Economic Evaluation of Inavolisib Combined With Palbociclib-Fulvestrant for PIK3CA-Mutated, HR+/HER2- Advanced Breast

Hanqing Zeng1, Li-Ying Song1, Ren Guo1

  • 1Department of Pharmacy, The Third Xiangya Hospital, Central South University, Changsha, Hunan, China.

Insights

The inavolisib regimen for PIK3CA-mutated, HR+/HER2- advanced breast cancer is not cost-effective in the U.S. Significant price reductions are needed for this PI3Kα inhibitor to meet willingness-to-pay thresholds.

Area of Science:

  • Oncology
  • Health Economics
  • Pharmacoeconomics

Background:

  • Inavolisib is a selective PI3Kα inhibitor approved for PIK3CA-mutated, HR+/HER2- advanced breast cancer (ABC).
  • The INAVO120 III trial confirmed its efficacy, but its high cost necessitates a value assessment.
  • Evaluating the cost-effectiveness of inavolisib plus palbociclib-fulvestrant is crucial for U.S. healthcare.

Purpose of the Study:

  • To assess the cost-effectiveness of inavolisib plus palbociclib-fulvestrant for PIK3CA-mutated, HR+/HER2- ABC.
  • To determine the incremental cost-effectiveness ratio (ICER) from a U.S. healthcare system perspective.
  • To identify necessary price reductions for the regimen to be considered cost-effective.

Main Methods:

  • A three-state Markov model simulated disease progression in PIK3CA-mutated, HR+/HER2- ABC patients.
  • Parametric survival models extrapolated long-term clinical outcomes, costs, and quality-adjusted life years (QALYs).
  • Sensitivity analyses and subgroup analyses assessed model robustness and benefit variations.

Main Results:

  • The inavolisib regimen yielded an additional 0.6 QALYs at an increased cost of $160,490.07, resulting in an ICER of $268,457.82 per QALY.
  • The regimen was not cost-effective within willingness-to-pay (WTP) thresholds of $100,000-$200,000 per QALY.
  • Inavolisib's price would need to decrease to 59.5%-86.5% of its current cost to meet WTP thresholds.

Conclusions:

  • The inavolisib regimen is not cost-effective for PIK3CA-mutated, HR+/HER2- ABC in the U.S. healthcare setting.
  • Price reductions for inavolisib are essential to improve its cost-effectiveness.
  • Adjusting decision thresholds based on patient characteristics could address treatment demand.

Related Concept Videos

PI3K/mTOR/AKT Signaling Pathway01:22

PI3K/mTOR/AKT Signaling Pathway

The mammalian target of rapamycin  (mTOR) is a serine/threonine kinase that regulates growth, proliferation, and cell survival in response to hormones, growth factors, or nutrient availability. This kinase exists in two structurally and functionally distinct forms: mTOR complex 1  (mTORC1) and mTOR complex 2  (mTORC2). The first form (mTORC1) is composed of a rapamycin-sensitive Raptor and proline-rich Akt substrate, PRAS40. In contrast,  mTORC2 consists of a...
6.5K
Treatment Resistent Cancers02:56

Treatment Resistent Cancers

1.5K
Treatment Resistant Cancers02:56

Treatment Resistant Cancers

Cancer is the second leading cause of death in the United States. A cancer cell is genetically unstable and hence can mutate faster. They can also modify their microenvironment and escape immune surveillance. The difficulties in treating cancer are further compounded by the emergence of rapid resistance to anticancer drugs. The most common ways to attain resistance in cancer cells include alteration in drug transport and metabolism, modification of drug target, elevated DNA damage response, or...
3.9K
Combination Therapies and Personalized Medicine02:50

Combination Therapies and Personalized Medicine

Combining two or more treatment methods increases the life span of cancer patients while reducing damage to vital organs or tissue from the overuse of a single treatment. Combination therapy also targets different cancer-inducing pathways, thus reducing the chances of developing resistance to treatment.
The combination of the drug acetazolamide and sulforaphane is a good example of combination therapy to treat cancer. The cells in the interior of a large tumor often die due to the hypoxic and...
6.4K
FDA Approved Drugs: Changes to Approved Drugs01:26

FDA Approved Drugs: Changes to Approved Drugs

Post-approval, manufacturers may modify an approved new or generic drug product. Such modifications can encompass alterations in the Active Pharmaceutical Ingredient (API), manufacturing process, formulation, batch size, manufacturing site, and container closure system (FDA Guidance for Industry, April 2004). Often, a drug product may undergo multiple changes.These modifications require careful evaluation to determine their potential impact on the drug product's identity, strength, quality,...
336
Targeted Cancer Therapies02:57

Targeted Cancer Therapies

The targeted cancer therapies, also known as “molecular targeted therapies,” take advantage of the molecular and genetic differences between the cancer cells and the normal cells. It needs a thorough understanding of the cancer cells to develop drugs that can target specific molecular aspects that drive the growth, progression, and spread of cancer cells without affecting the growth and survival of other normal cells in the body.
There are several types of targeted therapies against...
9.2K