- Original research
- Open Access
Experimental α-particle radioimmunotherapy of breast cancer using 227Th-labeled p-benzyl-DOTA-trastuzumab
EJNMMI Research volume 1, Article number: 18 (2011)
The aim of the present study was to explore the biodistribution, normal tissue toxicity, and therapeutic efficacy of the internalizing low-dose rate alpha-particle-emitting radioimmunoconjugate 227Th-trastuzumab in mice with HER2-expressing breast cancer xenografts.
Biodistribution of 227Th-trastuzumab and 227Th-rituximab in nude mice bearing SKBR-3 xenografts were determined at different time points after injection. Tumor growth was measured after administration of 227Th-trastuzumab, 227Th-rituximab, cold trastuzumab, and saline. The toxicity of 227Th-trastuzumab was evaluated by measurements of body weight, blood cell, and clinical chemistry parameters, as well as histological examination of tissue specimens.
The tumor uptake reached peak levels of 34% ID/g (4.6 kBq/g) 3 days after injection of 400 kBq/kg of 227Th-trastuzumab. The absorbed radiation dose to tumor was 2.9 Gy, while it was 2.4 Gy to femur due to uptake of the daughter nuclide 223Ra in bone; the latter already explored in clinical phases I and II trials without serious toxicity. A significant dose-dependent antitumor effect was observed for dosages of 200, 400, and 600 kBq/kg of 227Th-trastuzumab but no effect of 400 and 600 kBq/kg 227Th-rituximab (non-tumor binding). No serious delayed bone marrow or normal organ toxicity was observed, but there was a statistical significant reduction in blood cell parameters for the highest-dose group of 227Th-trastuzumab treatment.
Internalizing 227Th-trastuzumab therapy was well tolerated and resulted in a dose-dependent inhibition of breast cancer xenograft growth. These results warrant further preclinical studies aiming at a clinical trial in breast cancer patients with metastases to bone.
Metastatic breast cancer patients have poor prognosis despite recent therapeutic advances . The human epidermal growth factor receptor-2 (HER-2/neu) is a transmembrane receptor tyrosine kinase that is over-expressed in 25% to 30% of metastatic breast cancers and associated with more aggressive disease . Trastuzumab (Herceptin®) is a humanized monoclonal antibody (mAb) directed against this antigen and shows clinical activity in women both with HER2/neu-overexpressing primary and metastatic breast cancer .
Tumor cell-targeted alpha emitters have the potential to improve therapy of hematological malignancies and micrometastatic disease. Alpha particles have a short path length (50 to 80 μm) and high linear energy transfer (LET approximately 100 keV/μm) and, thus, deliver a high amount of DNA-damaging energy to cells in close vicinity of their decay. However, no alpha-emitting radioimmunoconjugate (RIC) has reached phase III clinical trial yet due to poor physical or chemical characteristics, supply limitations, and high production costs for the most promising alpha emitters . Recently, we have suggested 227Th as a novel radionuclide for alpha-particle radioimmunotherapy (RIT), as this radionuclide can be produced in clinically relevant amounts from β-decay of the long-term generator 227Ac [5, 6]. 227Ac can be produced by thermal neutron irradiation of 226Ra in a nuclear reactor. The yield of 227Ac after purification is relatively high and 226Ra is highly available, making the process cost efficient. 227Ac has a half-life of 21.8 years and thus, would serve as a generator nuclide for 227Th production for decades .
Thorium-227 decays via its alpha- and beta-emitting daughters 223Ra, 219Rn, 215Po, 211Pb, 211Bi, and 207Tl to stable 207 Pb. The long half-life of 227Th (T 1/2 = 18.7 days) permits the tumor targeting and normal tissue clearance of a 227Th-labeled RIC to occur before larger amounts of the daughter nuclide 223Ra is generated. Upon decay, 223Ra will detach from the antibody. Importantly, clinical trials have not shown worrisome toxicity of 223Ra injected as a therapy for prostate cancer bone metastases [8, 9]. Previously, we have shown that 227Th conjugated to the monoclonal antibody rituximab was effective in treatment of mice with lymphoma xenografts and had a relatively low normal tissue toxicity [7, 10, 11].
The conjugation of trastuzumab with different alpha-particle-emitting radionuclides, i.e., 211At, 225Ac, and 213Bi, has already been investigated by other groups [12–16]. The purpose of the present study was to determine the biodistribution, therapeutic effect, and toxicity of the low-dose rate alpha-particle-emitting RIC 227Th-trastuzumab on HER2-expressing SKBR-3 xenografts. In vitro experiments have shown internalization of the 227Th-trastuzumab/HER2 complex, retention of 227Th, and a high toxic effect against single tumor cells . The increased cytotoxic effect created by alpha particles may offer the opportunity to both improve the overall response rate of the trastuzumab treatment and also to treat patients with a lower HER2 expression.
Material and methods
Production of 227Th and radiolabeling of monoclonal antibodies
227Ac was produced through thermal neutron irradiation of 226Ra followed by β- decay of 227Ra (T 1/2 = 42.2 min) to 227Ac . 227Th was selectively retained from a 227Ac decay mixture in 7 M HNO3 by anion exchange chromatography .
Radiolabeling of trastuzumab (Herceptin®, Hoffmann-La Roche, Basel, Switzerland) and rituximab (MabThera, Hoffmann-La Roche) with 227Th was performed at Algeta ASA, Oslo, Norway. The antibodies were conjugated with p-SCN-Bn-DOTA at pH 9 (sodium borate buffer) at 37°C over night. The number of DOTA molecules per antibody was approximately four as determined by LC/MS analysis. The conjugate was purified with a spin filter (Amicon, Millipore, USA) using 0.9% NaCl as running buffer removing daughter nuclides and non-chelated 227Th. The purified antibody was distributed to microcentrifuge tubes (1 mg/tube) and freeze dried to keep a larger batch under stable conditions over a long period of time. The freeze-dried conjugate was dissolved in sodium acetate buffer pH 5.5 and added about 4 MBq of newly purified 227Th in 0.01 M HCl. The reaction was done over night at 42°C in a thermomixer (Eppendorf, Hamburg, Germany). The chelate was purified on a NAP5 column (GE Healthcare, Little Chalfont, UK) using PBS as running buffer. The specific activity was 1000-1600 kBq/mg with regard to 227Th.
The immunoreactive fraction (IRF) of the radioimmunoconjugate 227Th-trastuzumab was estimated by measuring the cell bound activity in a one point assay. SKOV-3 cells (2 × 107 cells/ml) in 200 μl PBS were used. Four million SKOV-3 cells in one vial of cells were blocked by incubating with 150 μg/ml cold trastuzumab for 15 min at 37°C. The cells in another vial were not blocked. About 500 cpm of 227Th-trastuzumab was added to each vial and the cells were incubated for 2 h before washing and measurement of radioactivity with an automated gamma counter (Wizard, Packard Instrument Co., Downers Grove, IL, USA). IRF was 70% to 90%.
All procedures and experiments involving animals in this study were approved by the National Animal Research Authority and carried out according to the European Convention for the Protection of Vertebrates used for Scientific Purposes. The animals were maintained under pathogen-free conditions. Food and water were supplied ad libitum. Eight to 12 weeks old, institutionally bred female Balb/C nu/nu (NCR) mice, with an average weight of 20 to 27 g at the start of study, were used. Mice were anesthetized with subcutaneous injection of 0.05 ml Zoletil® mix (Virbac, Carros Cedex, France) before HER-2-positive breast cancer (SKBR-3) tumor fragments from xenografted animals (1 × 1 × 1 mm) were implanted subcutaneously. The xenografted tumor line originated from HER-2-positive breast cancer (SKBR-3) cells from American Type Culture Collection (Manassas, VA). Mice with growing tumors of diameters between 4 and 8 mm were included in the experiments. Mice were killed by cervical dislocation.
Biodistribution of 227Th-labeled antibodies
The conjugates 227Th-trastuzumab and 227Th-rituximab were administered by tail vein injection of 100 μl (15 kBq) solution to each animal. For each conjugate and time point, a total of four to six animals were autopsied. Tumor and organs were measured for radioactivity content and weighed. Samples of the injectates (10%) were used as references in the measurement procedure.
Thorium-227 and 223Ra were measured using a solid-state photon well detector (GCW6021, Canberra, Meridan, CT, USA) coupled to a digital gamma ray spectrometer and analyzed using the computer software Apex™ version 1 (Canberra). For 227Th, the 236 keV (abundance 17.6%) and 256 keV (abundance 9.5%) γ-ray lines were used and for 223Ra the 154 keV (abundance 5.7%), 269 keV (abundance 13.9%), 324 keV (abundance 4%), and 338 keV (abundance 2.8%) γ-ray lines were used.
Calculation of absorbed dose
The total number of disintegrations, i.e., the cumulated activity, in various tissues from the time of injection of the preparation until no activity was left in the body was estimated by calculation of the area under the activity concentration versus time curves (AUC). For 227Th-labeled antibodies, the absorbed radiation doses were calculated assuming dose contributions coming only from α-particle emissions with a mean α-energy (Eα) of 5.9 MeV for 227Th and 26.4 MeV for 223Ra with its daughters in equilibrium, and that there was a 100% absorption of the absorbed dose from the α-particle within a tissue, i.e., absorbed fraction equal to unity (ø = 1). For α-particle radiation uniform distribution of radionuclides in the various tissues as well as no cross irradiation was assumed. Thus, the total absorbed dose to each organ was estimated by: Dose = AUC0 ∞ · Eα (227Th) + AUC0 ∞ · Eα (223Ra + daughters). Also for blood, the absorbed dose was calculated assuming 100% absorption of the α-particles, i.e., ø = 1. This was obviously a simplification since in the capillaries there will probably be escape of α-particles beyond the blood.
Mice were injected with a single dose of NaCl (control; n = 10), 20 μg (n = 5), 100 μg (n = 6), or 250 μg (n = 5) of cold trastuzumab; 200 kBq/kg (n = 10), 400 kBq/kg (n = 11), and 600 kBq/kg (n = 12) of 227Th-trastuzumab; and 400 kBq/kg (n = 9) and 600 kBq/kg (n = 10) 227Th-rituximab in 100 μl solution. Tumor growth and mouse weight were assessed three times a week in the first week before injection and the 3 weeks after injection; thereafter, weight, growth, and survival were assessed twice a week. Caliper measurements of perpendicular tumor diameters were used to estimate tumor volume by assuming ellipsoid shape. Mice with tumor diameter larger than 20 mm were killed. Mantley Cox log rank test was used to test for significant differences in surviving fraction of mice, which is defined as the fraction of mice that did not have to be sacrificed due to tumor diameter above 20 mm.
Evaluation of toxicity
Toxicity was evaluated in all treatment groups except 227Th-rituximab. Approximately 100 to 200 μl of blood was collected from the vena saphena lateralis in 500 μl EDTA-coated tubes (Microtainer K2E tubes, Becton, Dickinson, NJ, USA) for blood cell counting. Blood samples were taken before and at 3, 6, and 8 to 10 weeks after start of the study. For control, a group of ten mice without tumor was injected with NaCl and sampled at the same time points for blood cell count. While for clinical chemistry data, the samples from this control group were taken after 8 weeks. Blood cells were counted in an automatic blood counter (Scil Vet ABC, Horiba ABX, Montpellier, France). In addition, when mice were sacrificed due to tumor size or weight loss, blood samples were collected by heart puncture into EDTA-coated tubes and also lithium heparin-coated tubes (Microtainer LH tubes, Becton, Dickinson) for analysis of clinical chemistry parameters. Clinical chemistry strips were used to assess the serum aspartate aminotransferase (AST), alanine aminotransferase (ALT), alkaline phosphatase (ALP), and urea level (Reflotron, Roche Diagnostics GmbH, Mannheim, Germany). Full blood samples (30 μl) were analyzed by a clinical chemistry analyzer (Reflovet, Roche Diagnostics).
At the end of the study, the lung, heart, kidney, spleen, small intestine, large intestine, liver, femur, skull, and tumor were fixed with formalin, cut in 5-μm slices, stained with hematoxylin and eosin, and analyzed by a pathologist to detect any pathological changes. Slides from cold trastuzumab and 227Th-trastuzumab groups were compared to the slides of control groups.
Mice bearing tumor xenografts were injected with 15 kBq of 227Th-trastuzumab, corresponding to approximately 600 kBq/kg. Four animals were sacrificed by cervical dislocation 4 and 8 days after injection. Tumors were removed and immediately frozen in liquid nitrogen. Tissue sections of thickness 5 μm were used for exposure of Kodak Biomax MR-1 single-sided emulsion or Kodak Medical General Purpose Blue x-ray film (Eastman Kodak Company, Rochester, NY, USA). Films were exposed for 6 to 11 days at -80°C prior to development. Film patterns were compared to hematoxylin and eosin (H/E)-stained tissue sections.
Biodistribution and dosimetry of 227Th -trastuzumab and 227Th-rituximab
The in vivo biodistribution profiles of 227Th-trastuzumab, 227Th-rituximab, and the daughter nuclide 223Ra in nude mice with SKBR-3 xenografts at different time points after administration are shown in Figure 1. The maximum uptake of 227Th-trastuzumab in tumor (4.6 kBq/g) occurred 3 days after injection (Figure 1a). There was a large difference between the amount of activity in tumor and in normal organs for 227Th-trastuzumab. The uptake of non-tumor binding 227Th-rituximab (Figure 1b) in tumor was significantly lower than the uptake of 227Th-trastuzumab (Figure 1a). The 227Th daughter nuclide 223Ra was mainly localized to bone (femur and skull) but there were also some retention of 223Ra in spleen, kidneys, and in tumor (Figure 1c, d).
The absorbed radiation dose in tumor was 2.9 ± 0.8 Gy for 227Th-trastuzumab (Figure 2a) and 0.7 ± 0.1 Gy for 227Th-rituximab (Figure 2b); both normalized to injections of 400 kBq/kg. Radiation doses were less than 2 Gy for all organs for both RICs, except for femur (2.4 ± 0.6 Gy) and skull (2.7 ± 0.6 Gy) in mice treated with 227Th-trastuzumab.
Growth of SKBR-3 tumor xenografts in mice treated with alpha-particle-emitting 227Th-trastuzumab was compared with cold trastuzumab, non-tumor binding 227Th-rituximab, as well as saline (controls; Figure 3). There was a large variability in tumor growth within treatment groups. Table 1 shows growth delays calculated from average tumor growth curves. The mean tumor growth in mice treated with cold trastuzumab (20, 100, and 250 μg/mice or approximately 0.8, 4, and 10 mg/kg body weight) or 400 and 600 kBq/kg 227Th-rituximab was similar to the growth of the untreated controls. The dosage groups for cold trastuzumab and for 227Th-rituximab in Table 1 and Figure 3b, c were pooled since there was no difference between them. For 200 and 400 kBq/kg 227Th-trastuzumab, some of the tumors responded well to the treatment, while others did not (Figure 3d, e). The average delays to grow to a normalized tumor volume of 500 mm3 were 7 and 23 days, respectively (Table 1). For 600 kBq/kg 227Th-trastuzumab, all tumors responded to the treatment (Figure 3f) and the average growth delay to reach a tumor volume of 500 mm3 was 45 days (Table 1).
The surviving fraction of the different dosages of 227Th-trastuzumab was not significantly different from each other (p > 0.05), but there was a significant difference in survival between the 227Th-trastuzumab treatment groups and control groups (NaCl and trastuzumab; p < 0.001) (Figure 4a). Mean and median survival times were significantly different for mice in the dosage groups 400 and 600 kBq/kg 227Th-trastuzumab as compared to mice in the NaCl (control) group (p < 0.05; Table 2). None of the dosages of cold trastuzumab had an effect on survival (p = 0.40). Hence, the data were pooled into one group. The survival of mice treated with non-tumor-binding 227Th-rituximab was not significantly different from the survival of the control group (p > 0. 6; Figure 4b). In addition, no significant differences (p > 0.05) in mean and median survival times between control and 227Th-rituximab treatment groups were observed (Table 2).
Toxicity of 227Th-trastuzumab
White blood cell (WBC), platelet cell (PLT) counts, and clinical chemistry parameters of control mice and mice treated with 227Th-trastuzumab are shown in Figures 5 and 6. Figure 5a, b shows WBC and PLT counts of individual mice as well as mean values at 0, 3, 6, and 9 weeks time points from each treatment groups. In the control groups mice without tumor was also included in order to get measurements at longer follow-up. The WBC count was significantly lower in the control (NaCl) group at time 0 as compared to 3 weeks after injection. WBC decreased significantly for treatment with 400 kBq/kg (p < 0.001, t test) and 600 kBq/kg (p < 0.001, t test) of 227Th-trastuzumab as compared to WBC in the cold trastuzumab group and control mice after 3 weeks (Figure 5a) but not as compared with the 0 time point. After 6 weeks, only the 600 kBq/kg 227Th-trastuzumab group was significantly different from control (p = 0.008, t test).
No significant difference in PLT count was found for the 200 kBq/kg 227Th-trastuzumab treatment group when compared to control at any time point (Figure 5b). The PLT count was significantly lower for the 400 kBq/kg (p = 0.017, t test) and 600 kBq/kg (p = 0.003, t test) 227Th-trastuzumab treatments as compared to control after 3 weeks. At 6 weeks, the PLT counts had recovered. However, at 9 weeks, the PLT count was significantly lower than the control for the 400 kBq/kg 227Th-trastuzumab group (p = 0.038, t test) and for the cold trastuzumab group (p < 0.001, t test) as compared to control mice.
Urea, AST, ALT, and ALP levels in blood from control mice were compared with blood from mice treated with cold trastuzumab, 200, 400, and 600 kBq/kg of 227Th-trastuzumab (Figure 6a, b, c, d). Urea levels were within the normal range and were not significantly different from control. One mouse in each RIT group and one control mouse showed high ALT levels, i.e., above normal range. Another mouse treated with 200 kBq/kg 227Th-trastuzumab group had a very high AST levels as compared to mice in all other treatment groups. Large variations in ALP levels were observed among all treatment groups but were within the normal range. Therapy related pathological changes were not observed in any organ upon histological examination.
Figure 7 shows no morphological differences in normal bone marrow for a mouse treated with NaCl (Figure 7a) and a mouse treated with 600 kBq/kg of 227Th-trastuzumab up to 72 days (Figure 7b). Body weights of animals were measured throughout the study but no significant differences between the treatment groups were observed (data not shown).
Autoradiography of SKBR-3 tumor xenografts showed that the distribution patterns of radioactivity after injection of 600 kBq/kg of 227Th-trastuzumab were inhomogeneous (Figure 8). The smallest of the tumors analyzed showed highest concentration of radioactivity present as a rim corresponding to areas with viable tumor tissue close to the well perfused connective tissue capsule surrounding the tumor (Figure 8a). The tumor in Figure 8b had localized hotspots. On the corresponding H/E-stained tissue section, the hotspots with high 227Th-trastuzumab uptake matched areas with high density of blood vessels and/or large blood vessels, with areas of necrotic tissue and loosely bound cells in between. A similar correspondence was also seen in tissue sections taken at later time points (Figures 8c, d).
The present study of alpha-particle-emitting 227Th-trastuzumab showed a significant dose-dependent inhibition of tumor growth of human SKBR-3 breast cancer xenografts in mice, leading to long-term survival with low toxicity.
In RIT with 227Th the distribution of free daughter nuclides also has to be considered, as the daughter nuclide 223Ra detaches from the DOTA-trastuzumab construct upon alpha-particle emission from 227Th. The biodistribution study showed that 223Ra re-localized to bone and to spleen. It should be noticed that the 18.7-day half-life of 227Th allows for excretion of a large fraction of 227Th-trastuzumab before 223Ra is formed. The uptake in spleen was probably related to mouse-specific calcification of the spleen . Radium-223 has a half-life of 11.4 days and is excreted from the blood via the intestines with a major part of the 223Ra ending up in the hydroxyapatite of bone [8, 20, 21]. The half-lives of the 223Ra-daughters are in the millisecond to minute range. They are therefore likely to contribute mainly to the absorbed radiation dose in the vicinity of the site of 223Ra decay. Thus, as shown in Figure 2 the absorbed doses to bone were comparable to the doses in tumor.
Microautoradiography studies of 227Th-rituximab have shown that there probably is a contribution to the bone marrow absorbed dose from 223Ra and daughters on the bone surface . One could suspect that localization in bone would give a high contribution to bone marrow toxicity, but clinical studies of 223Ra have shown that it is well tolerated by breast and prostate cancer patients , with data from repeated dosing suggesting no more damage on red bone marrow compared to placebo . This lack of toxicity is probably due to the short path length of alpha emission, as previous data have shown that the beta-emitter strontium-89 is strikingly more toxic, although presumably localizing in an identical way in bone tissue . Therefore, we suggest that localization of small amounts of 223Ra in bone tissue would be acceptable. Furthermore, because of the long half-life of 227Th and internalization of HER-2 antigen after binding to 227Th- trastuzumab complex much of the 227Th will be excreted or internalized before 223Ra is formed and thereby reducing relocalization of 223Ra to bone. We also suggest that an optimized chelator will reduce the small amounts of free 227Th, indicated by the present biodistribution data.
No severe bone marrow toxicity was observed in this study even when therapeutically effective amounts were administered. A dosage of 600 kBq/kg of 227Th-rituximab is equal to an absorbed radiation dose in tumor of around 1 Gy. One could expect a small therapeutic effect of this dose since there was a significant therapeutic effect of 200 kBq/kg (1.45 Gy) of 227Th-trastuzumab. However, there was no therapeutic effect of even the highest dosage of 227Th-rituximab, showing that the antibody has to bind to the cells to get the emitted alpha particles close enough to the tumor cell nucleus. This is in analogy with the lack of bone marrow toxicity, discussed above, i.e., the low bone marrow toxicity might be due to the lack of binding of 227Th-trastuzumab or 223Ra to bone marrow cells.
In the present study, the tumor volumes were 8 to 16 times larger than the size of micrometastases (< 2 mm in diameter) in breast cancer patients. However, in a previous study we treated single SKBR-3 cells and achieved up to two log reduction in clonogenic survival and growth inhibition . Therefore, one relevant clinical setting for 227Th-trastuzumab might be adjuvant treatment of breast cancer patients with micrometastases. Due to the 223Ra (daughter) affinity to bone, patients with a high risk of developing bone metastasis might be an intriguing application [22, 23].
There was a dosage-dependent increase in tumor growth inhibition but not for survival. This may be related to individual differences in tumor vascularization and the presence of necrosis. In the 200 kBq/kg group we observed a variable therapeutic effect, while in the 400 and 600 kBq/kg groups we got a more prominent and similar therapeutic effect.
Radiolabeled antibody therapy for solid tumor has been less successful as compared to hematological tumors. The reasons are that the solid tumors are generally less sensitive to radiation and are more difficult to target due to macromolecule transport barriers, e.g., vascular supply limitation, high interstitial pressure, and vascular permeability limitation. Targeted delivery of high LET α-particles after administration of 227Th-trastuzumab may not be the only reason behind the successful growth inhibition of SKBR-3 tumor xenografts. The autoradiography images indicated that 227Th-trastuzumab in some tumors, were located close to the tumor vasculature. Targeting the tumor vasculature or vasculature near the tumor cells with α-emitting radionuclides has previously been shown to yield a therapeutic effect on solid tumors [24, 25].
The tumors treated in the present study were much larger than the range of alpha particles. However, the autoradiogaphy images indicated hot spots of 227Th-trastuzumab activity in perfused areas within the tumor xenografts, which might result in destruction of the blood vessels and eradication of tumors due to lack of nutrients. Furthermore, there was also some retention of free 223Ra in tumor. This is a small ion with several α-emitting daughter radionuclides that might surmount the macromolecular transport barriers of solid tumors and result in high LET α-irradiation of tumor cells not reached by the larger molecule 227Th-trastuzumab. Thus, the antitumor effect might have been a combined effect of tumor cell kill by both 227Th-trastuzumab, 223Ra, and daughters and destruction of the blood vessels that delivers nutrients and oxygen to the tumor cells.
At two samplings, the dosage-dependent decrease in the WBC count was significantly lower for mice in one or both of the two highest dosages groups compared to control mice; both for the 400 and 600 kBq/kg 227Th-trastuzumab groups at 3 weeks after injection, and for the 600 kBq/kg227Th-trastuzumab at 6-week time points. However, the blood values were within the normal physiological range for nude mice for all dosages of 227Th-trastuzumab. Furthermore, the most striking change in the WBC count is the increase for the control group from 0 to 3, 6, and 9 weeks. If the WBC count at 3, 6, and 9 weeks are compared with the WBC count of the control at 0 weeks there is no significant difference. The reason for this increase is unknown, but it might be related to an undetected infection in one cage of the control mice. Therefore, we conclude that the 227Th-trastuzumab treatment had no pathological effect on the WBC count.
There was a dosage-dependent decrease in PLT count at 3 weeks after injection, but the PLT count had recovered after 6 weeks. At the 9-week time point, the PLT count was significantly lower than the control for the 400 kBq/kg 227Th-trastuzumab group and the cold trastuzumab group. However, this decrease was probably related to a combination of biological variation and the low number of mice in these two groups (5 and 1, respectively). It should also be pointed out that control mice without tumor xenografts were used in order to get blood samples for the controls at the later time points.
Liver enzymes and urea levels in the blood did not show any dose-dependent changes following injection of 227Th-trastuzumab with levels in the highest dosage group similar to that of control. Other treatment groups showed random increase or decrease of some enzymes when compared with control. This may be related to one mouse within each group with very high value of the parameter in question. Since there were no dose-dependent changes and since there were no significant changes between the control and the 600 kBq/kg group for any parameters, these changes might be due to other factors than the 227Th-trastuzumab treatment.
In conclusion, 227Th-trastuzumab inhibits growth of breast cancer xenografts in a dose-dependent manner. Possibly due to the longer half-life, single dosing was efficacious; not excluding that improved efficacy might be obtained with multiple doses, as has been shown clinically with a more short-lived alpha emitter . The limited toxicity of the treatment was mainly related to reversible bone marrow depression. Further preclinical studies of 227Th-trastuzumab involving mice with breast cancer micrometastases and, if possible, metastasis to bone are warranted.
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The authors are grateful to Katrine B. Melhus, Camilla Mollatt, and Anne. K. Hjelmerud of Norwegian Radium Hospital, and Åsmund Larsen and Ellen M. Brevik of Algeta ASA, for technical assistance. We thank Lars Abrahamsen and Thomas Ramdahl at Algeta ASA for valuable comments on the manuscript.
JB is an employee of Algeta ASA which owns the patents for using 227Th in radioimmunotherapy. JD and OSB own a small amount of shares in Algeta ASA.
NA designed and performed the invivo studies and carried out interpretation and analysis of data including dosimetry calculation and writing of manuscript. JB performed radiolabeling and contributed in manuscript writing. JN and NA carried out histopathological studies of slides. HH carried out the autoradiography studies including interpretation and analysis of these data, and contributed to performing experiments and writing of parts of the manuscript. ØSB contributed to the study design, interpretation and analyses of data as well as writing of the manuscript. JD contributed to the study design, interpretation and analyses of data, writing the manuscript as well as performing experiments and dosimetry calculations. All authors read and approved the final manuscript.
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