177Lu-PSMA-617 for the Treatment of Advanced Clear Cell Renal Cell Carcinoma, LASER Trial

Inclusion Criteria

• Histologically or cytologically confirmed advanced or metastatic renal cell carcinoma with a clear cell component. Patients with sarcomatoid histology are eligible
• Participants must have measurable disease, defined as at least one lesion that can be accurately measured in at least one dimension (longest diameter to be recorded for non-nodal lesions and short axis for nodal lesions) as ≥ 20 mm (≥ 2 cm) by chest x-ray or as ≥ 10 mm (≥ 1 cm) with CT scan, MRI, or calipers by clinical exam
• Age ≥ 18 years
• Prior receipt of at least one immune checkpoint inhibitor and at least one tyrosine kinase inhibitor in the neoadjuvant, adjuvant or metastatic settings. Prior treatment with radium Ra 223 (Ra-223) is permitted providing that the last dose was ≥ 90 days prior to study entry
• Presence of ≥ 1 PSMA-positive metastatic lesion (with PSMA uptake > liver) on baseline/screening gallium Ga 68 gozetotide (68Ga-PSMA-11) PSMA-PET/CT (within 28 days of planned cycle 1 day 1 [C1D1]), and the absence of any PSMA-negative lesions (defined as those with PSMA uptake ≤ liver in any lymph node with short axis ≥ 2.5 cm, any metastatic solid organ lesion with short axis ≥ 1 cm and any metastatic bone lesion with a soft tissue component of ≥ 1 cm in short axis). All patients considered for the study should have their PSMA-PET imaging reviewed in a multidisciplinary meeting with Medical Oncology and Nuclear Medicine to confirm eligibility
• Eastern Cooperative Oncology Group (ECOG) performance status ≤ 2
• Absolute neutrophil count (ANC) >= 1.5×10^9/L
• Platelets >= 100×10^9/L
• Hemoglobin >= 9g/dL (>= 90g/L), independent of transfusions
• Total bilirubin =< 1.5 × upper limit of normal (ULN) OR < 2 × ULN if known or suspected Gilbert’s syndrome
• Alanine aminotransferase (ALT) and aspartate aminotransferase (AST) =< 3 × ULN OR =< 5 × ULN if liver metastases present
• Estimated glomerular filtration rate (eGFR) >= 50 mL/min/1.73 m^2 (based on Cockcroft-Gault formula OR 24 hour urine collection
• The effects of 177Lu-PSMA-617 on the developing human fetus are unknown. For this reason and because radiopharmaceutical therapies are known to be teratogenic, women of child-bearing potential and men must agree to use adequate contraception (hormonal or barrier method of birth control; abstinence) prior to study entry and for the duration of study participation. Should a woman become pregnant or suspect she is pregnant while she or her partner is participating in this study, she should inform her treating physician immediately. Female partners of child-bearing potential should also use highly effective birth control methods throughout the male participant’s study treatment and for at least 14 weeks following the last dose of 177Lu-PSMA-617. Men treated or enrolled on this protocol must also agree to use adequate contraception prior to the study, for the duration of study participation, and at least 14 weeks following the last dose of 177Lu-PSMA-617
• Ability to understand and the willingness to sign a written informed consent document. (Providing consents in as many languages as possible is encouraged)

Exclusion Criteria

• Prior PSMA-targeted therapy (eg. 177Lu-PSMA-617)
• Participants who have had radiotherapy within 4 weeks prior to planned cycle 1 day 1 of study treatment
• Participants who have received anti-neoplastic intervention or experimental antineoplastic therapy within 14 days of planned cycle 1 day 1 of study therapy
• Participants who are receiving any other investigational agents
• Participants with untreated brain metastases. Participants with treated brain metastases are eligible if follow-up brain imaging at least 4 weeks after central nervous system (CNS)-directed therapy shows no evidence of progression and ongoing corticosteroids are not required. Participants with new or progressive brain metastases (active brain metastases) or leptomeningeal disease are eligible if the treating physician determines that immediate CNS specific treatment is not required and is unlikely to be required during the first cycle of therapy
• Participants who have not recovered from adverse events due to prior anti-cancer therapy (i.e., have residual toxicities > grade 1) with the exception of alopecia. Sensory neuropathy grade ≤ 2 is acceptable
• History of allergic reactions attributed to compounds of similar chemical or biologic composition to 177Lu-PSMA-617
• Symptomatic cord compression, or clinical or radiologic findings indicative of impending cord compression
• Concurrent active malignancy whose natural history or treatment has the potential to interfere with safety or efficacy assessment of the investigational regimen. Patients with non-melanomatous skin cancer, superficial bladder cancer, cancer not needing active therapy for at least 2 years, cancer for which the treating investigator deems the subject to be in remission, or any prior malignancy that was treated with curative intent (no evidence of disease for at least 3 years) are permitted to enroll Nota bene (NB) – participants who are found to have suspected prostate cancer on the basis of PSMA-PET/CT performed for screening (eg. PSMA avid disease in the prostate) are eligible to proceed on study on the basis of clinical judgement by the treating physician. Prostate (or other) biopsy is not required to confirm evidence of prostate cancer, if suspected, prior to proceeding with study therapy as long as the treating physician deems renal cell carcinoma (RCC) to be a more pressing treatment priority
• The participant has serious and/or uncontrolled preexisting medical condition(s) that, in the judgment of the investigator, would preclude participation in this study (for example, interstitial lung disease, severe dyspnea at rest or requiring oxygen therapy, severe renal impairment [e.g. estimated creatinine clearance < 30ml/min], history of major surgical resection involving the stomach or small bowel, or preexisting Crohn’s disease or ulcerative colitis or a preexisting chronic condition resulting in baseline grade 2 or higher diarrhea)
• Females that are pregnant and/or lactating