shown the ability to detect single micrometastatic cells in bone marrow aspirates from OS patients, in which a strong correlation was detected between the TP-3 bound OS cells and poor therapeutic response following relapse (, ). In the present study, the TP-3 mAb itself did not initiate any cytotoxicity on OHS multicellular spheroids, which is in agreement with a previous study ().
In contrast, the cytotoxic effect was significantly improved when spheroids were treated with ≥ 2.7 kBq/ml of the 212Pb-TCMC-TP-3 radioimmunoconjugate (p < 0.005, Figure 2 and Supplementary Table 3). The therapeutic efficacy of 211At-TP-3 was extensively explored three decades ago and showed promising potential for OS in vitro and in vivo, similar to a more recent study evaluating a 213Bi radioimmunoconjugate (–, , ). Unfortunately, challenges related to the production of 211At and the very short half-life of 213Bi limits the applicability of these radionuclides in targeted therapy. TP-3 immunotoxins have previously showed to be effective in clonogenic OS cells in vitro, and in a subcutaneous as well as in a soft-tissue sarcoma model in vivo (–). SCID mice xenografted with OHS cells were treated with 1.0 mg/kg of a TP-3 immunotoxin and 67 ± 19% of the mice were tumor-free at 150 days, compared to the control mice which had a median survival of 19 days (). Despite these encouraging data, immunogenicity and nonspecific toxicity is known to limit the clinical success of immunotoxins (). Nevertheless, TP-3 seems highly promising for targeted therapies because of the high expression levels of p80 on the OS cell surface and the limited normal-tissue distribution (, ).
An important advantage with the 3D spheroid model is the possibility to observe the treatment response over an extended period, and thereby observe the repopulation potential of surviving cells. After 1 week, the volume of spheroids treated with 2.7 kBq/ml of 212Pb-TCMC-TP-3 for 1 h looked similar as spheroids treated with 4.5 and 9 kBq/ml (Figure 2B). Yet, regrowth of the spheroids was seen from week 2. After 4 h incubation with 2.7 kBq/ml of the 212Pb-TCMC-TP-3 single alpha solution, spheroids were disintegrated and no viable cells were observed at week 3 (Figure 2). This cytotoxic effect is similar to a study investigating comparable activities of 212Pb in 3D prostate cancer spheroids (). A study by Ballangrud et al. investigated the therapeutic effect of a 213Bi labeled mAb in multicellular prostate cancer spheroids with a diameter of 200 μm, and showed that the penetration time of the radioimmunoconjugate was around 3 h (). This supports the results observed herein, where a substantial increased cytotoxic effect was seen in spheroids (diameter of 253 ± 98 μm) treated with 2.7 kBq/ml of 212Pb-TCMC-TP-3 when the treatment duration increased from 1 to 4 h (Figure 2). These results are also in agreement with Hjelstuen et al. who demonstrated that 6 h was required for the 125I labeled mAb to reach the inner center of an OHS spheroid with a diameter of 400–450 μm (). Nevertheless, because of the short half-life of 213Bi (t1/2 ≈ 46 min), 76% of the decay in Ballangrud’s study had already occurred by the time that the radioimmunoconjugate reached the inner core of the spheroid (). This highlights the benefit of labeling a targeting molecule with 212Pb, as it has a long enough half-life for the majority of the deposited energy from the total decay to be emitted within the spheroid. However, it is important to mention that the OS tumor microenvironment is highly complex and the penetration time will also depend on other factors such as density and vascularity enabling diffusion of the targeting complex ().
The growth inhibition of spheroids observed 3 weeks after 4 h treatment with 2.7–4.5 kBq/ml of the 212Pb-TCMC-TP-3 single alpha solution (Figure 2 and Supplementary Figure 4) and 5 kBq/ml of the 224Ra/212Pb-TCMC-TP-3 dual alpha solution (Figure 3 and Supplementary Table 2) corresponds to 13.5–22.5 MBq of 212Pb and 25 MBq of 224Ra per patient (∼ 5 L blood). Subbiah et al. recommended an activity of 100 kBq/kg of 223RaCl2 for the phase II study in OS patients (). Assuming similar clinical dosing of 224Ra as for 223Ra (taken the different half-lives into account), this would translate into a clinically relevant dosage of 315 kBq/kg of 224Ra. In equilibrium with daughters, the 212Pb-immunoconjugate in the dual alpha solution would then be given in a dosage of approximately 24 MBq per patient (∼ 70 kg). This falls within the activity range of the 212Pb-TCMC-TRA radioimmunoconjugate (13–47 MBq) that was evaluated as safe for patients with HER2 overexpressing intraperitoneal cancer (). This suggests that 224Ra/212Pb-TCMC-TP-3 induces cytotoxic effects at clinically relevant activity doses, although activity conversions from mouse to human also may be based on body surface area and not only on radioactivity per gram of bodyweight or blood ().
Limitations of this study include the use of non-osteoblastic OHS spheroids, leading to an insignificant improvement in cytotoxicity from the naturally bone-seeking 224Ra itself. Therefore, the dual alpha solution with TP-3 required similar activities to disintegrate spheroids as the single alpha solution, meaning that the antitumor effect of the multicellular spheroids was likely linked to the delivery of the radiation emitted from the specifically bound 212Pb-TCMC-TP-3. Preincubation of OS cells in a calcifying medium can force the cells into an osteoblastic-like state, which will enhance the similarity of a true OS microenvironment such as observed in patients, and thereby potentially initiate an effect of 224Ra (). This should be evaluated in future studies using multicellular spheroid models of OS. Furthermore, following the protocol of Jacques et al., establishing a murine model with bone sarcoma would be the next step to fully explore the potential of the dual alpha in vivo (). Nonetheless, previous dual alpha studies have verified that 224Ra accumulates in bone (, ). In fact, in a preclinical breast cancer study, a 224RaCl2 solution with the 212Pb-daughter chelated to the bone-seeking EDTMP demonstrated similar therapeutic effect as a comparable in vivo study with 223RaCl2, but with significantly fewer radium atoms (, , ). A 224Ra solution without a chelating agent for the lead-daughter, such as for the approved 223RaCl2, will also have bone-seeking properties, but since 212Pb have a half-life that allows trans-organ redistribution if let free in physiological liquids like blood, saliva or lymphatic liquid, the toxicity impact from 212Pb is important to consider and will be minimized by the conjugation to TP-3 or EDTMP. An experimental limitation in this study includes adding activities from the single and dual alpha solutions to spheroids of different size. Ideally, the single and dual alpha experiments should be performed simultaneously with similar spheroid size at day 0. This should be considered in future studies.
Conclusion
This study demonstrated high cytotoxicity at clinically relevant activities of the single and dual alpha solutions in spheroids mimicking micrometastatic OS disease. These results warrant further exploration in preclinical models to evaluate the therapeutic efficacy and cytotoxicity of the 224Ra/212Pb-TCMC-TP-3 dual alpha solution in an osteoblastic OS environment.
Statements
Data availability statement
The original contributions presented in this study are included in the article/Supplementary material, further inquiries can be directed to the corresponding author.
Author contributions
AJKT, AJ, ØSB, and RHL: conceptualization. AJKT, AJ, VYS, ØSB, and RHL: designing the work. AJKT and AJ: in vitro experiments. AJKT, AJ, and VYS: analyzing the data. AJ, AJKT, VYS, ØSB, M-ER, and RHL: interpretation of results and drafting the manuscript and revising it critically for important intellectual content. All authors read and agreed to the published version of the manuscript.
Funding
The research was funded by the Norwegian Research Council (Industrial Ph.D. project numbers: 260639 and 329538, Oslo, Norway) and the South-Eastern Norway Regional Health Authority (project number: 2020028, Oslo, Norway).
Acknowledgments
We thank Li-Wei Ma at the Department of Radiation Biology, The Norwegian Radiation Hospital, Oslo, Norway for the contribution with the spheroids experiments and Petras Juzenas at the Department of Pathology, and The Norwegian Radiation Hospital, Oslo, Norway for contribution with the flow cytometry experiment and analysis.
Conflict of interest
Authors ØSB and RHL hold ownership interest in ArtBio AS. The remaining authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Publisher’s note
All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.
Supplementary material
The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fmed.2022.1058863/full#supplementary-material
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Summary
Keywords
targeted alpha therapy, osteosarcoma, dual alpha therapy, radium-224, lead-212, TP-3 antibody
Citation
Tornes AJK, Stenberg VY, Larsen RH, Bruland ØS, Revheim M-E and Juzeniene A (2022) Targeted alpha therapy with the 224Ra/212Pb-TCMC-TP-3 dual alpha solution in a multicellular tumor spheroid model of osteosarcoma. Front. Med. 9:1058863. doi: 10.3389/fmed.2022.1058863
Received
30 September 2022
Accepted
04 November 2022
Published
23 November 2022
Volume
9 - 2022
Edited by
Antonio Paulo, Universidade de Lisboa, Portugal
Reviewed by
Alice D’Onofrio, Universidade de Lisboa, Portugal; Yongkang Gai, Huazhong University of Science and Technology, China; Julie Bolcaen, iThemba Laboratory, South Africa
Updates
Copyright
© 2022 Tornes, Stenberg, Larsen, Bruland, Revheim and Juzeniene.
This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Anna Julie Kjøl Tornes, anna.julie.kjol.tornes@rr-research.no
This article was submitted to Nuclear Medicine, a section of the journal Frontiers in Medicine
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