Cost-Effectiveness of Nivolumab in Recurrent Metastatic Head and Neck Squamous Cell Carcinoma

Mahdi Zargar1, Thomas McFarlane1,2, Kelvin K W Chan2,3,4

  • 1University of Waterloo School of Pharmacy, Waterloo, Ontario, Canada.

The Oncologist
|October 13, 2017
PubMed
Abstract

Insights

Nivolumab offers clinical benefits for recurrent, metastatic head and neck squamous cell carcinoma (r/m HNSCC) but is not cost-effective at its current price. Cost-effectiveness may be achieved with a price reduction or for patients with high programmed death-ligand 1 expression.

Area of Science:

  • Oncology
  • Health Economics
  • Pharmacoeconomics

Background:

  • Limited treatment options and poor prognosis exist for platinum-refractory, recurrent, metastatic head and neck squamous cell carcinoma (r/m HNSCC).
  • Nivolumab, an anti-programmed cell death protein 1 (PD-1) antibody, demonstrated improved overall survival (OS) in the CheckMate 141 trial for this patient population.
  • Cost-effectiveness of nivolumab compared to standard therapies in r/m HNSCC requires evaluation.

Purpose of the Study:

  • To determine the cost-effectiveness of nivolumab versus docetaxel for treating platinum-refractory, recurrent, metastatic head and neck squamous cell carcinoma (r/m HNSCC).
  • To identify patient subgroups for whom nivolumab may be more cost-effective.

Main Methods:

  • A state transition model was developed for HNSCC patients progressing after platinum chemotherapy.
  • Treatment effects and adverse events were sourced from the CheckMate 141 trial.
  • A Canadian perspective, 5-year time horizon, and 1.5% discount rate were applied.

Main Results:

  • Nivolumab extended mean OS by 4 months and improved quality-adjusted life years (QALYs) by 0.13 compared to docetaxel.
  • The incremental cost-effectiveness ratio (ICER) for nivolumab was $144,744/QALY, exceeding the $100,000/QALY willingness-to-pay threshold.
  • Nivolumab could be cost-effective with a 20% price reduction or for patients with programmed death-ligand 1 (PD-L1) expression >5%.

Conclusions:

  • Nivolumab provides clinical benefits for r/m HNSCC but is not cost-effective at its current list price.
  • A value-based price estimate suggests potential cost-effectiveness with price adjustments.
  • Further research is needed to identify reliable biomarkers for nivolumab cost-effectiveness.

Related Concept Videos

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...
3.8K
Cancer Therapies02:49

Cancer Therapies

Cancer therapies are various modes of treatment, such as surgery, radiation therapy, and chemotherapy that are administered to cancer patients.
However, cancer treatments can pose several challenges, as therapies used to kill cancer cells are generally also toxic to normal cells. Moreover, cancer cells mutate rapidly and can develop resistance to chemical agents or radiation therapy. Besides, all types of cancer cells may not respond to the same therapy. Some cancer cells respond to one...
10.2K
Chemotherapy-Induced Nausea and Vomiting: Neurokinin-1 Receptor Antagonists01:28

Chemotherapy-Induced Nausea and Vomiting: Neurokinin-1 Receptor Antagonists

Neurokinin 1 (NK1) receptors are distributed across the GI tract, vagal afferents, and key CNS regions including the central vomiting center and chemoreceptor trigger zone (CTZ) Chemotherapy agents stimulate enterochromaffin cells in the gastrointestinal (GI) tract to release large amounts of substance P (SP). SP is a neuropeptide released by specific sensory nerves in response to many different stressors, including those in the GI mucosa affected by chemotherapy.  SP binds and activates...
663
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...
9.0K
Chemotherapy-Induced Nausea and Vomiting: Dopamine Receptor Antagonists01:29

Chemotherapy-Induced Nausea and Vomiting: Dopamine Receptor Antagonists

Dopamine receptor antagonists, also known as antipsychotic agents, are critical in managing chemotherapy-induced vomiting. These antiemetic agents block dopamine receptors in the chemoreceptor trigger zone (CTZ), inhibiting signal transmission to the vomiting center. Antipsychotic agents encompass phenothiazines (PTZ), butyrophenones, benzamides, and thienobenzodiazepines (Zyprexa), which are utilized for their antiemetic and sedative properties.
Phenothiazines, such as prochlorperazine...
945