# Targeted therapy acts to sensitize stereotactic body radiotherapy for pulmonary oligometastases from colorectal cancer

**Authors:** Xiye Sun, Pei Shu, Yali Shen, Zhiping Li, Ning Liu, Ganlu Ouyang, Yuanling Tang, Meijuan Huang, Xin Wang

PMC · DOI: 10.3389/fonc.2025.1464707 · Frontiers in Oncology · 2025-05-08

## TL;DR

Adding targeted drugs like cetuximab or bevacizumab to radiotherapy improves survival and control of lung metastases in colorectal cancer patients.

## Contribution

This study shows that combining targeted therapy with radiotherapy improves outcomes for pulmonary metastases from colorectal cancer.

## Key findings

- Combining SBRT with cetuximab or bevacizumab significantly improved local control and survival rates.
- Tumor size <2 cm and higher BED10 correlated with better local control.
- All regimens were well tolerated, though targeted therapies increased toxicity.

## Abstract

Stereotactic body radiation therapy (SBRT) is used to manage lung metastases arising from colorectal cancer (CRC), but its effectiveness is constrained by the radioresistance of CRCs. Here, we explored whether concurrent therapy with cetuximab or bevacizumab could improve the prognosis of CRC patients with pulmonary oligometastases.

CRC patients with oligometastatic lung tumors (OLTs) treated with concurrent chemoradiotherapy from March 2011 to March 2023 were retrospectively analyzed. Treatment outcomes for local control rate (LCR), progression-free survival (PFS), overall survival (OS), and toxicities were assessed.

Sixty-nine patients were included, with a median follow-up of 34 months. The 1-year LCRs for SBRT + chemotherapy, SBRT + chemotherapy + bevacizumab, and SBRT + chemotherapy + cetuximab were 63.3%, 96.2%, and 94.4%, respectively. Incorporating bevacizumab or cetuximab significantly prolonged median OS compared to chemotherapy (61 vs. 46 vs. 24 months). Substantial differences in median PFS were noted, with durations of 5, 23, and 8 months for SBRT + chemotherapy, SBRT + chemotherapy + bevacizumab, and SBRT + chemotherapy + cetuximab, respectively. Our univariate analysis revealed that patients under targeted therapy of bevacizumab or cetuximab were linked to prolonged OS and PFS (p < 0.05). Tumor size <2 cm and median biologically effective dose (BED10) ≥100 Gy were correlated with higher local control rates (p < 0.05). Furthermore, comprehensive multivariate analysis confirmed that tumor sizes of <2 cm were linked to better local control (p < 0.05). All three combination regimens were well tolerated, and the occurrence of toxicities was higher in treatments involving targeted therapy.

Combining concurrent chemoradiotherapy with cetuximab or bevacizumab improves treatment outcomes, with manageable toxicity. Given the limited sample size of this study, larger studies such as prospective trials are needed.

## Linked entities

- **Diseases:** colorectal cancer (MONDO:0005575)

## Full-text entities

- **Diseases:** Tumor (MESH:D009369), lung metastases (MESH:D009362), CRC (MESH:D015179), toxicities (MESH:D064420), lung tumors (MESH:D008175)
- **Chemicals:** bevacizumab (MESH:D000068258), cetuximab (MESH:D000068818)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

1 figure with captions in the complete paper: https://tomesphere.com/paper/PMC12095014/full.md

## References

47 references — full list in the complete paper: https://tomesphere.com/paper/PMC12095014/full.md

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Source: https://tomesphere.com/paper/PMC12095014