# Synergistic effects of radiotherapy and immunotherapy: improving oncological outcomes

**Authors:** Xueqin Chen, Wen Liu, Yuzhu Wang, Zhengliang Yue, Jiajie Wang, Yun Liu, Lifan Xu, Jianjun Hu

PMC · DOI: 10.3389/fimmu.2026.1771355 · Frontiers in Immunology · 2026-02-04

## TL;DR

This review explores how combining radiotherapy and immunotherapy can improve cancer treatment by understanding their synergistic effects and optimizing their use.

## Contribution

The paper introduces the dose–immune window hypothesis and highlights AI's role in optimizing RT–immunotherapy combinations.

## Key findings

- Radiotherapy and immunotherapy have distinct but complementary mechanisms in cancer treatment.
- The dose–immune window hypothesis explains how radiation doses can modulate immune responses for synergy with immunotherapy.
- Artificial intelligence is advancing treatment planning and patient stratification in RT–immunotherapy combinations.

## Abstract

Radiotherapy (RT) and immunotherapy, which are cornerstone modalities in the realm of oncology, involve distinct mechanistic pathways and possess unique therapeutic potential. RT achieves localized tumor control by inducing DNA damage and disrupting the tumor microenvironment (TME), whereas immunotherapy—particularly immune checkpoint inhibitors (ICIs)—reactivates dormant antitumor immune responses to exert systemic effects. Across randomized evaluations, evidence for RT–immunotherapy superiority over standard regimens remains inconsistent, with multiple studies failing to show improvement in primary survival endpoints. This result highlights the need for the refined optimization of combinatorial strategies. In this review, we summarize the underlying mechanisms of RT–immunotherapy synergy and actionable strategies to increase therapeutic efficacy. Notably, we elaborate on the dose–immune window hypothesis, which delineates how distinct radiation doses modulate immune responses to achieve synergy with immunotherapy, and we highlight recent advances in artificial intelligence (AI) for optimizing treatment planning, patient stratification, and toxicity predictions. Overall, this review underscores the potential of RT–immunotherapy combinations and provides a framework for precision-based optimization, aiming to guide clinical practice and inspire future research in improving oncological outcomes.

## Full-text entities

- **Genes:** TLR4 (toll like receptor 4) [NCBI Gene 7099] {aka ARMD10, CD284, TLR-4, TOLL}, NT5E (5'-nucleotidase ecto) [NCBI Gene 4907] {aka CALJA, CD73, E5NT, NT, NT5, NTE}, AKT1 (AKT serine/threonine kinase 1) [NCBI Gene 207] {aka AKT, PKB, PKB-ALPHA, PRKBA, RAC, RAC-ALPHA}, Cxcl10 (C-X-C motif chemokine ligand 10) [NCBI Gene 15945] {aka C7, CRG-2, INP10, IP-10, IP10, Ifi10}, CCR7 (C-C motif chemokine receptor 7) [NCBI Gene 1236] {aka BLR2, CC-CKR-7, CCR-7, CD197, CDw197, CMKBR7}, Calr (calreticulin) [NCBI Gene 12317] {aka CRT, Calregulin}, STAT3 (signal transducer and activator of transcription 3) [NCBI Gene 6774] {aka ADMIO, ADMIO1, APRF, HIES}, TLR2 (toll like receptor 2) [NCBI Gene 7097] {aka CD282, TIL4}, IL10 (interleukin 10) [NCBI Gene 3586] {aka CSIF, GVHDS, IL-10, IL10A, TGIF}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, FCGR1A (Fc gamma receptor Ia) [NCBI Gene 2209] {aka CD64, CD64A, FCG1, FCGR1, FCRI, FcgammaRI}, AR (androgen receptor) [NCBI Gene 367] {aka AIS, AR8, DHTR, HPCX3, HUMARA, HYSP1}, BATF3 (basic leucine zipper ATF-like transcription factor 3) [NCBI Gene 55509] {aka JDP1, JUNDM1, SNFT}, LOXL2 (lysyl oxidase like 2) [NCBI Gene 4017] {aka LOR, LOR2, WS9-14}, PDCD1 (programmed cell death 1) [NCBI Gene 5133] {aka ADMIO4, AIMTBS, CD279, PD-1, PD1, SLEB2}, HLA-C (major histocompatibility complex, class I, C) [NCBI Gene 3107] {aka D6S204, HLA-JY3, HLAC, HLC-C, MHC, PSORS1}, CCL22 (C-C motif chemokine ligand 22) [NCBI Gene 6367] {aka A-152E5.1, ABCD-1, DC/B-CK, MDC, SCYA22, STCP-1}, CXCL16 (C-X-C motif chemokine ligand 16) [NCBI Gene 58191] {aka CXCLG16, SR-PSOX, SRPSOX}, CXCR3 (C-X-C motif chemokine receptor 3) [NCBI Gene 2833] {aka CD182, CD183, CKR-L2, CMKAR3, GPR9, IP10-R}, IL1B (interleukin 1 beta) [NCBI Gene 3553] {aka IL-1, IL1-BETA, IL1F2, IL1beta}, ARG1 (arginase 1) [NCBI Gene 383], NFKB1 (nuclear factor kappa B subunit 1) [NCBI Gene 4790] {aka CVID12, EBP-1, KBF1, NF-kB, NF-kB1, NF-kappa-B1}, CTLA4 (cytotoxic T-lymphocyte associated protein 4) [NCBI Gene 397286], ICAM1 (intercellular adhesion molecule 1) [NCBI Gene 3383] {aka BB2, CD54, P3.58}, MMP2 (matrix metallopeptidase 2) [NCBI Gene 4313] {aka CLG4, CLG4A, MMP-2, MMP-II, MONA, TBE-1}, STING1 (stimulator of interferon response cGAMP interactor 1) [NCBI Gene 340061] {aka ERIS, MITA, MPYS, NET23, SAVI, STING}, Itgae (integrin alpha E, epithelial-associated) [NCBI Gene 16407] {aka A530055J10, CD103, aM290, alpha-E1, alpha-M290}, TRBV20OR9-2 (T cell receptor beta variable 20/OR9-2 (non-functional)) [NCBI Gene 6962] {aka CDR3, TCRBV20S2, TCRBV2O, TCRBV2S2O}, HAO1 (hydroxyacid oxidase 1) [NCBI Gene 54363] {aka GO, GOX, GOX1, HAOX1}, Cd4 (CD4 antigen) [NCBI Gene 12504] {aka L3T4, Ly-4}, Il6 (interleukin 6) [NCBI Gene 16193] {aka Il-6}, VEGFA (vascular endothelial growth factor A) [NCBI Gene 7422] {aka L-VEGF, MVCD1, VEGF, VPF}, ATR (ATR checkpoint kinase) [NCBI Gene 545] {aka FCTCS, FRP1, MEC1, SCKL, SCKL1}, CD86 (CD86 molecule) [NCBI Gene 942] {aka B7-2, B7.2, B70, BU63, CD28LG2, CD86 v6}, CCR5 (C-C motif chemokine receptor 5) [NCBI Gene 1234] {aka CC-CKR-5, CCCKR5, CCR-5, CD195, CKR-5, CKR5}, CCL28 (C-C motif chemokine ligand 28) [NCBI Gene 56477] {aka CCK1, MEC, SCYA28}, Tgfb1 (transforming growth factor, beta 1) [NCBI Gene 21803] {aka TGF-beta1, TGFbeta1, Tgfb, Tgfb-1}, PDE5A (phosphodiesterase 5A) [NCBI Gene 8654] {aka CGB-PDE, CN5A, PDE5}, CCR2 (C-C motif chemokine receptor 2) [NCBI Gene 729230] {aka CC-CKR-2, CCR-2, CCR2A, CCR2B, CD192, CKR2}, NBN (nibrin) [NCBI Gene 4683] {aka AT-V1, AT-V2, ATV, NBS, NBS1, P95}, TFRC (transferrin receptor) [NCBI Gene 7037] {aka CD71, IMD46, T9, TFR, TFR1, TR}, CHEK1 (checkpoint kinase 1) [NCBI Gene 1111] {aka CHK1, OZEMA21}, CNGB1 (cyclic nucleotide gated channel subunit beta 1) [NCBI Gene 1258] {aka CNCG2, CNCG3L, CNCG4, CNG4, CNGB1B, GAR1}, IRF3 (interferon regulatory factor 3) [NCBI Gene 3661] {aka IIAE7}, MOK (MOK protein kinase) [NCBI Gene 5891] {aka RAGE, RAGE-1, RAGE1, STK30}, TREX1 (three prime repair exonuclease 1) [NCBI Gene 11277] {aka AGS1, CRV, DRN3, HERNS, RVCLS}, CTAG1A (cancer/testis antigen 1A) [NCBI Gene 246100] {aka CT6.1, ESO1, LAGE-2, LAGE2A, NY-ESO-1}, CTLA4 (cytotoxic T-lymphocyte associated protein 4) [NCBI Gene 1493] {aka ALPS5, CD, CD152, CELIAC3, CTLA-4, GRD4}, TGFB1 (transforming growth factor beta 1) [NCBI Gene 7040] {aka CAEND1, CED, DPD1, IBDIMDE, LAP, TGF-beta1}, CD274 (CD274 molecule) [NCBI Gene 574058] {aka PDL1}, FLNB (filamin B) [NCBI Gene 2317] {aka ABP-278, ABP-280, FH1, FLN-B, FLN1L, LRS1}, MRC1 (mannose receptor C-type 1) [NCBI Gene 4360] {aka CD206, CLEC13D, CLEC13DL, MMR, MRC1L1, bA541I19.1}, CD8A (CD8 subunit alpha) [NCBI Gene 925] {aka CD8, CD8alpha, IMD116, Leu2, p32}, CXCL11 (C-X-C motif chemokine ligand 11) [NCBI Gene 6373] {aka H174, I-TAC, IP-9, IP9, SCYB11, SCYB9B}, VCAM1 (vascular cell adhesion molecule 1) [NCBI Gene 7412] {aka CD106, INCAM-100}, CSF2 (colony stimulating factor 2) [NCBI Gene 1437] {aka CSF, GMCSF}, CGAS (cyclic GMP-AMP synthase) [NCBI Gene 115004] {aka C6orf150, D4, MB21D1, h-cGAS}, JUNB (JunB proto-oncogene, AP-1 transcription factor subunit) [NCBI Gene 3726] {aka AP-1}, CD27 (CD27 molecule) [NCBI Gene 939] {aka S152, S152. LPFS2, T14, TNFRSF7, Tp55}, PPARG (peroxisome proliferator activated receptor gamma) [NCBI Gene 5468] {aka CIMT1, FPLD3, GLM1, NR1C3, PPARG1, PPARG2}
- **Diseases:** NLR (MESH:D015467), melanoma (MESH:D008545), fibrosis (MESH:D005355), prostate cancer (MESH:D011471), inflammation (MESH:D007249), liver lesions (MESH:D008107), PDAC (MESH:C537768), mPC (MESH:D021441), pancreatic cancer (MESH:D010190), cervical cancer (MESH:D002583), pain (MESH:D010146), abdominopelvic malignancies (MESH:D009369), adenocarcinoma (MESH:D000230), thoracic disease (MESH:D013896), RP (MESH:D017564), lymphopenia (MESH:D008231), lung cancer (MESH:D008175), neurotoxicity (MESH:D020258), LARC (MESH:D012004), lung injury (MESH:D055370), HNC (MESH:D006258), castration-resistant prostate cancer (MESH:D064129), Obesity (MESH:D009765), hypoxic (MESH:D002534), gastric cancer (MESH:D013274), pneumonitis (MESH:D011014), dermatitis (MESH:D003872), specific (MESH:D000080888), thyroiditis (MESH:D013966), metabolic abnormalities (MESH:D008659), malignant pleural mesothelioma (MESH:D000086002), esophagitis (MESH:D004941), Hypoxia (MESH:D000860), medulloblastoma (MESH:D008527), NSCLC (MESH:D002289), HNSCC (MESH:D000077195), squamous cell carcinoma (MESH:D002294), lymphopenic (MESH:C565427), bone metastases (MESH:D009362), neutropenia (MESH:D009503), ICD (MESH:D003643), neurological injury (MESH:D020196), III (MESH:C537189), brain necrosis (MESH:D001927), endocrine and other (MESH:D004700), mucosal and salivary toxicity (MESH:D012466), colitis (MESH:D003092), esophageal and gastrointestinal toxicities (MESH:D005767), TABN (MESH:D016609), acidosis (MESH:D000138), AEs (MESH:D064420), nodal (MESH:D013611), vascular damage (MESH:D057772), TNBC (MESH:D064726), abdominal malignancies (MESH:D000007), mucosal injury (MESH:D052016), ALC (MESH:D009845), PAC (MESH:C537560), hepatitis (MESH:D056486), RIL (MESH:D009381)
- **Chemicals:** gold (MESH:D006046), adenosine (MESH:D000241), platinum (MESH:D010984), O2 (MESH:D010100), avelumab (MESH:C000609138), lactate (MESH:D019344), water (MESH:D014867), MnO2 (MESH:C016552), tislelizumab (MESH:C000707970), aspirin (MESH:D001241), ipilimumab (MESH:D000074324), sodium glycididazole (MESH:C000603632), cyclophosphamide (MESH:D003520), nitric oxide (MESH:D009569), bile acids (MESH:D001647), pemetrexed (MESH:D000068437), H2O2 (MESH:D006861), CA184-043 (-), carboplatin (MESH:D016190), sildenafil (MESH:D000068677), ATRA (MESH:D014212), pembrolizumab (MESH:C582435), tungsten oxide (MESH:C511604), cGAMP (MESH:C584311), capecitabine (MESH:D000069287), ursodeoxycholic acid (MESH:D014580), GSH (MESH:D005978), ATP (MESH:D000255), OH (MESH:C031356), Durvalumab (MESH:C000613593), lipid (MESH:D008055), PBS (MESH:D007854), Nivolumab (MESH:D000077594), ROS (MESH:D017382), ICE (MESH:D007053), indole (MESH:C030374), DAMP (MESH:C116255), glucose (MESH:D005947)
- **Species:** Mus musculus (house mouse, species) [taxon 10090], C. minuta [taxon 212553], Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12913551/full.md

## References

193 references — full list in the complete paper: https://tomesphere.com/paper/PMC12913551/full.md

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Source: https://tomesphere.com/paper/PMC12913551