18F-FDG PET/CT as a Noninvasive Biomarker for Assessing Adequacy of Treatment and Predicting Relapse in Patients Treated for Pulmonary Tuberculosis

被引:26
作者
Lawal, Ismaheel O. [1 ,2 ]
Fourie, Bernard P. [3 ]
Mathebula, Matsontso [4 ,5 ]
Moagi, Ingrid [4 ,5 ]
Lengana, Thabo [1 ,2 ]
Moeketsi, Nontando [4 ,5 ]
Nchabeleng, Maphoshane [4 ,5 ]
Hatherill, Mark [6 ,7 ]
Sathekge, Mike M. [1 ,2 ]
机构
[1] Univ Pretoria, Dept Nucl Med, Private Bag X169, ZA-0001 Pretoria, South Africa
[2] Steve Biko Acad Hosp, Private Bag X169, ZA-0001 Pretoria, South Africa
[3] Univ Pretoria, Dept Med Microbiol, Pretoria, South Africa
[4] Sefako Makgatho Univ Med Sci, Dept Med Microbiol, Pretoria, South Africa
[5] MeCRU, Pretoria, South Africa
[6] Univ Cape Town, Inst Infect Dis, Dept Pathol, South African TB Vaccine Initiat, Cape Town, South Africa
[7] Univ Cape Town, Div Immunol, Dept Pathol, Cape Town, South Africa
基金
英国医学研究理事会;
关键词
tuberculosis; relapse; F-18-FDG PET/CT; end-of-treatment; residual metabolic activity; POSITRON-EMISSION-TOMOGRAPHY; MESSENGER-RNA; PHARMACOKINETICS; MOXIFLOXACIN; RIFAMPICIN; EXPOSURE; RISK; MICE;
D O I
10.2967/jnumed.119.233783
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
Microbial culture is the gold standard for determining the effectiveness of tuberculosis treatment. End-of-treatment (EOT) F-18-FDG PET/CT findings are variable among patients with negative microbial culture results after completing a standard regimen of antituberculous treatment (ATT), with some patients having a complete metabolic response to treatment whereas others have residual metabolic activity (RMA). We herein determine the impact of findings on EOT F-18-FDG PET/CT on tuberculosis relapse in patients treated with a standard regimen of ATT for drug-sensitive pulmonary tuberculosis (DS-PTB). Methods: Patients who completed a standard regimen of ATT for DS-PTB and were declared cured based on a negative clinical and bacteriologic examination were prospectively recruited to undergo EOT F-18-FDG PET/CT. Images were assessed for the presence of RMA. Patients were subsequently followed up for 6 mo looking for symptoms of tuberculosis relapse. When new symptoms developed, relapse was confirmed with bacteriologic testing. Repeat F-18-FDG PET/CT was done in patients who relapsed. Results: Fifty-three patients were included (mean age, 37.81 +/- 11.29 y), with 62% being male and 75% HIV-infected. RMA was demonstrated in 33 patients (RMA group), whereas 20 patients had a complete metabolic response to ATT (non-RMA group). There was a higher prevalence of lung cavitation in the RMA group (P = 0.035). The groups did not significantly differ in age, sex, presence of HIV infection, body mass index, or hemoglobin level (P > 0.05). On follow-up, no patients in the non-RMA group developed tuberculosis relapse. Three patients in the RMA group developed relapse. All patients who developed tuberculosis relapse had bilateral disease with lung cavitation. Conclusion: A negative EOT F-18-FDG PET/CT result is protective against tuberculosis relapse. Nine percent of patients with RMA after ATT may experience tuberculosis relapse within 6 mo of completing ATT. Bilateral disease with lung cavitation is prevalent among patients with tuberculosis relapse.
引用
收藏
页码:412 / 417
页数:6
相关论文
共 31 条
[1]   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
[2]  
[Anonymous], TUBERCULOSIS RES TRE
[3]  
[Anonymous], 2014, NAT TUB MAN GUID 201
[4]   High-dose rifampicin, moxifloxacin, and SQ109 for treating tuberculosis: a multi-arm, multi-stage randomised controlled trial [J].
Boeree, Martin J. ;
Heinrich, Norbert ;
Aarnoutse, Rob ;
Diacon, Andreas H. ;
Dawson, Rodney ;
Rehal, Sunita ;
Kibiki, Gibson S. ;
Churchyard, Gavin ;
Sanne, Ian ;
Ntinginya, Nyanda E. ;
Minja, Lilian T. ;
Hunt, Robert D. ;
Charalambous, Salome ;
Hanekom, Madeleine ;
Semvua, Hadija H. ;
Mpagama, Stellah G. ;
Manyama, Christina ;
Mtafya, Bariki ;
Reither, Klaus ;
Wallis, Robert S. ;
Venter, Amour ;
Narunsky, Kim ;
Mekota, Anka ;
Henne, Sonja ;
Colbers, Angela ;
van Balen, Georgette Plemper ;
Gillespie, Stephen H. ;
Phillips, Patrick P. J. ;
Hoelscher, Michael .
LANCET INFECTIOUS DISEASES, 2017, 17 (01) :39-49
[5]   A nested case-control study on treatment-related risk factors for early relapse of tuberculosis [J].
Chang, KC ;
Leung, CC ;
Yew, WW ;
Ho, SC ;
Tam, CM .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2004, 170 (10) :1124-1130
[6]   PET/CT imaging correlates with treatment outcome in patients with multidrug-resistant tuberculosis [J].
Chen, Ray Y. ;
Dodd, Lori E. ;
Lee, Myungsun ;
Paripati, Praveen ;
Hammoud, Dima A. ;
Mountz, James M. ;
Jeon, Doosoo ;
Zia, Nadeem ;
Zahiri, Homeira ;
Coleman, M. Teresa ;
Carroll, Matthew W. ;
Lee, Jong Doo ;
Jeong, Yeon Joo ;
Herscovitch, Peter ;
Lahouar, Saher ;
Tartakovsky, Michael ;
Rosenthal, Alexander ;
Somaiyya, Sandeep ;
Lee, Soyoung ;
Goldfeder, Lisa C. ;
Cai, Ying ;
Via, Laura E. ;
Park, Seung-Kyu ;
Cho, Sang-Nae ;
Barry, Clifton E., III .
SCIENCE TRANSLATIONAL MEDICINE, 2014, 6 (265)
[7]   Noninvasive Pulmonary [18F]-2-Fluoro-Deoxy-D-Glucose Positron Emission Tomography Correlates with Bactericidal Activity of Tuberculosis Drug Treatment [J].
Davis, Stephanie L. ;
Nuermberger, Eric L. ;
Um, Peter K. ;
Vidal, Camille ;
Jedynak, Bruno ;
Pomper, Martin G. ;
Bishai, William R. ;
Jain, Sanjay K. .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2009, 53 (11) :4879-4884
[8]   Determination of [11C] Rifampin Pharmacokinetics within Mycobacterium tuberculosis-Infected Mice by Using Dynamic Positron Emission Tomography Bioimaging [J].
DeMarco, Vincent P. ;
Ordonez, Alvaro A. ;
Klunk, Mariah ;
Prideaux, Brendan ;
Wang, Hui ;
Zhuo, Zhang ;
Tonge, Peter J. ;
Dannals, Robert F. ;
Holt, Daniel P. ;
Lee, Carlton K. K. ;
Weinstein, Edward A. ;
Dartois, Veronique ;
Dooley, Kelly E. ;
Jain, Sanjay K. .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2015, 59 (09) :5768-5774
[9]   Relapse in persons treated for drug-susceptible tuberculosis in a population with high coinfection with human immunodeficiency virus in New York City [J].
Driver, CR ;
Munsiff, SS ;
Li, JH ;
Kundamal, N ;
Osahan, SS .
CLINICAL INFECTIOUS DISEASES, 2001, 33 (10) :1762-1769
[10]   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