Share:
Share this content in WeChat
X
Clinical Article
Study on the detection efficiency of 18F-PSMA-1007 PET/CT and mp-MRI in prostate cancer and its correlation with pathological grade
ZHOU Yunshu  CHEN Xiaohua  CHEN Zhiqiang  ZHANG Ruodi  LIU Shili  WANG Zhuo  ZHANG Shaoru  LI Peng  LI Yanmei 

Cite this article as: ZHOU Y S, CHEN X H, CHEN Z Q, et al. Study on the detection efficiency of 18F-PSMA-1007 PET/CT and mp-MRI in prostate cancer and its correlation with pathological grade[J]. Chin J Magn Reson Imaging, 2024, 15(2): 71-76, 96. DOI:10.12015/issn.1674-8034.2024.02.010.


[Abstract] Objective To explore the comparison of the detection efficacy of 18-fluoro-labeled prostate specific membrane antigen (18F-PSMA-1007) positron emission tomography (PET)/computed tomography (CT) and multi-parameter magnetic resonance imaging (mp-MRI) alone and combined with prostate cancer (PCa) and the correlation between maximum standardized uptake value (SUVmax), apparent diffusion coefficient (ADC), SUVmax/ADC, T1, T2, proton density (PD) value and pathological grade of PCa.Materials and Methods A retrospective analysis was made on 50 patients suspected of PCa who were scheduled to undergo biopsy or surgery in our hospital from April 2020 to September 2022, of which 42 cases were diagnosed with PCa. According to the International Society of Urological Pathology (ISUP), the patients were divided into 5 groups. According to ISUP classification, there were 25 cases in high grade group (≥4 grade) and 17 cases in low grade group (1-3 grade). The differences of SUVmax, ADC and SUVmax/ADC in different grade groups were compared. Spearman correlation analysis was used to analyze the correlation among SUVmax value, ADC value, SUVmax/ADC, T1, T2, PD value and ISUP classification. Taking pathology as the gold standard, the efficacy of 18F-PSMA-1007 PET/CT and mp-MRI alone or in combination in the detection of benign and malignant prostate was analyzed. The diagnostic efficacy of SUVmax, ADC, SUVmax/ADC and combined parameters was evaluated by drawing receiver operating characteristic (ROC) and calculating the area under the curve (AUC), sensitivity and specificity, and the differences of AUC values were compared by DeLong test.Results There were significant differences in ADC, SUVmax, SUVmax/ADC between high-grade group and low-grade group (all P<0.001). Correlation analysis showed that there was a negative correlation between ADC and SUVmax in 50 cases of prostate diseases (r=-0.516, P<0.05), a negative correlation between ADC and ISUP in 42 cases of diagnosed PCa (r=-0.616, P<0.05), and a positive correlation between SUVmax, SUVmax/ADC and ISUP (r=0.549, r=0.639, all P<0.05). Magnetic resonance image compilation (MAGiC) sequence was completed in 20 cases, in which T1, T2, PD values were not correlated with ISUP (r=0.045, r=0.202, r=0.028, all P>0.05), T1 and T2 values were positively correlated with ADC (r=0.616, r=0.756, all P<0.05), while PD values were negatively correlated with ADC (r=-0.506, P<0.05). There was no significant correlation between SUVmax and T1, T2, PD (r=-0.132, r=-0.422, r=0.230, all P>0.05). ROC curve analysis showed that the AUC of SUVmax was 0.940 and the difference was statistically significant (P<0.001). With SUVmax=7.80 as the critical value, the sensitivity and specificity for the diagnosis of PCa were 83.33% and 100.00%, and the AUC of ADC was 0.970 and the difference was statistically significant (P<0.001). When ADC was 1.20×10-3 mm2/s, the sensitivity and specificity for the diagnosis of PCa were 95.24% and 87.50%, respectively. The AUC of SUVmax/ADC combined diagnosis of PCa was 0.970, and the difference was statistically significant (P<0.001). With SUVmax/ADC=6.43×103 as the critical value, the sensitivity and specificity of PCa diagnosis were 90.48% and 100.00%, respectively. The AUC of combining the two parameters was 0.976, and the difference was statistically significant (P<0.001). Taking 0.85 as the critical value, the sensitivity of diagnosing PCa was 90.48%, and the specificity was 100.00%.Conclusions The combination of 18F-PSMA-1007 PET/CT and mp-MRI can improve the diagnostic efficiency of PCa. ADC value, SUVmax and SUVmax/ADC can distinguish between low-risk and medium-high-risk PCa.
[Keywords] prostate cancer;prostate specific membrane antigen;diffusion weighted imaging;maximum standardized uptake value;apparent diffusion coefficient;magnetic resonance imaging;neoplasm grading

ZHOU Yunshu1   CHEN Xiaohua1   CHEN Zhiqiang2, 3*   ZHANG Ruodi1   LIU Shili1   WANG Zhuo1   ZHANG Shaoru1   LI Peng3   LI Yanmei4  

1 School of Clinical Medicine, Ningxia Medical University, Yinchuan 750004, China

2 Department of Radiology, the First Affiliated Hospital of Hainan Medical University, Haikou 570102, China

3 Department of Radiology, General Hospital of Ningxia Medical University, Yinchuan 750004, China

4 Department of Nuclear Medicine, General Hospital of Ningxia Medical University, Yinchuan 750004, China

Corresponding author: CHEN Z Q, E-mail: zhiqiang_chen99@163.com

Conflicts of interest   None.

Received  2023-09-15
Accepted  2023-12-26
DOI: 10.12015/issn.1674-8034.2024.02.010
Cite this article as: ZHOU Y S, CHEN X H, CHEN Z Q, et al. Study on the detection efficiency of 18F-PSMA-1007 PET/CT and mp-MRI in prostate cancer and its correlation with pathological grade[J]. Chin J Magn Reson Imaging, 2024, 15(2): 71-76, 96. DOI:10.12015/issn.1674-8034.2024.02.010.

[1]
MILLER K D, NOGUEIRA L, DEVASIA T, et al. Cancer treatment and survivorship statistics, 2022[J]. CA Cancer J Clin, 2022, 72(5): 409-436. DOI: 10.3322/caac.21731.
[2]
SEKHOACHA M, RIET K, MOTLOUNG P, et al. Prostate cancer review: genetics, diagnosis, treatment options, and alternative approaches[J/OL]. Molecules, 2022, 27(17): 5730 [2023-03-11]. https://pubmed.ncbi.nlm.nih.gov/36080493/. DOI: 10.3390/molecules27175730.
[3]
HUANG H, SUN P Y, ZOU K Y, et al. Current situation and prospect of primary prevention of cancer in China[J]. Zhonghua Zhong Liu Za Zhi, 2022, 44(9): 942-949. DOI: 10.3760/cma.j.cn112152-20220209-00083.
[4]
STABILE A, GIGANTI F, ROSENKRANTZ A B, et al. Multiparametric MRI for prostate cancer diagnosis: current status and future directions[J]. Nat Rev Urol, 2020, 17(1): 41-61. DOI: 10.1038/s41585-019-0212-4.
[5]
KUMAR V, BORA G S, KUMAR R, et al. Multiparametric (mp) MRI of prostate cancer[J]. Prog Nucl Magn Reson Spectrosc, 2018, 105: 23-40. DOI: 10.1016/j.pnmrs.2018.01.001.
[6]
LEE C H, TAN T W, TAN C H. Multiparametric MRI in active surveillance of prostate cancer: an overview and a practical approach[J]. Korean J Radiol, 2021, 22(7): 1087-1099. DOI: 10.3348/kjr.2020.1224.
[7]
BRATAN F, NIAF E, MELODELIMA C, et al. Influence of imaging and histological factors on prostate cancer detection and localisation on multiparametric MRI: a prospective study[J]. Eur Radiol, 2013, 23(7): 2019-2029. DOI: 10.1007/s00330-013-2795-0.
[8]
HOFMAN M S, LAWRENTSCHUK N, FRANCIS R J, et al. Prostate-specific membrane antigen PET-CT in patients with high-risk prostate cancer before curative-intent surgery or radiotherapy (proPSMA): a prospective, randomised, multicentre study[J]. Lancet, 2020, 395(10231): 1208-1216. DOI: 10.1016/S0140-6736(20)30314-7.
[9]
FAROLFI A, CALDERONI L, MATTANA F, et al. Current and emerging clinical applications of PSMA PET diagnostic imaging for prostate cancer[J]. J Nucl Med, 2021, 62(5): 596-604. DOI: 10.2967/jnumed.120.257238.
[10]
GLEMSER P A, ROTKOPF L T, ZIENER C H, et al. Hybrid imaging with[68Ga]PSMA-11 PET-CT and PET-MRI in biochemically recurrent prostate cancer[J/OL]. Cancer Imaging, 2022, 22(1): 53 [2023-04-11]. https://pubmed.ncbi.nlm.nih.gov/36138437/. DOI: 10.1186/s40644-022-00489-9.
[11]
HOFFMANN M A, MÜLLER-HÜBENTHAL J, ROSAR F, et al. Primary staging of prostate cancer patients with[18F]PSMA-1007 PET/CT compared with[68Ga]Ga-PSMA-11 PET/CT[J/OL]. J Clin Med, 2022, 11(17): 5064 [2023-04-17]. https://pubmed.ncbi.nlm.nih.gov/36078994/. DOI: 10.3390/jcm11175064.
[12]
JIAO J H, KANG F, ZHANG J L, et al. Establishment and prospective validation of an SUVmax cutoff value to discriminate clinically significant prostate cancer from benign prostate diseases in patients with suspected prostate cancer by 68Ga-PSMA PET/CT: a real-world study[J]. Theranostics, 2021, 11(17): 8396-8411. DOI: 10.7150/thno.58140.
[13]
BRUCKMANN N M, RISCHPLER C, KIRCHNER J, et al. Correlation between contrast enhancement, standardized uptake value (SUV), and diffusion restriction (ADC) with tumor grading in patients with therapy-naive neuroendocrine neoplasms using hybrid 68Ga-DOTATOC PET/MRI[J/OL]. Eur J Radiol, 2021, 137: 109588 [2023-04-19]. https://pubmed.ncbi.nlm.nih.gov/33639542/. DOI: 10.1016/j.ejrad.2021.109588.
[14]
CHINNAPPAN S, CHANDRA P, KUMAR J S, et al. SUVmax/ADC ratio as a molecular imaging biomarker for diagnosis of biopsy-Naïve primary prostate cancer[J]. Indian J Nucl Med, 2021, 36(4): 377-384. DOI: 10.4103/ijnm.ijnm_62_21.
[15]
HEPP T, KALMBACH L, KOLB M, et al. T2 mapping for the characterization of prostate lesions[J]. World J Urol, 2022, 40(6): 1455-1461. DOI: 10.1007/s00345-022-03991-8.
[16]
SONG N, WANG T, ZHANG D, et al. The value of relaxation time quantitative technique from synthetic magnetic resonance imaging in the diagnosis and invasion assessment of prostate cancer[J]. Natl Med J China, 2022, 102(15): 1093-1099. DOI: 10.3760/cma.j.cn112137-20211018-02304.
[17]
CERESER L, EVANGELISTA L, GIANNARINI G, et al. Prostate MRI and PSMA-PET in the primary diagnosis of prostate cancer[J/OL]. Diagnostics, 2023, 13(16): 2697 [2023-10-21]. https://pubmed.ncbi.nlm.nih.gov/37627956/. DOI: 10.3390/diagnostics13162697.
[18]
WANG Y S, GALANTE J R, HAROON A, et al. The future of psma pet and wb MRI as next-generation imaging tools in prostate cancer[J]. Nat Rev Urol, 2022, 19(8): 475-493. DOI: 10.1038/s41585-022-00618-w.
[19]
HOPE T A, EIBER M, ARMSTRONG W R, et al. Diagnostic accuracy of 68Ga-PSMA-11 PET for pelvic nodal metastasis detection prior to radical prostatectomy and pelvic lymph node dissection: a multicenter prospective phase 3 imaging trial[J]. JAMA Oncol, 2021, 7(11): 1635-1642. DOI: 10.1001/jamaoncol.2021.3771.
[20]
YI N, WANG Y J, ZANG S M, et al. Ability of 68 ga-psma pet/ct suvmax to differentiate isup gg2 from gg3 in intermediate-risk prostate cancer: a single-center retrospective study of 147 patients[J]. Cancer Med, 2023, 12(6): 7140-7148. DOI: 10.1002/cam4.5516.
[21]
EMMETT L, PAPA N, BUTEAU J, et al. The PRIMARY score: using intraprostatic 68Ga-PSMA PET/CT patterns to optimize prostate cancer diagnosis[J]. J Nucl Med, 2022, 63(11): 1644-1650. DOI: 10.2967/jnumed.121.263448.
[22]
SACHPEKIDIS C, AFSHAR-OROMIEH A, KOPKA K, et al. 18F-PSMA-1007 multiparametric, dynamic PET/CT in biochemical relapse and progression of prostate cancer[J]. Eur J Nucl Med Mol Imaging, 2020, 47(3): 592-602. DOI: 10.1007/s00259-019-04569-0.
[23]
HU S Q, ZHANG Y. Application of 68Ga-PSMA-11 and 18F-PSMA-1007 in prostate cancer[J]. J N Med, 2022, 53(1): 5-9.
[24]
MITTLMEIER L M, BRENDEL M, BEYER L, et al. Feasibility of different tumor delineation approaches for 18F-PSMA-1007 PET/CT imaging in prostate cancer patients[J/OL]. Front Oncol, 2021, 11: 663631 [2023-05-19]. https://pubmed.ncbi.nlm.nih.gov/34094956/. DOI: 10.3389/fonc.2021.663631.
[25]
TSECHELIDIS I, VRACHIMIS A. PSMA PET in imaging prostate cancer[J/OL]. Front Oncol, 2022, 12: 831429 [2023-05-16]. https://pubmed.ncbi.nlm.nih.gov/35155262/. DOI: 10.3389/fonc.2022.831429.
[26]
ZHANG J, LI S D. Correlation analysis between ADC minimum, rADC minimum and Fuhrman classification of renal clear cell carcinoma[J]. Chin J Magn Reson Imag, 2020, 11(9): 793-796. DOI: 10.12015/issn.1674-8034.2020.09.015.
[27]
KUS A A. The utility of ADC parameters in the diagnosis of clinically significant prostate cancer by 3.0-Tesla diffusion-weighted magnetic resonance imaging[J]. Pol J Radiol, 2021, 86: 262-268. DOI: 10.5114/pjr.2021.106071.
[28]
FALASCHI Z, TRICCA S, ATTANASIO S, et al. Non-timely clinically applicable ADC ratio in prostate mpMRI: a comparison with fusion biopsy results[J]. Abdom Radiol, 2022, 47(11): 3855-3867. DOI: 10.1007/s00261-022-03627-w.
[29]
MAI J L, ABUBRIG M, LEHMANN T, et al. T2 mapping in prostate cancer[J]. Invest Radiol, 2019, 54(3): 146-152. DOI: 10.1097/RLI.0000000000000520.
[30]
CHATTERJEE A, DEVARAJ A, MATHEW M, et al. Performance of T2 maps in the detection of prostate cancer[J]. Acad Radiol, 2019, 26(1): 15-21. DOI: 10.1016/j.acra.2018.04.005.
[31]
KLINGEBIEL M, SCHIMMÖLLER L, WEILAND E, et al. Value of T2 mapping MRI for prostate cancer detection and classification[J]. J Magn Reson Imaging, 2022, 56(2): 413-422. DOI: 10.1002/jmri.28061.
[32]
PARATHITHASAN N, PERRY E, TAUBMAN K, et al. Combination of MRI prostate and 18F-DCFPyl PSMA PET/CT detects all clinically significant prostate cancers in treatment-naive patients: an international multicentre retrospective study[J]. J Med Imaging Radiat Oncol, 2022, 66(7): 927-935. DOI: 10.1111/1754-9485.13382.
[33]
SONNI I, FELKER E R, LENIS A T, et al. Head-to-head comparison of 68Ga-PSMA-11 PET/CT and mpMRI with a histopathology gold standard in the detection, intraprostatic localization, and determination of local extension of primary prostate cancer: results from a prospective single-center imaging trial[J]. J Nucl Med, 2022, 63(6): 847-854. DOI: 10.2967/jnumed.121.262398.
[34]
ZHOU C C, TANG Y X, DENG Z H, et al. Comparison of 68Ga-PSMA PET/CT and multiparametric MRI for the detection of low- and intermediate-risk prostate cancer[J/OL]. EJNMMI Res, 2022, 12(1): 10 [2023-05-26]. https://pubmed.ncbi.nlm.nih.gov/35147810/. DOI: 10.1186/s13550-022-00881-3.
[35]
CHOW K M, SO W Z, LEE H J, et al. Head-to-head comparison of the diagnostic accuracy of prostate-specific membrane antigen positron emission tomography and conventional imaging modalities for initial staging of intermediate- to high-risk prostate cancer: a systematic review and meta-analysis[J]. Eur Urol, 2023, 84(1): 36-48. DOI: 10.1016/j.eururo.2023.03.001.
[36]
SZIGETI F, SCHWEIGHOFER-ZWINK G, MEISSNITZER M, et al. Incremental impact of[68Ga]Ga-PSMA-11 PET/CT in primary N and M staging of prostate cancer prior to curative-intent surgery: a prospective clinical trial in comparison with mpMRI[J]. Mol Imaging Biol, 2022, 24(1): 50-59. DOI: 10.1007/s11307-021-01650-9.
[37]
SANDGREN K, STRANDBERG S N, JONSSON J H, et al. Histopathology-validated lesion detection rates of clinically significant prostate cancer with mpMRI, [68 Ga]PSMA-11-PET and[11 C]Acetate-PET[J]. Nucl Med Commun, 2023, 44(11): 997-1004. DOI: 10.1097/MNM.0000000000001743.
[38]
PRIVÉ B M, ISRAËL B, SCHILHAM M G M, et al. Evaluating F-18-PSMA-1007-PET in primary prostate cancer and comparing it to multi-parametric MRI and histopathology[J]. Prostate Cancer Prostatic Dis, 2021, 24(2): 423-430. DOI: 10.1038/s41391-020-00292-2.

PREV Development of a nomogram based on diffusion weighted imaging of peritumoral liver tissue to predict local progression of recurrent hepatocellular carcinoma after hepatectomy
NEXT Differential diagnosis of MRI apparent diffusion coefficient for high-risk prostate cancer in the transition zone and its correlation with pathological grading group
  



Tel & Fax: +8610-67113815    E-mail: editor@cjmri.cn