News from the FDA/CDC

FDA Approves Tarlatamab for Extensive-Stage Small Cell Lung Cancer


 

The US Food and Drug Administration has granted accelerated approval to tarlatamab-dlle (Imdelltra) for extensive-stage small cell lung cancer (SCLC) with disease progression on or after platinum-based chemotherapy.

Tarlatamab is a first-in-class bispecific T-cell engager (BiTE) that binds delta-like ligand 3 on the surface of cells, including tumor cells, and CD3 expressed on the surface of T cells. It causes T-cell activation, release of inflammatory cytokines, and lysis of DLL3-expressing cells, according to labeling.

Approval was based on data from 99 patients in the DeLLphi-301 trial with relapsed/refractory extensive-stage SCLC who had progressed after platinum-based chemotherapy. Patients with symptomatic brain metastases, interstitial lung disease, noninfectious pneumonitis, and active immunodeficiency were excluded.

The overall response rate was 40%, and median duration of response 9.7 months. The overall response rate was 52% in 27 patients with platinum-resistant SCLC and 31% in 42 with platinum-sensitive disease.

Continued approval may depend on verification of clinical benefit in a confirmatory trial.

Labeling includes a box warning of serious or life-threatening cytokine release syndrome and neurologic toxicity, including immune effector cell–associated neurotoxicity syndrome.

The most common adverse events, occurring in 20% or more of patients, were cytokine release syndrome, fatigue, pyrexia, dysgeusia, decreased appetite, musculoskeletal pain, constipation, anemia, and nausea.

The most common grade 3 or 4 laboratory abnormalities included decreased lymphocytes, decreased sodium, increased uric acid, decreased total neutrophils, decreased hemoglobin, increased activated partial thromboplastin time, and decreased potassium.

The starting dose is 1 mg given intravenously over 1 hour on the first day of the first cycle followed by 10 mg on day 8 and day 15 of the first cycle, then every 2 weeks until disease progression or unacceptable toxicity.

M. Alexander Otto is a physician assistant with a master’s degree in medical science and a journalism degree from Newhouse. He is an award-winning medical journalist who worked for several major news outlets before joining Medscape. Alex is also an MIT Knight Science Journalism fellow. Email: aotto@mdedge.com

A version of this article appeared on Medscape.com.

Recommended Reading

The Long, Controversial Search for a ‘Cancer Microbiome’
MDedge Hematology and Oncology
The DEA Plans to Reschedule Marijuana: What Happens Next?
MDedge Hematology and Oncology
Terminal Cancer: What Matters to Patients and Caregivers
MDedge Hematology and Oncology
Do Health-Related Social Needs Raise Mortality Risk in Cancer Survivors?
MDedge Hematology and Oncology
Do Patients Benefit from Cancer Trial Participation?
MDedge Hematology and Oncology
National Mine Safety Group Issues Rule to Reduce Silica Exposure
MDedge Hematology and Oncology
Can a Risk Score Predict Kidney Injury After Cisplatin?
MDedge Hematology and Oncology
New mRNA Vaccines in Development for Cancer and Infections
MDedge Hematology and Oncology
Survey Spotlights Identification of Dermatologic Adverse Events From Cancer Therapies
MDedge Hematology and Oncology
Chatbots Seem More Empathetic Than Docs in Cancer Discussions
MDedge Hematology and Oncology