Assessment of PSMA Expression of Healthy Organs in Different Stages of Prostate Cancer Using [68Ga]Ga-PSMA-11-PET Examinations

. 2024 Apr 16 ; 16 (8) : . [epub] 20240416

Status PubMed-not-MEDLINE Jazyk angličtina Země Švýcarsko Médium electronic

Typ dokumentu časopisecké články

Perzistentní odkaz   https://www.medvik.cz/link/pmid38672596

The efficacy of radioligand therapy (RLT) targeting prostate-specific membrane antigen (PSMA) is currently being investigated for its application in patients with early-stage prostate cancer (PCa). However, little is known about PSMA expression in healthy organs in this cohort. Collectively, 202 [68Ga]Ga-PSMA-11 positron emission tomography (PET) scans from 152 patients were studied. Of these, 102 PET scans were from patients with primary PCa and hormone-sensitive biochemically recurrent PCa and 50 PET scans were from patients with metastatic castration-resistant PCa (mCRPC) before and after three cycles of [177Lu]Lu-PSMA-RLT. PSMA-standardized uptake values (SUV) were measured in multiple organs and PSMA-total tumor volume (PSMA-TTV) was determined in all cohorts. The measured PET parameters of the different cohorts were normalized to the bloodpool and compared using t- or Mann-Whitney U tests. Patients with early-stage PCa had lower PSMA-TTVs (10.39 mL vs. 462.42 mL, p < 0.001) and showed different SUVs in the thyroid, submandibular glands, heart, liver, kidneys, intestine, testes and bone marrow compared to patients with advanced CRPC, with all tests showing p < 0.05. Despite the differences in the PSMA-TTV of patients with mCRPC before and after [177Lu]Lu-PSMA-RLT (462.42 mL vs. 276.29 mL, p = 0.023), no significant organ differences in PET parameters were detected. These suggest different degrees of PSMA-ligand binding among patients with different stages of PCa that could influence radiotoxicity during earlier stages of disease in different organs when PSMA-RLT is administered.

Zobrazit více v PubMed

Rawla P. Epidemiology of Prostate Cancer. World J. Oncol. 2019;10:63–89. doi: 10.14740/wjon1191. PubMed DOI PMC

Wasim S., Park J., Nam S., Kim J. Review of Current Treatment Intensification Strategies for Prostate Cancer Patients. Cancers. 2023;15:5615. doi: 10.3390/cancers15235615. PubMed DOI PMC

Chang S.S. Overview of Prostate-Specific Membrane Antigen. Rev. Urol. 2004;6((Suppl. S10)):S13–S18. PubMed PMC

Freedland S.J., Humphreys E.B., Mangold L.A., Eisenberger M., Dorey F.J., Walsh P.C., Partin A.W. Risk of prostate cancer-specific mortality following biochemical recurrence after radical prostatectomy. JAMA. 2005;294:433–439. doi: 10.1001/jama.294.4.433. PubMed DOI

Kupelian P.A., Buchsbaum J.C., Elshaikh M., Reddy C.A., Zippe C., Klein E.A. Factors affecting recurrence rates after prostatectomy or radiotherapy in localized prostate carcinoma patients with biopsy Gleason score 8 or above. Cancer. 2002;95:2302–2307. doi: 10.1002/cncr.10977. PubMed DOI

Shore N.D., Moul J.W., Pienta K.J., Czernin J., King M.T., Freedland S.J. Biochemical recurrence in patients with prostate cancer after primary definitive therapy: Treatment based on risk stratification. Prostate Cancer Prostatic Dis. 2023:1–10. doi: 10.1038/s41391-023-00712-z. PubMed DOI PMC

Chandrasekar T., Yang J.C., Gao A.C., Evans C.P. Mechanisms of resistance in castration-resistant prostate cancer (CRPC) Transl. Androl. Urol. 2015;4:365–380. doi: 10.3978/j.issn.2223-4683.2015.05.02. PubMed DOI PMC

Kirby M., Hirst C., Crawford E.D. Characterising the castration-resistant prostate cancer population: A systematic review. Int. J. Clin. Pract. 2011;65:1180–1192. doi: 10.1111/j.1742-1241.2011.02799.x. PubMed DOI

Silver D.A., Pellicer I., Fair W.R., Heston W.D., Cordon-Cardo C. Prostate-specific membrane antigen expression in normal and malignant human tissues. Clin. Cancer Res. 1997;3:81–85. PubMed

Hofman M.S., Lawrentschuk N., Francis R.J., Tang C., Vela I., Thomas P., Rutherford N., Martin J.M., Frydenberg M., Shakher R., 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. Lancet. 2020;395:1208–1216. doi: 10.1016/S0140-6736(20)30314-7. PubMed DOI

Afshar-Oromieh A., Holland-Letz T., Giesel F.L., Kratochwil C., Mier W., Haufe S., Debus N., Eder M., Eisenhut M., Schäfer M., et al. Diagnostic performance of 68Ga-PSMA-11 (HBED-CC) PET/CT in patients with recurrent prostate cancer: Evaluation in 1007 patients. Eur. J. Nucl. Med. Mol. Imaging. 2017;44:1258–1268. doi: 10.1007/s00259-017-3711-7. PubMed DOI PMC

Sartor O., de Bono J., Chi K.N., Fizazi K., Herrmann K., Rahbar K., Tagawa S.T., Nordquist L.T., Vaishampayan N., El-Haddad G., et al. Lutetium-177–PSMA-617 for Metastatic Castration-Resistant Prostate Cancer. N. Engl. J. Med. 2021;385:1091–1103. doi: 10.1056/NEJMoa2107322. PubMed DOI PMC

Rasul S., Hacker M., Kretschmer-Chott E., Leisser A., Grubmüller B., Kramer G., Shariat S., Wadsak W., Mitterhauser M., Hartenbach M., et al. Clinical outcome of standardized 177Lu-PSMA-617 therapy in metastatic prostate cancer patients receiving 7400 MBq every 4 weeks. Eur. J. Nucl. Med. 2020;47:713–720. doi: 10.1007/s00259-019-04584-1. PubMed DOI PMC

Hofman M.S., Emmett L., Sandhu S., Iravani A., Joshua A.M., Goh J.C., Pattison D.A., Tan T.H., Kirkwood I.D., Ng S., et al. [177Lu]Lu-PSMA-617 versus cabazitaxel in patients with metastatic castration-resistant prostate cancer (TheraP): A randomised, open-label, phase 2 trial. Lancet. 2021;397:797–804. doi: 10.1016/S0140-6736(21)00237-3. PubMed DOI

Ferdinandus J., Fendler W.P., Farolfi A., Washington S., Mohammad O., Pampaloni M.H., Scott P.J., Rodnick M., Viglianti B.L., Eiber M., et al. PSMA PET Validates Higher Rates of Metastatic Disease for European Association of Urology Biochemical Recurrence Risk Groups: An International Multicenter Study. J. Nucl. Med. 2022;63:76–80. doi: 10.2967/jnumed.121.262821. PubMed DOI PMC

Grubmüller B., Senn D., Kramer G., Baltzer P., D’Andrea D., Grubmüller K.H., Mitterhauser M., Eidherr H., Haug A.R., Wadsak W., et al. Response assessment using 68Ga-PSMA ligand PET in patients undergoing 177Lu-PSMA radioligand therapy for metastatic castration-resistant prostate cancer. Eur. J. Nucl. Med. Mol. Imaging. 2019;46:1063–1072. doi: 10.1007/s00259-018-4236-4. PubMed DOI PMC

Grubmüller B., Huebner N.A., Rasul S., Clauser P., Pötsch N., Grubmüller K.H., Hacker M., Hartenbach S., Shariat S.F., Hartenbach M., et al. Dual-Tracer PET-MRI-Derived Imaging Biomarkers for Prediction of Clinically Significant Prostate Cancer. Curr. Oncol. 2023;30:1683–1691. doi: 10.3390/curroncol30020129. PubMed DOI PMC

Privé B.M., Janssen M.J.R., van Oort I.M., Muselaers C.H.J., Jonker M.A., van Gemert W.A., de Groot M., Westdorp H., Mehra N., Verzijlbergen J.F., et al. Update to a randomized controlled trial of lutetium-177-PSMA in Oligo-metastatic hormone-sensitive prostate cancer: The BULLSEYE trial. Trials. 2021;22:768. doi: 10.1186/s13063-021-05733-4. PubMed DOI PMC

Dhiantravan N., Emmett L., Joshua A.M., Pattison D.A., Francis R.J., Williams S., Sandhu S., Davis I.D., Vela I., Neha N., et al. UpFrontPSMA: A randomized phase 2 study of sequential 177 Lu-PSMA-617 and docetaxel vs docetaxel in metastatic hormone-naïve prostate cancer (clinical trial protocol) BJU Int. 2021;128:331–342. doi: 10.1111/bju.15384. PubMed DOI

Kostos L.K., Buteau J.P., Kong G., Yeung T., Di Iulio J., Fahey M.T., Fettke H., Furic L., Hofman M.S., Azad A. LuCAB: A phase I/II trial evaluating cabazitaxel in combination with [177Lu]Lu-PSMA-617 in patients (pts) with metastatic castration-resistant prostate cancer (mCRPC) J. Clin. Oncol. 2023;41:TPS278. doi: 10.1200/JCO.2023.41.6_suppl.TPS278. DOI

Sandhu S., Joshua A.M., Emmett L., Crumbaker M., Bressel M., Huynh R., Banks P.D., Wallace R., Hamid A., Inderjeeth A.J., et al. LuPARP: Phase 1 trial of 177Lu-PSMA-617 and olaparib in patients with metastatic castration resistant prostate cancer (mCRPC) J. Clin. Oncol. 2023;41:5005. doi: 10.1200/JCO.2023.41.16_suppl.5005. PubMed DOI

Eapen R.S., Buteau J.P., Jackson P., Mitchell C., Oon S.F., Alghazo O., McIntosh L., Dhiantravan N., Scalzo M.J., O’Brien J., et al. Administering [177Lu]Lu-PSMA-617 Prior to Radical Prostatectomy in Men with High-risk Localised Prostate Cancer (LuTectomy): A Single-centre, Single-arm, Phase 1/2 Study. Eur. Urol. 2023;85:217–226. doi: 10.1016/j.eururo.2023.08.026. PubMed DOI

Seitzer K.E., Seifert R., Kessel K., Roll W., Schlack K., Boegemann M., Rahbar K. Lutetium-177 Labelled PSMA Targeted Therapy in Advanced Prostate Cancer: Current Status and Future Perspectives. Cancers. 2021;13:3715. doi: 10.3390/cancers13153715. PubMed DOI PMC

Peters S.M.B., Hofferber R., Privé B.M., de Bakker M., Gotthardt M., Janssen M., de Lange F., Muselaers C.H.J., Mehra N., Witjes J.A., et al. [68Ga]Ga-PSMA-11 PET imaging as a predictor for absorbed doses in organs at risk and small lesions in [177Lu]Lu-PSMA-617 treatment. Eur. J. Nucl. Med. 2022;49:1101–1112. doi: 10.1007/s00259-021-05538-2. PubMed DOI PMC

Kluge K., Haberl D., Einspieler H., Rasul S., Gutschmayer S., Kenner L., Kramer G., Grubmüller B., Shariat S., Haug A., et al. Antihormonal-Treatment Status Affects68Ga-PSMA-HBED-CC PET Biodistribution in Patients with Prostate Cancer. J. Nucl. Med. 2023;64:1730–1736. doi: 10.2967/jnumed.123.265980. PubMed DOI

Gafita A., Wang H., Robertson A., Armstrong W.R., Zaum R., Weber M., Yagubbayli F., Kratochwil C., Grogan T.R., Nguyen K., et al. Tumor Sink Effect in 68Ga-PSMA-11 PET: Myth or Reality? J. Nucl. Med. Off. Publ. Soc. Nucl. Med. 2022;63:226–232. doi: 10.2967/jnumed.121.261906. PubMed DOI PMC

Tuncel M., Telli T., Tuncalı M., Karabulut E. Predictive factors of tumor sink effect: Insights from 177Lu-Prostate-specific membrane antigen therapy. Ann. Nucl. Med. 2021;35:529–539. doi: 10.1007/s12149-021-01593-9. PubMed DOI

Groener D., Wichert J., Adams M., Mader N., Klimek K., Ngoc C.N., Baumgarten J., Happel C., Mandel P., Chun F.K.H., et al. Impact of [177Lu]Lu-PSMA-617 Radioligand Therapy on Reference Organ Uptake Assessed by [68Ga]Ga-PSMA-11-PET/CT. Cancers. 2023;15:3878. doi: 10.3390/cancers15153878. PubMed DOI PMC

Lyons K., Seghers V., Sorensen J.I.L., Zhang W., Paldino M.J., Krishnamurthy R., Rohren E.M. Comparison of Standardized Uptake Values in Normal Structures Between PET/CT and PET/MRI in a Tertiary Pediatric Hospital: A Prospective Study. Am. J. Roentgenol. 2015;205:1094–1101. doi: 10.2214/AJR.15.14304. PubMed DOI

Huber R., Sher A., Crisan A., Faulhaber P. Comparisons of SUVs in normal structures between PET/CT and PET/MRI. J. Nucl. Med. 2014;55((Suppl. 1)):1506. PubMed

Jentjens S., Mai C., Bidakhvidi N.A., De Coster L., Mertens N., Koole M., Everaerts W., Joniau S., Oyen R., Van Laere K., et al. Prospective comparison of simultaneous [68Ga]Ga-PSMA-11 PET/MR versus PET/CT in patients with biochemically recurrent prostate cancer. Eur. Radiol. 2022;32:901–911. doi: 10.1007/s00330-021-08140-0. PubMed DOI

Freitag M.T., Radtke J.P., Afshar-Oromieh A., Roethke M.C., Hadaschik B., Gleave M., Bonekamp D., Kopka K., Eder M., Heusser T., et al. Local recurrence of prostate cancer after radical prostatectomy is at risk to be missed in 68Ga-PSMA-11-PET of PET/CT and PET/MRI: Comparison with mpMRI integrated in simultaneous PET/MRI. Eur. J. Nucl. Med. Mol. Imaging. 2017;44:776–787. doi: 10.1007/s00259-016-3594-z. PubMed DOI

Najít záznam

Citační ukazatele

Pouze přihlášení uživatelé

Možnosti archivace

Nahrávání dat ...