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          Use of 18F-FDG PET/CT for Imaging TB Patients and Related Conditions (HIV/AIDS, Tuberculosis): Focus on Drug Resistant Extrapulmonary Tuberculosis

          Closed for Proposals

          Project Type

          Coordinated Research Project

          Project Code

          E15021

          CRP

          2055

          Approved Date

          13/02/2014

          Project Status

          Closed

          Start Date

          04/04/2014

          Expected End Date

          04/12/2018

          Completed Date

          06/11/2018

          Description

          Over 95% of TB deaths occur in low- and middle-income Member States, where TB is among the top three causes of death for women in reproductive age. This disease has become or is becoming a medical emergency not only in developing Member States but also in some high-income countries, because of migration of people from low-income to higher-income areas, because of frequent co-infection with HIV/AIDS, and because of the development of drug-resistant strains of TB (3). Aim of this study is to engage Member States in a coordinated research project to develop a comprehensive TB imaging strategy through the use 18F-FDG PET/CT for imaging TB patients with special focus on: (a) extrapulmonary TB (b) multi drug resistant TB (MDR-TB) and (c) monitor response to therapy (Baseline 18F-FDG PET scan and repeat scan at 2 months and 6months post therapy) in order to reduce rates and deaths from TB especially drug resistant TB. Radionuclide imaging of infection has for long time relied almost exclusively on single-photon-emitting agents, evolving from early applications of 67Ga-citrate scintigraphy to scintigraphy with autologous leukocytes, labelled either directly (by in vitro incubation with agents such as 111In-Oxine or 99mTc-HMPAO before reinfusion) or indirectly (e.g., administering radiolabeled antibodies binding to surface antigens expressed by granulocytes)(1-2). The latest entry for radionuclide imaging of infection in the clinical setting is represented by PET with 18F-FDG, based on nonspecific enhanced glucose consumption of inflammatory cells and/or growing bacteria at the site(s) of infection(1-2). Nearly 11% of all deaths from infectious diseases are caused by tuberculosis (TB). This will contribute to the overall improvement of health care by accurate and early diagnosis of intractable TB infections in high risk patients through a multicentre imaging trial using 18F-FDG by increasing the detection rate of respiratory, abdominal, CNS, and postoperative infections ?related to TB. Overall, infectious disease constitutes a big burden to healthcare systems not only because of the direct costs related to treatments, but also in terms of parameters describing the overall economic and social burden deriving from associated disabilities and chronic debilitating illnesses, such as the disability-adjusted life years and the health-adjusted life expectancy. The top infectious diseases causing deaths worldwide are lower respiratory infections (including pneumonia and influenza), chronic obstructive pulmonary disease, diarrheal diseases, HIV/AIDS, and tuberculosis (TB). While the impact of radionuclide imaging in the first four such infectious conditions is rather limited, special attention should be paid to the potential role of nuclear medicine imaging in certain stages of TB infection. Such role is not to be seen in the diagnostic approach to TB, but rather in subsequent stages, for characterization of the disease and for assessing its response to therapy.

          Objectives

          A comprehensive TB imaging strategy using F-18 FDG PET/CT will be developed and introduced especially with developing Member States in order to reduce rates and deaths from MDR and extrapulmonary TB.

          Specific Objectives

          To assess the adequacy of 18F-FDG PET/CT for post-therapy surveillance

          To monitor therapy response, with emphasis on the possibility of an interim scan (2 months after starting therapy) to predict response with respect to the final scan at 6 months, or 9 to 12 months

          Use 18F-FDG PET/CT for imaging TB patients for: (a) the diagnosis of extrapulmonary TB (c) Use of 18F-FDG PET/CT as biomarker to monitor response to TB therapy, cure and relapse (Baseline 18F-FDG PET scan and repeat scan at 2 months and 6months post therapy)

          Impact

          Before the initiation of this project, PET imaging in EPTB was not considered by the treating physicians. From the data of patients included in this project, PET imaging has been found to be very useful and is now routinely performed especillay Pott's spine and TBM cases. Further emphasis can be given on MDRTB based on PET scan finding

          This multi-centre trial shows that 18F-FDG PET-CT imaging can be used as a biomarker to evaluate the full extent of disease which is superior to current practice of conventional CT imaging.

          The utility of PET/CT as an efficient health technology tool further validated.

          Relevance

          PET/CT imaging technology using short-lived radiotracers produced by cyclotron allow for the timely identification of functional and metabolic changes in the patient’s whole body, which precede morphological and structural changes with the application of the appropriate PET radiotracers. 18F-FDG used for PET/CT Imaging is known to accumulate at sites of infection, inflammation and in autoimmune and granulomatous diseases. This CRP provided participants from member Sates to be bale to participate in a multicentre trial and be able to validate the clinical utility of nuclear technique such PET/CT in the management of tuberculosis.

          CRP Publications

          India
          Peer reviewed research journal/ Clinical nuclear medicine, 42(6), pp.e304-e305.
          2017. Rangan, K., Ravina, M., Yadav, N., Suraj, A.S. and Gambhir, S., 2017. 18F-FDG PET/CT of Tuberculosis Meningitis and Carotid Pseudoaneurysm. Clinical nuclear medicine, 42(6), pp.e304-e305.
          A 26-year-old woman presented with a headache, left-sided weakness of the body, and pulsatile swelling above the sternal notch. She was treated for abdominal tuberculosis in the past, two years later she developed miliary tuberculosis and was put on modified regimen of antitubercular drugs in view of drug induced hepatitis. Ultrasound neck revealed saccular aneurysm measuring 4 x 3 cm, located in between common carotid arteries with an eccentric thrombus. MRI brain revealed multiple tuberculoma with thick basal meningeal enhancement. Cerebrospinal fluid was positive for Mycobacterium tuberculosis. F-FDG PET/CT was done to delineate the extent of the disease.

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