Ablative Radioembolization of Renal Cell Carcinoma Trial
- Conditions
- Renal Cell Carcinoma (RCC)Radioembolization
- Registration Number
- NCT06642220
- Lead Sponsor
- Derek W. Cool
- Brief Summary
Renal cell carcinoma (RCC), the most common type of kidney cancer, is typically treated with surgery; however, there is no established therapy for patients who are not surgical candidates and who have tumours greater than 4.0 cm in size. Selective internal radiation therapy (SIRT) or radioembolization using radioactive spheres containing 90-Yttrium (Y-90) is successful at treating large tumours with high doses of radiation within the liver and might be similarly effective for treating larger RCC tumours in patients, particularly those who are not surgical candidates.
This prospective study will enroll 16 participants with RCC who are not candidates for surgery and treat them with Y-90 radioembolization using a high-dose therapy to see if it is an effective cancer therapy. Primary outcome will be RCC treatment response 1 year after the Y-90 radioembolization. Additionally, the safety, tolerability, and impact on kidney function of the therapy will be monitored for all participants. Patients will be followed for a total of 5 years to evaluate long-term outcome in cancer control and safety of the treatment.
- Detailed Description
Renal cell carcinoma (RCC) is the 8th most common cancer in the United States with 81,610 new cases diagnosed each year. 70% of new RCC cases are localized, non-metastatic at initial diagnosis; however, the risk of disease recurrence or progression to metastatic disease is higher for larger tumors and those with higher grade disease. The standard therapy for localized renal cell carcinoma (RCC) is surgery - either partial or radical nephrectomy. However, a substantial proportion of patients with RCC are not good surgical candidates, as the average age at diagnosis is 64-year-old, and obesity, smoking, hypertension and renal disease known risk factors. Currently there are no established standard-of-care therapies for patients who are not eligible for surgery.
Unmet Clinical Need:
There is a need to establish a definitive, minimally-invasive therapy patients for with large, non-metastatic RCC who are not surgical candidates. For non-surgical candidates with small RCC (\< 4 cm or T1a) percutaneous ablation has been established as an effective minimally-invasive curative therapy. However, there is currently no minimally-invasive standard of care therapy for patients with larger localized RCC (\> 4 cm) who are not surgical candidates, despite these patients being at higher risk for developing metastatic disease. Percutaneous ablation can be performed in patients with tumors \> 4 cm; however, long term outcomes have not been established and those ablations carry higher risks of major bleeding complications than ablation of tumours \< 4 cm. SBRT has shown some promising progression-free survival data for localized RCC; however, the radiation resistance of RCC cells require higher treatment doses to achieve cytotoxic effect. The achievable therapeutic dose of SBRT is currently limited to 30-60 Gy, often due to required reductions in the externally delivered dose to protect the commonly adjacent radiosensitive colon and/or small bowel that routinely abut the kidney.
Selective internal radiation therapy (SIRT) or Yittrium-90 (Y-90) radioembolization is an endovascular therapy whereby beads loaded with the radioactive Yittrium-90 atom are injected through a catheter into the artery or arteries supplying the tumor to deliver the radiation dose internally. Radioactive decay of the Y-90 atom within the tumor's arterial bed, deposits radiation dose within 2.5 mm (maximum 11 mm) of the bead location. As such, the internal delivery of radiation, rather than external delivery of SBRT, allows for higher doses to be delivered to the tumour without exposing adjacent vulnerable organs to significant dose. Y-90 radioembolization has great success treating hepatocellular carcinoma (HCC) in the liver, commonly achieving tumor dose levels that are nearly ten times higher than SBRT (e.g. 300-500 Gy vs. 40-50 Gy). Furthermore, it has become a standard of care therapy for HCC with recent inclusion in the major international treatment guidelines. Y-90 tumor dosage of \>400 Gy is the typical target with one major explant study showing complete pathological necrosis of HCC tumors when this dose was achieved8.
RCC is a good potential disease target for Y-90 radioembolization as RCC is commonly hypervascular (similar to HCC) and the kidney is an end organ typically supplied by a single renal artery. Furthermore, the radioresistant tumour biology requires high radiation doses to achieve oncologic effect, which may be best achieved with the internal radiation delivery approach.
Existing Safety Data of Y-90 in the kidney:
Health Canada approval of Y-90 radioembolization is currently only for treatment of malignancies in the liver, where it is currently a standard of care therapy for treatment of HCC. The safety of Y-90 radioembolization in the kidney has been shown in preclinical studies as well as the RESIRT Phase I trial, which is the first and only human clinical trial of Y-90 radioembolization for RCC. The 21-patient RESIRT dose-escalation study had a heterogeneous patient population with both metastatic and non-metastatic RCC. The safety study showed no dose-limiting toxicity or reduction in renal function for treatment between 75-300 Gy; however, the secondary outcome of treatment response showed partial response in only 10% of patients without any complete response. The limited treatment response is potentially related to the administered dose being lower than the 400 Gy target used in the liver for complete pathologic necrosis. For HCC, complete pathologic necrosis from Y-90 SIRT requires an achieved tumour dose of ≥400 Gy. Within the liver, Y-90 administration of tumour doses ranging between 500-1000 Gy have been tolerated without serious adverse events.
Given the known radioresistance of RCC, it is reasonable to expect that a similar or higher dose than HCC would be required to achieve an ablative therapy (i.e. ≥ 400 Gy). The RESIRT trial used resin beads for Y-90 delivery (SIRspheres, Australia) and arterial bed stasis (not permitting additional bead administration) occurred in 52% of the treated patients, which might have limited higher achievable RCC doses. Glass-sphere beads loaded with Y-90 (Therasphere, Boston Scientific) will be used instead of resin, which have higher Y-90 radiation activity per bead than the resin counterparts (2,500 Bq/bead vs. 50 Bq/bead). The higher activity per bead should overcome the maximum dose limitation in the RESIRT trial to achieve the 400+ Gy dose likely required to for complete pathologic necrosis. This is supported by a recent case report where radioembolization with Y-90 loaded on glass spheres achieved complete tumor response after delivering 1,050 Gy into a 1.5 cm RCC without any reported adverse events.
Planned Study:
A single-centre, phase II clinical trial is proposed to evaluate the oncologic efficacy of Y-90 radioembolization treatment within the kidney for patients with large (\>4.0 cm), non-metastatic (localized) RCC who are not candidates or refuse the standard of care surgery. It is proposed that Y-90 radioembolization therapy with an ablative dose (400-600 Gy) into RCC within the kidney will achieve positive oncologic response and be tolerated clinically.
Recruitment & Eligibility
- Status
- NOT_YET_RECRUITING
- Sex
- All
- Target Recruitment
- 16
- Patients willing to participate and provide written consent
- Patients 18 years of age and older
- Eastern Cooperative Oncology Group (ECOG) performance status (PS) ≤2
- Biopsy confirmed RCC > 4.0 cm and no renal vein or IVC involvement (T1b or T2 disease)
- Not suitable for or declining standard of care nephrectomy or partial nephrectomy
- Adequate hepatic function, defined by the following laboratory results:
- Aspartate aminotransferase (AST) and alanine aminotransferase (ALT) ≤2.5 × upper limit of normal (ULN) (or ≤5 × ULN if presence of liver metastases)
- Total bilirubin ≤3 × ULN
- Serum albumin ≥3.0 g/dL unless prothrombin time (PT) is within the normal range
- Adequate hematologic function, defined by the following laboratory results:
- Hemoglobin concentration ≥8.0 g/dL
- Absolute neutrophil count (ANC) ≥1000 cells/µL (≥1000 cells/mm3 )
- Platelets >50 × 109 /L (100 × 103 /mm3 )
- For women of childbearing potential (WOCBP):
- Negative serum pregnancy test within 48 hours prior to the first dose of study treatment
- Agreement to use barrier contraception and a second form of highly effective contraception (Clinical Trials Facilitation Group [CTFG] 2020) while receiving study treatment and for 7 months following their last dose of study treatment. Alternatively, total abstinence is also considered a highly effective contraception method when this is in line with the preferred and usual lifestyle of the subject. Periodic abstinence (e.g., calendar, ovulation, symptothermal, post-ovulation methods) and withdrawal are not acceptable methods of contraception.
- Sexually active male subjects must use a condom during intercourse while receiving treatment and for at least 120 days after the last dose of the study treatment and should not father a child during this period.
- Male study subjects whose sexual partners are WOCBP must also agree to use a second form of highly effective contraception (CTFG 2020) while receiving 90Y and for at least 4 months following their last dose. Alternatively, total abstinence is also considered a highly effective contraception method when this is in line with the preferred and usual lifestyle of the subject.
- Vasectomized men are also required to use a condom during intercourse, including with a male partner, to prevent delivery of the drug via seminal fluid.
- Evidence of metastatic disease on CT or MRI
- Severely impaired renal function (GFR ≤ 30) and not on dialysis
- Bilateral RCC without plan for definitive therapy of the contralateral lesion
- RCC that is locally recurrent at prior surgery or ablation site (new location in same or contralateral kidney is permitted)
- Prior or concurrent kidney radiation therapy or systemic immunotherapy/TKI
- Lung shunt with estimated lung radiation dose > 30 Gy for single dose or > 50 Gy total.
- Planning angiogram cone beam CT from all accessible feeding arteries shows lack of perfusion to all or portions of the RCC tumour such that, in the investigator's opinion, Y-90 radioembolization would result in substantial RCC tumour being untreated or receive an inadequate dose.
- Contraindication to arterial renal angiogram, or both CT and MRI contrast medium
- History of severe allergy to CT contrast medium or any study product ingredients that cannot be managed medically
- History of chronic lung disease with baseline oxygen saturation < 90% or requiring home oxygen therapy.
- Congestive heart failure with ejection fraction < 40%
- Presence of active infection, defined by the investigator as clinically significant.
- Any chronic condition that is severe or unstable and, in the opinion of the investigator, would put the patient at unacceptable risk of adverse event related to the Y-90 radioembolization procedure. Such conditions include but are not limited to: unstable angina, congestive heart failure, interstitial lung disease, severe gastrointestinal disease with diarrhea.
- Life expectancy > 1 year
- Pregnant or breast-feeding patient
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- SINGLE_GROUP
- Primary Outcome Measures
Name Time Method Oncologic tumor response at 12 months From treatment until 12 months follow-up imaging Assessment the cancer treatment response within the 12 months after treatment. Oncologic response will be based on the modified RECIST (mRECIST) criteria.
- Secondary Outcome Measures
Name Time Method Treatment-related Adverse Events Evaluated from Y-90 therapy until 30 days, 1 year & 5 year follow-up Clinician assessment will occur at 4-weeks, 3-months, 6-months \& 12-months post-treatment and annually to 5 years. All adverse events will be categorized and graded based on Common Terminology Criteria for Adverse Events (CTCAE) grading system. All adverse events will be further classified based on relatedness to either a) the Therapeutic Intervention and b) Y-90 Radiation Dose by the following: a) unrelated, b) unlikely to be related, c) possibly related, d) probably related, e) definitely related.
Therapeutic Intervention: Includes all procedure-related adverse events during the planning angiogram or Y-90 therapy procedures (all Y-90 Radiation Dose adverse events included as well).
Y-90 Radiation Dose: Subset of Therapeutic Intervention that includes only those adverse events related to the Y-90 radiation therapy. Examples of dose-related events might include post-procedure fatigue/malaise, radiation colitis, acute kidney injury not related to a catheter arterial injury.Safety and tolerability of ablative doses (400-600 Gy) of Y-90 spheres administered in the kidney Evaluated from Y-90 therapy until 30 days, 1 year & 5 year follow-up Tolerability of the radiation will be characterized by dose-limiting toxicity (DLT) events. The DLT review period will be 30 days after Y-90 procedure. Any serious adverse event that is possibly, probably or definitely related to Y-90 Radiation Dose will be classified as a dose-limiting toxicity (DLT) event. Complications related only to catheter arterial embolization procedure (example puncture site bleeding, artery dissection, etc) or the planning angiogram will not be considered a DLT. Greater \> 1 in 6 patients experiencing DLT events will declare the maximally administered dose and require a reduction in the target dose to 300 Gy.
If no DLT events occur during the DLT review period for the first three patients or 1 in the first 6 patients, then the tumour target dose for future participants can be increased up to a maximum of 600 Gy (range 400-600 Gy) at the treating physician's discretion.Impact on global renal function Will be evaluated at the time of Y-90 therapy as well as after Y-90 therapy at 3 months (10-16 weeks), 6 months (24-30 weeks), 12 months (50-56 weeks), & 2-, 3-, 4-, 5-years time points Assessment of global renal function will be based on the glomerular filtration rate (GFR), calculated using the CKD-EPI Creatinine Equation (2021). GFR will be collected at baseline and at each clinical follow-up post-therapy to assess for change.
Local Progression free survival out to 5 years Greater than 1 year after Y-90 therapy, up to 5 years post therapy. Local progression-free survival will be evaluated looking only at the response of the treated RCC tumor based on the modified RECIST (mRECIST) criteria. This will be evaluated out to 5 years.
Patient-reported outcomes Collected at enrollment and then at 7-days, 14-days, 30-days & 3 months after Y-90 therapy. Patient-defined symptomatic adverse events: Self-reported by participants using the National Cancer Institute's Patient-Reported Outcomes Common Terminology Criteria for Adverse Events (PRO-CTCAE) form.
Overall Side Effect Impact: Measured by the Functional Assessment of Cancer Therapy-GP5 (FACT-GP5) question from the FACT-G questionnaire - "I am bothered by side effects of treatment". Pain intensity measured by 11-point Numerical Pain Rating Score.
Health-related quality of life measures: Quality of life and health utility will be self-reported using the NIH-developed PRO Measurement Information System® (PROMIS®) PROMIS-16 Profile v2.1. This profile evaluates eight health domains (physical function, fatigue, pain interference, depression, anxiety, ability to participate in social roles and activities, sleep disturbance, and cognitive function) and can generate a global preference-based score that can be used to estimate quality-adjusted life years (QALY) in cost-utility analysis.Change in Split Renal Function Will be calculated at the time of Y-90 therapy (baseline) as well as after Y-90 therapy at 3 months (10-16 weeks), 6 months (24-30 weeks), 12 months (50-56 weeks), & 2-, 3-, 4-, 5-years Estimation of the split renal function in all participants with two kidneys will be calculated based on established renal parenchymal volume equation calculated from the CT or MR scans. Changes in the split renal function following therapy will be collected at each imaging follow up
Progression free survival out to 5 years Greater than 1 year after Y-90 therapy, up to 5 years post therapy. Progression-free survival will be evaluated based on the modified RECIST (mRECIST) criteria.
Overall survival out to 5 years Greater than 1 year after Y-90 therapy, up to 5 years post therapy Overall survival will be calculated.
Metastasis-free survival out to 5 years Greater than 1 year after Y-90 therapy, up to 5 years post therapy Metastasis-free survival oncologic response will be calculated.
Oncologic Response based on PSMA PET scans at enrollment, and 3 months and 12 months after Y-90 therapy Optional Exploratory outcome - Gallium Prostate specific membrane antigen (PSMA) PET-CT be performed at baseline, 3 months and 12 months to assess the impact of Y-90 therapy on the PSMA avidity of RCC tumor. Functional imaging of PSMA PET might provide an earlier assessment of RCC tumour response as compared to the conventional contrast-enhanced CT or MRI assessment.
Change in renal volume and morphology post-therapy From enrollment until 5-years post-therapy Shape-based 3D volumetric assessment of the treated kidney will be evaluated at different time points to identify long-term changes to the kidney volume and contour shape that are potentially treatment related.
Procedure Costs Will be recorded immediately after the planning angiogram procedure and again after the Y-90 therapy procedure. All procedure-related costs for the interventional radiology angiogram procedure (in CAD) will be recorded (e.g. Y-90 particles, disposable catheters, wires, total time in interventional radiology suite) for both the planning angiogram and the Y-90 therapy procedures.
Procedure Time Will be recorded immediately after the planning angiogram procedure and again after the Y-90 therapy procedure. The time of the interventional radiology procedure will be recorded. Including a) total room time (time between patient entering and leaving room) and b) total angiogram procedure time (from arterial puncture until final catheter removal) for both the planning angiogram and Y-90 therapy procedures will be recorded.
Trial Locations
- Locations (1)
London Health Sciences Centre - Victoria Hospital
🇨🇦London, Ontario, Canada