Abstract

Radiotherapy (RT) primarily aims to locally destroy the tumor via the induction of DNA damage in the tumor cells. However, the so-called abscopal, namely systemic and immune–mediated, effects of RT move over more and more in the focus of scientists and clinicians since combinations of local irradiation with immune therapy have been demonstrated to induce anti-tumor immunity. We here summarize changes of the phenotype and microenvironment of tumor cells after exposure to irradiation, chemotherapeutic agents, and immune modulating agents rendering the tumor more immunogenic. The impact of therapy-modified tumor cells and damage-associated molecular patterns on local and systemic control of the primary tumor, recurrent tumors, and metastases will be outlined. Finally, clinical studies affirming the bench-side findings of interactions and synergies of radiation therapy and immunotherapy will be discussed. Focus is set on combination of radio(chemo)therapy (RCT) with immune checkpoint inhibitors, growth factor inhibitors, and chimeric antigen receptor T-cell therapy. Well-deliberated combination of RCT with selected immune therapies and growth factor inhibitors bear the great potential to further improve anti-cancer therapies.

Highlights

  • The current review focuses on induction of immunogenic cancer cell death by RT and on interactions of RT with selected immune therapies to induce a long-lasting, local, and systemic tumor control

  • While NCT00461110 investigates agonistic anti-CD137 (BMS-663513) treatment in combination with chemo-radiation (RT, paclitaxel, carboplatin) in non-small cell lung carcinoma (NSCLC) patients, NTC00351325 focuses on a combination therapy of Bristol-Myers Squibb (BMS)-663513 with CT in patients suffering from recurrent ovarian carcinoma

  • One of the challenges for researchers and clinicians is to identify treatments that will overcome or bypass the cell death resistance mechanisms established by the tumor cells, and those of the microenvironment [68]

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Summary

Systemic Effects of Radiotherapy

Radiation, together with surgery and chemotherapeutics, is one of the most important tools in cancer treatment with the primary goal to achieve local control of tumor growth. Since abscopal sounds a bit mystic, one should rather term it systemic immune-mediated effects of RT nowadays Such reactions have been observed in many pre-clinical studies as well as in clinical settings for several tumor entities, including melanoma, hepatocellular, renal-cell, and mammary carcinomas, chronic lymphocytic leukemia (CLL), or malignant lymphomas [for further reading, see Ref. A combined treatment of RT with the DC growth factor Flt-3 induced immune-mediated anti-tumor responses outside the irradiation field [89]. A murine model of stereotactic body radiation therapy (SBRT) of lung cancer showed significant enhancement of tumorfree survival through intensified tumor antigen-specific CD8+ T-cell responses under RT combined with adjuvant anti-OX40 therapy [111]. While NCT00461110 investigates agonistic anti-CD137 (BMS-663513) treatment in combination with chemo-radiation (RT, paclitaxel, carboplatin) in non-small cell lung carcinoma (NSCLC) patients, NTC00351325 focuses on a combination therapy of BMS-663513 with CT (paclitaxel, carboplatin) in patients suffering from recurrent ovarian carcinoma

BMS AstraZeneca
Tumor type
Improved PFS
RCT with concurrent and adjuvant cetuximab
RTK inhibitor
Growth Factors as Targets for Cancer
Growth Factor Inhibitors and RT
Findings
Summary

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