Standardized Uptake Values Derived from <sup>18</sup>F-FDG PET May Predict Lung Cancer Microvessel Density and Expression of KI 67, VEGF, and HIF-1<i>α</i> but Not Expression of Cyclin D1, PCNA, EGFR, PD L1, and p53

Surov, Alexey; Meyer, Hans Jonas; Wienke, Andreas

doi:https://doi.org/10.1155/2018/9257929

Contrast Media & Molecular Imaging

On this page

Abstract Introduction Materials and Methods Results Discussion Data Availability Ethical Approval Conflicts of Interest Authors’ Contributions References Copyright Related Articles

Special Issue

Imaging Diagnostic and Pathology in the Management of Oncological-Patients

View this Special Issue

Research Article | Open Access

Volume 2018 | Article ID 9257929 | https://doi.org/10.1155/2018/9257929

Standardized Uptake Values Derived from ¹⁸F-FDG PET May Predict Lung Cancer Microvessel Density and Expression of KI 67, VEGF, and HIF-1α but Not Expression of Cyclin D1, PCNA, EGFR, PD L1, and p53

Alexey Surov,¹Hans Jonas Meyer,¹and Andreas Wienke²

Academic Editor: Elena Bonanno

Received02 Mar 2018

Accepted26 Apr 2018

Published06 Jun 2018

Abstract

Background. Our purpose was to provide data regarding relationships between ¹⁸F-FDG PET and histopathological parameters in lung cancer. Methods. MEDLINE library was screened for associations between PET parameters and histopathological features in lung cancer up to December 2017. Only papers containing correlation coefficients between PET parameters and histopathological findings were acquired for the analysis. Overall, 40 publications were identified. Results. Associations between SUV and KI 67 were reported in 23 studies (1362 patients). The pooled correlation coefficient was 0.44. In 2 studies (180 patients), relationships between SUV and expression of cyclin D1 were analyzed (pooled correlation coefficient = 0.05). Correlation between SUV and HIF-1α was investigated in 3 studies (288 patients), and the pooled correlation coefficient was 0.42. In 5 studies (310 patients), associations between SUV and MVD were investigated (pooled correlation coefficient = 0.54). In 6 studies (305 patients), relationships between SUV and p53 were analyzed (pooled correlation coefficient = 0.30). In 6 studies (415 patients), associations between SUV and VEGF expression were investigated (pooled correlation coefficient = 0.44). In 5 studies (202 patients), associations between SUV and PCNA were investigated (pooled correlation coefficient = 0.32). In 3 studies (718 patients), associations between SUV and expression of PD L1 were analyzed (pooled correlation coefficient = 0.36). Finally, in 5 studies (409 patients), associations between SUV and EGFR were investigated (pooled correlation coefficient = 0.38). Conclusion. SUV may predict microvessel density and expression of VEGF, KI 67, and HIF-1α in lung cancer.

1. Introduction

Lung cancer is one of the most frequent malignancies in humans [1]. It is the largest cause of cancer deaths in the United States [1].

Multiple histopathological factors influence tumor biology in lung cancer. According to the literature, different molecular markers play a key role here [2]. Previous reports investigated numerous biomarkers and suggested that some histopathological parameters can predict tumor behavior in lung cancer [2–5]. It has been shown that they provide information about tumor proliferation, aggressiveness, prognosis, and therapy response [2–5]. According to the literature, following biomarkers are relevant in lung cancer: proliferation index KI 67, hypoxia-inducible factor- (HIF-) 1α, tumor suppressor protein p53, vascular endothelial growth factor (VEGF), epidermal growth factor receptor (EGFR), proliferating cell nuclear antigen (PCNA), PD L1, and several cyclins [2–10]. For instance, it has been shown that tumors with high expression of KI 67 and/or VEGF were associated with a worse prognosis [3, 4]. Similar results were also reported for expression of HIF-1α and p53 [5–7].

Furthermore, some reports analyzed associations between imaging parameters and histopathological features in lung cancer [11–14]. Especially parameters of positron emission tomography (PET) like standardized uptake values (SUV) were in focus of the studies. However, the reported data were inconsistent. While some authors found such significant relationships, others did not. Therefore, it is unclear whether SUV can be used as a surrogate parameter reflecting histopathological features in lung cancer or not.

The purpose of this meta-analysis was to provide evident data about associations between SUV and histopathological parameters in lung cancer.

2. Materials and Methods

2.1. Data Acquisition

The strategy of data acquisition is shown in Figure 1. MEDLINE library was screened for associations between PET parameters and histopathological findings in lung cancer up to December 2017.

For associations between PET and different biomarkers, the following search words were used:(i)PET and KI 67: “lung cancer AND PET OR positron emission tomography AND KI 67 OR KI67 OR ki67 OR ki-67 OR mitotic index OR proliferation index OR MIB 1 OR MIB-1 OR mitosis index” (192 items)(ii)PET and expression of p53: “lung cancer AND PET or positron emission tomography AND p53 OR tumor suppressor protein” (51 items)(iii)PET and expression of VEGF: “lung cancer AND PET or positron emission tomography AND VEGF OR vascular endothelial growth factor” (82 items)(iv)PET and expression of EGFR: “lung cancer AND PET or positron emission tomography AND EGFR OR epidermal growth factor receptor” (345 items)(v)PET and expression of HIF-1α: “lung cancer AND PET or positron emission tomography AND HIF-1α OR HIF1α OR HIF-1 alpha OR HIF1 alpha OR hypoxia-inducible factor” (38 items)(vi)PET and expression of PCNA: “lung cancer AND PET or positron emission tomography AND PCNA OR proliferating cell nuclear antigen” (23 items)(vii)PET and expression of cyclins: “lung cancer AND PET or positron emission tomography AND cyclin” (22 items)(viii)PET and microvessel density: “lung cancer AND PET or positron emission tomography AND microvessel density OR MVD” (34 items)(ix)PET and expression of PD L1: “lung cancer AND PET or positron emission tomography AND programmed cell death-ligand 1 OR PD L1” (15 items).

Secondary references were also recruited. Overall, 802 records were identified. After exclusion of doublets, review articles, case reports, non-English publications, and articles, which not contain correlation coefficients between PET and histopathological parameters, there were 40 articles [11–50].

The following data were extracted from the literature: authors, year of publication, number of patients, histopathological parameters, and correlation coefficients, according to our previous descriptions [51–53].

The Preferred Reporting Items for Systematic Reviews and Meta-Analyses statement (PRISMA) was used for the research [54].

2.2. Meta-Analysis

The methodological quality of the acquired 40 studies was independently checked by two observers (Alexey Surov and Hans Jonas Meyer) using the Quality Assessment of Diagnostic Studies (QUADAS) instrument according to previous descriptions [55]. Table 1 shows the results of QUADAS proving.

Associations between PET and histopathological findings were analyzed by Spearman’s correlation coefficient. The reported Pearson’s correlation coefficients in some studies were converted into Spearman’s correlation coefficients according to the previous description [56].

Furthermore, the meta-analysis was undertaken by using RevMan 5.3 (Computer Program, version 5.3, The Cochrane Collaboration, 2014, The Nordic Cochrane Centre, Copenhagen). Heterogeneity was calculated by means of the inconsistency index I² [57, 58]. Additionally, DerSimonian and Laird random-effects models with inverse-variance weights were used without any further correction [59].

3. Results

3.1. KI 67

Associations between ¹⁸F-FDG PET and KI 67 were reported in 23 studies (1362 patients) [11–33]. The calculated correlation coefficients between SUV_max and KI 67 ranged from −0.23 to 0.81 (Figure 2). The pooled correlation coefficient was 0.44 (95% CI = (0.35; 0.54)).

3.2. Cyclin D1

In 2 studies (180 patients), relationships between 18F-FDG PET and expression of cyclin D1 were analyzed [34, 35]. The pooled correlation coefficient between these parameters was 0.05 (95% CI = (−0.36; 0.46)) (Figure 3).

3.3. HIF-1α

Associations between ¹⁸F-FDG PET and HIF-1α were investigated in 3 studies (288 patients) [36–38]. The reported correlation coefficients ranged from −0.19 to 0.99 (Figure 4). The pooled correlation coefficient was 0.42 (95% CI = (0.06; 0.78)).

3.4. Microvessel Density (MVD)

Associations between ¹⁸F-FDG PET and MVD were investigated in 5 studies (310 patients) [25,37–40]. The reported correlation coefficients ranged from −0.23 to 0.91 (Figure 5). The pooled correlation coefficient was 0.54 (95% CI = (0.29; 0.80)).

3.5. P53

In 6 studies (305 patients), relationships between ¹⁸F-FDG PET and p53 were analyzed [13,22,34,41–43]. The pooled correlation coefficient between these parameters was 0.30 (95% CI = (0.13; 0.47)) (Figure 6).

3.6. VEGF

There were 6 studies (415 patients) which investigated associations between SUV and expression of VEGF in lung cancer [13, 18, 34, 37, 38, 44]. The reported correlation coefficients ranged from −0.13 to 0.77 (Figure 7). The pooled correlation coefficient was 0.44 (95% CI = (0.14; 0.73)).

3.7. PCNA

There were 5 studies (202 patients) which investigated associations between ¹⁸F-FDG PET and PCNA in lung cancer [22,40,45–47]. The reported correlation coefficients ranged from 0.04 to 0.83 (Figure 8). The pooled correlation coefficient was 0.32 (95% CI = (0.05; 0.60)).

3.8. EGFR

There were 5 studies (409 patients) which investigated associations between ¹⁸F-FDG PET and expression of EGFR in lung cancer [13, 34, 38, 42, 44]. The reported correlation coefficients ranged from 0.04 to 0.83 (Figure 9). The pooled correlation coefficient was 0.38 (95% CI = (0.10; 0.66)).

3.9. PD L1

In 3 studies (718 patients), relationships between ¹⁸F-FDG PET and expression of PD L1 were analyzed [48–50]. The pooled correlation coefficient between these parameters was 0.36 (95% CI = (0.22; 0.50)) (Figure 10).

4. Discussion

Analysis of interactions between imaging findings, in particular, between PET and histopathology can significantly improve oncologic diagnostics [60]. The possibility to characterize histological tissues by imaging can also personalize anticancer treatment [60]. Although PET is an established investigation of lung cancer in clinical practice, only few reports analyzed the question if there are relationships between PET findings and different histopathological parameters. However, this is a key question. In fact, if PET parameters do correlate with several histopathological findings reflecting proliferation or other features of lung cancer, then PET values can also be used as biomarkers.

Our meta-analysis showed that SUV can reflect different histopathological parameters in lung cancer. As shown, SUV correlated moderately with KI 67. This finding is not surprisingly. KI 67 is a nonhistone, nuclear protein synthesized throughout the whole cell cycle except the G0 phase and has been shown to be responsible for cell proliferation [61]. It is an established biomarker in lung cancer for prediction of tumor behavior. Our data are in agreement with those of previous investigations and also analyzed relationships between expression of KI 67 and SUV in lung cancer [62, 63]. However, we found weak correlations between SUV_max and other proliferation markers, namely, PCNA (0.32). This finding is difficult to explain. Theoretically, SUV reflects metabolic activity and, therefore, might correlate stronger with several proliferation biomarkers. Obviously, metabolic activity and proliferation are not associated directly.

Similarly, our analysis found only slight correlation between SUV_max and expression of EGFR (0.38). EGFR is a cell membrane tyrosine kinase receptor [64, 65]. As reported previously, EGFR signaling is critical in development and cellular homeostasis, proliferation, and growth [64–66]. EGFR is overexpressed in most lung cancers [64–66]. Overexpression of EGFR is associated with a poor prognosis in non-small-cell lung cancer [66]. In addition, EGFR overexpression is also associated with chemoresistance in non-small-cell lung cancer [64, 66]. The present meta-analysis showed that SUV_max cannot be used as a surrogate marker for EGFR expression in lung cancer.

Furthermore, we analyzed associations between SUV_max and expression of p53. As seen, these parameters correlate weakly (0.30). According to the literature, p53 is a protein encoded by the TP53 gene and plays a key role in tumor suppression and in the cellular response to DNA damage [2, 5]. Some authors indicated that high expression of p53 can be used as a predictor for better overall survival [2]. However, in the study of Tsao et al., p53 protein overexpression was a significant prognostic marker of shortened survival [5]. Relationships between SUV_max and p53 were analyzed in 6 previous studies with divergent results [13,22,34,41–43]. Our data suggest that SUV cannot be used as a surrogate marker for expression of p53.

Programmed cell death-ligand 1 or PD L1 is another very important biomarker in lung cancer [67]. PD L1 is an immune modulator that promotes immunosuppression by binding to PD-1 receptor [68]. PD L1 on the surface of tumor cells inhibits an immune-mediated attack by binding to PD-1 on cytotoxic T-cells [68, 69]. According to the literature, high expression of PD L1 is associated with shorter overall survival in patients with non-small cell lung cancer [70]. Therefore, prediction of PD L1 expression by imaging may be of interest in clinical practice. Our analysis identified only a slightly correlation (0.36) between SUV_max and PD L1 expression in lung cancer; that is, SUV_max cannot be used as a surrogate marker for PD L1 status.

Our analysis also showed that SUV_max cannot predict expression of cyclin D1 in lung cancer. As reported previously, data of the role of this protein are inconsequent. For example, Gautschi et al. found a strong pathological role for cyclin D1 deregulation in bronchial neoplasia [71]. However, Zhang et al. suggested in their meta-analysis that the expression of cyclin D1 is unlikely to be useful as a prognostic marker for NSCLC in clinical practice from current evidence [72].

The present meta-analysis identified a moderate pooled correlation between SUV_max and hypoxia-inducible factor-1 alpha (HIF-1α). According to the literature, HIF-1α characterizes cellular responses to hypoxic stress [6, 7]. It has been reported that patients with lung cancer and positive HIF-1α expression in tumor tissues had lower overall survival rate than patients with negative HIF-1α expression [6, 7]. Furthermore, in a recent meta-analysis, it was suggested that HIF-1α expression may be a prognostic biomarker for lung cancer [6]. In addition, it is discussed that HIF-1α might be a target for therapy in lung cancer [7]. Therefore, associations between PET parameters and HIF-1α may be also of clinical importance.

Similarly, we calculated a moderate pooled correlation between SUV_max and expression of VEGF. Previous reports indicated that VEGF overexpression is associated with poor prognosis for NSCLC patients [3]. Furthermore, VEGF plays an important role in sustaining the development and progression of lung cancer [73]. Notably, some reports indicated a great potential of anti-VEGF agents in therapy of lung cancer [74]. Therefore, possible relationships between VEGF expression and SUV in lung cancer may play a significant role to plane chemotherapy. In fact, if SUV or other PET parameters may predict VEGF expression and tumors with overexpression, respectively, then PET may also be used for therapy control with anti-VEGF agents.

Finally, the strongest correlation was found between SUV_max and microvessel density (0.54). This finding seems to be logical. In fact, high metabolic activity may induce a high perfusion, which is associated with more vessels. SUV may identify hypervascularized tumor areas. Therefore, SUV may be used for evaluation of response to therapy with angiogenesis inhibitors.

The present meta-analysis also identified several other problems. Overall, most analyzed biomarkers are associated with SUV. This finding suggests that SUV_max may reflect different histopathological features in lung cancer. However, as mentioned above, the calculated pooled correlations are slightly-to-moderate. Therefore, our analysis showed that SUV_max cannot be used as an ultimate one-to-one surrogate marker for different receptor expressions in lung cancer.

Some reports suggested that other PET parameters like metabolic tumor volume or total lesion glycolysis are more sensitive than SUV_max [75]. In fact, pretreatment SUV is commonly used as a relative measure of ¹⁸FDG uptake and is considered a prognostic factor for risk stratification in different malignancies. However, as suggested previously, it does not reflect the heterogeneity of a tumor [76]. Therefore, to overcome this drawback of SUV, other PET parameters, such as metabolic tumor volume and total lesion glycolysis that reflect metabolic volume and activity, have been proposed as quantitative indexes of tumor metabolism [76, 77]. According to the literature, these parameters can be used as prognostic factors for survival in several malignant diseases like non-small lung cancer, pleural mesothelioma, and ovarian cancer [77–79]. Clearly, further researches are needed to investigate possible associations between several PET parameters and histopathology in lung cancer.

Furthermore, lung cancer involves several carcinomas with different histopathological features and behavior. Presumably, different subtypes of lung cancer may have also different associations between PET and histopathology. This question should also be analyzed by further investigations.

There were also other problems. Only 40 reports with small number of patients investigated associations between PET parameters and histopathological features in lung cancer. Furthermore, most of the acquired studies were retrospective. Finally, according the QUADAS criteria, all involved studies showed partial verification bias, differential verification bias, and incorporation bias. Also, most of the studies had clinical review bias and diagnostic review bias. Clearly, further prospective studies with more patients are needed to investigate associations between PET and histopathology in lung cancer.

Some recent reports indicated that other histopathological markers like tumor-infiltrating CD8-positive T lymphocytes, cyclooxygenase-2, and survivin play also a great role in lung cancer [3, 4]. However, there were either no data or in each case only one report about relationships between PET and these histopathological factors. This should be also the purpose for further investigations.

In conclusion, our meta-analysis showed that SUV_max may predict microvessel density and expression of VEGF, KI 67, and HIF-1α in lung cancer. There were no significant associations between SUV_max and expression of cyclin D1, EGFR, PD L1, PCNA, and p53.

Data Availability

The data used to support the findings of this study are available from the corresponding author upon request.

Ethical Approval

The study was approved by the institutional review board of the University of Leipzig. All procedures performed in the study were in accordance with the ethical standards of the institutional research committee and with the 1964 Helsinki Declaration and its later amendments or comparable ethical standards.

Conflicts of Interest

There are no conflicts of interest.

Authors’ Contributions

Alexey Surov conceptualized the data. Alexey Surov, Hans Jonas Meyer, and Andreas Wienke performed data curation. Alexey Surov, Hans Jonas Meyer, and Andreas Wienke did formal analysis. Alexey Surov, Hans Jonas Meyer, and Andreas Wienke investigated the data. Alexey Surov, Hans Jonas Meyer, and Andreas Wienke designed the methodology. Alexey Surov administered the project. Alexey Surov, Hans Jonas Meyer, and Andreas Wienke collected resources. Alexey Surov, Hans Jonas Meyer, and Andreas Wienke designed the software. Alexey Surov helped in supervision. Alexey Surov validated the data. Alexey Surov, Hans Jonas Meyer, and Andreas Wienke visualized the data. Alexey Surov wrote the original draft. Alexey Surov, Hans Jonas Meyer, and Andreas Wienke wrote, reviewed, and edited the data. All authors contributed equally to this work.

References

R. Siegel, D. Naishadham, and A. Jemal, “Cancer statistics,” CA: A Cancer Journal for Clinicians, vol. 62, no. 1, pp. 10–29, 2012.
View at: Publisher Site | Google Scholar
S. Wallerek and J. B. Sørensen, “Biomarkers for efficacy of adjuvant chemotherapy following complete resection in NSCLC stages I-IIIA,” European Respiratory Review, vol. 24, no. 136, pp. 340–355, 2015.
View at: Publisher Site | Google Scholar
H. Jiang, W. Shao, and W. Zhao, “VEGF-C in non-small cell lung cancer: meta-analysis,” Clinica Chimica Acta, vol. 427, pp. 94–99, 2014.
View at: Publisher Site | Google Scholar
B. Martin, M. Paesmans, C. Mascaux et al., “Ki-67 expression and patients survival in lung cancer: systematic review of the literature with meta-analysis,” British Journal of Cancer, vol. 91, no. 12, pp. 2018–2025, 2004.
View at: Publisher Site | Google Scholar
M. S. Tsao, S. Aviel-Ronen, K. Ding et al., “Prognostic and predictive importance of p53 and RAS for adjuvant chemotherapy in non small-cell lung cancer,” Journal of Clinical Oncology, vol. 25, no. 33, pp. 5240–5247, 2007.
View at: Publisher Site | Google Scholar
S. L. Yang, Q. G. Ren, L. Wen, and J. L. Hu, “Clinicopathological and prognostic significance of hypoxia-inducible factor-1 alpha in lung cancer: a systematic review with meta-analysis,” Journal of Huazhong University of Science and Technology, vol. 36, no. 3, pp. 321–327, 2016.
View at: Publisher Site | Google Scholar
W. Ren, D. Mi, K. Yang et al., “The expression of hypoxia-inducible factor-1α and its clinical significance in lung cancer: a systematic review and meta-analysis,” Swiss Medical Weekly, vol. 143, p. w13855, 2013.
View at: Publisher Site | Google Scholar
R. T. Adamson, “Biomarkers and molecular profiling in non-small cell lung cancer: an expanding role and its managed care implications,” American Journal of Managed Care, vol. 19, no. 19, pp. s398–s404, 2013.
View at: Google Scholar
X. Li, X. Liu, D. Cui, X. Wu, and R. Qian, “Clinical significance of nucleostemin and proliferating cell nuclear antigen protein expression in non-small cell lung cancer,” Journal of B.U.ON.: Official Journal of the Balkan Union of Oncology, vol. 20, no. 4, pp. 1088–1093, 2015.
View at: Google Scholar
S. Singhal, A. Vachani, D. Antin-Ozerkis, L. R. Kaiser, and S. M. Albelda, “Prognostic implications of cell cycle, apoptosis, and angiogenesis biomarkers in non-small cell lung cancer: a review,” Clinical Cancer Research, vol. 11, no. 11, pp. 3974–3986, 2005.
View at: Publisher Site | Google Scholar
M. H. Cherk, S. S. Foo, A. M. Poon et al., “Lack of correlation of hypoxic cell fraction and angiogenesis with glucose metabolic rate in non-small cell lung cancer assessed by 18F-fluoromisonidazole and 18F-FDG PET,” Journal of Nuclear Medicine, vol. 47, no. 12, pp. 1921–1926, 2006.
View at: Google Scholar
J. Zhang, L. B. Cui, X. Tang et al., “DW MRI at 3.0 T versus FDG PET/CT for detection of malignant pulmonary tumors,” International Journal of Cancer, vol. 134, no. 3, pp. 606–611, 2014.
View at: Publisher Site | Google Scholar
I. Apostolova, K. Ego, I. G. Steffen et al., “The asphericity of the metabolic tumour volume in NSCLC: correlation with histopathology and molecular markers,” European Journal of Nuclear Medicine and Molecular Imaging, vol. 43, no. 13, pp. 2360–2373, 2016.
View at: Publisher Site | Google Scholar
A. K. Buck, G. Halter, H. Schirrmeister et al., “Imaging proliferation in lung tumors with PET: 18F-FLT versus 18F-FDG,” Journal of Nuclear Medicine, vol. 44, no. 9, pp. 1426–1431, 2003.
View at: Google Scholar
A. Del Gobbo, A. Pellegrinelli, G. Gaudioso et al., “Analysis of NSCLC tumour heterogeneity, proliferative and 18F-FDG PET indices reveals Ki67 prognostic role in adenocarcinomas,” Histopathology, vol. 68, no. 5, pp. 746–751, 2016.
View at: Publisher Site | Google Scholar
B. Han, S. Lin, L. J. Yu, R. Z. Wang, and Y. Y. Wang, “Correlation of ¹⁸F-FDG PET activity with expressions of survivin, Ki67, and CD34 in non-small-cell lung cancer,” Nuclear Medicine Communications, vol. 30, no. 11, pp. 831–837, 2009.
View at: Publisher Site | Google Scholar
H. Kaida, A. Kawahara, M. Hayakawa et al., “The difference in relationship between ¹⁸F-FDG uptake and clinicopathological factors on thyroid, esophageal, and lung cancers,” Nuclear Medicine Communications, vol. 35, no. 1, pp. 36–43, 2014.
View at: Publisher Site | Google Scholar
K. Kaira, N. Oriuchi, K. Shimizu et al., “Correlation of angiogenesis with ¹⁸F-FMT and ¹⁸F-FDG uptake in non-small cell lung cancer,” Cancer Science, vol. 100, no. 4, pp. 753–758, 2009.
View at: Publisher Site | Google Scholar
S. Kuyumcu, I. Adalet, Y. Sanli, C. Turkmen, Z. G. Ozkan, and D. Yilmazbayhan, “Somatostatin receptor scintigraphy with 111In-octreotide in pulmonary carcinoid tumours correlated with pathological and 18FDG PET/CT findings,” Annals of Nuclear Medicine, vol. 26, no. 9, pp. 689–697, 2012.
View at: Publisher Site | Google Scholar
L. P. Liu, X. X. Zhang, L. B. Cui et al., “Preliminary comparison of diffusion-weighted MRI and PET/CT in predicting histological type and malignancy of lung cancer,” Clinical Respiratory Journal, vol. 11, no. 2, pp. 151–158, 2017.
View at: Publisher Site | Google Scholar
S. Murakami, H. Saito, Y. Sakuma et al., “Correlation of 18F-fluorodeoxyglucose uptake on positron emission tomography with Ki-67 index and pathological invasive area in lung adenocarcinomas 30 mm or less in size,” European Journal of Radiology, vol. 75, no. 2, pp. e62–e66, 2010.
View at: Publisher Site | Google Scholar
H. Nakamura, T. Hirata, H. Kitamura, and J. Nishikawa, “Correlation of the standardized uptake value in FDG-PET with the expression level of cell-cycle-related molecular biomarkers in resected non-small cell lung cancers,” Annals of Thoracic and Cardiovascular Surgery, vol. 15, no. 3, pp. 304–310, 2009.
View at: Google Scholar
X. C. Nguyen, W. W. Lee, J. H. Chung et al., “FDG uptake, glucose transporter type 1, and Ki-67 expressions in non-small-cell lung cancer: correlations and prognostic values,” European Journal of Radiology, vol. 62, no. 2, pp. 214–219, 2007.
View at: Publisher Site | Google Scholar
S. Park, E. Lee, S. Rhee et al., “Correlation between semi-quantitative (18)F-FDG PET/CT parameters and Ki-67 expression in small cell lung cancer,” Nuclear Medicine and Molecular Imaging, vol. 50, no. 1, pp. 24–30, 2016.
View at: Publisher Site | Google Scholar
A. W. Sauter, S. Winterstein, D. Spira et al., “Multifunctional profiling of non-small cell lung cancer using 18F-FDG PET/CT and volume perfusion CT.,” Journal of Nuclear Medicine, vol. 53, no. 4, pp. 521–529, 2012.
View at: Publisher Site | Google Scholar
H. Shibata, H. Nomori, K. Uno et al., “11C-acetate for positron emission tomography imaging of clinical stage IA lung adenocarcinoma: comparison with ¹⁸F-fluorodeoxyglucose for imaging and evaluation of tumor aggressiveness,” Annals of Nuclear Medicine, vol. 23, no. 7, pp. 609–616, 2009.
View at: Publisher Site | Google Scholar
M. Soussan, J. Cyrta, C. Pouliquen et al., “Fluorine 18 fluorodeoxyglucose PET/CT volume-based indices in locally advanced non-small cell lung cancer: prediction of residual viable tumor after induction chemotherapy,” Radiology, vol. 272, no. 3, pp. 875–884, 2014.
View at: Publisher Site | Google Scholar
H. Vesselle, A. Salskov, E. Turcotte et al., “Relationship between non-small cell lung cancer FDG uptake at PET, tumor histology, and Ki-67 proliferation index,” Journal of Thoracic Oncology, vol. 3, no. 9, pp. 971–978, 2008.
View at: Publisher Site | Google Scholar
H. Vesselle, R. A. Schmidt, J. M. Pugsley et al., “Lung cancer proliferation correlates with [F-18]fluorodeoxyglucose uptake by positron emission tomography,” Clinical Cancer Research, vol. 6, no. 10, pp. 3837–3844, 2000.
View at: Google Scholar
F. L. Wang, Y. Y. Tan, X. M. Gu et al., “Comparison of positron emission tomography using 2-[18F]-fluoro-2-deoxy-D-glucose and 3-deoxy-3-[18F]-fluorothymidine in lung cancer imaging,” Chinese Medical Journal, vol. 129, no. 24, pp. 2926–2935, 2016.
View at: Publisher Site | Google Scholar
K. Watanabe, H. Nomori, T. Ohtsuka et al., “[F-18]Fluorodeoxyglucose positron emission tomography can predict pathological tumor stage and proliferative activity determined by Ki-67 in clinical stage IA lung adenocarcinomas,” Japanese Journal of Clinical Oncology, vol. 36, no. 7, pp. 403–409, 2006.
View at: Publisher Site | Google Scholar
Y. Yamamoto, Y. Nishiyama, S. Ishikawa et al., “Correlation of ¹⁸F-FLT and ¹⁸F-FDG uptake on PET with Ki-67 immunohistochemistry in non-small cell lung cancer,” European Journal of Nuclear Medicine and Molecular Imaging, vol. 34, no. 10, pp. 1610–1616, 2007.
View at: Publisher Site | Google Scholar
C. S. Yap, J Czernin, M. C. Fishbein et al., “Evaluation of thoracic tumors with ¹⁸F-fluorothymidine and ¹⁸F-fluorodeoxyglucose-positron emission tomography,” Chest, vol. 129, no. 2, pp. 393–401, 2006.
View at: Publisher Site | Google Scholar
M. D. Taylor, P. W. Smith, W. K. Brix et al., “Fluorodeoxyglucose positron emission tomography and tumor marker expression in non-small cell lung cancer,” Journal of Thoracic and Cardiovascular Surgery, vol. 137, no. 1, pp. 43–48, 2009.
View at: Publisher Site | Google Scholar
W. Yang, Y. Zhang, Z. Fu et al., “Imaging of proliferation with ¹⁸F-FLT PET/CT versus ¹⁸F-FDG PET/CT in non-small-cell lung cancer,” European J Nuclear Medicine and Molecular Imaging, vol. 37, no. 7, pp. 1291–1299, 2010.
View at: Publisher Site | Google Scholar
T. Furukawa, Y. Miyata, K. Kushitani et al., “Association between [¹⁸F]-fluoro-2-deoxyglucose uptake and expressions of hypoxia-induced factor 1α and glucose transporter 1 in non-small cell lung cancer,” Japanese Journal of Clinical Oncology, vol. 45, no. 12, pp. 1154–1161, 2015.
View at: Publisher Site | Google Scholar
K. Kaira, M. Endo, M. Abe et al., “Biologic correlates of ¹⁸F-FDG uptake on PET in pulmonary pleomorphic carcinoma,” Lung Cancer, vol. 71, no. 2, pp. 144–150, 2011.
View at: Publisher Site | Google Scholar
K. Kaira, M. Serizawa, Y. Koh et al., “Biological significance of 18F-FDG uptake on PET in patients with non-small-cell lung cancer,” Lung Cancer, vol. 83, no. 2, pp. 197–204, 2014.
View at: Publisher Site | Google Scholar
N. Xing, Z. L. Cai, S. H. Zhao, L. Yang, B. X. Xu, and F. L. Wang, “The use of CT perfusion to determine microvessel density in lung cancer: comparison with FDG-PET and pathology,” Chinese Journal of Cancer Research, vol. 23, no. 2, pp. 118–122, 2011.
View at: Publisher Site | Google Scholar
Z. J. Zhang, J. H. Chen, L. Meng et al., “¹⁸F-FDG uptake as a biologic factor predicting outcome in patients with resected non-small-cell lung cancer,” Chinese Medical Journal, vol. 120, no. 2, pp. 125–131, 2007.
View at: Google Scholar
O. Araz, E. Demirci, E. Y. Ucar et al., “Roles of Ki-67, p53, transforming growth factor-β and lysyl oxidase in the metastasis of lung cancer,” Respirology, vol. 19, no. 7, pp. 1034–1039, 2014.
View at: Publisher Site | Google Scholar
L. Bai, C. Guo, J. Wang et al., “¹⁸F-fludrodeoxyglucose maximal standardized uptake value and metabolic tumor burden are associated with major chemotherapy-related tumor markers in NSCLC patients,” OncoTargets and Therapy, vol. 9, pp. 6315–6324, 2016.
View at: Publisher Site | Google Scholar
X. Y. Duan, W. Wang, J. S. Wang, J Shang, J. G. Gao, and Y. M. Guo, “Fluorodeoxyglucose positron emission tomography and chemotherapy-related tumor marker expression in non-small cell lung cancer,” BMC Cancer, vol. 13, no. 1, p. 546, 2013.
View at: Publisher Site | Google Scholar
X. Liu, H. Zhang, X. Yu et al., “The correlation of expression of VEGF and EGFR with SUV of (18)FDG-PET-CT in non-small cell lung cancer,” Contemporary Oncology, vol. 18, no. 5, pp. 334–339, 2014.
View at: Publisher Site | Google Scholar
K. Higashi, Y. Ueda, A. Sakurai et al., “Correlation of Glut-1 glucose transporter expression with [(18)F]FDG uptake in non-small cell lung cancer,” European Journal of Nuclear Medicine, vol. 27, no. 12, pp. 1778–1785, 2000.
View at: Publisher Site | Google Scholar
A. H. Khandani, K. D. Whitney, S. M. Keller, C. R. Isasi, and M. Donald Blaufox, “Sensitivity of FDG PET, GLUT1 expression and proliferative index in bronchioloalveolar lung cancer,” Nuclear Medicine Communications, vol. 28, no. 3, pp. 173–177, 2007.
View at: Publisher Site | Google Scholar
M. Mamede, T. Higashi, M. Kitaichi et al., “[18F]FDG uptake and PCNA, Glut-1, and Hexokinase-II expressions in cancers and inflammatory lesions of the lung,” Neoplasia, vol. 7, no. 4, pp. 369–379, 2005.
View at: Publisher Site | Google Scholar
K. Takada, G. Toyokawa, T. Okamoto et al., “Metabolic characteristics of programmed cell death-ligand 1-expressing lung cancer on ¹⁸F-fluorodeoxyglucose positron emission tomography/computed tomography,” Cancer Medicine, vol. 6, no. 11, pp. 2552–2561, 2017.
View at: Publisher Site | Google Scholar
M. Zhang, D. Wang, Q. Sun et al., “Prognostic significance of PD-L1 expression and ¹⁸F-FDG PET/CT in surgical pulmonary squamous cell carcinoma,” Oncotarget, vol. 8, no. 31, pp. 51630–51640, 2017.
View at: Publisher Site | Google Scholar
E. Lopci, L. Toschi, F. Grizzi et al., “Correlation of metabolic information on FDG-PET with tissue expression of immune markers in patients with non-small cell lung cancer (NSCLC) who are candidates for upfront surgery,” European Journal of Nuclear Medicine and Molecular Imaging, vol. 43, no. 11, pp. 1954–1961, 2016.
View at: Publisher Site | Google Scholar
A. Surov, H. J. Meyer, and A. Wienke, “Can imaging parameters provide information regarding histopathology in head and neck squamous cell carcinoma? A meta-analysis,” Translational Oncology, vol. 11, no. 2, pp. 498–503, 2018.
View at: Publisher Site | Google Scholar
A. Surov, H. J. Meyer, and A. Wienke, “Correlation between apparent diffusion coefficient (ADC) and KI 67 in different tumors: a meta-analysis. Part 1: ADC_mean,” Oncotarget, vol. 8, no. 43, pp. 75434–75444, 2017.
View at: Publisher Site | Google Scholar
A. Surov, H. J. Meyer, and A. Wienke, “Correlation between apparent diffusion coefficient (ADC) and cellularity is different in several tumors: a meta-analysis,” Oncotarget, vol. 8, no. 35, pp. 59492–59499, 2017.
View at: Publisher Site | Google Scholar
D. Moher, A. Liberati, J. Tetzlaff, and D. G. Altman, “Preferred reporting items for systematic reviews and meta-analyses: the PRISMA statement,” PLoS Medicine, vol. 6, no. 7, Article ID e1000097, 2009.
View at: Publisher Site | Google Scholar
P. Whiting, A. W. Rutjes, J. B. Reitsma, P. M. Bossuyt, and J. Kleijnen, “The development of QUADAS: a tool for the quality assessment of studies of diagnostic accuracy included in systematic reviews,” BMC Medical Research Methodology, vol. 3, no. 1, p. 25, 2003.
View at: Publisher Site | Google Scholar
A. Chalkidou, D. B. Landau, E. W. Odell, V. R. Cornelius, M. J. O'Doherty, and P. K. Marsden, “Correlation between Ki-67 immunohistochemistry and ¹⁸F-fluorothymidine uptake in patients with cancer: a systematic review and meta-analysis,” European Journal of Cancer, vol. 48, no. 18, pp. 3499–3513, 2012.
View at: Publisher Site | Google Scholar
M. M. Leeflang, J. J. Deeks, C. Gatsonis, and P. M. Bossuyt, “Systematic reviews of diagnostic test accuracy,” Annals of Internal Medicine, vol. 149, no. 12, pp. 889–897, 2008.
View at: Publisher Site | Google Scholar
J. Zamora, V. Abraira, A. Muriel, K. Khan, and A. Coomarasamy, “Meta-DiSc: a software for meta-analysis of test accuracy data,” BMC Medical Research Methodology, vol. 6, no. 1, p. 31, 2006.
View at: Publisher Site | Google Scholar
R. DerSimonian and N. Laird, “Meta-analysis in clinical trials,” Controlled Clinical Trials, vol. 7, no. 3, pp. 177–188, 1986.
View at: Publisher Site | Google Scholar
M. Scimeca, N. Urbano, R. Bonfiglio, O. Schillaci, and E. Bonanno, “Management of oncological patients in the digital era: anatomic pathology and nuclear medicine teamwork,” Future Oncology, 2018.
View at: Publisher Site | Google Scholar
C. Schlüter, M. Duchrow, C. Wohlenberg et al., “The cell proliferation-associated antigen of antibody Ki-67: a very large, ubiquitous nuclear protein with numerous repeated elements, representing a new kind of cell cycle-maintaining proteins,” Journal of Cell Biology, vol. 123, no. 3, pp. 513–522, 1993.
View at: Publisher Site | Google Scholar
S. M. Deng, W. Zhang, B. Zhang, Y. Y. Chen, J. H. Li, and Y. W. Wu, “Correlation between the uptake of ¹⁸F-fluorodeoxyglucose (18F-FDG) and the expression of proliferation-associated antigen Ki-67 in cancer patients: a meta-analysis,” PLoS One, vol. 10, no. 6, Article ID e0129028, 2015.
View at: Publisher Site | Google Scholar
G. Shen, H. Ma, F. Pang, P. Ren, and A. Kuang, “Correlations of ¹⁸F-FDG and ¹⁸F-FLT uptake on PET with Ki-67 expression in patients with lung cancer: a meta-analysis,” Acta Radiologica, vol. 59, no. 2, pp. 188–195, 2018.
View at: Publisher Site | Google Scholar
L. M. Sholl, “Biomarkers in lung adenocarcinoma: a decade of progress,” Archives of Pathology & Laboratory Medicine, vol. 139, no. 4, pp. 469–480, 2015.
View at: Publisher Site | Google Scholar
S. V. Sharma, D. W. Bell, J. Settleman, and D. A. Haber, “Epidermal growth factor receptor mutations in lung cancer,” Nature Reviews Cancer, vol. 7, no. 3, pp. 169–181, 2007.
View at: Publisher Site | Google Scholar
M. Tateishi, T. Ishida, T. Mitsudomi, S. Kaneko, and K. Sugimachi, “Immunohistochemical evidence of autocrine growth factors in adenocarcinoma of the human lung,” Cancer Research, vol. 50, no. 21, pp. 7077–7080, 1990.
View at: Google Scholar
K. Inamura, “Update on immunohistochemistry for the diagnosis of lung cancer,” Cancers, vol. 10, pii: E72, no. 3, 2018.
View at: Publisher Site | Google Scholar
P. C. Tumeh, C. L. Harview, J. H. Yearley et al., “PD-1 blockade induces responses by inhibiting adaptive immune resistance,” Nature, vol. 515, no. 7528, pp. 568–571, 2014.
View at: Publisher Site | Google Scholar
S. Simon and N. Labarriere, “PD-1 expression on tumor-specific T cells: friend or foe for immunotherapy?” Oncoimmunology, vol. 7, p. e1364828, 2017.
View at: Publisher Site | Google Scholar
R. Brody, Y. Zhang, M. Ballas et al., “PD-L1 expression in advanced NSCLC: insights into risk stratification and treatment selection from a systematic literature review,” Lung Cancer, vol. 112, pp. 200–215, 2017.
View at: Publisher Site | Google Scholar
O. Gautschi, D. Ratschiller, M. Gugger, D. C. Betticher, and J. Heighway, “Cyclin D1 in non-small cell lung cancer: a key driver of malignant transformation,” Lung Cancer, vol. 55, no. 1, pp. 1–14, 2007.
View at: Publisher Site | Google Scholar
L. Q. Zhang, F. Jiang, L. Xu et al., “The role of cyclin D1 expression and patient’s survival in non-small-cell lung cancer: a systematic review with meta-analysis,” Clinical Lung Cancer, vol. 13, no. 3, pp. 188–195, 2012.
View at: Publisher Site | Google Scholar
V. M. Villaflor and R. Salgia, “Targeted agents in non-small cell lung cancer therapy: what is there on the horizon?” Journal of Carcinogenesis, vol. 12, p. 7, 2013.
View at: Publisher Site | Google Scholar
D. Frezzetti, M. Gallo, M. R. Maiello et al., “VEGF as a potential target in lung cancer,” Expert Opinion on Therapeutic Targets, vol. 21, no. 10, pp. 959–966, 2017.
View at: Publisher Site | Google Scholar
A. Sharma, A. Mohan, A. S. Bhalla et al., “Role of various metabolic parameters derived from baseline ¹⁸F-FDG PET/CT as prognostic markers in non-small cell lung cancer patients undergoing platinum-based chemotherapy,” Clinical Nuclear Medicine, vol. 43, no. 1, pp. e8–e17, 2018.
View at: Publisher Site | Google Scholar
J. H. Hong, H. H. Kim, E. J. Han et al., “Total lesion glycolysis using ¹⁸F-FDG PET/CT as a prognostic factor for locally advanced esophageal cancer,” Journal of Korean Medical Science, vol. 31, no. 1, pp. 39–46, 2016.
View at: Publisher Site | Google Scholar
S. Liao, B. C. Penney, K. Wroblewski et al., “Prognostic value of metabolic tumor burden on ¹⁸F-FDG PET in nonsurgical patients with non-small cell lung cancer,” European Journal of Nuclear Medicine and Molecular Imaging, vol. 39, no. 1, pp. 27–38, 2012.
View at: Publisher Site | Google Scholar
H. Y. Lee, S. H. Hyun, K. S. Lee et al., “Volume-based parameter of ¹⁸F-FDG PET/CT in malignant pleural mesothelioma: prediction of therapeutic response and prognostic implications,” Annals of Surgical Oncology, vol. 17, no. 10, pp. 2787–2794, 2010.
View at: Publisher Site | Google Scholar
H. H. Chung, H. W. Kwon, K. W. Kang et al., “Prognostic value of preoperative metabolic tumor volume and total lesion glycolysis in patients with epithelial ovarian cancer,” Annals of Surgical Oncology, vol. 19, no. 6, pp. 1966–1972, 2012.
View at: Publisher Site | Google Scholar

Copyright

Copyright © 2018 Alexey Surov 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.

PDF Download Citation

Download other formats

Order printed copies

Views

1450

Downloads

1185

Citations