ICER Publishes Final Evidence Report on Gene Therapy for Metachromatic Leukodystrophy


— Independent appraisal committee voted that across all patient subpopulations, arsa-cel demonstrated a net health benefit when compared to usual care; arsa-cel would achieve common thresholds for cost-effectiveness if priced between $2.3M and $3.9M —

BOSTON, October 30, 2023 – The Institute for Clinical and Economic Review (ICER) today released a Final Evidence Report assessing the comparative clinical effectiveness and value of atidarsagene autotemcel (“arsa-cel”, Orchard Therapeutics) for metachromatic leukodystrophy (MLD). ICER’s report on these therapies was the subject of the September 2023 public meeting of the of the CTAF (CTAF), one of ICER’s three independent evidence appraisal committees.


Downloads: Final Evidence Report | Report-at-a-Glance | Policy Recommendations


“MLD is a devastating disease for children and their caregivers,” said ICER’s Chief Medical Officer, David Rind, MD. “It is extremely rare, and most doctors have never seen a case. We again see a gene therapy potentially filling the promise of treating a disease that was previously untreatable, delivering remarkable clinical benefits and extending life. If the manufacturer prices arsa-cel in line with its price in Europe, despite being very expensive, arsa-cel would be cost-effective.”


ICER’s Virtual Public Meeting: Voting Results on Clinical Effectiveness and Contextual Considerations


ICER assessed, and the independent appraisal committee voted on, the evidence of arsa-cel for three types of MLD:


1.      For children with presymptomatic late infantile MLD:


  • All panelists (13-0) found that current evidence is adequate to demonstrate a net health benefit for atidarsagene autotemcel (arsa-cel) when compared to usual care.


2.      For children with presymptomatic early juvenile MLD:


  • All panelists (13-0) found that current evidence is adequate to demonstrate a net health benefit for atidarsagene autotemcel (arsa-cel) when compared to usual care.


3.      For children with symptomatic early juvenile MLD:


  • A majority of panelists (12-1) found that current evidence is adequate to demonstrate a net health benefit for atidarsagene autotemcel (arsa-cel) when compared to usual care.


For children with presymptomatic late infantile MLD or presymptomatic early juvenile MLD, panel members also weighed potential benefits and disadvantages beyond the direct health effects and broader contextual considerations. Voting highlighted the following as particularly important for payers and other policymakers to note:


  • The acuity of need for treatment of individual patients based on short-term risk of death or progression to permanent disability;


  • The magnitude of the lifetime impact on individual patients of MLD;


  • The likelihood that these new treatments will improve patients’ broader ability to achieve major life goals related to education, work, or family life;


  • The likelihood that these new treatments will improve caregivers’ quality of life and/or ability to achieve major life goals related to education, work, or family life.


ICER’s Virtual Public Meeting: Voting Results on Long-Term Value for Money


Arsa-cel has not yet been approved by the FDA, and the manufacturer has not announced a US price if approved. ICER has calculated a health-benefit price benchmark (HBPB), meaning a price range that matches the clinical benefit patients are expected to receive, for arsa-cel to be between $2.3M to $3.9M


Consistent with ICER’s process, because there is no firm estimate yet of a potential launch price for the treatment, the panel did not take separate votes on the treatment’s long-term value for money.


Key Policy Recommendations:


ICER’s independent assessment of value informs the critical decisions that stakeholders across the US health system need to make around pricing and coverage. Following the voting session, a policy roundtable of experts — including the manufacturer, clinical experts, patient advocates, and representatives from US payers — convened to discuss the pricing implications and recommendations to ensure fair access. Key recommendations stemming from the roundtable discussion include:


  • In the context of a rapidly progressive disease such as MLD, when a treatment has a high likelihood of being approved by the FDA, payers should be evaluating evidence and preparing policies in advance to avoid a new-to-market block on insurance coverage.


  •  Payers should cover fertility preservation in concert with coverage of gene therapies.


  • Manufacturers should actively engage with independent value assessment efforts to allow public dialogue on access and fair pricing with broad input from patients and other stakeholders. Orchard Therapeutics has set a good example for other developers of transformative gene therapies.


ICER’s detailed set of policy recommendations, including comprehensive considerations for establishing evidence-based prior authorization criteria, is available in the Final Evidence Report and in the standalone Policy Recommendations document.

About ICER


The Institute for Clinical and Economic Review (ICER) is an independent non-profit research institute that produces reports analyzing the evidence on the effectiveness and value of drugs and other medical services. ICER’s reports include evidence-based calculations of prices for new drugs that accurately reflect the degree of improvement expected in long-term patient outcomes, while also highlighting price levels that might contribute to unaffordable short-term cost growth for the overall health care system.


ICER’s reports incorporate extensive input from all stakeholders and are the subject of public hearings through three core programs: the California Technology Assessment Forum (CTAF), the Midwest Comparative Effectiveness Public Advisory Council (Midwest CEPAC), and the New England Comparative Effectiveness Public Advisory Council (New England CEPAC). These independent panels review ICER’s reports at public meetings to deliberate on the evidence and develop recommendations for how patients, clinicians, insurers, and policymakers can improve the quality and value of health care. For more information about ICER, please visit ICER’s website.