18F-FDG PET/CT in Tuberculosis Can Interim PET/CT Predict the Clinical Outcome of the Patients?

被引:15
作者
Sood, Apurva [1 ]
Mittal, Bhagwant Rai [1 ]
Modi, Manish [2 ]
Chhabra, Rajesh [3 ]
Verma, Roshan [4 ]
Rana, Nivedita [1 ]
Parihar, Ashwin Singh [1 ]
Satapathy, Swayamjeet [1 ]
Kumar, Rajender [1 ]
机构
[1] Post Grad Inst Med Educ & Res, Dept Nucl Med, Chandigarh 160012, India
[2] Post Grad Inst Med Educ & Res, Dept Neurol, Chandigarh, India
[3] Post Grad Inst Med Educ & Res, Dept Neurosurg, Chandigarh, India
[4] Post Grad Inst Med Educ & Res, Dept Otolaryngol & Head & Neck Surg, Chandigarh, India
关键词
F-18-FDG PET; CT; tuberculosis; interim PET; treatment response;
D O I
10.1097/RLU.0000000000002968
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
Purpose of the Report Tuberculosis (TB) is a major health problem. Activated macrophages in TB lesions show high metabolic activity and can be assessed using F-18-FDG PET/CT. This retroprospective study was done to evaluate the utility of F-18-FDG PET/CT in initial assessment and therapeutic response in patients with TB. Materials and Methods Eighty-seven patients (male-to-female ratio, 46:41) diagnosed with pulmonary TB and extrapulmonary TB underwent whole-body F-18-FDG PET/CT for initial assessment and a follow-up scan 3 to 4 months after initiation of antitubercular therapy (ATT). Visual and semiquantitative (SUVmax) analyses were used for scan assessment. Treatment responses on interim scans were categorized as complete metabolic response (CMR), favorable response to therapy (FRT), stable disease (SD), and disease progression (DP). CMR, FRT, and SD cases were considered as responders and DP cases as nonresponders. Treatment response was correlated with clinical outcome (mortality) and ATT duration. Results Baseline F-18-FDG PET/CT scans were positive in all the patients and detected additional disease sites than suspected clinically in 72% patients. On interim PET/CT, 13 patients showed CMR, 43 showed FRT, 8 showed SD, and 23 showed DP. A longer duration of ATT was seen in nonresponders (P <= 0.001) than responders. During follow-up, 9/87 patients died, out of which 8 patients were of DP group and 1 patient belonged to SD. Nonresponders showed 35% mortality compared with 1.6% in the responder group (P <= 0.001). Conclusions F-18-FDG PET/CT is a valuable imaging modality for disease mapping and assessing therapeutic response. Treatment response in the interim PET/CT done at 3 to 4 months predicted the duration of ATT and clinical outcome of the patients.
引用
收藏
页码:276 / 282
页数:7
相关论文
共 22 条
[1]  
Aggarwal Ashish, 2013, Surg Neurol Int, V4, pS323, DOI 10.4103/2152-7806.112619
[2]   Tuberculosis [J].
Ankrah, Alfred O. ;
Glaudemans, Andor W. J. M. ;
Maes, Alex ;
Van de Wiele, Christophe ;
Dierckx, Rudi A. J. O. ;
Vorster, Mariza ;
Sathekge, Mike M. .
SEMINARS IN NUCLEAR MEDICINE, 2018, 48 (02) :108-130
[3]  
[Anonymous], 2010, TREATM TUB GUID 4 ED
[4]   HIV-associated opportunistic CNS infections: pathophysiology, diagnosis and treatment [J].
Bowen, Lauren N. ;
Smith, Bryan ;
Reich, Daniel ;
Quezado, Martha ;
Nath, Avindra .
NATURE REVIEWS NEUROLOGY, 2016, 12 (11) :662-674
[5]   Tuberculosis: a radiologic review [J].
Burrill, Joshua ;
Williams, Christopher J. ;
Bain, Gillian ;
Conder, Gabriel ;
Hine, Andrew L. ;
Misra, Rakesh R. .
RADIOGRAPHICS, 2007, 27 (05) :1255-1273
[6]   Corticosteroids for prevention of mortality in people with tuberculosis: a systematic review and meta-analysis [J].
Critchley, Julia A. ;
Young, Fiona ;
Orton, Lois ;
Garner, Paul .
LANCET INFECTIOUS DISEASES, 2013, 13 (03) :223-237
[7]   Potential role of F18 FDG PET-CT as an imaging biomarker for the noninvasive evaluation in uncomplicated skeletal tuberculosis: a prospective clinical observational study [J].
Dureja, Sugandha ;
Sen, Ishita Barat ;
Acharya, Shankar .
EUROPEAN SPINE JOURNAL, 2014, 23 (11) :2449-2454
[8]   Evolving role of positron emission tomography in the management of patients with inflammatory and other benign disorders [J].
El-Haddad, G ;
Zhuang, HM ;
Gupta, N ;
Alavi, A .
SEMINARS IN NUCLEAR MEDICINE, 2004, 34 (04) :313-329
[9]   Multidrug-resistant and extensively drug-resistant tuberculosis: a threat to global control of tuberculosis [J].
Gandhi, Neel R. ;
Nunn, Paul ;
Dheda, Keertan ;
Schaaf, H. Simon ;
Zignol, Matteo ;
van Soolingen, Dick ;
Jensen, Paul ;
Bayona, Jaime .
LANCET, 2010, 375 (9728) :1830-1843
[10]  
Golden MP, 2005, AM FAM PHYSICIAN, V72, P1761