# Dual blockade immunotherapy targeting PD-1/PD-L1 and CTLA-4 in lung cancer

**Authors:** Weishi Cheng, Kai Kang, Ailin Zhao, Yijun Wu

PMC · DOI: 10.1186/s13045-024-01581-2 · Journal of Hematology & Oncology · 2024-07-27

## TL;DR

This paper reviews dual immunotherapy targeting PD-1/PD-L1 and CTLA-4 in lung cancer, aiming to improve treatment efficacy while managing side effects.

## Contribution

The paper provides novel insights into combining dual blockade immunotherapy with other strategies to optimize lung cancer treatment.

## Key findings

- Dual blockade immunotherapy enhances immune responses against cancer cells by targeting PD-1/PD-L1 and CTLA-4.
- Combination therapy increases efficacy but also raises the risk of immune-related adverse events.
- Bispecific antibodies offer a feasible approach to dual targeting with reduced toxicity.

## Abstract

Cancer immunotherapies, represented by immune checkpoint inhibitors (ICIs), have reshaped the treatment paradigm for both advanced non-small cell lung cancer and small cell lung cancer. Programmed death receptor-1/programmed death receptor ligand-1 (PD-1/PD-L1) and cytotoxic T lymphocyte-associated antigen-4 (CTLA-4) are some of the most common and promising targets in ICIs. Compared to ICI monotherapy, which occasionally demonstrates treatment resistance and limited efficacy, the dual blockade immunotherapy targeting PD-1/PD-L1 and CTLA-4 operates at different stages of T cell activation with synergistically enhancing immune responses against cancer cells. This emerging dual therapy heralds a new direction for cancer immunotherapy, which, however, may increase the risk of drug-related adverse reactions while improving efficacy. Previous clinical trials have explored combination therapy strategy of anti-PD-1/PD-L1 and anti-CTLA-4 agents in lung cancer, yet its efficacy remains to be unclear with the inevitable incidence of immune-related adverse events. The recent advent of bispecific antibodies has made this sort of dual targeting more feasible, aiming to alleviate toxicity without compromising efficacy. Thus, this review highlights the role of dual blockade immunotherapy targeting PD-1/PD-L1 and CTLA-4 in treating lung cancer, and further elucidates its pre-clinical mechanisms and current advancements in clinical trials. Besides, we also provide novel insights into the potential combinations of dual blockade therapies with other strategies to optimize the future treatment mode for lung cancer.

## Linked entities

- **Proteins:** PDCD1 (programmed cell death 1), CD274 (CD274 molecule), CTLA4 (cytotoxic T-lymphocyte associated protein 4)
- **Diseases:** lung cancer (MONDO:0005138), non-small cell lung cancer (MONDO:0005233), small cell lung cancer (MONDO:0008433)

## Full-text entities

- **Genes:** CTLA4 (cytotoxic T-lymphocyte associated protein 4) [NCBI Gene 1493] {aka ALPS5, CD, CD152, CELIAC3, CTLA-4, GRD4}, CD274 (CD274 molecule) [NCBI Gene 29126] {aka ADMIO5, B7-H, B7H1, PD-L1, PDCD1L1, PDCD1LG1}, PDCD1 (programmed cell death 1) [NCBI Gene 5133] {aka ADMIO4, AIMTBS, CD279, PD-1, PD1, SLEB2}
- **Diseases:** small cell lung cancer (MESH:D055752), Cancer (MESH:D009369), non-small cell lung cancer (MESH:D002289), lung cancer (MESH:D008175), toxicity (MESH:D064420)

## Full text

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## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11283714/full.md

## References

25 references — full list in the complete paper: https://tomesphere.com/paper/PMC11283714/full.md

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Source: https://tomesphere.com/paper/PMC11283714