# Abscopal effect induced by conventional fractionated radiotherapy following anti-PD-1 immunotherapy in pulmonary metastatic thymic squamous cell carcinoma: a case report and literature review

**Authors:** Minghui Cui, Jie He, Fang Zhang, Yiqian Zhang, Ang Gao, Jie Liu

PMC · DOI: 10.3389/fimmu.2026.1733066 · Frontiers in Immunology · 2026-02-18

## TL;DR

A patient with advanced thymic squamous cell carcinoma showed a rare abscopal effect after radiotherapy and immunotherapy, but severe lymphopenia limited treatment success.

## Contribution

This case report provides new clinical evidence that conventional radiotherapy can induce an abscopal effect in thymic squamous cell carcinoma.

## Key findings

- CFRT induced an abscopal effect in a patient with TSCC, reducing pleural lesions outside the radiation field.
- Severe lymphopenia following treatment may limit the durability of the abscopal effect in TSCC.
- Combined therapy outcomes can be optimized by monitoring and mitigating lymphopenia.

## Abstract

Radiotherapy (RT) can enhance immune control of distant metastases, known as the abscopal effect (AE), but it doesn’t significantly alter the immunosuppressive tumor microenvironment (TME), resulting in low AE incidence. Combining RT with immunotherapy (especially anti-PD-1/PD-L1 agents) has increased AE occurrences, though questions remain about this approach, particularly in tumors with low immunogenicity such as thymic squamous cell carcinoma (TSCC).

A 73-year-old woman with advanced TSCC and multiple metastases experienced disease progression after two therapies. Following palliative conventional fractionated radiotherapy (CFRT) (40Gy) for thoracic metastases, her pleural lesions outside the radiation field significantly reduced, indicating an AE. Despite subsequent immunotherapy and antiangiogenic drugs, treatment efficacy was unsatisfactory due to severe lymphopenia, possibly contributing to disease progression.

The rise of immunotherapy challenges traditional RT. To enhance AE occurrence in practice, factors like radiation dose, irradiation site, timing with ICIs, ICI drug choice, patient health, disease stage, and tumor traits must be considered. This case demonstrates that CFRT can induce an AE in TSCC but also highlights the associated risk of severe lymphopenia that may limit its durability. Monitoring and mitigating lymphopenia are crucial in optimizing combined therapy outcomes. This case provides new clinical evidence for treating recurrent TSCC with combined therapy, though more research on its immunological mechanisms is needed.

## Linked entities

- **Proteins:** PDCD1 (programmed cell death 1), CD274 (CD274 molecule)
- **Diseases:** thymic squamous cell carcinoma (MONDO:0003493), lymphopenia (MONDO:0003783)

## Full-text entities

- **Genes:** TGFB1 (transforming growth factor beta 1) [NCBI Gene 7040] {aka CAEND1, CED, DPD1, IBDIMDE, LAP, TGF-beta1}, ALB (albumin) [NCBI Gene 213] {aka FDAHT, HSA, PRO0883, PRO0903, PRO1341}, CD8A (CD8 subunit alpha) [NCBI Gene 925] {aka CD8, CD8alpha, IMD116, Leu2, p32}, PDCD1 (programmed cell death 1) [NCBI Gene 5133] {aka ADMIO4, AIMTBS, CD279, PD-1, PD1, SLEB2}, CGAS (cyclic GMP-AMP synthase) [NCBI Gene 115004] {aka C6orf150, D4, MB21D1, h-cGAS}, TLR4 (toll like receptor 4) [NCBI Gene 7099] {aka ARMD10, CD284, TLR-4, TOLL}, TREX1 (three prime repair exonuclease 1) [NCBI Gene 11277] {aka AGS1, CRV, DRN3, HERNS, RVCLS}, AREG (amphiregulin) [NCBI Gene 374] {aka AR, AREGB, CRDGF, SDGF}, STING1 (stimulator of interferon response cGAMP interactor 1) [NCBI Gene 340061] {aka ERIS, MITA, MPYS, NET23, SAVI, STING}, FOXP3 (forkhead box P3) [NCBI Gene 50943] {aka AIID, DIETER, IPEX, JM2, PIDX, XPID}, CD4 (CD4 molecule) [NCBI Gene 920] {aka CD4mut, IMD79, Leu-3, OKT4D, T4}, NFKB1 (nuclear factor kappa B subunit 1) [NCBI Gene 4790] {aka CVID12, EBP-1, KBF1, NF-kB, NF-kB1, NF-kappa-B1}, CD274 (CD274 molecule) [NCBI Gene 29126] {aka ADMIO5, B7-H, B7H1, PD-L1, PDCD1L1, PDCD1LG1}
- **Diseases:** lymphopenia (MESH:D008231), lung lesions (MESH:D008171), Tumors (MESH:D009369), CFRT (MESH:C563514), pleural lesion (MESH:D010995), dyspnea (MESH:D004417), lymphangitic carcinomatosis (MESH:D002277), superior vena cava syndrome (MESH:D013479), toxicity (MESH:D064420), lung metastases (MESH:D009362), respiratory and circulatory failure (MESH:D012769), atelectasis (MESH:D001261), infectious diseases (MESH:D003141), TSCC (MESH:D002294), NSCLC (MESH:D002289), abscopal lesion (MESH:D009059), autoimmune disorders (MESH:D001327), sternal mass (MESH:C537489), lymph node metastases (MESH:D008207), wheezing (MESH:D012135), ALC (MESH:D009845), pleural effusion (MESH:D010996), thymic cancer (MESH:D013953), pneumonia (MESH:D011014), RIL (MESH:D009381), chest tightness (MESH:D002637), AE (MESH:D065606), Thymoma (MESH:D013945)
- **Chemicals:** paclitaxel (MESH:D017239), carbon (MESH:D002244), AiRuiKa (-), nedaplatin (MESH:C053989), alcohol (MESH:D000438), apatinib (MESH:C553458), tegafur (MESH:D005641), anlotinib (MESH:C000625192), lobaplatin (MESH:C066228), camrelizumab (MESH:C000631724), Sintilimab (MESH:C000632826)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

61 references — full list in the complete paper: https://tomesphere.com/paper/PMC12957225/full.md

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Source: https://tomesphere.com/paper/PMC12957225