- Department of Radiology, The Fourth Hospital of Hebei Medical University, Shijiazhuang, China
Objective: This study aimed to evaluate the visibility of different subgroups of lung nodules of <3 cm using the pointwise encoding time reduction with radial acquisition (PETRA) sequence on 3T magnetic resonance imaging (MRI) in comparison with that obtained using low-dose computed tomography (LDCT).
Methods: The appropriate detection rate was calculated for each of the different subgroups of lung nodules of <3 cm. The mean diameter of each detected nodule was determined. The detection rates and diameters of the lung nodules detected by MRI with the PETRA sequence were compared with those detected by computed tomography (CT). The sensitivity of detection for the different subgroups of pulmonary nodules was determined based on the location, size, type of nodules and morphologic characteristics. Agreement of nodule characteristics between CT and MRI were assessed by intraclass correlation coefficient (ICC) and Kappa test.
Results: The CT scans detected 256 lung nodules, comprising 99 solid nodules (SNs) and 157 subsolid nodules with a mean nodule diameter of 8.3 mm. For the SNs, the MRI detected 30/47 nodules of <6 mm in diameter and 52/52 nodules of ≥6 mm in diameter. For the subsolid nodules, the MRI detected 30/51 nodules of <6 mm in diameter and 102/106 nodules of ≥6 mm in diameter. The PETRA sequence returned a high detection rate (84%). The detection rates of SN, ground glass nodules, and PSN were 82%, 72%, and 94%, respectively. For nodules with a diameter of >6 mm, the sensitivity of the PETRA sequence reached 97%, with a higher rate for nodules located in the upper lung fields than those in the middle and lower lung fields. Strong agreement was found between the CT and PETRA results (correlation coefficients = 0.97).
Conclusion: The PETRA technique had high sensitivity for different type of nodule detection and enabled accurate assessment of their diameter and morphologic characteristics. It may be an effective alternative to CT as a tool for screening and follow up pulmonary nodules.
Introduction
Pulmonary nodules are common findings in individuals with an elevated risk for lung cancer. According to the Fleischner Society, the risk of malignancy in nodules of <6 mm in diameter is extremely low, while nodules of >6 mm in diameter require multiple follow-ups or further evaluation (1, 2). The National Lung Screening Trial demonstrated the benefits of using multi-slice computed tomography (CT) for lung cancer screening in a high-risk population. This approach was shown to reduce lung cancer-associated mortality by up to 20% (3, 4). Results of NELSON trial showed that lung-cancer mortality was significantly lower among those who underwent volume CT screening than among those who underwent no screening (5). Although this technique has high spatial resolution and good contrast between air and lung tissues, repetitive use of CT increases the risk of developing cancer due to ionizing radiation exposure, particularly in patients who require reviews on multiple occasions over a prolonged period (6, 7).
Magnetic resonance imaging (MRI) is a non-ionizing technique, which is of particular interest for the assessment of lung diseases, including pneumonia and cystic fibrosis, in children or patients who require frequent follow-up examinations (8–11). Continuous technical developments in terms of stronger gradients, parallel imaging, and shorter echo times have led to increased interest in MRI as an alternative to CT for lung screening (12, 13).
Short echo times have been shown to be crucial in improving the quality of lung proton MRIs (14). The pointwise encoding time reduction with radial acquisition (PETRA) sequence is a noiseless prototype hybrid approach to ultrashort-echo-time three-dimensional imaging (15, 16). This technique offers several advantages over other conventional sequences, including three-dimensional isotropic imaging with submillimeter spatial resolution (17). Therefore, the present study was conducted to evaluate the detection and sizing of different subgroups of lung nodules using the PETRA sequence with a 3T MRI scanner and compare these results with CT findings.
Materials and Methods
The present prospective study was approved by the institutional review board and the federal agency for radiation protection. Written informed consent was obtained from each participant.
Patient Population
Between May 2017 and September 2018, patients from a lung cancer screening program, were enrolled for the present prospective study according to the recommendations of the Fleischner Society’s guidelines regarding relevant risk factors (18). Inclusion criteria: 1) patients diagnosed with lung cancer, and nodule<3cm in diameter; 2) patients with a time interval of <24 h between their CT scan and MRI; and 3) patients >18 years old. Exclusion criteria: 1) patients who had pacemakers; 2) patients who had metal implants; 3) patients with severe claustrophobia; and 4) patients suffering from severe emphysema and/or fibrosis.
CT Imaging Protocol
For acquisition, the patients were in the supine position on a 128-row multi-detector dual source CT (Definition Flash, Siemens Healthcare, Forchheim, Germany). The CT protocol used included the following parameters: tube voltage = 120 kV; 50 mAs; pitch = 1.2; field of view (FOV) = 300 mm; slice thickness = 1 mm; and kernel = B70f. The patients were asked to raise their arms and hold their breath, so the scanning range included the area from the chest entrance to the diaphragm, thus covering the whole lung. The scan time was 3.98 s, and the effective dose was 1.2–1.5 mSv.
CT Image Analysis
The CT images were evaluated in clinical routine by a radiologist with ten years of experience (N.Z.), who had no knowledge of the MRI findings. The location, size, and type of each lung nodule were recorded. In line with the literature (19–21), the nodules were classified into three groups according to density: solid nodules (SNs), partial solid nodules (PSNs), and ground glass nodules (GGNs).
Following the recommendations of the Fleischner Society (19), the nodules were categorized based on size: SNs of <6 mm, 6–8 mm, or >8 mm in diameter; and PSNs of <6 mm or ≥6 mm in diameter. Nodule size was defined as the mean value of the longest and shortest axial diameters. Furthermore, the nodules were categorized according to location as follows: left lung (upper and lower lobe groups); right lung (upper lobe group, middle lobe group, and lower lobe group); center group (distance from the peripheral pleura of >1 cm); and peripheral group (distance from the peripheral pleura of <1 cm). The largest level of each nodule was selected for measurement. All nodules were measured in the standard lung window setting (window center = −600 HU; window width = 1,200 HU).
The CT was considered the gold standard for recording the number of detected nodules. Thus, a false positive result was defined as a nodule diagnosed by MRI that was not observed in the CT images, and a false negative result was defined as a nodule diagnosed in the CT images that was not observed by MRI.
MRI Protocol
MRI was performed using a 3T MRI unit (Magnetom Skyra, Siemens Healthcare). A multi-channel phased-array receiver body coil was used for detection. The patients assumed the supine position, with their arms raised above their body, and they were instructed to breathe freely. The PETRA sequence parameters were as follows: TR = 3 ms; TE = 0.07 ms; matrix = 256 × 256; FOV = 400 × 400; slice thickness = 1.6 mm; and acquisition plane = axial. To reduce cardiac and breathing motion artifacts, respiratory gating was performed. The total scan time was 3 min.
MRI Analysis
The prospective MRI data analysis was performed by two radiologists with ten years (N.W., observer 1) and five years (Y.D., observer 2) of experience, respectively. All MRI datasets obtained from the 75 participants were pseudonymized and presented in random order. To eliminate detection bias, both of these observers were unaware of the CT findings. The recorded content for each nodule included the location of the nodule (including the lung lobe and segment), the position in the lung parenchyma (center or peripheral), and size. Morphologic characteristics in CT and MRI were assessed by both readers for each nodules. The characteristics including shape (round, oval or irregular), margins (smooth, nonsmooth, lobulated, spiculated, pleural tag) and attenuation (GGN, SN or PSN). Any disagreements between the radiologists’ findings were resolved by consensus interpretation.
To investigate intraobserver variation, observer 1 measured the nodules twice after one month. We used the average value of measurements the final reference value of MRI measurement to compare with CT.
Statistical Analysis
The statistical analysis was performed using SPSS 21 (IBM, Armonk, NY, USA). The sensitivity levels of detection for the different subgroups of pulmonary nodules were calculated according to location, size (based on the Fleischner Society’s nodule size categorization guide), and type. The measures of diagnostic performance were calculated for the nodule detection by MRI, and these results were then compared with the CT findings (the gold standard of nodule detection). Comparison of categorical variables was performed using Chi-square test and McNemar’s test. Morphologic features from CT and PETRA were compared using Kappa test, with the following levels of agreement (22): 0-0.20,poor; 0.21-0.40, fair; 0.41-0.60, moderate; 0.61-0.80, substantial; and 0.81-1.00, almost perfect agreement. The mean nodule diameters from the CT and PETRA findings were compared using Bland–Altman plots. Interobserver and intraobserver agreement rates were assessed by intraclass correlation coefficient (ICC). Receiver operating characteristic(ROC) analyses were performed to determine feasible threshold values for the mean diameter of detected nodules and to evaluate the usefulness of PETRA sequence. An error probability of P < 0.05 was considered to be statistically significant.
Results
General Characteristics
According to the recommendations of the Fleischner Society regarding relevant factors, a total of 82 patients from a lung cancer screening program (36 males and 46 females; mean age = 58; age range = 52–85) were enrolled for this prospective study. The exclusion criteria included patients who had contraindications to MRI, including pacemakers, metal implants, and severe claustrophobia, and patients with severe emphysema and/or fibrosis. Based on the inclusion and exclusion criteria, 75 patients who underwent low-dose CT (LDCT) and MRI (31 males and 44 females; mean age = 56.5; age range = 50–75) were ultimately included in the study.
Lung Nodule Detection Rates
The CT imaging revealed 256 lung nodules (mean diameter: 8.3 ± 4.6 mm) among the 75 sample patients, comprising 99 SNs, and 157 subsolid nodules (including 86 PSNs and 71 GGNs). Among the SNs, 47 nodules measured <6 mm in diameter, 20 nodules measured between 6 and 8 mm in diameter, and 32 nodules measured >8 mm in diameter. Among 157 subsolid nodules, 51 nodules measured <6 mm in diameter, and 106 nodules were >6 mm in diameter. The mean number of nodules per patient was 3, with a range of 1–20. From CT examination, the diameter of the nodules ranged from 2.4 to 24.3 mm. A breakdown of the patient characteristics is presented in Table 1.
The PETRA sequence accurately detected 214 of 256 pulmonary nodules, but it failed to identify 42 nodules, and the overall sensitivity was 84%. For pulmonary nodules >8 mm in diameter, the detection rate was 100% (Table 2). MRI had a higher detection rate for SNs (82%) and PSNs (94%) than for GGNs (72%) (Figures 1 and 2). ROC curve (Figure 3). Showed the diagnostic perfomance of PETRA sequence in detecting nodules, AUC=0.946. Nodules with a diameter greater than 6mm, the sensitivity and specificity of detecting are 85.5% and 99.5%.
![www.frontiersin.org](https://www.frontiersin.org/files/Articles/649625/fonc-11-649625-HTML/image_m/fonc-11-649625-t002.jpg)
Table 2 The sensitivity of the detection of different subgroups of pulmonary nodules (according to the Fleischner Society nodule size category) and different lobe.
![www.frontiersin.org](https://www.frontiersin.org/files/Articles/649625/fonc-11-649625-HTML/image_m/fonc-11-649625-g001.jpg)
Figure 1 A 50-year-old man with 8.8mm GGN (arrow) in the right upper lobe. The nodule is well depicted on the CT axial (A), coronal (B), and sagittal (C) image, and on the PETRA sequence axial (D), coronal (E), and sagittal (F) image. The arrows represent the locations of nodules.
![www.frontiersin.org](https://www.frontiersin.org/files/Articles/649625/fonc-11-649625-HTML/image_m/fonc-11-649625-g002.jpg)
Figure 2 A 52-year-old man with 14mm PSN (arrow) in the left lower lobe. The nodule is well visualized on the CT axial (A), coronal (B), and sagittal (C) image, and on the PETRA sequence axial (D), coronal (E), and sagittal (F) image. The arrows represent the locations of nodules.
![www.frontiersin.org](https://www.frontiersin.org/files/Articles/649625/fonc-11-649625-HTML/image_m/fonc-11-649625-g003.jpg)
Figure 3 Graph illustrating the result of ROC analyses. ROC analysis was performed according to the mean diameter of the nodules. ROC curve showed the diagnostic perfomance of PETRA sequence in detecting nodules, AUC=0.946. Nodules with a diameter greater than 6mm, the sensitivity and specificity of detecting are 85.5% and 99.5%.
The PETRA Had a Higher Sensitivity of for Nodules Located in the Peripheral Lobe
Compared with nodules located in the middle or lower lobes, the PETRA sequence had a higher detection ability in the upper lobe, and nodules located in the peripheral lobe were more easily detected. The undetected nodules were predominantly located close to the diaphragm or around the heart (Table 3).
The range of nodule diameters detected by MRI was 2.9–24.3 mm, and the mean diameter was 8.6 mm. The maximum diameter of the largest lesion not detected by MRI was 7.3 mm. For nodules >6 mm in diameter, the PETRA sequence achieved 97% sensitivity. All of the pulmonary nodules falsely reported by MRI had diameters of <6 mm.
There were nine false positive nodules identified by the PETRA sequence. The diameters of six of the false positive nodules were <6 mm, and five of the nine nodules were close to the diaphragm or around the heart. The sizes of the nodules undetected by MRI were as follows: 38 nodules of <6 mm diameter, and eight nodules of ≥6 mm diameter. Among these 42 undetected nodules, SNs, PSNs, and GGNs accounted for 40% (17/42), 12% (5/42), and 48% (20/42), respectively (Figure 4).
![www.frontiersin.org](https://www.frontiersin.org/files/Articles/649625/fonc-11-649625-HTML/image_m/fonc-11-649625-g004.jpg)
Figure 4 A 54-year-old man with 5.5mm GGN (arrow) in the right upper lobe. The nodule is well visualized on the CT axial (A), coronal (B), and sagittal (C) image, and is not detected in the PETRA sequence (D–F). The arrows represent the locations of nodules.
Strong Agreement Between CT and PETRA
There were good levels of both interobserver and intraobserver agreement regarding the mean diameters of pulmonary nodules measured by CT and MRI, and the ICC results were 0.990 and 0.992, respectively (Table 4). The Bland–Altman plots present the differences between mean diameters from the CT and MRI results for GGNs, PSNs and SNs respectively (Figure 5). The results of agreement between CT and MRI to assess the morphologic characteristics of detected nodules was found to be substantial or almost perfect. (K=0.816-1.00) (Table 5).
![www.frontiersin.org](https://www.frontiersin.org/files/Articles/649625/fonc-11-649625-HTML/image_m/fonc-11-649625-t004.jpg)
Table 4 Mean diameter of detected nodules for subgroups and agreement of measurements compared to CT.
![www.frontiersin.org](https://www.frontiersin.org/files/Articles/649625/fonc-11-649625-HTML/image_m/fonc-11-649625-g005.jpg)
Figure 5 Bland–Altman plot showing the agreement between the nodule mean diameter measurements by CT and PETRA for GGN (A), PSN (B) and (C) SN respectively. Dashed lines denote 95%CI, and solid lines denote mean.
![www.frontiersin.org](https://www.frontiersin.org/files/Articles/649625/fonc-11-649625-HTML/image_m/fonc-11-649625-t005.jpg)
Table 5 Comparison and agreement between CT and MRI to assess the morphologic characteristics of detected nodules.
Discussion
The value of MRI in patients with pulmonary nodules in terms of both lesion detection and characterization has been assessed in several studies (2, 23, 24). The reported sensitivity of nodule detection using MRI ranges between 40% and 93% (2, 15–21, 23–34). The PETRA sequence is a noiseless prototype hybrid approach to ultra-short-echo-time three-dimensional imaging (15, 18) that does not require a hardware change. The rapid imaging with ultra-short echo time enabled by PETRA may be useful for new clinical applications (17). Dournes et al. (17) demonstrated that the PETRA sequence offers advantages for lung imaging, including noiseless, free-breathing, and isotropic imaging. Ohno et al. (35) assessed the nodule detection capability of standard-dose CT, reduced-dose CT, and MRI with ultrashort echo time (UTE), and the sensitivity of the UTE technique was >90%. In the present study, the capability of the PETRA sequence in nodule detection was as effective as CT, and the PETRA sequence achieved high sensitivity (84%) for nodule detection. The sensitivity of MRI for the detection of pulmonary nodules with diameters of >6 mm was 97% (152/158), and for nodules with diameters of >8 mm, the sensitivity was 100%. For nodules with diameters of >6 mm and >8 mm, the detection rate reached 97% and 100%, respectively. The results of the present study are compatible with those presented by Ohno et al. (35). Furthermore, the present study indicated the superiority of the PETRA sequence in detecting GGNs (diameter of ≥6 mm; detection rate of 97%), which is also similar to the results reported by Ohno et al. (35). The present study demonstrated that PETRA can be an optimal sequence for the detection of lung lesions. This is consistent with the work of Dournes et al. (17), who highlighted the superior performance of PETRA compared with the T1-VIBE sequence (36). ROC curve showed the diagnostic perfomance of PETRA sequence in detecting nodules, AUC=0.946. Nodules with a diameter greater than 6mm, the sensitivity and specificity of detecting are 85.5% and 99.5%. According to the recommendations of the Fleischner Society guidelines, only nodules of ≥6 mm in diameter and growing nodules are associated with a risk of malignancy (Lung-RADS category 3 and 4) (37). Therefore, the results of the present study fit well with the sensitivity of MRI for nodule detection as reported in previous studies (30, 32, 38, 39).
In the present study, nine false positive nodules were identified by the PETRA sequence, giving a false positive rate of 3.5%. In other studies, false positive rates have ranged between 5% and 8.7% (28, 36). False positives have frequently been found in the T2-TSE sequence rather than in the T1-VIBE sequence, and the rate in the present study was lower than that in other sequences. Although the false positive nodules were <6 mm in diameter, they would likely not affect further treatment. The percentage of false positives depends on several factors, including scanning parameters, the CT analysis method, and nodule characteristics (40). The recommended method for reducing the false positive rate is to combine two or three sequences (33). Other recommended sequence including T2-STIR and T1-VIBE. Koyama et al. (41) had demonstrated that T2-STIR sequence was superior to T2 in term of nodule detection and lesion contrast because STIR technique make it possible for some T1-decay to be submitted for T2-decay, the contrast of tissues was higher in STIR sequence. The results of Cieszanowski et al. (42) showed that the nodules detection rate of T1-VIBE was 69%, and T1-VIBE could detect more calcified nodules than other sequences.
In the present study, 42/256 pulmonary nodules were not detected by MRI, comprising 17 SNs, 5 PSNs, and 20 GGNs, and the CT values of undetected GGNs were all below −400 HU. Among these undetected nodules, 38 were <6 mm in diameter, and the other eight are conjectured to have been missed due to respiratory motion artifacts or being adjacent to vessels. Most of the undetected nodules were located in the lower lobe and center of the lung parenchyma, an area which is greatly affected by respiratory and cardiac motion artifacts. Therefore, the density, size, and location of these nodules are important factors in influencing their detection.
PETRA showed good agreement for detecting morphologic features compared to CT. MRI could distinguish different subgroup nodules, similarly to CT image. Other shape and margins characteristics which could help to differentiate malignant and benign nodules were accurately detected by MRI with substantial to almost perfect. The results of our Bland–Altman analysis revealed a good agreement between the mean diameters of pulmonary nodules when measured by CT and MRI (ICC = 0.97); a similar finding was reported by Heye et al. (33). In the current study, a >1 mm difference between the CT and MRI measurements occurred in only 16 nodules (nine GGNs and seven PSNs), and the mean diameter of these nodules was more than 10 mm. For other nodules, differences between the mean diameter results did not exceed 1 mm. These results show higher levels of interobserver and intraobserver agreement in SNs compared with PSNs and GGNs, especially for nodules >6 mm. The present study found that the mean diameters measured by the MRI were mostly smaller than those returned by the CT, particularly for PSNs and GGNs. This is potentially due to the different conditions of patient examination; the CT required the patient to hold their breath, while the MRI was completed while the patient was breathing freely. In addition, the MRI method showed certain difficulties in determining the edge of the ground glass component with lower CT values, while nodules that differed by more than 1 mm presented with diameters of >10 mm, which did not affect follow-up or treatment during the lung cancer screening. The use of MRI (PETRA) in the follow-up study can lead to a reduction of X-ray irradiation. Therefore, MRI, particularly the PETRA sequence, is recommended as an alternative method for pulmonary nodule follow-up that can potentially be used for nodule detection and nodule type assessment.
There were a number of limitations in the present study. First, underlying lung diseases, including emphysema and pulmonary fibrosis, can affect the detection of nodules, but the present study did not assess the lung conditions of the enrolled patients. Second, the study group was comprised of only 75 patients. A larger population is required to confirm these results. Third, the study sample contained three calcified nodules, and the MRI method had limitations in identifying the calcification. Hence, there is a need to combine these results with other sequences for differentiation. Finally, due to the study restrictions, only one CT professional participated in this research; more professionals should be consulted in future studies.
Conclusion
MRI has a potential role in detecting and evaluating pulmonary nodules, demonstrating a high level of sensitivity and a low false positive rate. The PETRA sequence has high sensitivity, particularly for nodules with diameters of >8 mm and GGNs. Furthermore, PETRA shows good agreement with CT scanning in assessing nodule size. Therefore, MRI with PETRA is considered a useful technique for lung nodule detection and may be an effective alternative approach for follow-up regarding pulmonary nodules in lung cancer screening.
Data Availability Statement
The original contributions presented in the study are included in the article/supplementary material. Further inquiries can be directed to the corresponding author.
Ethics Statement
The studies involving human participants were reviewed and approved by The Fourth Hospital of Hebei Medical University. The patients/participants provided their written informed consent to participate in this study.
Author Contributions
HF and GS conceived the idea and conceptualized the study. HF, HL and YD collected the data. NZ and YW analyzed the data. HF drafted the manuscript, then GS reviewed the manuscript. All authors contributed to the article and approved the submitted version.
Conflict of Interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Acknowledgments
We are particularly grateful to all the people who have given us help on our article.
References
1. Liu Y, Wang H, Li Q, McGettigan MJ, Balagurunathan Y, Garcia AL, et al. Radiologic Features of Small Pulmonary Nodules and Lung Cancer Risk in the National Lung Screening Trial: A Nested Case-Control Study. Radiology (2018) 286(1):298–306. doi: 10.1148/radiol.2017161458
2. MacMahon H, Naidich DP, Goo JM, Lee KS, Leung ANC, Mayo JR, et al. Guidelines for Management of Incidental Pulmonary Nodules Detected on CT Images: From the Fleischner Society 2017. Radiology (2017) 284(1):228–43. doi: 10.1148/radiol.2017161659
3. National Lung Screening Trial Research T, Aberle DR, Adams AM, Berg CD, Black WC, Clapp JD, et al. Reduced Lung-Cancer Morality With Low-Dose Computed Tomographic Screening. N Eng J Med (2011) 365:395–409. doi: 10.1056/NEJMoa1102873
4. National Lung Screening Trial Research Team, Church TR, Black WC, Aberle DR, Berg CD, Clingan KL, et al. Results of Initial Low-Dose Computed Tomographic Screening for Lung Cancer. N Eng J Med (2013) 368(21):1980–91. doi: 10.1056/NEJMoa1209120
5. De Koning HJ, van der Aalst CM, de Jong PA, Scholten ET, Nackaerts K, Heuvelmans MA, et al. Reduced Lung-Cancer Mortality With Volume CT Screening in a Randomized Trial. N Engl J Med (2020) 382(6):503–13. doi: 10.1056/NEJMoa1911793
6. Sodickson A, Baeyens PF, Andriole KP, Prevedello LM, Nawfel RD, Hanson R, et al. Cumulative Radiation Exposure ,and Associated Radiation-Induced Cancer Risk From CT of Adults. Radiology (2009) 251(1):175–84. doi: 10.1148/radiol.2511081296
7. Marant-Micallef C, Shield KD, Vignat J, Cléro E, Kesminiene A, Hill C, et al. The Risk of Cancer Attributable to Diagnostic Medical Radiation: Estimation for France in 2015. Int J Cancer (2019) 144(12):2954–63. doi: 10.1002/ijc.32048
8. Kaireit TF, Sorrentino SA, Renne J, Schoenfeld C, Voskrebenzev A, Gutberlet M, et al. Functional Lung MRI for Regional Monitoring of Patients With Cystic Fibrosis. PloS One (2017) 12(12):e0187483. doi: 10.1371/journal.pone.0187483
9. Sodhi KS, Khandelwal N, Saxena AK, Singh M, Agarwal R, Bhatia A, et al. Rapid Lung MRI in Children With Pulmonary Infections: Time to Change Our Diagnostic Algorithms. J Magn Reso Imaging (2016) 43(5):1196–206. doi: 10.1002/jmri.25082
10. Dournes G, Menut F, Macey J, Fayon M, Chateil JF, Salel M, et al. Lung Morphology Assessment of Cystic Fibrosis Using MRI With Ultra-Short Echo Time At Submillimeter Spatial Resolution. Eur Radiol (2016) 26(11):3811–20. doi: 10.1007/s00330-016-4218-5
11. Nozawa K, Niwa T, Aida N. Imaging of Cystic Lung Lesions in Infants Using Pointwise Encoding Time Reduction With Radial Acquisition (PETRA). Magn Reson Med Sci (2019) 18(4):299–300. doi: 10.2463/mrms.bc.2018-0080
12. Usuda K, Funazaki A, Maeda R, Sekimura A, Motono N, Matoba M, et al. Economic Benefits and Diagnostic Quality of Diffusion-Weighted Magnetic Resonance Imaging for Primary Lung Cancer. Ann Thorac Cardiovasc Surg (2017) 23(6):275–80. doi: 10.5761/atcs.ra.17-00097
13. Basson L, Jarraya H, Escande A, Cordoba A, Daghistani R, Pasquier D, et al. Chest Magnetic Resonance Imaging Decreases Inter-Observer Variability of Gross Target Volume for Lung Tumors. Front Oncol (2019) 9:690. doi: 10.3389/fonc.2019.00690
14. Schoenmaekers J, Hofman P, Bootsma G, Westenend M, de Booij M, Schreurs W, et al. Screening for Brain Metastases in Patients With Stage III Non-Small-Cell Lung Cancer, Magnetic Resonance Imaging or Computed Tomography? A Prospective Study. Eur J Cancer (2019) 115:88–96. doi: 10.1016/j.ejca.2019.04.017
15. Ida M, Wakayama T, Nielsen ML, Abe T, Grodzki DM. Quiet T1-weighted Imaging Using PETRA: Initial Clinical Evaluation in Intracranial Tumor Patients. J Magn Reson Imaging (2014) 41(2):447–53. doi: 10.1002/jmri.24575
16. Grodzki DM, Jakob PM, Heismann B. Ultrashort Echo Time Imaging Using Pointwise Encoding Time Reduction With Radial Acquisition (PETRA). Magn Reson Med (2012) 67(2):510–8. doi: 10.1002/mrm.23017
17. Dournes G, Grodzki D, Macey J, Girodet PO, Fayon M, Chateil JF, et al. Quiet Submillimeter MR Imaging of the Lung is Feasible With a PETRA Sequence At 1.5T. Radiology (2016) 279(1):328. doi: 10.1148/radiol.2016164006
18. Bankier AA, Macmahon H, Goo JM, Rubin GD, Schaefer-Prokop CM, Naidich DP. Recommendations for Measuring Pulmonary Nodules At CT: A Statement, From the Fleischner Society. Radiology (2017) 285(2):584–600. doi: 10.1148/radiol.2017162894
19. MacMahon H, Austin JH, Gamsu G, Herold CJ, Jett JR, Naidich DP, et al. Guidelines for Management of Small Pulmonary Nodules Detected on CT Scans: A Statement From the Fleischner Society. Radiology (2005) 237(2):395–400. doi: 10.1148/radiol.2372041887
20. Naidich DP, Bankier AA, Macmahon H, Schaefer-Prokop CM, Pistolesi M, Goo JM, et al. Recommendations for the Management of Subsolid Pulmonary Nodules Detected At CT: A Statement From the Fleischner Society. Radiology (2013) 266(1):304–17. doi: 10.1148/radiol.12120628
21. Hansell DM, Bankier AA, MacMahon H, McLoud TC, Müller NL, Remy J. Fleischner Society: Glossary of Terms for Thoracic Imaging. Radiology (2008) 246(3):697–722. doi: 10.1148/radiol.2462070712
22. Landis JR, Koch GG. The Measurement of Observer Agreement for Categorical Data. Biometrics (1977) 33:159–74. doi: 10.2307/2529310
23. Bach PB, Mirkin JN, Oliver TK, Azzoli CG, Berry DA, Brawley OW, et al. Benefits and Harms of CT Screening for Lung Cancer: A Systematic Review. JAMA (2012) 307(22):2418–29. doi: 10.1001/jama.2012.5521
24. Yun SJ, Ryu CW, Choi NY, Kim HC, Oh JY, Yang DM. Comparison of Low- and Standard-Dose CT for the Diagnosis of Acute Appendicitis: A Meta-Analysis. AJR Am J Roentgenol (2017) 208(6):W198–207. doi: 10.2214/AJR.16.17274
25. Regier M, Schwarz D, Hense FO, Groth M, Kooijman H, Begemann PG, et al. Diffusion-Weighted MR Imaging for the Detection of Pulmonary Nodules At 1.5Tesla: Intraindividual Comparison With Multidetector Computed Tomography. J Med Imaging Radiat Oncol (2011) 55(3):266–74. doi: 10.1111/j.1754-9485.2011.02263.x
26. Wu NY, Cheng HC, Ko JS, Cheng YC, Lin PW, Lin WC, et al. Magnetic Resonance Imaging for Lung Cancer Detection: Experience in a Population of More Than 10,000 Healthy Individuals. BMC Cancer (2011) 11:242. doi: 10.1186/1471-2407-11-242
27. Biederer J, Schoene A, Freitag S, Reuter M, Heller M. Simulated Pulmonary Nodules Implanted in a Dedicated Porcine Chest Phantom: Sensitivity of MR Imaging for Detection. Radiology (2003) 227(2):475–83. doi: 10.1148/radiol.2272020635
28. Sommer G, Tremper J, Koenigkam SM, Delorme S, Becker N, Biederer J, et al. Lung Nodule Detection in a High-Risk Population: Comparison of Magnetic Resonance Imaging and Low-Dose Computed Tomography. Eur J Radiol (2014) 83(3):600–5. doi: 10.1016/j.ejrad.2013.11.012
29. Luboldt W, Wetter A, Eichler K, Vogl TJ, Wagner TO, Seemann MD. Determination of the Optimal MRI Sequence for the Detection of Malignant Lung Nodules. Eur J Med Res (2006) 11(8):336–42.
30. Schroeder T, Ruehm SG, Debatin JF, Ladd ME, Barkhausen J, Goehde SC. Detection of Pulmonary Nodules Using a 2D HASTE MR Sequence: Comparison With MDCT. AJR Am J Roentgenol (2005) 185(4):979–84. doi: 10.2214/AJR.04.0814
31. Yi CA, Jeon TY, Lee KS, Lee JH, Seo JB, Kim YK, et al. 3t MRI: Usefulness for Evaluating Primary Lung Cancer and Small Nodules in Lobes Not Containing Primary Tumors. AJR Am J Roentgenol (2007) 189(2):386–92. doi: 10.2214/AJR.07.2082
32. Vogt FM, Herborn CU, Hunold P, Lauenstein TC, Schröder T, Debatin JF, et al. Haste MRI Versus Chest Radiography in the Detection of Pulmonary Nodules:Comparison With MDCT. AJR Am J Roentgenol (2004) 183(1):71–8. doi: 10.2214/ajr.183.1.1830071
33. Heye T, Ley S, Heussel CP, Dienemann H, Kauczor HU, Hosch W, et al. Detection and Size of Pulmonary Lesions: How Accurate is MRI? A Prospective Comparison of CT and MRI. Acta Radiol (2012) 53(2):153–60. doi: 10.1258/ar.2011.110445
34. Stolzmann P, Veit-Haibach P, Chuck N, Rossi C, Frauenfelder T, Alkadhi H, et al. Detection Rate, Location, and Size of Pulmonary Nodules in Trimodality PET/CT-MR: Comparison of Low-Dose CT and Dixon-based MR Imaging. Invest Radiol (2013) 48(5):241–6. doi: 10.1097/RLI.0b013e31826f2de9
35. Ohno Y, Koyama H, Yoshikawa T, Kishida Y, Seki S, Takenaka D, et al. Standard-, Reduced- and No-Dose Thin-Section Radiologic Examinations: Comparison of Capability for Nodule Detection and Nodule Type Assessment in Patients Suspected of Having Pulmonary Nodules. Radiology (2017) 284(2):562–73. doi: 10.1148/radiol.2017161037
36. Meier-Schroers M, Homsi R, Schild HH, Thomas D. Lung Cancer Screening With MRI: Characterization of Nodules With Different Non-Enhanced MRI Sequence. Acta Radiol (2019) 60(2):168–76. doi: 10.1177/0284185118778870
37. American College of Radiology. Lung CT Screening Reporting and Data System(Lung-Rads) (2017). Available at: http://www.acr.org/Quality-Safety/Resources/LungRADS.
38. Biederer J, Mirsadraee S, Beer M, Molinari F, Hintze C, Bauman G, et al. MRI of the Lung(3/3)-Current Applications and Future Perspectives. Insights Imaging (2012) 3(4):373–86. doi: 10.1007/s13244-011-0142-z
39. Biederer J, Beer M, Hirsch W, Wild J, Fabel M, Puderbach M, et al. MRI of the Lung(2/3) Why...When ...How? Insights Imaging (2012) 3(4):355–71. doi: 10.1007/s13244-011-0146-8
40. Rubin GD, Lyo JK, Paik DS, Sherbondy AJ, Chow LC, Leung AN, et al. Pulmonary Nodules on Multidetector Row CT Scans: Performance Comparison of Radiologists and Computer Aided Detection. Radiology (2005) 234(1):274–83. doi: 10.1148/radiol.2341040589
41. Koyama H, Ohno Y, Kono A, Takenaka D, Maniwa Y, Nishimura Y, et al. Quantitative and Qualitative Assessment of non-Contrast-Enhanced Pulmonary MR Imaging for Management of Pulmonary Nodules in 161 Subjects. Eur Radiol (2008) 18:2120–31. doi: 10.1007/s00330-008-1001-2
Keywords: lung nodule, MRI, CT, PETRA, malignancy
Citation: Feng H, Shi G, Liu H, Du Y, Zhang N and Wang Y (2021) The Value of PETRA in Pulmonary Nodules of <3 cm Among Patients With Lung Cancer. Front. Oncol. 11:649625. doi: 10.3389/fonc.2021.649625
Received: 05 January 2021; Accepted: 15 April 2021;
Published: 18 May 2021.
Edited by:
Leonard Wee, Maastro Clinic, NetherlandsReviewed by:
Joost Verhoeff, University Medical Center Utrecht, NetherlandsTetsu Niwa, Tokai University School of Medicine, Japan
Copyright © 2021 Feng, Shi, Liu, Du, Zhang and Wang. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Gaofeng Shi, shigaofeng1245@163.com