Skip to main content
Oncology Letters logoLink to Oncology Letters
. 2019 Dec 4;19(1):700–706. doi: 10.3892/ol.2019.11180

Diagnostic value and clinical significance of MRI and CT in detecting lymph node metastasis of early cervical cancer

Lan Luo 1, Qian Luo 2,, Liang Tang 3
PMCID: PMC6924181  PMID: 31897185

Abstract

Diagnostic value and clinical significance of magnetic resonance imaging (MRI) and computed tomography (CT) in detecting lymph node metastasis of early cervical cancer were investigated. From April 2015 to April 2019, 160 patients with lymph node metastasis (stage I–II) of early cervical cancer in Jining No. 1 People's Hospital were retrospectively analyzed. All the patients underwent MRI, CT diagnosis and MRI combined with CT diagnosis before operation. Sensitivity, specificity and diagnostic accordance rate, the diagnostic value and clinical significance of MRI, CT and MRI combined with CT in the diagnosis of lymph node metastasis of early cervical cancer were compared. The sensitivity, specificity and diagnostic accordance rate of MRI in the diagnosis of lymph node metastasis of early cervical cancer in stage Ia-Ib were 75.00, 72.92 and 77.50%, respectively, which were significantly higher than those of PET/CT in the same period (P<0.05). The sensitivity, specificity and diagnostic accordance rate of MRI combined with CT in the diagnosis of early cervical cancer in stage Ia-Ib were 78.13, 87.50 and 83.75%, respectively, which were significantly higher than those of MRI or CT alone (P<0.05). However, the sensitivity, specificity and diagnostic accordance rate of MRI combined with CT in the diagnosis of lymph node metastasis of early cervical cancer in stage IIa-IIb were 91.66, 82.81 and 88.13%, respectively, which were significantly higher than those of MRI or CT alone (P<0.05). MRI is superior to CT in the diagnosis of lymph node metastasis of early cervical cancer. However, the diagnostic efficiency of combined scans of the two is far higher than that of MRI or CT alone, which has more diagnostic value. In clinic, MRI and CT should be combined to improve the diagnostic accuracy of diseases.

Keywords: MRI, CT, early cervical cancer, lymph node metastasis

Introduction

Cervical cancer is one of the main causes of cancer death in women (1), most of which is caused by human papillomavirus (HPV) infection (2). Approximately 86% of women who die from cervical cancer are in developing countries (3,4). According to the clinical stage standard issued by FIGO, cervical cancer was staged based on the depth of tumor invasion and the degree of invasion to surrounding tissues (5). Patients with cervical cancer with FIGO stage I–II were divided into early cervical cancer (6). Although these were not mentioned in FIGO stage, lymph node metastasis has a very close relationship with the prognosis of cervical cancer and is the most important in cervical cancers (7).

Clinically, various imaging methods are used to detect lymph node metastasis in cancer, including magnetic resonance imaging (MRI) and computed tomography (CT) (8). CT imaging is very common in various clinical diagnoses. Its clinical value in tumor diagnosis and differential diagnosis cannot be ignored, and it has non-invasive advantages (9,10). MRI has no radiation effect on human body. It can complete local and whole body scanning, which is more advanced and safe. Compared with CT, it also provides more anatomical details for diagnosis and the image contains more abundant texture information than CT images. Therefore, it is challenging to compare the advantages and disadvantages of MRI and CT. This needs to be analyzed on a case-by-case basis (11,12). In this study, we compared the diagnostic value and clinical significance of MRI and CT in detecting lymph node metastasis of early cervical cancer.

Patients and methods

Collection of baseline data

In this study, we selected 160 patients with lymph node metastasis of cervical cancer from April 2015 to April 2019, including 122 patients with squamous cell carcinoma, 18 patients with adenosquamous carcinoma, 10 patients with endometrioid adenocarcinoma and 10 patients with clear cell carcinoma. The age of patients ranged from 28 to 64 years, with an average age of 35.59±4.02 years. FIGO stage included 17 cases in stage Ia, 47 cases in stage Ib, 43 cases in stage IIa and 53 cases in stage IIb.

Inclusion criteria: i) The patient was diagnosed as cervical cancer by pathology after treatment in Jining No. 1 People's Hospital (Jining, China); ii) FIGO stage was stage I and II in patients. iii) Patients underwent plain scan to increase examination before operation (the scanning range included at least inferior diaphragm to pubic symphysis). iv) The patient had no other treatment before surgery. v) Patients selected radical hysterectomy bilateral salpingo-oophorectomy and pelvic lymphadenectomy, radical hysterectomy pelvic lymphadenectomy para-aortic lymphadenectomy. vi) Patients and their families signed informed consent forms in advance. The study was approved by the Ethics Committee of Jining No. 1 Hospital.

Exclusion criteria: i) Patients who received only plain scan or only pelvic plain scan and enhanced scan before operation. ii) The stage of FIGO was stage III or above and the postoperative pathology was cervical intraepithelial neoplasia. iii) Scan did not conform to the standard, patient examination preparation was not perfect or contrast agent injection factors did not conform to the diagnostic criteria. iv) The treatment method was radiotherapy, chemotherapy or other treatment methods. v) The patient received other preoperative treatment.

Examination methods

i) Main reagents and instruments: Siemens Verio 3.0T superconducting magnetic resonance was from Siemens. Gd-DTPA, a bolus contrast agent, 18F-deoxyglucose (18FDG), a CT imaging agent, were from Accdon. CT scanners were from Royal Philips Electronics. Sixty-four slice CT was from Siemens.

ii) CT examination methods: The patient should avoid, or consume only liquid food with little residue the day before the examination to ensure the formation of unformed feces. The enema was cleaned with warm water before examination for 1–2 h. Patients drank 600–800 ml warm boiled water to fill the bladder 30–60 min before examination to increase the contrast with the uterus. Retention enema was performed ~5 min before CT scan: In order to fully dilate the rectum, the patient was placed in the left lateral position, taking the tolerance dose as the degree, and injected ~400 ml warm water through the anus with the intestinal irrigator bag to increase the contrast between the large intestine and the uterus. Training the patient's breathing before examination: It is required to hold the breath after inhaling calmly during examination, and to breathe calmly if the breath cannot be held. Before the examination, the technical operator explained to the patient the matters needing attention and checked whether the patient had any foreign matters affecting diagnosis, such as metal. The most commonly used volume of continuous scanning method was adopted: The tube voltage was 120 kV, the tube current was 300 mA, the slice thickness was 5 mm, the interlayer spacing was 5 mm and the reconstruction thickness was 1 mm. The patient was placed in a supine position with both hands on the top of the head. The scanning range included at least inferior diaphragm to pubic symphysis. After conventional axial plain CT scan, the body position remained unchanged. Professional nurses injected 100 ml of nonionic contrast agent through superficial vein of the elbow with high pressure injector at an injection rate of 2.5–3.0 ml/sec. Arterial phased scan was performed ~30 sec later, mainly scanning the liver. Portal phase enhanced scan was performed ~65–75 sec, including whole abdomen or chest and abdomen and pelvic. Equilibrium phase can be added to scan when it was necessary according to lesion display and diagnostic needs.

iii) MRI examination methods: The examinee did not eat for 48 h, and drank a proper amount of water to fill the bladder before 9 a.m. on the examination day. Then scan of 4.0 mm/layer was performed. The examination sequences were as follows: sagittal SET1WI, TR/TE 364/15 msec; sagittal TSE T2WI, TR/TE 2890/108 msec; sagittal fat suppression T2W(ISTIR), TR/TE3840/103 msec, TI 115 msec; oblique transverse T2WI of scanning diameter line and perpendicular to uterine axis, TR/TE 4890/84 msec; Gd-DTPA T1WI transverse, TR/TE 397/15 msec; The sagittal scan parameters of T1WI were the same as those of plain scan.

The CT and MRI images were read by two radiologists with more than 10 years experience and no knowledge of the surgical and pathological results. The CT staging and MRI staging of cervical cancer were carried out according to the reading results.

Judgement of criterion

i) Image analysis of MRI diagnostic stage (Table I). ii) Image analysis of CT diagnosis of SC stage (Table II).

Table I.

Features of MRI of early cervical cancer in different stages.

Grouping Features
Stage Ia No evidence of mass lesion.
Stage Ib Tumor pierced cervical low signal intensity ring.
Stage IIa The tumor pierced the upper vagina but did not touch the parametrium.
Stage IIb The matrix of the cervix was destroyed and the parametrium tissues were invaded.

MRI, magnetic resonance imaging.

Table II.

Features of CT of early cervical cancer in different stages.

Grouping Features
Stage Ia No metastatic lymph nodes.
Stage Ib Metastatic lymph nodes appeared, but were not obvious.
Stage IIa Metastatic lymph nodes appeared but did not invade the parametrium.
Stage IIb Metastatic lymph nodes began to invade the parametrium.

CT, computed tomography.

Statistical methods

Data analysis was completed by SPSS 18.0. The counting data were expressed as [n(%)]. The χ2 test was used for univariate analysis and comparison of the diagnostic accuracy of SC at each stage. The difference was statistically significant at P<0.05.

Results

Baseline data

The basic conditions of 160 patients were investigated, such as age, obesity, smoking and drinking habits, histological classification, clinical stage (Fig. 1 and Table III). Degree of differentiation and lymph node metastasis of cervical cancer are shown in (Fig. 2).

Figure 1.

Figure 1.

Number of early cervical cancer patients tested with four different stages.

Table III.

Baseline clinical data of 160 SC patients.

Factors [n(%)]
Age (years)
  ≤50 105 (65.63)
  >50 55 (34.37)
Smoking
  Yes 81 (50.63)
  No 79 (49.67)
Drinking
  Yes 78 (48.75)
  No 82 (51.25)
Obesity
  Yes 80 (50.00)
  No 80 (50.00)
Histological classification of cervical cancer
  Squamous cell carcinoma 122 (76.25)
  Adenosquamous carcinoma 18 (11.25)
  Endometrioid adenocarcinoma 10 (6.25)
  Clear cell carcinoma 10 (6.25)
Clinical stage of cervical cancer
  Stage Ia 17 (10.63)
  Stage Ib 47 (29.37)
  Stage IIa 43 (26.87)
  Stage IIb 53 (33.13)
Differentiation degree
  Poorly differentiated 65 (40.63)
  Middle differentiated 45 (28.12)
  Well differentiated 50 (31.25)
Lymph node metastasis
  Yes 96 (60.00)
  No 64 (40.00)
Figure 2.

Figure 2.

Differentiation of tumors.

Diagnostic efficiency of MRI and CT in lymph node metastasis of early cervical cancer in different stages

i) Diagnostic efficacy of MRI and CT in lymph node metastasis of early cervical cancer in stage I

The sensitivity, specificity and diagnostic accordance rate of MRI in the diagnosis of early cervical cancer in stage I were 75.00%, 72.92 and 77.50%, respectively. The sensitivity, specificity and diagnostic accordance rate of CT in the diagnosis of early cervical cancer in stage I were 62.50, 56.25 and 58.75%, respectively. Comparing data of the two groups, the sensitivity, specificity and diagnostic accordance rates of MRI in the diagnosis of early cervical cancer in stage I were significantly higher than those of CT (P<0.05) (Tables IVVI).

Table IV.

Diagnostic efficacy of MRI in lymph node metastasis of early cervical cancer in stage I.

Pathological diagnostic results

Grouping Stage Ia-Ib Stage non-Ia-Ib Total
Ia-Ib phase by MRI diagnosis 54 26   80
Non-Ia-Ib phase by MRI diagnosis 10 70   80
Total 64 96 160

MRI, magnetic resonance imaging.

Table VI.

Comparison of diagnostic efficiency of MRI and CT in lymphatic metastasis of early cervical cancer in stage I.

Factors MRI CT χ2 value P-value
Sensitivity 75.00% (54/64) 62.50% (40/64) 7.850 0.005
Specificity 72.92% (70/96) 56.25% (54/96) 5.829 0.016
Diagnostic accordance rate 77.50% (124/160) 58.75% (94/160) 12.950 <0.001

MRI, magnetic resonance imaging; CT, computed tomography.

ii) Diagnostic efficacy of MRI and CT in lymphatic metastasis of early cervical cancer in stage II

The sensitivity, specificity and diagnostic accordance rate of MRI in the diagnosis of lymphatic metastasis of early cervical cancer in stage II were 79.17, 78.13 and 78.75%, respectively. The sensitivity, specificity and diagnostic accordance rate of CT in the diagnosis of lymphatic metastasis of early cervical cancer in stage II were 62.50, 68.75 and 60.00%, respectively. Comparing the data of the two groups, the sensitivity, specificity and diagnostic accordance rate of MRI in the diagnosis of lymphatic metastasis of early cervical cancer in stage II were significantly higher than those of CT in the diagnosis of lymphatic metastasis of early cervical cancer in stage II (P<0.05). However, there was no obvious difference in specificity (P>0.05) (Tables VIIIX).

Table VII.

Diagnostic efficacy of MRI in lymphatic metastasis of early cervical cancer in stage II.

Pathological diagnostic results

Grouping Stage IIa-IIb Stage non-IIa-IIb Total
IIa-IIb phase by MRI diagnosis 76 14   70
Non-IIa-IIb phase by MRI diagnosis 20 50   90
Total 96 64 160

MRI, magnetic resonance imaging.

Table IX.

Comparison of diagnostic efficiency of MRI and CT in lymphatic metastasis of early cervical cancer in stage II.

Factors MRI CT χ2 value P-value
Sensitivity 79.17% (76/96) 62.50% (60/96) 6.454 0.011
Specificity 78.13% (50/64) 68.75% (44/64) 1.442 0.230
Diagnostic accordance rate 78.75% (126/160) 58.75% (94/160) 14.890 <0.001

MRI, magnetic resonance imaging; CT, computed tomography.

Comparison of diagnostic efficiency between MRI combined with CT and MRI or CT alone in lymphatic metastasis of early cervical cancer in different stage

The sensitivity, specificity and diagnostic accordance rate of MRI combined with CT in the diagnosis of early cervical cancer in stage I were 78.13, 87.50 and 83.75%, respectively, which were significantly higher than the sensitivity and diagnostic accordance rate of MRI or CT alone (P<0.05). However, the sensitivity, specificity and diagnostic accordance rate of MRI combined with CT in the diagnosis of early cervical cancer in stage II were 91.66, 82.81 and 88.13%, respectively. There was no obvious difference in specificity (P>0.05), the specificity and diagnostic accordance rate were significantly higher than that of MRI or CT alone (P<0.05) (Tables XXII).

Table X.

Diagnostic efficacy of MRI combined with CT in lymphatic metastasis of early cervical cancer in stage I.

Pathological diagnostic results

Grouping Stage Ia-Ib Stage non-Ia-Ib Total
Ia-Ib phase by combined diagnosis 50 12   62
Non-Ia-Ib phase by combined diagnosis 14 84   98
Total 64 96 160

MRI, magnetic resonance imaging; CT, computed tomography.

Table XII.

Comparison of the diagnostic efficacy between combined diagnosis with MRI or CT alone.

Factors Combination MRI CT P-value
Stage Ia-Ib
  Sensitivity 78.13% (50/64) 75.00% (54/64) 62.50% (40/64) 0.013
  Specificity 87.50% (84/96) 72.92% (70/96) 56.25% (54/96) <0.001
  Diagnostic accordance rate 83.75% (134/160) 77.50% (124/160) 58.75% (94/160) <0.001
Stage IIa-IIb
  Sensitivity 91.66% (90/96) 79.17% (76/96) 62.50% (60/96) <0.001
  Specificity 82.81% (53/64) 78.13% (50/64) 68.75% (44/64) 0.161
  Diagnostic accordance rate 88.13% (143/160) 78.75% (126/160) 58.75% (94/160) <0.001

MRI, magnetic resonance imaging; CT, computed tomography.

Discussion

Cervical cancer is particularly harmful to women in developing countries, and screening its level is very important (13,14). However, two imaging techniques, CT and MRI, play a vital role in the early stage of cancer, treatment strategy and treatment of response evaluation (1517). In many studies on lung cancer, prostate cancer and breast cancer, MRI and CT are widely used (1820). These technologies have their own advantages and disadvantages, and are suitable for examining different tumors (21). Therefore, the purpose of this study was to compare the diagnostic value of the two imaging methods in the detection of lymph node metastasis of early cervical cancer.

In this study, different stages of patients with early cervical cancer were examined with MRI, and CT alone, and MRI combined with CT, and their diagnostic efficacy such as sensitivity, specificity, diagnostic accordance rate was compared. According to the results, the sensitivity, specificity and diagnostic accordance rate of MRI in the diagnosis of lymph node metastasis of early cervical cancer with stage I (Ia-Ib) were significantly higher than those of CT in the diagnosis of lymph node metastasis of early cervical cancer with stage I (Ia-Ib). In addition to specificity, the sensitivity, diagnostic accordance rate of MRI in the diagnosis of lymph node metastasis of early cervical cancer with stage II (IIa-IIb) were significantly higher than the sensitivity, specificity, and diagnostic accordance rate by CT diagnosis. In another study on cervical cancer, it was found that MRI is better than CT in diagnosing cervical cancer. It can not only be useful for the discovery of early cervical cancer, but also for reasonable staging (22). However, in the study of Li and Room (23) on invasive cervical cancer, MRI was shown to be better than CT in observing tumor size and boundary, the signal was easy to identify, and the diagnostic accordance rate for lymphatic metastasis was also very high. It was concluded that MRI has better diagnostic efficiency and higher clinical diagnostic value than CT in the diagnosis of lymph node metastasis of early cervical cancer.

In a study on lymphoma, it was found that MRI combined with CT has good examination effect (24). Therefore, in this study, we also carried out combined examination of MRI and CT on patients. According to the results, besides the specificity index for diagnosing lymph node metastasis of early cervical cancer in stage II (IIa-IIb), the sensitivity and diagnostic accordance rate of MRI combined with CT diagnosis were significantly higher than those of MRI and CT alone. CT has good density resolution, can avoid intestinal peristalsis and other effects to a certain extent. It is visual and has certain advantages in finding lymph node diffusion, but its diagnostic sensitivity to cancer staging is not strong, and its differentiation specificity for lesions is not high. However, MRI has higher tissue resolution and better tissue contrast. It can directly display the tumor condition and can change imaging parameters to improve its contrast, thus improving the prediction range of tumors (25). Complementary advantages of the two can have a better examination effect. Therefore, we conclude that the diagnostic value of MRI and CT combined diagnosis was higher than that each alone. In the study of Kim et al (26) on non-small cell lung cancer, the combination of MRI and CT was more helpful to significantly improve the sensitivity of detecting lymph node metastasis than CT alone. In a clinical study of calcified meningioma, it was found that CT combined with MRI diagnosis has a higher diagnostic accordance rate for tumors and a more comprehensive and obvious reflection on the characteristics of tumors (27). These are all similar to the results of the present study.

In conclusion, the diagnostic value of MRI in the clinical diagnosis of lymph node metastasis of early cervical cancer is significantly higher than that of CT and the sensitivity, specificity and diagnostic accordance rate are significantly improved when they are combined. Therefore, we consider that MRI and CT should be combined in clinic to improve the diagnostic accuracy of diseases.

Table V.

Diagnostic efficacy of CT lymph node metastasis of early cervical cancer in stage I.

Pathological diagnostic results

Grouping Stage Ia-Ib Stage non-Ia-Ib Total
Ia-Ib phase by CT diagnosis 40 42   82
Non-Ia-Ib phase by CT diagnosis 24 54   78
Total 64 96 160

CT, computed tomography.

Table VIII.

Diagnostic efficacy of CT in lymphatic metastasis of early cervical cancer in stage II.

Pathological diagnostic results

Grouping Stage IIa-IIb Stage non-IIa-IIb Total
IIa-IIb phase by CT diagnosis 60 20   88
Non-IIa-IIb phase by CT diagnosis 36 44   72
Total 96 64 160

CT, computed tomography.

Table XI.

Diagnostic efficacy of MRI combined with CT in lymphatic metastasis of early cervical cancer in stage II.

Pathological diagnostic results

Grouping Stage IIa-IIb Stage non-IIa-IIb Total
IIa-IIb phase by combined diagnosis 90 11 101
Non-IIa-IIb phase by combined diagnosis   6 53   59
Total 96 64 160

MRI, magnetic resonance imaging; CT, computed tomography.

Acknowledgements

Not applicable.

Funding

No funding was received.

Availability of data and materials

The datasets used and/or analyzed during the current study are available from the corresponding author on reasonable request.

Authors' contributions

LL wrote the manuscript, interpreted and analyzed the data. QL designed the study and performed the experiments. LT was responsible for the analysis and discussion of the data. All authors read and approved the final manuscript.

Ethics approval and consent to participate

The study was approved by the Ethics Committee of Jining No. 1 People's Hospital (Jining, China). Patients who participated in this research had complete clinical data. Signed informed consents were obtained from the patients and/or the guardians.

Patient consent for publication

Not applicable.

Competing interests

The authors declare that they have no competing interests.

References

  • 1.Small W, Jr, Bacon MA, Bajaj A, Chuang LT, Fisher BJ, Harkenrider MM, Jhingran A, Kitchener HC, Mileshkin LR, Viswanathan AN, et al. Cervical cancer: A global health crisis. Cancer. 2017;123:2404–2412. doi: 10.1002/cncr.30667. [DOI] [PubMed] [Google Scholar]
  • 2.Wentzensen N, Schiffman M, Palmer T, Arbyn M. Triage of HPV positive women in cervical cancer screening. J Clin Virol. 2016;76(Suppl 1):S49–S55. doi: 10.1016/j.jcv.2015.11.015. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 3.Denny L. Cervical cancer: Prevention and treatment. Discov Med. 2012;14:125–131. [PubMed] [Google Scholar]
  • 4.Sreedevi A, Javed R, Dinesh A. Epidemiology of cervical cancer with special focus on India. Int J Womens Health. 2015;7:405–414. doi: 10.2147/IJWH.S50001. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 5.Dornhöfer N, Höckel M. New developments in the surgical therapy of cervical carcinoma. Ann NY Acad Sci. 2008;1138:233–252. doi: 10.1196/annals.1414.029. [DOI] [PubMed] [Google Scholar]
  • 6.Tsili AC, Tsangou V, Koliopoulos G, Stefos T, Argyropoulou MI. Early-stage cervical carcinoma: The role of multidetector CT in correlation with histopathological findings. J Obstet Gynaecol. 2013;33:882–887. doi: 10.3109/01443615.2013.823927. [DOI] [PubMed] [Google Scholar]
  • 7.Hosaka M, Watari H, Mitamura T, Konno Y, Odagiri T, Kato T, Takeda M, Sakuragi N. Survival and prognosticators of node-positive cervical cancer patients treated with radical hysterectomy and systematic lymphadenectomy. Int J Clin Oncol. 2011;16:33–38. doi: 10.1007/s10147-010-0123-0. [DOI] [PubMed] [Google Scholar]
  • 8.Petersen LJ, Nielsen JB, Langkilde NC, Petersen A, Afshar-Oromieh A, De Souza NM, De Paepe K, Fisker RV, Arp DT, Carl J, et al. 68Ga-PSMA PET/CT compared with MRI/CT and diffusion-weighted MRI for primary lymph node staging prior to definitive radiotherapy in prostate cancer: a prospective diagnostic test accuracy study. World J Urol. 2019 doi: 10.1007/s00345-019-02846-z. doi: 10.1007/s00345-019-02846-z. [Epub ahead of print] [DOI] [PubMed] [Google Scholar]
  • 9.Kinahan PE, Townsend DW, Beyer T, Sashin D. Attenuation correction for a combined 3D PET/CT scanner. Med Phys. 1998;25:2046–2053. doi: 10.1118/1.598392. [DOI] [PubMed] [Google Scholar]
  • 10.Shin S, Pak K, Kim SJ, Kim H, Kim SJ. Pulmonary tumor embolism derived from stomach cancer observation with serial 18F-FDG PET/CT. Clin Nucl Med. 2015;40:270–272. doi: 10.1097/RLU.0000000000000596. [DOI] [PubMed] [Google Scholar]
  • 11.Nie D, Cao X, Gao Y, Wang L, Shen D. Estimating CT image from MRI data using 3D fully convolutional networks. Deep Learn Data Label Med Appl (2016) 2016;2016:170–178. doi: 10.1007/978-3-319-46976-8_18. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 12.Low RN, Gurney J. Diffusion-weighted MRI (DWI) in the oncology patient: Value of breathhold DWI compared to unenhanced and gadolinium-enhanced MRI. J Magn Reson Imaging. 2007;25:848–858. doi: 10.1002/jmri.20864. [DOI] [PubMed] [Google Scholar]
  • 13.Marth C, Landoni F, Mahner S, McCormack M, Gonzalez-Martin A, Colombo N, ESMO Guidelines Committee Cervical cancer: ESMO Clinical Practice Guidelines for diagnosis, treatment and follow-up. Ann Oncol. 2017;28(Suppl 4):iv72–iv83. doi: 10.1093/annonc/mdx220. [DOI] [PubMed] [Google Scholar]
  • 14.Landy R, Pesola F, Castañón A, Sasieni P. Impact of cervical screening on cervical cancer mortality: Estimation using stage-specific results from a nested case-control study. Br J Cancer. 2016;115:1140–1146. doi: 10.1038/bjc.2016.290. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 15.Lucia F, Visvikis D, Desseroit MC, Miranda O, Malhaire JP, Robin P, Pradier O, Hatt M, Schick U. Prediction of outcome using pretreatment 18F-FDG PET/CT and MRI radiomics in locally advanced cervical cancer treated with chemoradiotherapy. Eur J Nucl Med Mol Imaging. 2018;45:768–786. doi: 10.1007/s00259-017-3898-7. [DOI] [PubMed] [Google Scholar]
  • 16.Choi J, Kim HJ, Jeong YH, Lee JH, Cho A, Yun M, Lee JD, Kim YB, Kim YT, Kang WJ. The role of 18F-FDG PET/CT in assessing therapy response in cervix cancer after concurrent chemoradiation therapy. Nucl Med Mol Imaging. 2014;48:130–136. doi: 10.1007/s13139-013-0248-y. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 17.Patel CN, Nazir SA, Khan Z, Gleeson FV, Bradley KM. 18F-FDG PET/CT of cervical carcinoma. AJR Am J Roentgenol. 2011;196:1225–1233. doi: 10.2214/AJR.10.5084. [DOI] [PubMed] [Google Scholar]
  • 18.Kim HS, Lee KS, Ohno Y, van Beek EJ, Biederer J. PET/CT versus MRI for diagnosis, staging, and follow-up of lung cancer. J Magn Reson Imaging. 2015;42:247–260. doi: 10.1002/jmri.24776. [DOI] [PubMed] [Google Scholar]
  • 19.Shen G, Deng H, Hu S, Jia Z. Comparison of choline-PET/CT, MRI, SPECT, and bone scintigraphy in the diagnosis of bone metastases in patients with prostate cancer: A meta-analysis. Skeletal Radiol. 2014;43:1503–1513. doi: 10.1007/s00256-014-1903-9. [DOI] [PubMed] [Google Scholar]
  • 20.Sawicki LM, Grueneisen J, Schaarschmidt BM, Buchbender C, Nagarajah J, Umutlu L, Antoch G, Kinner S. Evaluation of 18F-FDG PET/MRI, 18F-FDG PET/CT, MRI, and CT in whole-body staging of recurrent breast cancer. Eur J Radiol. 2016;85:459–465. doi: 10.1016/j.ejrad.2015.12.010. [DOI] [PubMed] [Google Scholar]
  • 21.Cazzato RL, Garnon J, Shaygi B, Koch G, Tsoumakidou G, Caudrelier J, Addeo P, Bachellier P, Namer IJ, Gangi A. PET/CT-guided interventions: Indications, advantages, disadvantages and the state of the art. Minim Invasive Ther Allied Technol. 2018;27:27–32. doi: 10.1080/13645706.2017.1399280. [DOI] [PubMed] [Google Scholar]
  • 22.Yong HE. Comparative analysis of diagnostic value of imaging of cervical cancers by B-ultrasonography, CT and MRI. Acta Med Sin. 2009;03:413–415. [Google Scholar]
  • 23.Li LC, Room C. Clinical value of preoperative CT and MRI on diagnosing invasive cervical cancer. Han Shao Ji Bing Za Zhi. 2018;01:62–63. (In Chinese) [Google Scholar]
  • 24.Heacock L, Weissbrot J, Raad R, Campbell N, Friedman KP, Ponzo F, Chandarana H. PET/MRI for the evaluation of patients with lymphoma: Initial observations. AJR Am J Roentgenol. 2015;204:842–848. doi: 10.2214/AJR.14.13181. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 25.Bin D, Li ZL. Value analysis and efficacy observation of CT in combination with MRI on staging diagnosis of endometrial carcinoma. Chin J Ct Mri. 2016;04:107–109. [Google Scholar]
  • 26.Kim YN, Yi CA, Lee KS, Kwon OJ, Lee HY, Kim BT, Choi JY, Kim SW, Chung MP, Han J, et al. A proposal for combined MRI and PET/CT interpretation criteria for preoperative nodal staging in non-small-cell lung cancer. Eur Radiol. 2012;22:1537–1546. doi: 10.1007/s00330-012-2388-3. [DOI] [PubMed] [Google Scholar]
  • 27.Ren F, Gao L, Yao FM, Hu TB, Lin MJ. The technological efficacy of CT combined with MRI in diagnosing calcified meningioma. Health Res. 2014;3:259–260. [Google Scholar]

Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Data Availability Statement

The datasets used and/or analyzed during the current study are available from the corresponding author on reasonable request.


Articles from Oncology Letters are provided here courtesy of Spandidos Publications

RESOURCES