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FDA Grants Accelerated Approval to Adagrasib with Cetuximab for KRAS G12C-mutated Advanced Colorectal Cancer

Evidence for efficacy is based on the results from the KRYSTAL-1 study
15 Jul 2024
Targeted Therapy;  Molecular Oncology
Colon and Rectal Cancer

On 21 June 2024, the US Food and Drug Administration (FDA) granted accelerated approval to adagrasib (Krazati; Mirati Therapeutics, Inc.) plus cetuximab for adults with KRAS G12C-mutated locally advanced or metastatic colorectal cancer (CRC), as determined by an FDA-approved test, who have received prior treatment with fluoropyrimidine-, oxaliplatin-, and irinotecan-based chemotherapy.

Efficacy was evaluated in KRYSTAL-1, a multicentre, single-arm expansion cohort study. Eligible patients were required to have locally advanced or metastatic KRAS G12C-mutated CRC previously treated with fluoropyrimidine-, oxaliplatin-, and irinotecan-based chemotherapy, and a VEGF inhibitor, if eligible. Patients were treated with adagrasib 600 mg twice daily plus cetuximab administered either biweekly (500 mg/m2 every two weeks) or weekly (400 mg/m2 initial dose followed by 250 mg/m2 weekly). Tumour assessments were performed every 6 weeks. Adagrasib discontinuation required cetuximab discontinuation, however patients could continue adagrasib if cetuximab was discontinued.

The major efficacy outcome measures were confirmed overall response rate (ORR) and duration of response (DoR) according to RECIST v1.1 assessed by blinded independent central review. In the 94 enrolled patients, ORR was 34% (95% confidence interval [CI] 25%, 45%), all responses were partial responses, and median DoR was 5.8 months (95% CI 4.2, 7.6). Among responding patients, 31% had a DoR of at least 6 months.

The most common adverse reactions (≥20%) were rash, nausea, diarrhoea, vomiting, fatigue, musculoskeletal pain, hepatotoxicity, headache, dry skin, abdominal pain, decreased appetite, oedema, anaemia, cough, dizziness, constipation, and peripheral neuropathy.

The recommended adagrasib dose is 600 mg orally twice daily until disease progression or unacceptable toxicity. Refer to the cetuximab prescribing information for cetuximab dosage information.

This application was granted priority review and breakthrough therapy designation.

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 FDA’s Oncology Center of Excellence Project Facilitate.

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