Individualization Personalized Radiotherapy using Theranostic Isotopes

Martina Sollini

Department of Oncology, Medical University of Vienna, Vienna, Austria


DOI10.36648/2574-285X.9.4.84

Martina Sollini*

1Department of Oncology, Medical University of Vienna, Vienna, Austria

*Corresponding Author:
Martina Sollini,
Department of Oncology, Medical University of Vienna, Vienna, Austria
E-mail:
mertina@gmail.com

Received date: November 28, 2024, Manuscript No. IPIMP-24-20079; Editor assigned date: December 02, 2024, PreQC No. IPIMP-24-20079 (PQ); Reviewed date: December 16, 2024, QC No. IPIMP-24-20079; Revised date: December 23, 2024, Manuscript No. IPIMP-24-20079 (R); Published date: December 30, 2024, DOI: 10.36648/2574-285X.9.4.84

Citation: Sollini M (2024) Individualization Personalized Radiotherapy using Theranostic Isotopes. J Med Phys Appl Sci Vol.9.No.4: 84.

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Description

Personalized radiotherapy has emerged as a transformative approach in cancer treatment, aiming to improve therapeutic outcomes while minimizing side effects. This customized treatment strategy focuses on adapting the radiotherapy regimen to the specific needs and characteristics of individual patients, rather than applying a one-size-fits-all approach. Among the most potential advancements in personalized radiotherapy are theranostic isotopes, a combination of therapy and diagnostics that allow for precise targeting of cancer cells, real-time monitoring of treatment efficacy and individualization of radiation doses. Theranostic isotopes represent a innovative intersection of nuclear medicine and oncology, offering an integrated solution for both diagnosis and treatment. Theranostics is a term that combines "therapy" and "diagnostics," and it refers to the use of specific molecules or isotopes that can both detect disease and deliver therapeutic radiation. This dual functionality is pivotal in cancer treatment because it allows clinicians to track the progression of cancer in real-time and adjust treatment plans accordingly. Theranostic isotopes, such as those used in Positron Emission Tomography (PET) or Single-Photon Emission Computed Tomography (SPECT), are designed to bind specifically to cancer cells, enabling imaging and targeting of the tumors. Once bound, the therapeutic component of these isotopes can deliver radiation directly to the cancerous tissue, sparing surrounding healthy tissue and reducing adverse side effects. One of the key advantages of using theranostic isotopes in radiotherapy is their ability to provide personalized treatment. Traditional radiotherapy often uses a standardized approach based on tumor size, location and general patient characteristics.

Genetic mutations

However, each cancer is unique, with distinct genetic mutations, molecular profiles and responses to treatment. Theranostic isotopes allow clinicians to obtain detailed information about the tumor's biology and molecular characteristics, helping them to customize treatment plans to each patient’s needs. For instance, by using a radioactive isotope that binds to a particular protein or receptor found predominantly on cancer cells, clinicians can ensure that radiation is delivered precisely to the tumor site, reducing the likelihood of damage to healthy tissues. A key element of theranostic isotopes is their ability to work with advanced imaging techniques like PET, SPECT and Magnetic Resonance Imaging (MRI). These imaging modalities are vital for detecting the presence of tumors at an early stage and monitoring the progress of treatment in real time. Theranostic agents can be engineered to attach to specific molecules or receptors that are overexpressed on cancer cells, such as the Prostate-Specific Membrane Antigen (PSMA) in prostate cancer. This targeted binding not only provides high-resolution images but also allows physicians to track how well the radiotherapy is working. If the imaging reveals that the tumor is shrinking or responding to the therapy, clinicians can adjust the radiation dose or modify the treatment strategy accordingly. The integration of theranostic isotopes in radiotherapy also allows for better management of treatment-related toxicity.

Traditional radiotherapy

Traditional radiotherapy often requires high doses of radiation, which can lead to damage in surrounding healthy tissues, resulting in side effects such as fatigue, nausea and skin irritation. However, with theranostic isotopes, radiation can be delivered in a more focused and controlled manner. This localized targeting ensures that only the cancerous tissue is affected, preserving the surrounding healthy cells. Moreover, the use of advanced imaging techniques enables early detection of any adverse effects, allowing for prompt intervention and adjustments to the treatment plan. The ability to personalize treatment based on the molecular and genetic profile of the tumor is another significant advantage of theranostic isotopes. By tailoring radiotherapy to the individual’s specific cancer characteristics, clinicians can maximize the therapeutic effect while minimizing harm to healthy tissues. This individualized approach is particularly important in treating cancers that are difficult to target with traditional methods, such as metastatic or recurrent cancers. The precision provided by theranostics opens up new possibilities for treating a wide range of cancers, from solid tumors to hematologic malignancies, with a higher degree of accuracy and efficacy. Despite the promising potential of theranostic isotopes, there are still several challenges to overcome. One of the primary obstacles is the availability and production of these isotopes. While some isotopes, such as I-131, are more readily available, others, like Lu-177, require specialized facilities and infrastructure for their production. Additionally, theranostic agents must be carefully designed to ensure that the targeting molecules bind specifically to cancer cells without affecting normal cells. This requires extensive research and development to identify the most appropriate molecular markers and to optimize the conjugation of isotopes to targeting molecules.

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