Yttrium-90 Tabituximab barzuxetan: A Pioneering Radiolabelled Therapy for Synovial Sarcoma
Yttrium-90 Tabituximab barzuxetan is a radiolabelled drug designed for targeted synovial sarcoma treatment.
Medical radiotheranostics, a revolutionary concept in cancer care, integrates diagnosis and therapy, enhancing the precision and efficacy of treatments. This innovative approach utilises radiolabelled compounds that can both image and treat malignancies, offering a dual benefit that has significantly advanced the field of nuclear medicine.
The term ‘radiotheranostics’ combines ‘radiotherapy’ and ‘diagnostics’, reflecting its dual functionality. It involves the use of specific molecules that bind to cancer cells and are tagged with radioactive isotopes. These isotopes are carefully chosen so that their emitted radiation can be detected by imaging techniques such as Positron Emission Tomography (PET) or Single Photon Emission Computed Tomography (SPECT), allowing for precise tumour localisation. Following imaging, the same radioactive isotopes deliver targeted radiation therapy, destroying the cancer cells while minimising damage to surrounding healthy tissue.
One of the pivotal elements of radiotheranostics is the selection of appropriate targets on cancer cells, such as receptors or antigens that are overexpressed in certain tumour types. For example, the prostate-specific membrane antigen (PSMA) is used as a target in prostate cancer. Radiolabelled molecules that bind to PSMA can be visualised to assess the extent and location of the cancer and then used to deliver lethal doses of radiation directly to the tumour cells.
This targeted approach offers several advantages over traditional methods. Firstly, it allows for the assessment of the biodistribution of the radiopharmaceutical, ensuring that it accumulates sufficiently within the tumour before commencing therapeutic radiation. This leads to a more tailored treatment plan based on the individual’s specific disease presentation, which can result in improved efficacy and reduced side effects. Additionally, radiotheranostics can provide vital information on tumour response early in the treatment course, enabling adjustments to be made if necessary.
Another significant benefit of radiotheranostics is its potential in treating metastatic diseases, which are often difficult to manage with conventional therapies. For instance, Lutetium-177 PSMA therapy has shown promising results in patients with metastatic castration-resistant prostate cancer, providing a new lifeline where previous therapies have failed.
The future of medical radiotheranostics looks promising as research continues to evolve. New targets are being explored, and advances in molecular biology and imaging technology are likely to expand the range of cancers that can be treated with this method. Moreover, developing novel radiolabelled compounds that can be used for diagnostic and therapeutic purposes is set further to enhance the effectiveness and safety of cancer treatments, heralding a new era in personalised medicine. As this field grows, it holds the potential to significantly alter the landscape of cancer treatment, offering hope to those battling this complex disease.
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Yttrium-90 Tabituximab barzuxetan is a radiolabelled drug designed for targeted synovial sarcoma treatment.
Yttrium-90 OPS201, a receptor antagonist, delivers targeted beta radiation for effective neuroendocrine tumour therapy and research.
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Zevalin therapy combines monoclonal antibody targeting with Yttrium-90 radiation to treat non-Hodgkin’s lymphoma effectively.
Ferritarg therapy targets acidic ferritin in cancer cells, offering precision treatment for refractory Hodgkin’s disease and other malignancies.
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Yttrium-90 FAPi-46 targets fibroblast activation protein, providing effective radiotherapy for tumours and fibrotic diseases.
Yttrium-90 FAPi-04 is a promising radiotherapeutic targeting fibroblast activation protein in cancer-associated fibroblasts effectively.
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Yttrium-90 Epratuzumab Tetraxetan enhances Non-Hodgkin Lymphoma treatment through targeted radioimmunotherapy and durable responses.
Yttrium-90 Edotreotide delivers targeted beta radiation therapy to somatostatin receptor-positive neuroendocrine tumours with precision.
Yttrium-90 DOTA-FF-21101 targets P-Cadherin in solid tumours, delivering beta radiation for precise cancer treatment.
Yttrium-90 Besilesomab targets CD66-expressing cells, providing precise beta radiation therapy for systemic amyloid light chain amyloidosis.
Yttrium-90 Anditixafortide targets CXCR4-expressing tumours, delivering therapeutic β– radiation precisely, improving treatment outcomes significantly.
Radioactive isotopes emit targeted radiation that effectively destroys cancer cells while minimising harm to healthy tissues.
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Thorium-227 Anetumab Corixetan delivers targeted alpha radiation, effectively treating mesothelin-expressing tumours while sparing healthy tissues.
Terbium-161 PSMA-I&T combines precise PSMA targeting with beta and Auger emissions, revolutionising prostate cancer treatment efficacy.
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Tin-117m DTPA offers innovative treatment options for bone metastases, combining therapeutic efficacy with minimal collateral tissue damage.
Tin-117m DOTA-Annexin V revolutionises medicine by simultaneously imaging and treating vulnerable plaques, cancers, and neuroinflammation.
Samarium-153 DOTMP, a promising radiopharmaceutical, targets bone metastases effectively while allowing precise imaging for clinical monitoring.
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Rhenium-188 SSS/Lipiodol combines targeted delivery with beta radiation, offering hope for advanced hepatocellular carcinoma patients.
Rhenium-188 Colloidal Sulfide provides targeted radiation therapy, reducing joint inflammation and pain in large rheumatoid arthritis-affected joints.
Rhenium-188 HDD/Lipiodol therapy offers targeted radiopharmaceutical treatment for advanced hepatocellular carcinoma with portal vein thrombosis.
Rhenium-188 P2045 is a peptide-based radiopharmaceutical targeting somatostatin receptors for treating neuroendocrine and pancreatic cancers.
Rhenium-188 Etidronate effectively targets metastatic bone lesions, delivering therapeutic beta radiation while reducing associated pain.
Rhenium-188 ImDendrim combines targeted nitro-imidazole ligands and dendrimers to deliver beta radiation to hypoxic tumours.
Lead-203 DOTA-VMT-MCR1 binds MC1R with high specificity, facilitating targeted imaging and image-guided therapy for metastatic melanoma patients.
Lead-212 VMT-α-NET offers advanced targeted therapy for neuroendocrine tumours by harnessing precise alpha-particle radiation.
Lead-212 DOTAMTATE targets somatostatin receptors in neuroendocrine tumours, delivering potent alpha-emission therapy with minimal off-target toxicity.
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Phosphorus-32 Colloidal Chromic Phosphate delivers precise beta radiation for treating malignant effusions and cystic tumours.
Lutetium-177 XT033 combines PSMA targeting and Evans blue technology to improve metabolic stability and therapeutic effectiveness.
Lutetium-177 Vipivotide Tetraxetan is a groundbreaking radioligand therapy targeting PSMA, offering precise tumour treatment with minimal damage to healthy tissues.
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Lutetium-177 TLX250 targets CA-IX-expressing tumours, providing a selective radiotherapy approach for treating advanced renal cell carcinoma.
Lutetium-177 Satoreotide Tetratexan is a radiopharmaceutical targeting somatostatin receptors, providing advanced therapeutic options for neuroendocrine neoplasms effectively.
Lutetium-177 Rosopatamab is a radiopharmaceutical therapy combining targeted monoclonal antibodies with beta-emitting radioactive particles.
Lutetium-177 RM2 leverages GRPR targeting to deliver therapeutic beta radiation, minimising off-target effects and enhancing prostate cancer treatment outcomes.
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Lutetium-177 Rituximab offers a targeted radiopharmaceutical solution, delivering beta radiation to CD20-positive cells, ensuring effective and precise lymphoma therapy.
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RhPSMA revolutionises prostate cancer management with dual labelling, enabling precise imaging and effective targeted radiotherapy options.
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Lutetium-177 PSMA-R2 is a urea-based therapeutic agent targeting PSMA, effectively treating advanced prostate cancer patients.
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Lutetium-177 PSMA-ALB-56 is an innovative treatment optimising prostate cancer therapy through targeted radiopharmaceutical advancements.
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Lutetium-177 PNT6555, a FAP-targeted radiopharmaceutical, combines precision therapy with beta radiation for tumour-specific treatment.
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Lutetium-177 PNT2002 offers targeted radiotherapy for prostate cancer, combining precise tumour targeting with therapeutic and diagnostic capabilities.
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Lutetium-177 Pentixather targets CXCR4-expressing tumours, delivering precise beta radiation therapy to eliminate malignant cells effectively.
Lutetium-177 Oxodotreotide Treatment offers targeted neuroendocrine tumour therapy, improving progression-free survival and patient outcomes significantly.
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Lutetium-177 MVT-1075 radioimmunotherapy targets pancreatic cancer by utilising CA19-9 specificity, sialyl-Lewis a binding, and precision radiation delivery.
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Lutetium-177 Ludotadipep targets PSMA with enhanced stability, specificity, and reduced side-effects, revolutionising prostate cancer treatment.
Lutetium-177 LNC1010, a radiolabelled therapy, targets somatostatin receptors, delivering precise treatment with minimal side effects.
A novel radiolabelled drug, Lutetium-177 LNC1004, targets fibroblast activation protein, transforming cancer therapy through precision and innovation.
Radiopharmaceutical therapy in cancer offers targeted treatment, minimising side effects while enhancing patient outcomes.
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Betalutin combines the precision of CD37-targeting antibody Lilotomab with Lutetium-177, offering targeted and effective haematological cancer treatment.
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Targeting glioblastoma with Lutetium-177 ITM-31 offers precise intracavitary treatment, reducing recurrence by specifically addressing residual cancer cells post-surgery.
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Lutetium-177 iPSMA revolutionises prostate cancer treatment, delivering targeted beta radiation to metastatic cells with precision and minimal side effects.
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Targeting Neurotensin Receptor-1 with Lutetium-177 IPN-01087 demonstrates promising precision therapy, delivering beta radiation for treating invasive cancers like ductal pancreatic adenocarcinoma.
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Advancing prostate cancer treatment, Lutetium-177 HTK03170 and Gallium-68 HTK03149 enable targeted PSMA therapy, improving diagnosis and therapeutic outcomes.
Lutetium-177 FAPI-04 revolutionises cancer treatment by precisely targeting cancer-associated fibroblasts, enabling dual imaging and radiotherapy functionalities for enhanced outcomes.
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Revolutionising cancer therapy, Lutetium-177 FAP-2286 offers precise diagnostics and targeted treatment, addressing solid tumours and fibrotic conditions effectively.
Lutetium-177 EDTMP provides a cost-effective, accessible, and efficacious alternative for bone pain palliation in metastatic cancer patients.
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Lutetium-177 Edotreotide revolutionises neuroendocrine tumour treatment through targeted radioligand therapy, enhancing precision and improving patient outcomes.
Lutetium-177 EB-PSMA-617 represents an innovative radioligand therapy optimising tumour retention and therapeutic outcomes in metastatic prostate cancer.
Lutetium-177 DTPA-Omburtamab offers hope in neuroblastoma treatment by precisely targeting B7-H3, delivering localised radiation while sparing healthy tissues.
Lutetium-177 DPI-4452 pioneers precision radiotheranostics, revolutionising treatment for CAIX-expressing solid tumours through targeted imaging, therapy, and personalised oncology care advancements.
Lutetium-177 DOTAZOL offers a dual-function approach, combining targeted radiotherapy and bone modulation, enhancing treatment for prostate cancer-related bone metastases.
Lutetium-177 DOTA-EB-TATE enhances neuroendocrine tumour therapy by improving tumour uptake, retention, and pharmacokinetics through albumin-binding Evans blue moieties.
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Lutetium-177 DOTA-EB-FAPi revolutionises oncology by enhancing precision targeting of fibroblast activation protein, improving tumour uptake, and expanding therapeutic applications.
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Radiotheranostics in prostate cancer enables precise diagnosis and targeted treatment, improving patient outcomes significantly.
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Lutetium-177 Debio 1124, a second-generation theranostic agent, selectively targets CCK2R-expressing tumours, offering precision radiotherapy and personalised oncology advancements.
Lutetium-177 CTT1403, an innovative PSMA-targeted therapy with irreversible phosphoramidate-based binding, shows remarkable efficacy in treating metastatic prostate cancer, enhancing tumour uptake, internalisation, and therapeutic precision.
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Exploring Lutetium-177 AMTG highlights its innovative design, enhanced metabolic stability, and potential for effectively treating GRPR-positive prostate and breast tumours.
The rise and fall of Iodine-131 Tositumomab highlights challenges in balancing innovation, efficacy, infrastructure, and cost within radiopharmaceutical therapies.
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Iodine-131 TM601, a synthetic radiolabelled peptide, targets tumour cells expressing Annexin A2, delivering therapeutic radiation and exhibiting anti-angiogenic properties effectively.
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TLX101 is a revolutionary radiopharmaceutical targeting gliomas, offering dual imaging and therapy through tumour-selective uptake, enhancing treatment outcomes.
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Iodine-131 Sodium Iodide plays a pivotal role in diagnosing and treating thyroid diseases, including carcinomas, through targeted radiotherapy and imaging.
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Iodine-131 RPS-001, a radiolabelled small molecule targeting PSMA, shows promise in prostate cancer therapy through precision-directed beta radiation delivery.
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Iodine-131 Omburtamab offers targeted radiation therapy, significantly improving survival in neuroblastoma patients with CNS and leptomeningeal metastasis.
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Iodine-131 naxitamab (¹³¹I-3F8) targets GD2-expressing cancers, offering precise radioimmunotherapy for neuroblastoma, melanoma, and small cell lung carcinoma.
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Iodine-131 Metuximab (Licartin) selectively targets CD147 receptors, delivering beta radiation to hepatocellular carcinoma cells, improving treatment precision significantly.
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Iodine-131 Lipiodol has re-emerged as a promising therapy for hepatocellular carcinoma, particularly in non-resectable cases with portal vein thrombosis.
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Iodine-131 Iopofosine selectively delivers cytotoxic radiation to malignant cells by targeting the PI3K/Akt pathway, offering promising cancer therapy advancements.
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Iodine-131 Iobenguane revolutionises neuroendocrine tumour management by offering targeted imaging and therapy, significantly improving diagnosis, treatment, and patient outcomes.
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Alpha particles provide precise cancer treatment by delivering high-energy radiation, targeting tumour cells while sparing healthy tissue.
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Iodine-131 ICF01012, targeting melanin receptors, shows promise in the fight against metastasised melanomas, heralding a new era in treatment.
Iodine-131 chTNT, aiming to revolutionise oncology, shows promise in targeting and eradicating tumour cells with precision.
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Iodine-131 CAM-H2 heralds a new era in oncology, offering hope through precise targeting of HER2-expressing cancers with minimal side effects.
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Iodine-131 BA52, a melanin-binding therapeutic, offers new hope for patients with melanin-positive malignant melanomas.
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Iodine-131 Monoclonal Antibody 81C6 specifically targets glioma cells by honing in on the tenascin protein.
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Holmium-166 Phytate, initially developed for chronic synovitis, has shown significant promise in phase I/II clinical trials.
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Holmium-166 Chitosan, a groundbreaking radiopharmaceutical, offers new hope in treating hepatocellular carcinoma with targeted therapy.
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Holmium-166 microspheres, by delivering localized radiation, significantly enhance the therapeutic approach to inoperable liver cancer treatment.
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Copper-67 SARTATE emerges as a groundbreaking radiopharmaceutical in targeted cancer therapy, showcasing promising clinical trial results.
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Copper-67 SARbisPSMA offers new hope in targeting and treating prostate cancer with precision and effectiveness.
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The article explores the theranostic applications of Terbium radionuclides, highlighting their diagnostic and therapeutic potential in nuclear medicine.
Terbium Radionuclides for Theranostic Applications in Nuclear Medicine Read Post »
Copper-64 Diasparagine offers a promising breakthrough in targeting and treating aggressive brain tumours like glioblastoma.
213Bi-Lintuzumab demonstrated efficacy in AML treatment, offering a targeted approach with manageable side effects, yet development paused.
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213Bi-DOTATOC offers potent, targeted alpha therapy for tumours, advancing treatment with precision and reduced systemic toxicity.
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211At-MX35-F(ab’)2 shows promise in treating ovarian cancer through targeted therapy in ongoing clinical trials.
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The innovative 211At-MABG targets rare tumours like malignant pheochromocytoma and paragangliomas, promising a new era in treatment.
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Neuroblastoma Targeting Agents offer innovative diagnostic and therapeutic options, revolutionizing treatment with precise targeting and efficacy.
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Technetium-99m and Radium-223 are pivotal in managing bone metastases, enhancing both diagnostic accuracy and therapeutic efficacy.
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Utilising CXCR4 targeting agents with labelled ligands marks a breakthrough in treating haematological malignancies effectively.
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Estrogen receptor targeting agents, including Fluorine-18 and Iodine-131 analogues, revolutionise breast cancer diagnostics, therapeutics, and personalised patient management.
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FAPI revolutionises oncology with precise Gallium-68 diagnostics and targeted Lutetium-177 therapy for cancer.
Somatostatin Receptor Targeting Agents offer groundbreaking diagnostic and therapeutic solutions for neuroendocrine tumour management and care.
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PSMA targeting agents revolutionise prostate cancer care with precise diagnostics and targeted therapeutic approaches.
211At-BC8-B10, targeting CD45 in leukemia, combines BC8 antibody with Astatine-211, showing promising clinical trials.
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Astatine-211 in radiotheranostics offers targeted, effective cancer treatment, but faces production and safety challenges.
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211At-81C6-mAb, targeting tenascin in brain tumours, shows extended survival but needs further funding for development.
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225Ac-RYZ101 offers promising GEP-NET treatment, targeting tumours with alpha particles via somatostatin receptor-specific edotreotate.
225Ac-Rosopatamab, targeting metastatic prostate cancer, combines monoclonal antibodies with alpha radiation, showing promise in early trials.
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225Ac-PSMA-617 revolutionises prostate cancer treatment, offering targeted, effective therapy with promising clinical trial results.
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225Ac-MTI-201, targeting MC1R, offers groundbreaking, targeted treatment for uveal melanoma with minimal side effects.
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225Ac-Lintuzumab, targeting CD33, shows promise in AML treatment with potential expansion to other cancers.
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225Ac-FPI-2265, targeting PSMA, shows promise in treating advanced prostate cancer in the TATCIST clinical trial.
225Ac-FPI-2068 and 111In-FPI-2107 represent a major advancement in targeted alpha therapy for various solid tumours.
225Ac-FPI-2059 targets NTSR1 in cancer cells, offering a novel approach in pancreatic cancer treatment.
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225Ac-FPI-1434 advances in clinical trials, targeting IGF-1R in chemo-resistant solid tumors with promising results.
225Ac-DOTAZOL enhances 177Lu-radiotherapy in bone diseases, particularly effective in prostate cancer, as shown in preclinical studies.
225Ac-DOTATOC advances GEP-NET treatment, offering targeted, effective therapy for patients resistant to traditional methods.
225Ac-DOTA-YS5 targets CD46 in prostate cancer, promising precision and effectiveness in therapy.
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225Ac-DOTA-SP, a breakthrough in targeted alpha therapy, offers precise cancer treatment with minimal side effects, revolutionising oncological approaches.
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Radiotheranostic Pairs combine diagnostic imaging with targeted radiotherapy, revolutionising personalised cancer treatment through enhanced precision and efficacy.
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Radiotheranostics combines diagnostic imaging and targeted radiotherapy, using radiopharmaceuticals for personalised, precise cancer treatment and improved outcomes.
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Targeted Alpha Radionuclide Therapy precisely delivers potent alpha particles to tumors, maximising efficacy while sparing healthy tissues.
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World Theranostics Day honours Dr. Hertz’s groundbreaking radioiodine therapy, transforming disease treatment globally since 1941.
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Theragnomics melds theranostics and radiomics, promising targeted cancer therapies with improved outcomes through precision diagnostics and treatment adaptation.
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Thorium-227 emerges in nuclear medicine, revolutionizing cancer treatment through precise, effective radiotheranostic and therapeutic applications.
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Theranostics is a cutting-edge approach that integrates diagnosis and therapy, enabling personalised and precise disease management.
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Targeted radionuclide therapy was first used to treat cancer for an ‘over-active’ thyroid using radioactive iodine-131 seeds.
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The nuclear medicine imaging approach is to use theranostics for example Zevalin to establish tools for specific molecular targeting.
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