Lancet oncology. The Lancet Oncology Reprint ; Vol 6 (meghosszabbítva: ) -

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Stanford University Medical Center Summary: A way to scan young cancer patients' bodies for tumors without exposing them to radiation has been developed. The technique could reduce patients' risk of developing secondary cancers later in life. The new method is a modification of magnetic resonance imaging that employs a novel contrast agent to find tumors. The MRI-based method is as effective as cancer-detection scans that use lancet oncology radiation -- specifically, positron emission tomography-computed tomography -- the researchers found.

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Although whole-body PET-CT technology provides essential information for detecting cancer, it has one big drawback: A single scan exposes the patient to as much radiation as chest X-rays. This exposure is especially risky for children and teenagers, who are more vulnerable to radiation than adults because they are still growing.

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Children are also more likely to live long enough to develop a second cancer. These cancers originate in the immune system and the bones, respectively.

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Both cancers can spread throughout tissues such as bone marrow, lymph nodes, liver and spleen. In the past, several hurdles prevented physicians lancet oncology using whole-body MRIs to look for tumors.

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Lancet oncology scans take up to two hours. It combines PET images taken by monitoring the metabolism of radioactive glucose with CT images, which are essentially a series of X-rays from different angles.

Here, we present 5-year results of patient-reported quality of life. Randomisation was stratified by study centre, tumour type, and menopausal status, with a block size of ten and an automated dynamic algorithm. There was no masking of patients or investigators.

More importantly, in many organs, MRI does not distinguish healthy from cancerous tissue. And existing contrast agents -- chemicals injected into the body to make tumors visible -- leave the tissues too quickly to be used in a lengthy, whole-body MRI.

Injections of these iron nanoparticles are approved by the Food and Drug Administration to treat anemia, and the researchers obtained FDA permission for the experimental use.

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The nanoparticles are retained in the body for many days. On MRIs, they cause blood vessels to appear brighter, providing anatomic landmarks.

The nanoparticles also cause healthy bone marrow, lymph nodes, liver and spleen to appear darker, making tumors stand out.

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The images generated from the experimental MRIs provided comparable information to the Lancet oncology scans that study subjects received as part of their care. The two methods had similar levels of sensitivity, specificity and diagnostic accuracy. None of the patients experienced adverse reactions to the iron nanoparticles, though the FDA has previously noted a small risk of allergic reaction to the nanoparticles' coating.

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It's rare for patients to have adverse reactions to other contrast agents, too. Radiologists at several academic hospitals are searching for ways to reduce children's radiation exposure, Daldrup-Link said, adding that she is sharing the new technique with colleagues around the country.

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The other barrier to wide adoption of MRI-based tests is lack of a billing code, a hurdle the researchers hope will soon be resolved. But there are no technologic obstacles to use of the new technique.

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Future research will aim to validate the MRI-based method in larger, more diverse groups of cancer patients, as well as examine its possible use for monitoring tumors over the course of cancer treatment. The MRI-based method also holds promise for scanning patients after their treatment is complete, when the ability to monitor them without radiation would be especially valuable.

Original written by Lancet lancet oncology Digitale. Note: Content may be edited for style and length.