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Indication: For the treatment of adult patients with von Hippel-Lindau disease who require therapy for associated nonmetastatic renal cell carcinoma, central nervous system hemangioblastomas, or nonmetastatic pancreatic neuroendocrine tumours, not requiring immediate surgery
CADTH recommends that Welireg should be reimbursed by public drug plans for the treatment of adult patients with von Hippel-Lindau (VHL) disease who require therapy for associated nonmetastatic renal cell carcinoma (RCC), central nervous system (CNS) hemangioblastomas, or nonmetastatic pancreatic neuroendocrine tumours (pNET), not requiring immediate surgery if certain conditions are met.
Welireg should only be covered to treat adult patients with VHL disease who require therapy for associated nonmetastatic RCC, CNS hemangioblastomas, or nonmetastatic pNET, not requiring immediate surgery. Patients receiving Welireg should be in relatively good health.
Welireg should only be reimbursed if it is prescribed by specialists with expertise in VHL disease-associated tumours and if the cost of Welireg is reduced. Welireg should not be used in combination with other anti-tumour drugs.
VHL disease is an inherited genetic condition associated with tumours developing in multiple organs. VHL disease affects 1 in 36,000 live births and the prevalence is estimated to be 1 in 53,000 individuals.
Patients with VHL disease are closely monitored to check if tumours have developed, grown, and/or spread. Patients usually need multiple surgeries and radiation over the course of their lives to treat their tumours, and these treatments are invasive and associated with complications. There is a need for treatments that can prolong patients’ lives while avoiding the need for surgery and radiation.
Treatment with Welireg is expected to cost $17,920 per 28 days.
The CADTH pCODR Expert Review Committee (pERC) recommends that belzutifan be reimbursed for the treatment of adult patients with VHL disease who require therapy for associated nonmetastatic RCC, CNS hemangioblastomas, or nonmetastatic pancreatic neuroendocrine tumours (pNET), not requiring immediate surgery only if the conditions listed in Table 1 are met.
pERC recognized the unmet need of patients with VHL disease-associated tumours, for which no other systemic therapies are currently available. One phase II, single-arm, open-label trial (LITESPARK-004) demonstrated that treatment with belzutifan may result in a clinical benefit in objective response rate (ORR) for adult patients with VHL-associated nonmetastatic RCC (N = 61), with or without CNS hemangioblastomas (N = 50) and/or nonmetastatic pNET (N = 22), not requiring immediate surgery. At a median follow-up of 37.7 months, the ORR assessed by the independent review committee (IRC) was 63.9% (39/61) among patients with RCC, 44.0% (22/50) among those with CNS hemangioblastomas, and 90.9% (20/22) among those with pNET; the ORR was greater than the prespecified alternative hypothesis of 30% and considered clinically meaningful.
Patients indicated there is a need for treatments that can improve their physical condition (e.g., decrease or stabilize the size of tumours, reduce pain, improve breathing), offer long-term stability or reduction of disease, avoid surgery, and improve health-related quality of life (HRQoL). pERC concluded that belzutifan meets some of the needs identified by patients, such as a meaningful ORR and durable tumour response as measured by duration of response (DOR). pERC considered that belzutifan could potentially meet additional needs, such as an opportunity to avoid surgery, although this is uncertain due to the single-arm design of the LITESPARK-004 trial and limitations of the indirect treatment comparison (ITC).
Using the sponsor submitted price for belzutifan and publicly listed prices for all other drug costs, the incremental cost-effectiveness ratio (ICER) for belzutifan was $360,193 per quality-adjusted life-year (QALY) gained compared with active surveillance for the VHL-RCC cohort. The ICERs were similar in the VHL-CNS hemangioblastoma and VHL-pNET subgroup cohorts. At this ICER, belzutifan is not cost-effective at a $50,000 per QALY willingness to pay (WTP) threshold for the indicated population. A price reduction is required for belzutifan to be considered cost-effective at a WTP threshold of $50,000 per QALY gained.
Reimbursement Conditions and Reasons.
VHL disease, which is an inherited, autosomal dominant neoplasia syndrome caused by a germline mutation and/or deletion of the VHL gene, is associated with a variety of neoplasms such as hemangioblastomas of the CNS and retina, renal cysts and clear cell RCC, pheochromocytomas, pNET, epididymal and broad ligament cystadenomas, and endolymphatic sac tumours. VHL disease affects 1 in 36,000 live births. Approximately 20% of the cases are caused by de novo mutations and hence do not have a family history of VHL. The prevalence is estimated to be 1 in 53,000 individuals. In Canada, the estimated number of cases is 727.
The diagnosis of VHL disease is typically established through genetic testing to identify a germline pathogenic variant in the VHL gene. People with VHL disease can have tumours involving multiple organs many times in their life; their symptoms will depend on the location and size of the tumours. Tumours associated with VHL disease have the potential to metastasize. Active surveillance until treatment is indicated is currently the standard approach for VHL disease-associated tumours. Active surveillance aims to find and remove tumours as early as possible before they affect the patient’s health. Surgical resection is indicated for tumours with high symptom burden or those carrying a high risk of organ dysfunction or metastasis. Certain tumours can be treated with radiation. However, treatments such as surgery and irradiation can be morbid. There is a need among patients and clinicians for a systemic treatment which could be effective in treating VHL disease while causing less harm.
Health Canada has approved belzutifan for the treatment of adult patients with VHL disease who require therapy for associated nonmetastatic RCC, CNS hemangioblastomas, or nonmetastatic pNET, not requiring immediate surgery. Belzutifan is an antineoplastic drug. It is available as 40 mg tablets, and the dosage recommended in the product monograph is 120 mg (three 40 mg tablets) administered orally once daily, with or without food.
To make its recommendation, the committee considered the following information:
The Canadian VHL Alliance (CVHLA), The Canadian Organization for Rare Disorders (CORD), Kidney Cancer Canada, Pancreatic Cancer Canada, and the Canadian Neuroendocrine Tumour Society provided 1 joint input for the treatment of adult patients with VHL disease who require therapy for associated nonmetastatic RCC, CNS hemangioblastomas, and nonmetastatic pNET, not requiring immediate surgery. Patient input was gathered from online surveys and semistructured telephone interviews among patients living with VHL and their caregivers in December 2022. In total, 123 responses were gathered (72 from patients and 51 from caregivers), and 19 patients had experience with belzutifan.
Patients and caregivers described their ongoing physical and psychological struggles due to VHL, such as dismissal or misdiagnosis for initial symptoms; not getting a diagnosis until they had an advanced stage resulting in a tumour affecting vision, hearing, and walking; discomfort, pain, interference with daily activities; difficulties in adhering to tumour screening guidelines, scheduling tests, travelling for tumour screenings; and out of pocket payment due to noncoverage by public health care or private insurance. Surgical resection was reported as the primary treatment for symptomatic lesions. The majority of 92 respondents described their experiences with surgeries as undergoing multiple surgeries on multiple sites, some with life-threatening risks and side effects. Out of 98 respondents, 18 (18.4%) reported having 10 or more surgeries, and the average number of surgeries reported was 5.3.
While evaluating the importance of outcomes of new treatments, patients from the survey placed importance on the need for a treatment that can improve their physical condition by decreasing or stabilizing the size of tumours (weighted average rating: 4.8 on a scale from 1 not important to 5 extremely important), improving quality of life (weighted average rating: 4.63 on a scale from 0 not important to 5 extremely important), offering long-term stability or reduction of disease (weighted average rating: 4.86 on a scale from 0 not important to 5 extremely important), and offering the opportunity to avoid surgery (weighted average rating: 4.9 on a scale from 0 not important to 5 extremely important).
The patient groups suggested to provide all VHL patients with access to belzutifan based on an individual informed decision between the treating physician and the patient and their family.
The clinician input was provided by a panel of 3 clinical experts with expertise in treating VHL-associated RCC, CNS hemangioblastoma, and pNET from across Canada.
The clinical experts noted that prolonging survival and improving quality of life are critical goals for patients with VHL-associated nonmetastatic RCC, CNS hemangioblastoma, and/or nonmetastatic pNET. The current treatment paradigm for VHL disease involves genetic testing for VHL at diagnosis and active surveillance until treatment is indicated for associated tumours. Reactive treatments, such as surgery and radiation, can be morbid and are usually selected to respond to the conditions or symptoms developed. The clinical experts agreed that an effective systemic treatment would minimize the morbidity associated with surgical procedures in patients with VHL-associated nonmetastatic pNET and RCC, many of whom are younger. The clinical experts noted that belzutifan if reimbursed, would be the first systemic treatment for VHL-associated tumours, which would change the current treatment paradigm by helping patients delay or avoid the need for local therapies (e.g., surgery and radiation).
The clinical experts indicated that VHL is a rare disease, and all patients with VHL might benefit from belzutifan. The clinical experts did not specify any subset of the patient population for whom it is in the most need or identify any prognostic factors that might cause differential treatment effects. The clinical experts noted that before initiating treatment with belzutifan, genetic testing for diagnosing VHL should be required. The clinicians also noted that a genetic counsellor should be involved in the diagnosis of VHL disease.
The clinical experts noted several situations in which belzutifan may be discontinued, including intolerable adverse events (e.g., becoming transfusion dependent due to anemia), clinical disease progression (e.g., worsening of symptoms). The clinical experts indicated that strict stopping criteria based on radiographic disease progression alone would not be reasonable if patients were still experiencing clinical benefit. The clinical experts noted that due to the rarity of the VHL disease, it is highly likely that only specialists working in large medical centres (e.g., tertiary referral centres, specialized referral centre) in Canada may encounter patients with VHL. Thus, prescription may be limited to specialists (e.g., medical oncologist, neuro oncologists) working in these large centres.
Clinician group input was received from Ontario Health Cancer Care Ontario (OH-CCO) Genitourinary Cancer Drug Advisory Committee (GU DAC) (7 clinicians), and a group of subspecialists from Canada involved in VHL care (25 clinicians).
The clinician groups agreed with the clinical experts consulted by CADTH that belzutifan, the first systemic therapy option for VHL disease approved in Canada, fulfills an important unmet need for the treatment of patients with VHL and represents a shift in the current treatment paradigm. They also generally agreed upon treatment goals, patient population, assessing response, treatment discontinuation criteria, and prescribing conditions.
While the clinical experts considered genetic testing to be a prerequisite for initiating treatment with belzutifan, neither clinician group indicated whether genetic testing for VHL mutation or deletion was required. The clinician group indicated that belzutifan should be discontinued if the patient is pregnant.
Input was obtained from the drug programs that participate in the CADTH reimbursement review process. The clinical experts consulted by CADTH provided advice on the potential implementation issues raised by the drug programs.
Responses to Questions From the Drug Programs.
One sponsor conducted phase II, single-arm, open-label trial (LITESPARK-004, N = 61) was identified from the sponsor's systematic literature review. The primary objective of the LITESPARK-004 trial was to evaluate the efficacy of belzutifan (oral administration at the dose of 120 mg once daily in 3 40-mg tablets until disease progression or unacceptable toxicity) for the treatment of VHL disease-associated nonmetastatic RCC as measured by ORR assessed by an IRC as per Response Evaluation Criteria in Solid Tumours version 1.1 (RECIST v1.1). Secondary objectives included the evaluation of the efficacy of belzutifan for the treatment of VHL disease-associated non-RCC tumours (CNS hemangioblastoma and nonmetastatic pNET), as well as the assessment of the safety and tolerability (including AEs of special interest; anemia, hypoxia, secondary primary malignancies, hepatic safety). In terms of efficacy end points, tumour response and durability of response were assessed by ORR and DOR, respectively. Time-to-event outcomes, such as TTS, progression-free survival (PFS), time to response were also reported. Additionally, the LITESPARK-004 trial also measured end points such as disease control rate (DCR), best overall response, linear growth rate (LGR), and number of patients who developed metastases. No inferential statistical analyses were carried out in the LITESPARK-004 trial due to the single-arm study design, and data were summarized using descriptive statistics. The LITESPARK-004 trial is ongoing, and the data submitted by the sponsor to support this reimbursement request is based on the data cut-off date of April 1, 2022, as of which, the median follow-up duration was 37.7 months (range: 4.2 to 46.1).
Patients eligible to be included in the LITESPARK-004 trial were required to be at least 18 years of age, diagnosed with VHL disease based on a germline VHL alteration, and had at least 1 measurable RCC. Eligible patients could have other VHL disease-associated non-RCC tumours such as CNS hemangioblastoma and pNET. Patients who had an immediate need for surgical intervention for tumour treatment or evidence of metastatic disease were excluded. Efficacy results for RCC came from the total study population (n = 61), while efficacy results for CNS hemangioblastoma (n = 50) and pNET (n = 22) were from subsets of the total study population. At baseline, for the total study population (i.e., patients with RCC), the median age was 41.0 years (range: 19.0 to 66.0) with the majority being white (90.2%, 55/61), and the median age at time of VHL disease diagnosis was 32.0 years (range: 4.0 to 66.0). Characteristics were similar for the subpopulations of patients with CNS hemangioblastoma and pNET.
The efficacy results are from the April 1, 2022 data cut-off date.
Median TTS was not reached for patients with VHL disease associated nonmetastatic RCC, CNS hemangioblastoma, or nonmetastatic pNET at the data cut-off date. Seven (11.5%, 7/61) patients with RCC, 1 patient (2.0%, 1/51) with CNS hemangioblastoma, and none of the patients with pNET had surgery during the follow-up period.
The IRC-assessed median PFS (95% confidence interval [CI]) was 39.2 months (38.5 to not evaluable) for patients with VHL disease-associated nonmetastatic RCC. Median PFS was not reached for patients with VHL disease-associated CNS hemangioblastoma and those with nonmetastatic pNET at the data cut-off date.
IRC-assessed results showed that among 61 patients with RCC at baseline, 11 (18.0%) had events (i.e., progressive disease, death), and 50 (82%) patients were censored mostly due to no progression at the time of data cut-off or before end of treatment (43, 70.5%).
IRC-assessed results showed that among 50 patients with CNS hemangioblastoma at baseline, 11 (22.0%) had events (i.e., progressive disease, death), and 39 (78%) patients were censored (in which 34 [68%] were due to no progression at the time of data cut-off).
All of the 22 patients with pNET were censored due to no progression at the time of data cut-off.
At a median follow-up of 37.7 months, the IRC-assessed percentage of patients who had a complete response (CR) or partial response (PR) to belzutifan was 63.9% (39/61) among those with VHL-associated nonmetastatic RCC, 44% (22/50) among those with VHL-associated CNS hemangioblastomas, and 90.9% (20/22) among those with VHL-associated nonmetastatic pNET.
IRC-assessed median DOR (95% CI) was not reached for responders with VHL disease associated nonmetastatic RCC, CNS hemangioblastoma, or nonmetastatic pNET at the data cut-off date. For patients with RCC, 74.4% (29/39) of responders had a DOR of at least 18 months, 56.4% (22/39) had a DOR of at least 24 months, and 25.6% (10/39) had a DOR of at least 30 months. For patients with CNS hemangioblastoma, 63.6% (14/22) of responders had a DOR of at least 18 months, 59.1% (13/22) had a DOR of at least 24 months, and 54.5% (12/22) had a DOR of at least 30 months. For patients with pNET, 95.0% (19/20) of responders had a DOR of at least 18 months, 75.0% (15/20) had a DOR of at least 24 months, and 40.0% (8/20) had a DOR of at least 30 months.
Among 39 RCC patients with confirmed response, 32 (82.1%) were censored due to no progression at the time of data cut-off or before end of treatment. Out of 22 patients with CNS hemangioblastoma who showed confirmed response, 17 were censored due to no progression at the time of data cut-off or before end of treatment. All 20 patients with pNET who showed confirmed response had no progression at the time of data cut-off.
Treatment-emergent adverse events (TEAEs) were reported in all 61 (100%) patients in the LITESPARK-004 trial. The most commonly reported TEAE was anemia (90.2%), followed by fatigue (73.8%), headache (47.5%), dizziness (45.9%), and nausea (39.3%).
SAEs were reported in 18 (29.3%) patients.
Treatment discontinuation due to TEAEs was reported in 4 patients, 2 (i.e., dizziness, intracranial hemorrhage) of which were drug related.
Two patients died during the study due to acute toxic effects of fentanyl and suicide, respectively.
As of the data cut-off, 90.2% (55/61) patients had 229 episodes of anemia. The average number of episodes of anemia for each patient was 4.2. One (1.6%) and 2 (3.3%) patients developed hypoxia and secondary primary malignancies, respectively. None of the participants had drug-induced liver injury.
The LITESPARK-004 trial was a phase II, single-arm, open-label clinical trial. Given the rarity of the VHL disease and that active surveillance is the current standard of care for patients with VHL-associated nonmetastatic tumours, the single-arm design and small sample size was considered appropriate from the regulatory perspective to assess the efficacy and safety of belzutifan. However, the absence of an internal comparison group in the single-arm LITESPARK-004 trial hampered the causality establishment of the efficacy or safety outcomes observed in patients.
The LITESPARK-004 trial explicitly defined the hypothesis (i.e., a null hypothesis of an ORR of 15% or lower with an alternate hypothesis of ORR of 30% or higher), which was considered clinically meaningful by the clinical experts consulted by CADTH. The selection of ORR (defined as sum of CR and PR per RECIST v1.1) to measure antitumour activity and DOR in patients with CR or PR) to determine the durability of tumour response were appropriate. Additional time-to-event end points (i.e., TTS and PFS) were employed in the LITESPARK-004 trial, which were considered by the clinical experts as critical outcomes to assess the efficacy of belzutifan. However, RCTs are preferred over single-arm studies for time-to-event end points such as PFS due to their sensitivity to baseline differences in patient, disease, and other clinical characteristics, and results interpretation without a randomized reference could be problematic.15-17 The LITESPARK-004 trial also involved outcomes pre-and posttreatment with belzutifan (i.e., change in LGR) to demonstrate the efficacy of belzutifan. However, without formal statistical analysis, the role of chance could not be ruled out. For outcome measurement, in addition, to study investigators, an IRC was also involved in assessing radiographic outcomes to reduce the risk of bias in the measurement of the outcome for most of the efficacy end points in patients with VHL-associated nonmetastatic RCC and those with VHL-associated CNS hemangioblastoma.
Altogether, due to major limitations such as lack of comparison groups and lack of formal inferential statistical analyses, no definitive conclusions could be drawn from the LITESPARK-004 trial with respective to the efficacy and safety of belzutifan in patients with VHL-associated nonmetastatic RCC, CNS hemangioblastoma, or nonmetastatic pNET, all of whom did not require immediate surgery.
All participants in the LITESPARK-004 trial were required to have at least 1 RCC. Therefore, the LITESPARK-004 trial may not reflect results for participants with only CNS hemangioblastomas and/or pNETs. However, the clinical experts consulted by CADTH did not consider this a serious generalizability issue. According to the clinical experts, the inclusion and exclusion criteria of the LITESPARK-004 trial generally aligned with selection criteria in the Canadian settings when identifying suitable candidates for belzutifan. However, the clinical experts noted that the requirement for patients being of Eastern Cooperative Oncology Group (ECOG) performance status 0 or 1 might not be necessary in clinical practice to initiate belzutifan because they indicated ECOG status could be unstable and subjective. There were no study sites in Canada as the LITESPARK-004 trial was conducted in Denmark, France, UK, and the US. Over 90% of the patients in LITESPARK-004 were white, which is not representative of the racial profile in the patient population in Canada according to the clinical experts. The dosing and administration of belzutifan in the LITESPARK-004 trial were consistent with the product monograph. The clinical experts commented that concomitant medications/procedures in the LITESPARK-004 trial were also appropriate and commonly used in Canadian settings. The outcomes TTS, PFS, ORR, and DOR were commonly used in clinical trials of anticancer therapy and relevant to clinical practice, as per the clinical experts. These outcomes are also important to patients who indicated they want treatments that offer the opportunity to avoid surgery, decrease or stabilize the size of tumours, and result in long-term stability or reduction of disease. However, LGR was not commonly adopted in clinical practice and may not correlate with clinical benefit. The clinical expert specializing in CNS hemangioblastoma noted that in clinical practice, RANO criteria are adopted instead of RECIST v1.1 to assess tumour response in patients with CNS hemangioblastoma. The LITESPARK-004 trial did not assess some outcomes that are important to patients, such as symptoms and HRQoL.
A sponsor-conducted ITC was submitted to supplement the absence of comparative evidence of belzutifan for treating adult patients with VHL disease in the LITESPARK-004 trial. The ITC compared a real-world, retrospective, noninterventional cohort study of existing medical records of VHL patients managed and treated at the National Cancer Institute (NCI) in the US or Canada (the VHL Natural History Study) with the LITESPARK-004 trial. Patients with VHL-associated RCC from the VHL Natural History Study were reweighted to match the distribution of key baseline characteristics among patients with VHL-associated RCC in LITESPARK-004 and compared using the matching-adjusted indirect comparison (MAIC) method. The comparative treatment was active surveillance. The primary and only outcome assessed was time-to-RCC related surgery.
The weekly exponential rate of RCC surgery was estimated at 0.00487 (standard error [SE]: 0.00034) in the matched Natural History Study sample versus 0.00071 (SE: 0.0003) in the LITESPARK-004 population.
Findings from the sponsor-conducted ITC, which used the VHL Natural History Study to provide an external comparator for the LITESPARK-004 trial, were considered of high uncertainty. Although the estimated decrease in the rate of surgeries in the LITESPARK-004 trial relative to the VHL Natural History Study was large, several major limitations decreased CADTH’s confidence in the results. First, the selection criteria that informed the VHL Natural History Study subcohorts used in the ITC were intended to match with those from the LITESPARK-004 cohort but did not include some key criteria. Specifically, the Natural History Study cohort did not include restrictions on ECOG scores of 0 or 1; this difference incurs a risk of bias of the effectiveness that may favour belzutifan. Second, it was difficult to assess the degree of heterogeneity between the included studies based on the sponsor-provided technical report since reporting of study design and patient characteristics was limited. It is likely that the underlying assumption of the unanchored MAIC that all potential prognostic and effect-modifying factors were balanced across groups was violated, which would result in a high risk of confounding. Third, the outcome definition of RCC surgery within the Natural History Study cohort is subject to potential measurement error. Specifically, the clinical experts indicated that renography and cyst removal are not definitive surgical interventions for managing RCC. However, these were considered an RCC surgery outcome in the VHL Natural History Study. The magnitude of bias due to measurement error is unknown but may overestimate the estimated relative rate of RCC surgeries in favour of belzutifan. Finally, the analysis did not provide information specific to VHL-associated CNS hemangioblastoma and pNET populations.
The sponsor submitted the VHL Natural History Study39 to address the gap of no published clinical trial or observational data on the efficacy outcomes of the standard of care, which is active surveillance. This study provided the active surveillance efficacy data used for the ITC. The sponsor also provided a cross-sectional HRQoL survey41 to address the gap of the lack of HRQoL or utility values, which is summarized and critically appraised in Appendix 1. This study assessed the impact of VHL disease on HRQoL as measured using the EQ-5D in patients with RCC, CNS hemangioblastoma, or pNET. A total of 220 patients completed the survey. Overall, patients with VHL-associated tumours had a mean EQ-5D score of 0.771. Patients who participated in this study were not treated with belzutifan, therefore this study does not provide information related to the effect of treatment with belzutifan on the HRQoL of patients with VHL disease.
The VHL Natural History Study39, a retrospective real-world cohort study of growth kinetics and surgical patterns in patients with VHL disease and associated renal solid tumours, was conducted using data registered by the NCI in a Hereditary Database of patients with VHL syndrome. The Primary Study Population consisted of patients from the US and Canada treated at the NCI with confirmed VHL syndrome and at least one renal solid tumour with available measurement(s) during the study period (July 31, 2004 to June 30, 2020). Additional criteria were applied to closely match the study population to the 1 enrolled in the LITESPARK-004 trial.
Of 776 VHL patients in the NCI hereditary database, 308 patients with at least 1 solid renal tumour met the eligibility criteria and were included in the Primary Study Population. After applying additional eligibility criteria focusing on the tumour growth rate assessment, 247 patients (80.2%) were included in the Trial Population Subgroup.
Subgroups of 131 patients and 114 patients in the Primary Study Population and the Trial Population Subgroup, respectively, had at least 3 serial measurements for at least 1 solid renal tumour during the study period that qualified them for inclusion in the LGR Analysis Subgroups to address the primary research objective.
The median tumour-level LGR for the Primary Study Population and Trial Population Subgroup was 0.38 cm per year (interquartile range [IQR]: 0.30 to 0.49) and 0.37 cm/year (IQR: 0.29 to 0.47]), respectively.
Of the 308 patients in the Primary Study Population, 232 (75.3%) patients had at least 1 renal solid tumour reduction procedure during the study period, including 225 (73.1%) patients with surgical procedures (96% of which were partial nephrectomies), 16 (5.2%) patients with ablation procedures, and 1 (0.3%) patient who received a radiation procedure. In the Trial Population Subgroup, 184 (74.5%) patients underwent at least 1 renal solid tumour reduction procedure. The median number of tumour reduction procedures per patient in the Trial Population Subgroup was 2 (range: 1 to 9).
The 1-year, 2-year, 5-year, and 7-year intervention free survival probabilities for the first tumour reduction procedure were 79.0%, 69.9%, 38.3%, and 26.4%, respectively, for the Trial Population Subgroup. The median time to first tumour reduction procedure was 44.2 months (95% CI, 35.74 to 49.51) in the Trial Population Subgroup.
Of the 217 (70.5%) patients in the Primary Study Population with at least 1 partial nephrectomy, 413 partial nephrectomies were performed during follow-up, 124 (30.0%) of which were associated with complications. The median estimated blood loss, assessed among all surgical procedure types, was 1.5 L (IQR: 0.6 to 2.6). Two (0.9%) patients in the Primary Study Population with at least 1 renal tumour reduction procedure conducted at the National Institutes of Health (NIH) died within 30 days of the procedure (1 nephrectomy and 1 biopsy).
This real-world retrospective cohort study did not evaluate the effect of belzutifan and did not provide evidence about the efficacy of the treatment. There appears to be no a priori protocol for the analyses presented. The study was conducted using data registered by the NCI in a Hereditary Database of patients with VHL syndrome, but how these data were located (e.g., search methods) or selected is not specified.
Some of the limitations of this study were high level of missing data for some variables; unavailability of longitudinal measures of tumour growth for all tumours in a systematic manner (i.e., differences may have arisen due to variation in measurement across observers), since the measures were extracted from the registry directly; incomplete documentation of metastasis; and the possibility of misclassification. There is also a possibility of loss to follow-up of patients (i.e., left the registry), but no information was provided regarding this. Attempts were made to ensure that the Trial Population Subgroup would be similar to the population of the LITESPARK-004 trial based on the additional criteria that were applied. However, several criteria in the Natural History Study cohort approximate those of the pivotal trial due to insufficient access to information within the database. While demographics and clinical characteristics were similar for patients in the Trial Population Subgroup and patients in the LGR Analysis Subgroups, many demographic characteristics (i.e., race/ethnicity and ECOG performance status) were not reported in the Natural History Study report. One of the exclusion criteria was receiving systemic oncologic therapy or investigational therapy within 30 days on or before the Patient-Level Index Date. However, no specific information was given about the type of systemic or investigational therapy. Moreover, this exclusion criteria might have led to exclusion of patients with a better prognosis, thus affecting the results for the Trial Population Subgroup.
This study includes patients managed and treated at the NCI only. This may impact the overall generalizability of the study, as this may not be representative of all patients with VHL in Canada that fall within the Health Canada–approved indication. While this study presented data for renal tumours, patients also had other tumours associated with VHL. However, no additional information was provided for these tumours, which might have excluded some important clinical outcomes associated with VHL syndrome. Since the indication under review includes nonmetastatic pNETs and CNS hemangioblastomas in addition to nonmetastatic RCC, the unavailability of data related to these 2 tumours represents a gap in the evidence provided by this study. The authors of this study noted the potential risk of losing substantial sample size due to the eligibility criteria of recruiting patients with at least 3 serial measurements to assess tumour growth rate patterns.
Patient group, clinician group, clinical expert, and drug program input gathered in the course of this CADTH review, as well as relevant literature, were reviewed to identify ethical considerations relevant to the use of belzutifan for the treatment of adult patients with VHL disease who require therapy for associated nonmetastatic RCC, CNS hemangioblastomas, or nonmetastatic pNET, not requiring immediate surgery.
Cost and Cost-Effectiveness.
CADTH identified the following key limitations with the sponsor’s analysis: the submitted model was unnecessarily complex and difficult to validate, the number of patients eligible for treatment with belzutifan is uncertain and may be underestimated, the market shares for belzutifan were likely underestimated, the time on treatment for patients receiving belzutifan is uncertain, and the use of relative dose intensity to estimate drug costs is inappropriate.
Due to the lack of face validity and overly complex structure of the sponsor’s model, CADTH was unable to undertake a base case reanalysis using the sponsor’s model. CADTH used the sponsor’s epidemiologic approach to determine the base number of patients in year 1 based on the sponsor’s estimates of population growth, VHL prevalence, diagnosis rate, tumour type, eligibility to start treatment (e.g., do not require immediate surgery), and public drug coverage rate. Eligible patients in Years 2 and 3 were added using Canadian population growth and the same variables as above. The CADTH reanalysis used median time on treatment, and revised estimates of the diagnosis rate of VHL disease, patients eligible to start treatment, the public coverage rate, and relative dose intensity. Based on the CADTH reanalysis, the three-year budget impact on the public drug plans of introducing belzutifan for the treatment of adults with VHL disease who require therapy for associated nonmetastatic RCC, CNS Hb, or nonmetastatic pNET, not requiring immediate surgery is expected to be $52,864,610 (year 1: $13,881,930; year 2: $17,588,769; year 3: $21,393,912).
Dr. Maureen Trudeau (Chair), Mr. Daryl Bell, Dr. Jennifer Bell, Dr. Matthew Cheung; Dr. Winson Cheung, Dr. Michael Crump, Dr. Leela John, Dr. Christian Kollmannsberger, Mr. Cameron Lane, Dr. Catherine Moltzan, Ms. Amy Peasgood, Dr. Anca Prica, Dr. Adam Raymakers, Dr. Patricia Tang, Dr. Marianne Taylor, and Dr. W. Dominika Wranik.
Meeting date: July 12, 2023
Regrets: One expert committee member did not attend.
Conflicts of interest: None
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Indication: For the treatment of adult patients with von Hippel-Lindau disease who require therapy for associated nonmetastatic renal cell carcinoma, central nervous system hemangioblastomas, or nonmetastatic pancreatic neuroendocrine tumours, not requiring immediate surgery.
Sponsor: Merck Canada Inc.
Final recommendation: Reimburse with conditions
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