Contrast Media & Molecular Imaging
Volume 2018 (2018), Article ID 8194678, 6 pages
https://doi.org/10.1155/2018/8194678

Clinical Study

Comparing the Differential Diagnostic Values of ¹⁸F-Alfatide II PET/CT between Tuberculosis and Lung Cancer Patients

Xiaoqing Du,¹ Yu Zhang,¹ Liping Chen,¹ Baoming Mi,¹ Qingjun You,¹ Yuping Xu,² Donghui Pan,² Weixing Wan,¹ Min Yang,² and Chunjing Yu¹

¹Department of Nuclear Medicine, Affiliated Hospital of Jiangnan University (Wuxi No. 4 People’s Hospital), Wuxi, China
²Key Laboratory of Nuclear Medicine, Ministry of Health, Jiangsu Institute of Nuclear Medicine, Wuxi, China

Correspondence should be addressed to Chunjing Yu; ycj_wxd1978@163.com

Received 31 October 2017; Revised 27 December 2017; Accepted 31 December 2017; Published 19 February 2018

Academic Editor: Yuebing Wang

Copyright © 2018 Xiaoqing Du et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract.

Purpose. To compare the differential diagnostic values of ¹⁸F-Alfatide II PET/CT between tuberculosis and lung cancer patients and in patients with sarcoidosis and common inflammation. Methods. Nine inflammation patients (4 tuberculosis, 3 sarcoidosis, and 2 common inflammation) and 11 lung cancer patients were included in this study. All patients underwent ¹⁸F-FDG and ¹⁸F-Alfatide II PET/CT within 2 weeks, followed by biopsy and surgery. The maximized standard uptake value (SUVmax) and the mean standard uptake value (SUVmean) were evaluated. Results. The active tuberculosis lesions showed a high accumulation of ¹⁸F-FDG, but varying degrees of accumulation of ¹⁸F-Alfatide II, including negative results. The SUVmax of ¹⁸F-Alfatide II in malignant lesions was significantly higher than that in tuberculosis (4.08 ± 1.51 versus 2.63 ± 1.34, = 0.0078). Three patients with sarcoidosis showed negative results in ¹⁸F-Alfatide II PET/CT. Conclusions. The expression of is much lower in tuberculosis as compared to that in lung cancer, and accumulation of ¹⁸F-Alfatide II varied even in lesions of the same patient. The negative results of sarcoidosis patients led to the speculation that was not expressed in those lesions.

1. Introduction

Lung cancer is one of the largest malignant tumors with fast-growing morbidity and mortality. ¹⁸F-FDG PET/CT has been verified as a crucial tool for detecting, identifying, and staging lung cancer. However, the specificity of ¹⁸F-FDG PET/CT in lung cancer is controversial as some benign lesions such as tuberculosis and sarcoidosis also show a high accumulation of ¹⁸F-FDG. Thus, a new tracer with higher specificity in differentiating lung cancer and inflammation is essential.

The expression of integrin β3 on the surface of cancer cells and neovascularization endothelial cells is upregulated in cancer, inflammation, and wound [1]. ¹⁸F-Alfatide II is an annular dimer RGD (Arg-Gly-Asp) tracer targeting integrin β3. Previous studies reported that the uptake of Alfatide in lung cancer and tuberculosis lesions is markedly different [2, 3]. Thus, additional clinical data is needed to illustrate whether this new tracer is beneficial for the differentiation of tuberculosis from lung cancer.

The present study investigated the differential diagnostic value of ¹⁸F-Alfatide II PET/CT between tuberculosis and lung cancer patients. Also, the angiogenesis in sarcoidosis and chronic inflammations was investigated.

2. Materials and Methods

2.1. Radiopharmaceutical Preparation

The kit was provided by Jiangsu Institute of Nuclear Medicine. Synthesis of ¹⁸F-Alfatide II has been described previously [4].

2.2. Patients

The local institutional review board approved the ¹⁸F-Alfatide II PET/CT compliment protocol. Written informed consent was obtained from each patient. The cohort consisted of 9 patients [5 men and 4 women; aged 25–71 (55 ± 16) years] with suspected inflammations and 11 patients [10 men, 1 women; aged 48–78 (66 ± 9) years] with suspected lung cancer.

2.3. PET/CT Acquisition and Image Analysis

¹⁸F-FDG and ¹⁸F-Alfatide II PET/CT were performed at an interval of 2 weeks. Patients were required to fast at least 6 h before ¹⁸F-FDG (5.55 MBq/kg) intravenous injection. The acquisitions were conducted at 60 min after the injection. The patients were placed in a supine position on the scanner bed. Imaging data were acquired from the skull to the thigh, using PET/CT scanner, at 1.5 min/bed position. Low-dose CT was performed for attenuation correction and lesion localization. ¹⁸F-Alfatide II PET/CT was performed on the next day without any specific preparation before the examination. ¹⁸F-Alfatide II (248.27 ± 45.14 MBq) was injected intravenously in all patients. The acquisition procedure and parameters were identical to that as ¹⁸F-FDG PET/CT. Regions of interest (ROIs) were drawn manually on the site of lesions based on the corresponding CT images.

PET/CT Scanner was from Siemens (Biograph True Point PET/CT).

Visual analysis was used to evaluate the preliminary accumulation of ¹⁸F-Alfatide II and ¹⁸F-FDG in tuberculosis and lung cancer. Maximum standard uptake value (SUVmax), mean standard uptake value (SUVmean), and lesion/muscle (L/M) ratio recorded the uptake of the lesions in this study. The uptake of the right hip muscle was selected as a reference for lesions. All lesions were divided into different regions of head-neck, chest, abdomen, and pelvis. The largest lesion of each region was chosen to measure the uncountable lesions.

Two physicians evaluated the images independently, and the discrepancies were resolved by consultation.

2.4. Pathological Analysis and Follow-Up

Inflammation Group. Number 1 patient was confirmed as thoracic tuberculosis by biopsy. Number 2–4 patients, receiving PPD test, T-SPOT test, and antituberculosis treatment, were followed up for 16, 17, and 33 months, respectively; they were confirmed as lung tuberculosis, lymph node tuberculosis, and lung tuberculosis mixed with tuberculous pleurisy. Number 5 patient was confirmed as sarcoidosis by bronchoscope puncture biopsy. Number 6-7 patients, receiving no treatment and followed up for 17 and 28 months, respectively, were diagnosed as sarcoidosis. Number 8 patient was shown to have chronic inflammation accompanied by fibrosis as assessed by percutaneous lung biopsy. Number 9 patient was diagnosed with inflammation caused by common infection after 20 months’ follow-up based on CT (Table 1).

Table 1: Patient demographics (inflammation group).

Patient number
Age (years)
Sex
Histology

1
69
M
Thoracic tuberculosis

2
71
M
Lung tuberculosis

3
25
F
Lymph node tuberculosis

4
63
M
Lung tuberculosis + tuberculous pleurisy

5
66
F
Sarcoidosis

6
56
F
Sarcoidosis

7
32
F
Sarcoidosis

8
67
M
Chronic-inflammation with fibrosis

9
66
M
Common inflammation

Malignancy Group. Eight patients received surgery. One patient did not undergo surgery since the pulmonary trunk was invaded by cancer, and two patients were not recommended surgery as distant metastasis detected by PET/CT and MRI. All patients were confirmed by pathology; one distant metastasis patient received bronchoscopy biopsy, while the other underwent clavicle lymph node excision (Table 2).

Table 2: Patient demographics (malignancy group).

Patient number
Age (years)
Sex
Histology

1
65
M
Squamous cell carcinoma (SCC)

2
75
M
Adenocarcinoma

3
78
M
Squamous cell carcinoma (SCC)

4
72
M
Squamous cell carcinoma (SCC)

5
58
M
Squamous cell carcinoma (SCC)

6
57
M
Squamous cell carcinoma (SCC)

7
67
M
Squamous cell carcinoma (SCC)

8
48
M
Squamous cell carcinoma (SCC)

9
57
F
Adenocarcinoma

10
75
M
Adenocarcinoma

11
74
M
Adenocarcinoma

2.5. Statistical Analysis

Mean ± standard deviation (m ± SD) was used to express all quantitative data. Differences in SUVmax/SUVmean between patients with different diseases were compared and assessed by -test or Mann–Whitney test. All statistical analyses were carried out using SAS 9.2. < 0.05 indicated statistical significance.

3. Results

3.1. Safety

Patients did not report any subjective effects following the injected dose of ¹⁸F-Alfatide II. No adverse events were noted during the examination of ¹⁸F-Alfatide II PET/CT or follow-up (at least 6 months).

3.2. Visual Analysis Results

The accumulation of ¹⁸F-Alfatide II in tuberculosis was much lower than that of ¹⁸F-FDG (Figures 1 and 2), while no accumulation was observed in sarcoidosis lesions (Figure 3). Additionally, 2 chronic inflammations showed a high accumulation of ¹⁸F-Alfatide II.

(a)

(b)

Figure 1: -FDG (a) and -Alfatide II (b) PET/CT images of a thoracic tuberculosis patient. T2, T3, and T4 showed intense -FDG uptake and mild -Alfatide II uptake. The white arrows indicate tuberculosis lesions in T4.

(a)

(b)

Figure 2: -FDG (a) and -Alfatide II (b) PET/CT images of a lymph node tuberculosis patient. Lymph nodes tuberculosis lesions showed intense -FDG uptake and no -Alfatide II uptake. The white arrows indicate tuberculosis lesions in porta hepatis lymph nodes.

(a)

(b)

Figure 3: -FDG (a) and -Alfatide II (b) PET/CT images of a sarcoidosis patient. All lesions showed intense -FDG uptake and no -Alfatide II uptake. The white arrows indicate sarcoidosis lesions in mediastinum and hilus pulmonis.

All lung cancer patients in this study showed a high accumulation of ¹⁸F-Alfatide II, including brain and bone metastasis. The results were similar to that in the previous reports [5].

3.3. Preliminary Diagnostic Value of ¹⁸F-FDG PET/CT and ¹⁸F-Alfatide II PET/CT in Tuberculosis

The SUVmax of tuberculosis was calculated as 7.53 ± 2.88 and 2.63 ± 1.34 for ¹⁸F-FDG and ¹⁸F-Alfatide II, respectively. The SUVmean of tuberculosis was 4.58 ± 1.73 and 1.86 ± 1.0, respectively.

3.4. Preliminary Diagnostic Value of ¹⁸F-FDG PET/CT and ¹⁸F-Alfatide II PET/CT in Chronic Inflammation

The SUVmax of two patients with chronic inflammation was 10.80 and 1.62 for ¹⁸F-FDG and 9.13 and 5.75 for ¹⁸F-Alfatide II, respectively. The SUVmean was 5.33, 0.99 and 5.12, 2.65, respectively.

3.5. Preliminary Diagnostic Value of ¹⁸F-FDG PET/CT and ¹⁸F-Alfatide II PET/CT in Sarcoidosis

The SUVmax of ¹⁸F-FDG and ¹⁸F-Alfatide II in sarcoidosis was calculated as 8.82 ± 5.17 and 1.77 ± 0.69, respectively, while SUVmean was 5.34 ± 3.08 and 1.28 ± 0.63, respectively.

3.6. Preliminary Diagnostic Value of ¹⁸F-FDG PET/CT and ¹⁸F-Alfatide II PET/CT in Lung Cancer

The SUVmax of ¹⁸F-FDG and ¹⁸F-Alfatide II in lung cancer was 12.04 ± 4.67 and 4.08 ± 1.51, respectively, while SUVmean was 4.55 ± 1.98 and 1.99 ± 0.81, respectively.

3.7. Difference between the SUVmax of Malignant Lesions and Tuberculosis Lesions

The lesion-to-lesion analysis showed that the SUVmax of ¹⁸F-Alfatide II in malignant lesions was 4.08 ± 1.51, which was significantly higher than that in tuberculosis (2.63 ± 1.34, = 0.0078).

3.8. Difference between the SUVmean of Malignant Lesions and Tuberculosis Lesions

The SUVmean of ¹⁸F-Alfatide II in malignant lesions was 1.99 ± 0.81 without any statistically significant difference from that of tuberculosis (1.86 ± 1.0, = 0.3820).

3.9. Preliminary Diagnostic Value of ¹⁸F-FDG and ¹⁸F-Alfatide II PET/CT in Inflammations (Active TB, Chronic Inflammation, and Sarcoidosis) and Lung Cancer

See Table 3.

Table 3: SUVmax and SUVmean of lesions.

¹⁸F-FDG
¹⁸F-Alfatide II
¹⁸F-FDG
¹⁸F-Alfatide II

SUVmax
SUVmax
SUVmean
SUVmean

Tuberculosis
7.53 ± 2.88
2.63 ± 1.34
4.58 ± 1.73
1.86 ± 1.0

Lung cancer
12.04 ± 4.67
4.08 ± 1.51
4.55 ± 1.98
1.99 ± 0.81

Sarcoidosis
8.82 ± 5.17
1.77 ± 0.69
5.34 ± 3.08
1.28 ± 0.63

Chronic inflammation 1
10.80
9.13
5.33
5.12

Chronic inflammation 2
1.62
5.75
0.99
2.65

4. Discussion

Integrin is overexpressed not only in various tumor cells and tumor neovasculature [6] but also in chronic inflammatory diseases, such as inflammatory bowel disease (IBD) and rheumatoid arthritis (RA) [7, 8]. Previous studies reported that angiogenesis and chronic inflammation are interrelated [7, 9]. Jackson et al. [10] suggested that several resident cells (fibroblasts, monocytes-macrophages, neutrophils, and lymphocytes) can promote angiogenesis when the microenvironment becomes hypoxic or inflammatory, thereby facilitating the migration of inflammatory cells to inflammatory sites and the supply of nutrients and oxygen to the proliferating tissue. The frequent dual functionality of angiogenic factors such as and VEGF reflects the close relationship between angiogenesis and inflammation [11]. Cao et al. [12] demonstrated specific uptake of in the chronic inflammation of mouse ear using ⁶⁴Cu-DOTA-RGD tetramer PET imaging.

Chin et al. [13] carried out a PET imaging study with ¹⁸F-FPP(RGD)₂ in a healthy woman volunteer, and no unusual or adverse patient symptoms were found on the day of imaging as well as during follow-up. Wan et al. [2] did not record any adverse events associated with ¹⁸F-Alfatide in the first subject during the study, in which nine lung cancer patients were investigated. No adverse events occurred in all patients during or after the ¹⁸F-Alfatide II PET/CT imaging in the current study. All these investigations revealed that using RGD tracers labeled by ¹⁸F is safe for patients.

Tuberculosis is a major global health problem with an estimated 8.6 million new cases worldwide in 2012 [14]. The tuberculous granuloma is an organized collection of differentiated macrophages surrounded by T-lymphocytes, B-lymphocytes, dendritic cells, fibroblasts, and extracellular matrix components [15]. Some studies demonstrated expression in lung granulomas and lymph nodes of sarcoid patients [16]. Rojas et al. [17] found that the mycobacterial glycolipid phosphatidylinositol mannoside interacts directly with integrin VLA-5 on CD4⁺ T-lymphocytes, resulting in fibronectin binding and T-cell migration. Several studies have reported increased levels of VEGF in granulomatous disease, such as pulmonary tuberculosis [18–21] and Crohn’s disease [22]. Hur et al. [23] reported that median concentration of serum VEGF-A was significantly higher in tuberculosis patients than that in the latent tuberculosis infection and control groups. Four patients with active tuberculosis showed varying degree of accumulation of ¹⁸F-Alfatide II in this study, including negative results, and even the positive lesions showed a low accumulation of ¹⁸F-Alfatide II than that of ¹⁸F-FDG. Kang et al. [3] reported that tuberculosis granuloma and the surrounding vasculature epithelium showed baseline expression as assessed by immunohistochemistry. The diversity in the current study revealed different expression of in all tuberculosis lesions.

All lung cancer lesions and the metastases in the brain and bone showed an increased RGD uptake. A significant difference was noted in SUVmax between the lung cancer and tuberculosis groups, which indicated that RGD PET/CT might differentiate lung cancer from tuberculosis.

Sarcoidosis is an immunological, granulomatous disorder affecting multiple systems. The presence of noncaseating granulomas in involved organs is a pathological feature [24]. The common sites of the disease are lung, mediastinum, and hilus pulmonis lymph node [25, 26]. The precise pathogenesis is yet unknown, which might include various factors: environmental, occupational exposure, the presence of infectious agents, and genetic susceptibility [27–29]. Various studies suggested that angiogenic factors contribute to the pathogenesis of sarcoidosis [30, 31]. Agostini et al. [32] and Antoniou et al. [31] indicated the presence of angiogenesis in the pathogenesis of granulomatous and pulmonary fibrosis. Tzouvelekis et al. [33] revealed an abundant expression of VEGF and ING4 within the granulomatous tissue, localized in the epithelioid and giant cells. Three sarcoidosis patients, in this study, showed negative results in ¹⁸F-Alfatide II PET/CT, thereby indicating the lack of expression in sarcoidosis. Kambouchner et al. [34] proposed the presence of an avascular microenvironment within sarcoid lesions. Tzouvelekis et al. [33] speculated that abundant expression of VEGF might be implicated in the inflammatory than the angiogenic cascade of sarcoidosis. Murdoch et al. supported this speculation with respect to the pleiotropic properties of VEGF in promoting the Th1-dependent immunity via facilitation of monocyte recruitment and T-cell migration to sites of ongoing inflammation [35]. The results from the current study were in agreement with the theory by Kambouchner et al. and Tzouvelekis et al.

Furthermore, the present study comprised 2 common infection patients: one patient showed high accumulation of ¹⁸F-Alfatide II as well as ¹⁸F-FDG, while the other showed a high accumulation of ¹⁸F-Alfatide II compared to ¹⁸F-FDG. Winter et al. [36] speculated that integrin was a potential marker of inflammation and angiogenesis in atherosclerotic lesions. Srivatsa et al. and Hansson both observed persistently high levels of expression between 7 and 21 days following injury in the neointima, media, and adventitia [37, 38]. Other studies demonstrated the expression of integrin on activated macrophages by different methods [39–41]. When acute inflammation transforms into subacute and chronic inflammation, macrophages are gradually increased in number in lesions than the neutrophils. Thus, the high accumulation of ¹⁸F-Alfatide II in the 2 patients in this study indicated the chronic inflammatory stage, which was confirmed by fibrosis tested by percutaneous lung biopsy in one lesion. Storgard et al. [42] reported that the treatment with cyclic RGD peptide c(RGDfV), an integrin antagonist, significantly inhibited the disease progression in an experimental RA model. Taken together, ¹⁸F-Alfatide II PET/CT may not only detect chronic inflammation but also allow the evaluation of angiogenesis and neovascularization during chronic inflammation and guide the selection of patients for antiangiogenesis therapy.

Nevertheless, the present study has some deficiencies. (1) Early experimental design was not perfect; for example, we did not recruit lymphoma patients to compare with sarcoidosis in ¹⁸F-Alfatide II PET/CT. (2) The number of patients was small. (3) Further investigations are essential.

5. Conclusion

The accumulation of lung cancer and tuberculosis exhibits distinct difference, which might be valuable in differentiating the two diseases. Three sarcoidoses showed negative results, and thus, we speculated the lack of expression within sarcoidosis. ¹⁸F-Alfatide II might be valuable in the evaluation of angiogenesis and neovascularization during chronic inflammation, which could guide the selection of patients for antiangiogenesis therapy and evaluate the clinical effect of the treatment.

Conflicts of Interest

The authors declare that they have no conflicts of interest.

Acknowledgments

This work was supported by the Natural Science Foundation of China (81471691).

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