"Never doubt that a small group of thoughtful, committed citizens can change the world. Indeed, it is the only thing that ever has."

Margaret Mead

Review article
peer-reviewed

A Review of 177Lutetium-PSMA and 225Actinium-PSMA as Emerging Theranostic Agents in Prostate Cancer



Abstract

The development of prostate-specific membrane antigen (PSMA) ligands labeled with radionuclides is a ground-breaking achievement in the management of prostate cancer. With the increasing use of 68Gallium-PSMA and 18F-DCFPyL (Pylarify) and their approval by the Food and Drug Administration (FDA), other PSMA agents and their unique characteristics are also being studied. Two other PSMA agents, namely 177Lutetium-PSMA (177Lu-PSMA) and 225Actinium-PSMA (225Ac-PSMA), are currently drawing the researcher’s attention mainly due to their theranostic importance. Studies focusing on the essential characteristics of these two emerging radiotracers are relatively lacking. Hence, this review article, beginning with a brief introduction, intends to provide insights on the mechanism, efficacy, adverse effects, usefulness, including theranostic implications, and limitations of these two emerging PSMA agents. The 177Lu-PSMA is commercially accessible, is well tolerated, and has been found to lower prostate-specific antigen (PSA) levels while improving patients’ quality of life. It also reduces pain and the requirement for analgesics and is safe for advanced diseases. However, despite its potential advantages, around one-third of patients do not respond satisfactorily to this costly treatment; it is still challenging to personalize this therapy and predict its outcome. Similarly, 225Ac is compatible with antibody-based targeting vectors, releasing four extremely hazardous high-energy emissions with a longer half-life of 10 days. It has made 225Ac-PSMA therapy useful for tumors resistant to standard treatments, with a better response than 177Lu-PSMA. Dosimetry studies show a good biochemical response without toxicity in patients with advanced metastatic castration-resistant prostate cancer (mCRPC). However, it can potentially cause significant damage to healthy tissues if not retained at the tumor site. Encapsulating radionuclides in a nano-carrier, hastening the absorption by tumor cells, and local delivery might all help reduce the harmful consequences. Both have advantages and disadvantages. The choice of PSMA agents may rely on desired qualities, cost, and convenience, among other factors. Further research is warranted in order to better understand their ideal use in clinical settings.

Introduction & Background

Prostate cancer is the most prevalent cancer among American men, after skin cancer. The American Cancer Society (ACS) estimates that approximately one in eight men will be diagnosed with prostate cancer in their lifetime. It is more prevalent in older men and non-Hispanic black men, with an average age of 66 years at diagnosis. Moreover, it is the second leading cause of cancer-related mortality among American men after lung cancer. Approximately one in 41 men will eventually die from prostate cancer, according to an estimate by ACS [1]. Prostate cancer can be deadly, but most men diagnosed with it do not succumb to it. More than 3.1 million men diagnosed with prostate cancer in the United States are still alive today [1]. Prostate cancer is generally indolent, with numerous treatment options such as androgen deprivation therapy, radical surgical resection, radiotherapy, chemotherapy, and immunotherapy. However, its prognosis becomes poor when it aggressively metastasizes despite the initial treatment, eventually progressing into metastatic castration-resistant prostate cancer (mCRPC) [2]. Here comes the emerging role of prostate-specific membrane antigen (PSMA)-targeted radioligand therapy (PRLT) as a promising treatment modality for managing mCRPC. Several small-molecule PSMA ligands that can be conjugated to radioisotopes, such as 18F, 68Ga, 177Lu, and 225Ac, among others, have been developed [3]. FDA approved 68Gallium PSMA (68Ga-PSMA) in 2020, and [18F]DCFPyL, a Fluorine-18 labeled PSMA ligand, popularly known as Pylarify in 2021 as the first and second PSMA-based PET tracer for management of patients with prostate cancer who had a biochemical recurrence. Recently, PSMA-based radiotracers such as 177Lutetium-PSMA (177Lu-PSMA) and 225Actinium-PSMA (225Ac-PSMA) have become available with unique diagnostic and therapeutic benefits. It involves using PSMA molecules radiolabeled with the beta (β) and gamma (γ) emitters) such as 177Lu and the α-emitter such as 225Ac. The 177Lu emits a cytotoxic β-particle useful for targeted therapies and γ-particles whose emissions can be quantified to assist with the diagnostic evaluation [4]. Similarly, targeted alpha-particle therapy (TAT) uses alpha-particles released by 225Ac and can potentially treat metastases in soft tissues [5,6]. In light of the rapidly evolving adoption of [18F]DCFPyL and 68Ga-PSMA globally, there is a relative scarcity of literature to highlight the advantages and limitations of 177Lu-PSMA and 225Ac-PSMA, which are currently being studied extensively. This review article aims to shed light on the pros and cons of these two emerging PSMA agents, 177Lu-PSMA and 225Ac-PSMA, which are gradually gaining popularity, mainly due to their theranostic importance.

Review

177Lu-PSMA

177Lu-PSMA-617 radioligand therapy ([RLT] which is regarded as the mainstay 177Lu-labeled PSMA agent in this review) has demonstrated its ability to target prostate cancer cells while sparing most normal tissues in patients that have been identified using imaging to confirm radionuclide binding with the prostate cancer cells [7]. Anderson et al. reported the first clinical use of 177Lu in 1960 when three patients with myelomatosis were treated with intravenous injections of 177Lu as lutetium chloride and citrate [8]. Keeling and Vaughan published a study on 177Lu hydroxyapatite (HA) particles to investigate the mechanism of uptake of bone minerals using in vitro techniques in 1988, which was the first publication on 177Lu [9]. However, the potential application of 177Lu as a therapeutic radionuclide was established with the introduction of 177Lu-DOTATATE, a radiopharmaceutical that targets neuroendocrine tumors [10,11]. The significant rise in interest in 177Lu as a therapeutic radionuclide can be due to its favorable nuclear properties and adaptable chemistry, which results in stable compounds with good in vivo properties. However, the ease with which 177Lu may be produced in high activity levels with high specific activity in many current nuclear reactors worldwide is the single most crucial reason contributing to its rising interest and use in nuclear medicine [12]

Mechanism of 177Lu-PSMA

The beta-particle radiation delivered by 177Lu-PSMA-617 is preferential to PSMA-positive cells and the tissues surrounding them [4,12]. The internalization of the radioligand makes it possible for radioactivity to accumulate in the tumor tissue, allowing for inside-out irradiation. 177Lu-PSMA-617 has a half-life of six to eight days [8]. Figure 1 demonstrates its efficacy in prostate cancer.

177Lu-PSMA RLT appears safe, even in patients with advanced disease [13]. Because most prostate cancer patients had repeated relapses before receiving PSMA-RLT therapy, the results are pretty encouraging [11,14,15]. An average of 7.5 to 15 months is recorded for overall survival (OS) and 4.5 to 13.7 months for progression-free survival (PFS) [16]. Important findings of studies assessing OS and objective remission (complete remission and partial remission) are presented in Table 1. However, it is worth noting that the response rate is fluctuating [16]. Nearly one-third of patients do not respond satisfactorily to this expensive treatment. At the later stages of the disease, the therapy options available to individuals who have experienced a relapse following PSMA-RLT are much restricted. This demands further individualization of therapy and better prediction of clinical outcomes [11].

Author Total number of patients Frequency of best PSA decline of ≥50% (%) Frequency of objective remission* (%) Median overall survival (months)
Kratochwil et al. [17] 30 43% NR NR
Kulkarni et al.  [15] 119 58% 29% 70% at 15 months
Ahmadzadehfar et al. [18] 22 60% NR 14
Brauer et al. [19] 59 53% NR 8
Fendler et al. [20] 15 47% 27% NR
Rahbar et al. [21] 145 49% NR NR
Rahbar et al. [22] 104 33% NR 14
Peters and Stahel [23] 10 50% 30% NR
Yadav et al. [24] 31 71% 82% 16
Khreish et al. [25] 252 48% NR 13.4
Sartor et al. [26] 551 46% NR 15.3
Hofman et al. [27] 98 66% NR NR

Adverse effects of 177Lu-PSMA 

Anemia, neutropenia, and thrombocytopenia were some treatment-induced hematologic toxicities reported in a prospective study by Hofman et al. [27]. Extensive bone marrow metastases, previous chemotherapy, and older patients (likely associated with reduced renal function) are all factors that might amplify hematopoietic damage. Patients with renal impairment should get a modified activity dosage to protect the red marrow [28]. Transient xerostomia is a treatment-related side effect that may have a negative impact on quality of life. Nephrotoxicity can occur. However, severe cases of renal failure are rare [14,24]. According to the findings of Barber et al., grade I-II renal toxicity (as determined by estimated glomerular filtration rate) was seen in 42/167 individuals; 26 of these patients had reduced baseline renal function. Not a single patient reported having grade III-IV renal toxicity [29]. In their series, many additional investigations found no evidence of treatment-induced nephrotoxicity [30-32]. Old age, systemic hypertension, and pre-existing renal impairment are risk factors for 177Lu-PSMA renal toxicity [33]. A case of tumor lysis syndrome due to 177Lu-PSMA treatment has been reported [34]. Table 2 illustrates the percentage of occurrence of these common side effects in various studies.

Study Total number of patients Hematologic toxicity Nephrotoxicity Salivary gland toxicity
Anemia Neutropenia Thrombocytopenia
Ahmadzaehfar et al. [35] 24 38% 21% 17% 12.5% 9%
Baum et al. [36] 56 5% 16% 0% 0% 4%
Heck et al. [37] 22 32% 5% 25% NR 37%
Kratochwil et al. [17] 30 10% 27% 7% 0% 7%
Kulkarni et al. [17] 119 4% NR NR NR NR
Rahbar et al. [38] 74 36% 16% 23% 5.4% 9%
Rahbar et al. [39] 28 20% 11% 23% 4.5% 0%
Brauer et al. [19] 59 85% 38% 47% 85% 85%
Yadav et al. [24] 31 7% 3% 0% 0% 0%
Hofman et al. [40] 30 26% 30% 30% NR 87%

Limitations of 177Lu-PSMA 

According to the findings of a recent meta-analysis, around 37% of patients show biochemical progression and are resistant to the treatment provided by 177Lu-PSMA-617 [41]. Alternative treatment options are required for patients who do not respond to 177Lu-PSMA and are unfit or exhausted from receiving the approved therapies. Additionally, many patients who respond to 177Lu-PSMA will ultimately progress. Patients whose prostate cancer has spread throughout the bone marrow and has induced bone marrow failure may not be good candidates for 177Lu-PSMA due to the extended route length of 177Lu, which may cross 20 to 60 cells resulting in bone marrow failure [42]. This necessitates the understanding of major properties of alternative PSMA agents such as 225Ac-PSMA.

225Ac-PSMA

Although alpha emitters can be more efficacious than beta emitters, only a limited number of alpha-emitting radionuclides are commercially accessible and possess the necessary properties for use in medical settings. In the last decade, the radioactive metals 225Actinium (t1/2 = 10 days) and 227Thorium (t1/2 = 19 days) have emerged as potentially useful alpha emitters that might be used in the development of future targeted radiotherapeutics [43].

TAT is a new approach aiming to take advantage of alpha-particles therapeutic potential for metastases in soft tissues [5,6]. To selectively administer cytotoxic alpha radiation to cancer cells, radionuclides that generate alpha radiation are coupled to tumor-targeting vectors utilizing bifunctional chelators [44]. 225Ac, one of the radionuclides suitable for such an application, has a long half-life of 10 days, is compatible with antibody-based targeting vectors, and emits four high-energy emissions that are very harmful to cells. This makes it a better option for use in TAT. 225Ac is easily complexable with the DOTA chelator under temperatures of 80-90°C, which can be achieved by microwave or other methods [45]. But initial research suggested that the chelator macropa (mcp) would be even more appropriate [46]. Additionally, 213Bismuth is produced when 225Ac decays, and this latter compound also emits 440 keV rays, which may be used to image the therapeutic biodistribution. It should be noted that it is unclear if the detected radioactive decay reflects liberated daughter radioisotopes or intact radiopharmaceuticals [47,48]. The relatively long half-life of 225Ac enables centralized manufacturing and shipping of the irradiated targets to other users allowing its widespread use.

Excellent response to 225Ac-PSMA was first reported by Kratochwil et al. in two patients who had previously failed 177Lu-PSMA treatment [32]. Patients with advanced mCRPC have shown a satisfactory biochemical response and low toxicities with 225Ac-PSMA-617 TAT, according to dosimetry studies [49].

Mechanism of 225Ac-PSMA

Alpha emitters such as 225Ac-PSMA can treat cancer more effectively than beta emitters such as 177Lu-PSMA because of the narrow range of alpha radiation in human tissue (less than 0.1 mm), which corresponds to just a few cell diameters. This, in turn, enables the selective destruction of cancer cells being targeted while preserving the healthy tissues around them. In addition, the high energy of alpha particles, which may be many MeV, along with the strong linear energy transfer that comes with it, causes a significant increase in the number of cells killed. As a consequence, alpha radiation can kill cells that, under normal circumstances, would be resistant to treatment with beta or gamma irradiation or chemotherapeutic drugs, hence making alpha radiation a viable treatment option for tumors that are resistant to conventional therapies [50] (Figure 2).

Efficacy of 225Ac-PSMA

The Prostate Cancer Clinical Trials Working Group 3 recommends using a PSA drop of more than 50% as a standard for measuring therapeutic success in patients with mCRPC [52]. Recent meta-analyses by Lee et al. revealed that approximately 61%percent of patients showed more than a 50% PSA decline after receiving 225Ac-PSMA RLT and that 84% of patients showed any PSA decline after receiving 225Ac-PSMA RLT [53]. It has a greater response than what was shown in a prior meta-analysis for 177Lu-PSMA RLT: 46% by Yadav et al. [41] and 57 % by Hofman et al. in a previous phase two clinical trial of 177Lu-PSMA-617 [54]. After receiving 177Lu-PSMA RLT, the median PFS and OS were found to be 11 months and 14 months, respectively, in a study by Yadav et al. [41]. This is a longer period than what Lee et al. found; the median PFS and OS were 8 months and 12 months, respectively, following 225Ac-PSMA RLT [53]. PFS, OS, and other characteristics of some important studies related to 225Ac-PSMA included in this review article have been listed in Table 3.

Author Total number of patients Frequency of best PSA decline of ≥50% (%) Frequency of objective remission (%) Median overall survival (months)
Kratochwil et al. [55] 14 63% NR NR
Kratochwil et al. [56] 38 82% 13% >12
Sathekge et al. [57] 17 70% NR NR
Sathekge et al. [58] 73 65% NR 18
Khreish et al. [59] 20 49% 21% 12
Yadav et al. [60] 28 39% 9% 17

Adverse effects of 225Ac-PSMA

The majority of patients who were treated with 225Ac-PSMA reported that xerostomia was the most prevalent adverse effect [56-58]. It was so severe that 10% of participants in previous research gave up on treatment. The treatment dose of 225Ac-PSMA was gradually adjusted in subsequent studies based on the patient's ability to tolerate the severity of dry mouth without compromising antitumor activity [57,58,61]. This has resulted in a less severe case of xerostomia being recorded in more recent studies, and no patient has had to stop treatment as a direct result of xerostomia. Sialendoscopy with dilation, isotonic saline irrigation, and steroid injection improved salivary gland function in individuals with intolerable xerostomia [62].

In a study conducted by Feuerecker et al., patients exhibited anemia of grade III/IV, thrombocytopenia, and leukopenia at varying rates: 35%, 19%, and 27%, respectively [63]. Feuerecker et al. [63] documented grade I/II impairment of kidney function in 19% of patients but without clinical relevance, similar to what Sathekge et al. described [58]. The most significant disadvantage associated with 225Ac is its high price. In addition, the recoiled daughters of 225Ac have the potential to cause significant damage to healthy tissues if they are not retained at the tumor site. Harmful effects produced by the daughters that create alpha particles could be minimized by encapsulation in a nano-carrier, rapid absorption of the radionuclides by tumor cells, and local delivery of the radionuclides to the tumor location [64].

Conclusions

The discovery of various PSMA ligands labeled with radionuclides is a novel diagnostic and therapeutic option in the management of prostate cancer. Their uses are growing rapidly globally, owing to their diagnostic superiority over other conventional imaging modalities and some PSMA agents having an additional advantage of theranostic value. 177Lu-PSMA emits a cytotoxic β-particle useful for targeted therapies and γ-particles whose emissions can be quantified to assist with diagnostic evaluation and dosimetry studies. The 177Lu-PRLT (PRLT) has demonstrated its promising results in mCRPC with reductions in PSA level, relief from pain, and reduced need for analgesics. Moreover, it has been found to be superior to other third-line systemic treatments. However, patients with prostate cancer that have metastases to the bone marrow may not be suitable candidates for 177Lu-PSMA as 177Lu can pass through 20 to 60 cells causing bone marrow failure. 225Ac-PSMA, an α-emitter, is another promising agent owing to its ability to kill both single cancer cells and clusters of cancer cells with only minor collateral damage to healthy, non-targeted cells, as shown in both preclinical and clinical studies. There is growing evidence that 225Ac-PSMA TAT is superior to 177Lu-PSMA RLT in terms of tumor control. However, there is also evidence that co-radiation to the salivary glands is more common with the former. 

Clearly, both of these agents have their own pros and cons. Hence, the choice of PSMA agents might depend on the desired properties of the agent, the cost of treatment, and the convenience of adopting that agent, among others. It is still unknown whether PSMA RLT can benefit patients with nonexistent or low PSMA expression, thereby limiting a suitable and effective therapy plan in this setting. Conducting high-quality, multicenter, prospective, randomized controlled studies to assess the efficacy, safety, and survival benefits of these PSMA-targeted radioligands with one another, as well as with traditional therapies, might help us better understand their ideal clinical utility.


References

  1. Key statistics for prostate cancer. Accessed. (2022). Accessed: August 19, 2022: https://www.cancer.org/cancer/prostate-cancer/about/key-statistics.html..
  2. Halabi S, Vogelzang NJ, Kornblith AB, Ou SS, Kantoff PW, Dawson NA, Small EJ: Pain predicts overall survival in men with metastatic castration-refractory prostate cancer. J Clin Oncol. 2008, 26:2544-9. 10.1200/JCO.2007.15.0367
  3. Eiber M, Fendler WP, Rowe SP, et al.: Prostate-specific membrane antigen ligands for imaging and therapy. J Nucl Med. 2017, 58:67S-76S. 10.2967/jnumed.116.186767
  4. Afshar-Oromieh A, Hetzheim H, Kratochwil C, et al.: The theranostic PSMA ligand PSMA-617 in the diagnosis of prostate cancer by PET/CT: biodistribution in humans, radiation dosimetry, and first evaluation of tumor lesions. J Nucl Med. 2015, 56:1697-705. 10.2967/jnumed.115.161299
  5. Kim YS, Brechbiel MW: An overview of targeted alpha therapy. Tumour Biol. 2012, 33:573-90. 10.1007/s13277-011-0286-y
  6. Dekempeneer Y, Keyaerts M, Krasniqi A, et al.: Targeted alpha therapy using short-lived alpha-particles and the promise of nanobodies as targeting vehicle. Expert Opin Biol Ther. 2016, 16:1035-47. 10.1080/14712598.2016.1185412
  7. Rowe SP, Gorin MA, Pomper MG: Imaging of prostate-specific membrane antigen with small-molecule pet radiotracers: from the bench to advanced clinical applications. Annu Rev Med. 2019, 70:461-77. 10.1146/annurev-med-062117-073027
  8. Anderson J, Farmer FT, Haggith JW, Hill M: The treatment of myelomatosis with lutecium 177. Br J Radiol. 1960, 33:374-8. 10.1259/0007-1285-33-390-374
  9. Keeling AA, Vaughan ATM: Factors influencing the adsorption of Lutetium-177 on hydroxyapatite. Int J Rad Appl Instrum B. 1988, 15:489-92. 10.1016/S0969-8051(88)80003-9
  10. Bodei L, Mueller-Brand J, Baum RP, et al.: The joint IAEA, EANM, and SNMMI practical guidance on peptide receptor radionuclide therapy (PRRNT) in neuroendocrine tumours. Eur J Nucl Med Mol Imaging. 2013, 40:800-16. 10.1007/s00259-012-2330-6
  11. Kwekkeboom DJ, Bakker WH, Kooij PP, et al.: [177Lu-DOTAOTyr3]octreotate: comparison with [111In-DTPAo]octreotide in patients. Eur J Nucl Med. 2001, 28:1319-25. 10.1007/s002590100574
  12. Banerjee S, Pillai MR, Knapp FF: Lutetium-177 therapeutic radiopharmaceuticals: linking chemistry, radiochemistry, and practical applications. Chem Rev. 2015, 115:2934-74. 10.1021/cr500171e
  13. Awang ZH, Essler M, Ahmadzadehfar H: Radioligand therapy of metastatic castration-resistant prostate cancer: current approaches. Radiat Oncol. 2018, 13:98. 10.1186/s13014-018-1037-7
  14. Violet J, Jackson P, Ferdinandus J, et al.: Dosimetry of 177Lu-PSMA-617 in metastatic castration-resistant prostate cancer: correlations between pretherapeutic imaging and whole-body tumor dosimetry with treatment outcomes. J Nucl Med. 2019, 60:517-23. 10.2967/jnumed.118.219352
  15. Kulkarni HR, Singh A, Schuchardt C, et al.: PSMA-based radioligand therapy for metastatic castration-resistant prostate cancer: the bad Berka experience since 2013. J Nucl Med. 2016, 57:97S-104S. 10.2967/jnumed.115.170167
  16. Yordanova A, Linden P, Hauser S, et al.: Outcome and safety of rechallenge [177Lu]Lu-PSMA-617 in patients with metastatic prostate cancer. Eur J Nucl Med Mol Imaging. 2019, 46:1073-80. 10.1007/s00259-018-4222-x
  17. Kratochwil C, Giesel FL, Stefanova M, et al.: PSMA-targeted radionuclide therapy of metastatic castration-resistant prostate cancer with 177Lu-labeled PSMA-617. J Nucl Med. 2016, 57:1170-6. 10.2967/jnumed.115.171397
  18. Mohan R: Prostate Cancer: Leading-edge Diagnostic Procedures and Treatments. InTech, Rijeka, Croatia; 2016.
  19. Bräuer A, Grubert LS, Roll W, Schrader AJ, Schäfers M, Bögemann M, Rahbar K: 177Lu-PSMA-617 radioligand therapy and outcome in patients with metastasized castration-resistant prostate cancer. Eur J Nucl Med Mol Imaging. 2017, 44:1663-70. 10.1007/s00259-017-3751-z
  20. Fendler WP, Reinhardt S, Ilhan H, et al.: Preliminary experience with dosimetry, response and patient reported outcome after 177Lu-PSMA-617 therapy for metastatic castration-resistant prostate cancer. Oncotarget. 2017, 8:3581-90. 10.18632/oncotarget.12240
  21. Rahbar K, Ahmadzadehfar H, Kratochwil C, et al.: German multicenter study investigating 177Lu-PSMA-617 radioligand therapy in advanced prostate cancer patients. J Nucl Med. 2017, 58:85-90. 10.2967/jnumed.116.183194
  22. Rahbar K, Boegemann M, Yordanova A, Eveslage M, Schäfers M, Essler M, Ahmadzadehfar H: PSMA targeted radioligand therapy in metastatic castration resistant prostate cancer after chemotherapy, abiraterone and/or enzalutamide. A retrospective analysis of overall survival. Eur J Nucl Med Mol Imaging. 2018, 45:12-9. 10.1007/s00259-017-3848-4
  23. Peters S, Stahel RA: Successes and Limitations of Targeted Cancer Therapy. Karger Medical and Scientific Publishers, Basel; 2014.
  24. Yadav MP, Ballal S, Tripathi M, Damle NA, Sahoo RK, Seth A, Bal C: 177Lu-DKFZ-PSMA-617 therapy in metastatic castration resistant prostate cancer: safety, efficacy, and quality of life assessment. Eur J Nucl Med Mol Imaging. 2017, 44:81-91. 10.1007/s00259-016-3481-7
  25. Khreish F, Ghazal Z, Marlowe RJ, et al.: 177 Lu-PSMA-617 radioligand therapy of metastatic castration-resistant prostate cancer: Initial 254-patient results from a prospective registry (REALITY Study). Eur J Nucl Med Mol Imaging. 2022, 49:1075-85. 10.1007/s00259-021-05525-7
  26. Sartor O, de Bono J, Chi KN, et al.: Lutetium-177-PSMA-617 for metastatic castration-resistant prostate cancer. N Engl J Med. 2021, 385:1091-103. 10.1056/NEJMoa2107322
  27. Hofman MS, Emmett L, Sandhu 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. 10.1016/S0140-6736(21)00237-3
  28. Lawal IO, Bruchertseifer F, Vorster M, Morgenstern A, Sathekge MM: Prostate-specific membrane antigen-targeted endoradiotherapy in metastatic prostate cancer. Curr Opin Urol. 2020, 30:98-105. 10.1097/MOU.0000000000000685
  29. Barber TW, Singh A, Kulkarni HR, Niepsch K, Billah B, Baum RP: Clinical outcomes of 177Lu-PSMA radioligand therapy in earlier and later phases of metastatic castration-resistant prostate cancer grouped by previous taxane chemotherapy. J Nucl Med. 2019, 60:955-62. 10.2967/jnumed.118.216820
  30. Heck MM, Tauber R, Schwaiger S, et al.: Treatment outcome, toxicity, and predictive factors for radioligand therapy with 177Lu-PSMA-I&T in metastatic castration-resistant prostate cancer. Eur Urol. 2019, 75:920-6. 10.1016/j.eururo.2018.11.016
  31. McBean R, O'Kane B, Parsons R, Wong D: Lu177-PSMA therapy for men with advanced prostate cancer: Initial 18 months experience at a single Australian tertiary institution. J Med Imaging Radiat Oncol. 2019, 63:538-45. 10.1111/1754-9485.12891
  32. van Kalmthout L, Braat A, Lam M, et al.: First experience with 177Lu-PSMA-617 therapy for advanced prostate cancer in the Netherlands. Clin Nucl Med. 2019, 44:446-51. 10.1097/RLU.0000000000002561
  33. Yordanova A, Becker A, Eppard E, et al.: The impact of repeated cycles of radioligand therapy using [177Lu]Lu-PSMA-617 on renal function in patients with hormone refractory metastatic prostate cancer. Eur J Nucl Med Mol Imaging. 2017, 44:1473-9. 10.1007/s00259-017-3681-9
  34. Huang K, Brenner W, Prasad V: Tumor lysis syndrome: a rare but serious complication of radioligand therapies. J Nucl Med. 2019, 60:752-5. 10.2967/jnumed.118.217380
  35. Ahmadzadehfar H, Eppard E, Kürpig S, et al.: Therapeutic response and side effects of repeated radioligand therapy with 177Lu-PSMA-DKFZ-617 of castrate-resistant metastatic prostate cancer. Oncotarget. 2016, 7:12477-88. 10.18632/oncotarget.7245
  36. Baum RP, Kulkarni HR, Schuchardt C, et al.: 177Lu-labeled prostate-specific membrane antigen radioligand therapy of metastatic castration-resistant prostate cancer: safety and efficacy. J Nucl Med. 2016, 57:1006-13. 10.2967/jnumed.115.168443
  37. Heck MM, Retz M, D'Alessandria C, et al.: Systemic radioligand therapy with (177)Lu labeled prostate specific membrane antigen ligand for imaging and therapy in patients with metastatic castration resistant prostate cancer. J Urol. 2016, 196:382-91. 10.1016/j.juro.2016.02.2969
  38. Rahbar K, Schmidt M, Heinzel A, et al.: Response and tolerability of a single dose of 177Lu-PSMA-617 in patients with metastatic castration-resistant prostate cancer: a multicenter retrospective analysis. J Nucl Med. 2016, 57:1334-8. 10.2967/jnumed.116.173757
  39. Rahbar K, Bode A, Weckesser M, Avramovic N, Claesener M, Stegger L, Bögemann M: Radioligand therapy with 177Lu-PSMA-617 as a novel therapeutic option in patients with metastatic castration resistant prostate cancer. Clin Nucl Med. 2016, 41:522-8. 10.1097/RLU.0000000000001240
  40. Hofman MS, Violet J, Hicks RJ, et al.: [177Lu]-PSMA-617 radionuclide treatment in patients with metastatic castration-resistant prostate cancer (LuPSMA trial): a single-centre, single-arm, phase 2 study. Lancet Oncol. 2018, 19:825-33. 10.1016/S1470-2045(18)30198-0
  41. Yadav MP, Ballal S, Sahoo RK, Dwivedi SN, Bal C: Radioligand therapy with 177Lu-PSMA for metastatic castration-resistant prostate cancer: a systematic review and meta-analysis. AJR Am J Roentgenol. 2019, 213:275-85. 10.2214/AJR.18.20845
  42. Morgenstern A, Apostolidis C, Kratochwil C, Sathekge M, Krolicki L, Bruchertseifer F: An overview of targeted alpha therapy with 225Actinium and 213Bismuth. Curr Radiopharm. 2018, 11:200-8. 10.2174/1874471011666180502104524
  43. Reissig F, Bauer D, Zarschler K, et al.: Towards targeted alpha therapy with Actinium-225: chelators for mild condition radiolabeling and targeting PSMA-a proof of concept study. Cancers (Basel). 2021, 13:1974. 10.3390/cancers13081974
  44. Price EW, Orvig C: Matching chelators to radiometals for radiopharmaceuticals. Chem Soc Rev. 2014, 43:260-90. 10.1039/c3cs60304k
  45. Levy MY, Cicic D, Bergonio G, Berger M: Trial in progress: phase I study of Actinium-225 (225Ac)-Lintuzumab in patients with refractory multiple myeloma. Clin Lymphoma Myeloma Leuk. 2017, 17:329-30. 10.1016/j.clml.2017.07.141
  46. Thiele NA, Brown V, Kelly JM, et al.: An eighteen-membered macrocyclic ligand for Actinium-225 targeted alpha therapy. Angew Chem Int Ed Engl. 2017, 56:14712-7. 10.1002/anie.201709532
  47. McDevitt MR, Ma D, Simon J, Frank RK, Scheinberg DA: Design and synthesis of 225Ac radioimmunopharmaceuticals. Appl Radiat Isot. 2002, 57:841-7. 10.1016/s0969-8043(02)00167-7
  48. Maguire WF, McDevitt MR, Smith-Jones PM, Scheinberg DA: Efficient 1-step radiolabeling of monoclonal antibodies to high specific activity with 225Ac for α-particle radioimmunotherapy of cancer. J Nucl Med. 2014, 55:1492-8. 10.2967/jnumed.114.138347
  49. Kratochwil C, Haberkorn U, Giesel FL: 225Ac-PSMA-617 for therapy of prostate cancer. Semin Nucl Med. 2020, 50:133-40. 10.1053/j.semnuclmed.2020.02.004
  50. Pretze M, Kunkel F, Runge R, et al.: Ac-EAZY! towards GMP-compliant module syntheses of 225Ac-labeled peptides for clinical application. Pharmaceuticals (Basel). 2021, 14:652. 10.3390/ph14070652
  51. Kratochwil C, Bruchertseifer F, Giesel FL, et al.: 225Ac-PSMA-617 for PSMA-targeted α-radiation therapy of metastatic castration-resistant prostate cancer. J Nucl Med. 2016, 57:1941-4. 10.2967/jnumed.116.178673
  52. Scher HI, Morris MJ, Stadler WM, et al.: Trial design and objectives for castration-resistant prostate cancer: updated recommendations from the Prostate Cancer Clinical Trials Working Group 3. J Clin Oncol. 2016, 34:1402-18. 10.1200/JCO.2015.64.2702
  53. Lee DY, Kim YI: Effects of 225Ac-labeled prostate-specific membrane antigen radioligand therapy in metastatic castration-resistant prostate cancer: a meta-analysis. J Nucl Med. 2022, 63:840-6. 10.2967/jnumed.121.262017
  54. Hofman MS, Emmett L, Violet J, et al.: TheraP: a randomized phase 2 trial of 177 Lu-PSMA-617 theranostic treatment vs cabazitaxel in progressive metastatic castration-resistant prostate cancer (Clinical Trial Protocol ANZUP 1603). BJU Int. 2019, 124:5-13. 10.1111/bju.14876
  55. Kratochwil C, Bruchertseifer F, Rathke H, et al.: Targeted α-therapy of metastatic castration-resistant prostate cancer with 225Ac-PSMA-617: dosimetry estimate and empiric dose finding. J Nucl Med. 2017, 58:1624-31. 10.2967/jnumed.117.191395
  56. Kratochwil C, Bruchertseifer F, Rathke H, Hohenfellner M, Giesel FL, Haberkorn U, Morgenstern A: Targeted α-therapy of metastatic castration-resistant prostate cancer with 225Ac-PSMA-617: swimmer-plot analysis suggests efficacy regarding duration of tumor control. J Nucl Med. 2018, 59:795-802. 10.2967/jnumed.117.203539
  57. Sathekge M, Bruchertseifer F, Knoesen O, et al.: 225Ac-PSMA-617 in chemotherapy-naive patients with advanced prostate cancer: a pilot study. Eur J Nucl Med Mol Imaging. 2019, 46:129-38. 10.1007/s00259-018-4167-0
  58. Sathekge M, Bruchertseifer F, Vorster M, et al.: Predictors of overall and disease-free survival in metastatic castration-resistant prostate cancer patients receiving 225Ac-PSMA-617 radioligand therapy. J Nucl Med. 2020, 61:62-9. 10.2967/jnumed.119.229229
  59. Khreish F, Ebert N, Ries M, et al.: 225Ac-PSMA-617/177Lu-PSMA-617 tandem therapy of metastatic castration-resistant prostate cancer: pilot experience. Eur J Nucl Med Mol Imaging. 2020, 47:721-8. 10.1007/s00259-019-04612-0
  60. Yadav MP, Ballal S, Sahoo RK, Tripathi M, Seth A, Bal C: Efficacy and safety of 225Ac-PSMA-617 targeted alpha therapy in metastatic castration-resistant Prostate Cancer patients. Theranostics. 2020, 10:9364-77. 10.7150/thno.48107
  61. Sathekge MM, Bruchertseifer F, Lawal IO, et al.: Treatment of brain metastases of castration-resistant prostate cancer with 225Ac-PSMA-617. Eur J Nucl Med Mol Imaging. 2019, 46:1756-7. 10.1007/s00259-019-04354-z
  62. Rathke H, Kratochwil C, Hohenberger R, et al.: Initial clinical experience performing sialendoscopy for salivary gland protection in patients undergoing 225Ac-PSMA-617 RLT. Eur J Nucl Med Mol Imaging. 2019, 46:139-47. 10.1007/s00259-018-4135-8
  63. Feuerecker B, Tauber R, Knorr K, et al.: Activity and adverse events of Actinium-225-Psma-617 in advanced metastatic castration-resistant prostate cancer after failure of Lutetium-177-PSMA. Eur Urol. 2021, 79:343-50. 10.1016/j.eururo.2020.11.013
  64. de Kruijff RM, Wolterbeek HT, Denkova AG: A critical review of alpha radionuclide therapy-how to deal with recoiling daughters?. Pharmaceuticals (Basel). 2015, 8:321-36. 10.3390/ph8020321

Review article
peer-reviewed

A Review of 177Lutetium-PSMA and 225Actinium-PSMA as Emerging Theranostic Agents in Prostate Cancer


Author Information

Mohammad R. Alam

Department of Internal Medicine, Argakhachi Hospital Pvt. Ltd, Sandhikharka, NPL

Shashi B. Singh Corresponding Author

Department of Radiology, KIST Medical College and Teaching Hospital, Kathmandu, NPL

Shreeya Thapaliya

Department of Internal Medicine, Kathmandu Medical College Teaching Hospital, Kathmandu, NPL

Shreeya Shrestha

Department of Internal Medicine, Manipal College of Medical Sciences, Pokhara, NPL

Sulav Deo

Department of Internal Medicine, Suraksha Hospital, Biratnagar, NPL

Kishor Khanal

Department of Cardiology, Memorial Healthcare System, Pembroke Pines, USA


Ethics Statement and Conflict of Interest Disclosures

Conflicts of interest: In compliance with the ICMJE uniform disclosure form, all authors declare the following: Payment/services info: All authors have declared that no financial support was received from any organization for the submitted work. Financial relationships: All authors have declared that they have no financial relationships at present or within the previous three years with any organizations that might have an interest in the submitted work. Other relationships: All authors have declared that there are no other relationships or activities that could appear to have influenced the submitted work.

Acknowledgements

Shashi Bhushan Singh contributed equally to work and should be considered co-first author.



Review article
peer-reviewed

A Review of 177Lutetium-PSMA and 225Actinium-PSMA as Emerging Theranostic Agents in Prostate Cancer


Figures etc.

SIQ
8.0
RATED BY 4 READERS
CONTRIBUTE RATING

Scholarly Impact Quotient™ (SIQ™) is our unique post-publication peer review rating process. Learn more here.