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Plain language summary: tarlatamab for patients with previously treated small cell lung cancer
Myung-Ju Ahn1, Byoung Chul Cho2, Enriqueta Felip3
1Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, South Korea.
What Is This Summary About?:
This is a summary of a phase 2 clinical study called DeLLphi-301. The study looked at how effective and safe a medicine called tarlatamab was in participants with small cell lung cancer (SCLC). Participants previously received at least two other treatments for their SCLC. Tarlatamab is a new medicine that locates a protein called DLL3 on the cancer, which allows T cells to attack the cancer. T cells belong to the body's natural defense system known as the immune system. The DeLLphi-301 study separated participants into two groups to receive tarlatamab 10 mg or 100 mg to determine which dose best shrank SCLC with minimal side effects. All participants received a small first dose (1 mg tarlatamab) to decrease the risk of an immune system reaction called cytokine release syndrome (CRS). Tarlatamab was given through the participant's vein once every 2 weeks. This method of administration is known as intravenous (IV) infusion.
What Were The Results Of The Dellphi-301 Study?:
In the group given 10 mg tarlatamab, 40% of participants responded to treatment (cancer shrank). In the group given 100 mg tarlatamab, 32% of participants responded to treatment (cancer shrank). After taking tarlatamab at either dose, 59% of participants lived for at least 6 months without their cancer growing or getting worse.The most common side effect was CRS, which occurred in 51% of participants in the group given 10 mg tarlatamab and 61% of participants in the group given 100 mg tarlatamab. Other common side effects were decreased appetite, fever, constipation, and anemia. Some participants had a type of immune reaction called immune effector cell-associated neurotoxicity syndrome (ICANS). A small number of participants (3%) stopped taking tarlatamab because of side effects related to tarlatamab.
What Do The Results From The Dellphi-301 Study Mean?:
The study found that tarlatamab given every 2 weeks shrank SCLC in participants with SCLC who received previous treatments. Participants given the 10 mg tarlatamab dose had fewer side effects than those given the 100 mg tarlatamab dose.Clinical Trial Registration: NCT05740566 (DeLLphi-304) (ClinicalTrials.gov).
Insights
Tarlatamab demonstrated efficacy in shrinking small cell lung cancer (SCLC) in a Phase 2 trial. The 10 mg dose showed a favorable side effect profile compared to the 100 mg dose.
Area of Science:
- Oncology
- Immunotherapy
Background:
- Small cell lung cancer (SCLC) is an aggressive malignancy with limited treatment options.
- Tarlatamab targets the DLL3 protein, prevalent on SCLC cells, to facilitate T-cell-mediated cancer attack.
Purpose of the Study:
- To evaluate the efficacy and safety of tarlatamab in patients with previously treated SCLC.
- To determine the optimal dose of tarlatamab (10 mg vs. 100 mg) for SCLC treatment.
Main Methods:
- Phase 2 clinical trial (DeLLphi-301) involving participants with advanced SCLC.
- Intravenous (IV) infusion of tarlatamab every two weeks, with an initial low dose to mitigate cytokine release syndrome (CRS).
Main Results:
- Response rates were 40% for 10 mg tarlatamab and 32% for 100 mg tarlatamab.
- 59% of participants experienced at least 6 months progression-free survival.
- Common side effects included CRS (51-61%), decreased appetite, fever, constipation, and anemia; 3% discontinued treatment due to side effects.
Conclusions:
- Tarlatamab effectively shrinks SCLC in patients with prior treatments.
- The 10 mg dose of tarlatamab exhibited a better safety profile with comparable efficacy to the 100 mg dose.
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