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FDA Approves Pembrolizumab as Adjuvant Treatment for NSCLC

Evidence for efficacy is based on the results from the KEYNOTE-091 study
02 Feb 2023
Immunotherapy
Non-Small Cell Lung Cancer

On 26 January 2023, the US Food and Drug Administration (FDA) approved pembrolizumab (Keytruda, Merck) for adjuvant treatment following resection and platinum-based chemotherapy for stage IB (T2a ≥4 cm), II, or IIIA non-small cell lung cancer (NSCLC).

Full prescribing information for Keytruda is available here.

Efficacy was evaluated in KEYNOTE-091 (NCT02504372), a multicentre, randomised, triple-blind, placebo-controlled study. Patients had not received neoadjuvant radiotherapy or chemotherapy. Patients were randomised (1:1) to receive pembrolizumab 200 mg or placebo intravenously every 3 weeks for up to 1 year. Stratification factors included receipt of adjuvant chemotherapy and region of the world. Of the 1177 patients randomised, 1010 (86%) received adjuvant platinum-based chemotherapy following complete resection.

The major efficacy outcome measure was investigator-assessed disease-free survival (DFS). The study met its primary endpoint, demonstrating a statistically significant improvement in DFS in the overall population. In an exploratory subgroup analysis of the 167 patients who did not receive adjuvant chemotherapy, the DFS hazard ratio (HR) was 1.25 (95% confidence interval [CI] 0.76, 2.05). For patients who received adjuvant chemotherapy, median DFS was 58.7 months in the pembrolizumab arm (95% CI 39.2, not reached) and 34.9 months in the placebo arm (95% CI 28.6, not reached) with HR 0.73 (95% CI 0.60, 0.89).

The adverse reactions observed in KEYNOTE-091 were generally similar to those occurring in other patients with NSCLC receiving KEYTRUDA as a single agent, with the exception of hypothyroidism (22%), hyperthyroidism (11%), and pneumonitis (7%). Two fatal adverse reactions of myocarditis occurred.

The recommended pembrolizumab dose is 200 mg every 3 weeks or 400 mg every 6 weeks until disease recurrence, unacceptable toxicity, or up to 12 months.

This review was conducted under Project Orbis, an initiative of the FDA Oncology Center of Excellence (OCE). Project Orbis provides a framework for concurrent submission and review of oncology drugs among international partners. For this review, FDA collaborated with the Australian Therapeutic Goods Administration, Health Canada, and Switzerland’s Swissmedic. The application reviews are ongoing at the other regulatory agencies.

This review used the Assessment Aid, a voluntary submission from the applicant to facilitate the FDA’s assessment.

Healthcare professionals should report all serious adverse events suspected to be associated with the use of any medicine and device to FDA’s MedWatch Reporting System.

For assistance with single-patient INDs for investigational oncology products, healthcare professionals may contact OCE’s Project Facilitate.

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