Combining Radiotherapy and Immunotherapy in Lung Cancer: Can We Expect Limitations Due to Altered Normal Tissue Toxicity?

Abstract

In recent decades, technical advances in surgery and radiotherapy, as well as breakthroughs in the knowledge on cancer biology, have helped to substantially improve the standard of cancer care with respect to overall response rates, progression-free survival, and the quality of life of cancer patients. In this context, immunotherapy is thought to have revolutionized the standard of care for cancer patients in the long term. For example, immunotherapy approaches such as immune checkpoint blockade are currently increasingly being used in cancer treatment, either alone or in combination with chemotherapy or radiotherapy, and there is hope from the first clinical trials that the appropriate integration of immunotherapy into standard care will raise the success rates of cancer therapy to a new level. Nevertheless, successful cancer therapy remains a major challenge, particularly in tumors with either pronounced resistance to chemotherapy and radiation treatment, a high risk of normal tissue complications, or both, as in lung cancer. Chemotherapy, radiotherapy and immunotherapy have the capacity to evoke adverse effects in normal tissues when administered alone. However, therapy concepts are usually highly complex, and it is still not clear if combining immunotherapy with radio(chemo)therapy will increase the risk of normal tissue complications, in particular since normal tissue toxicity induced by chemotherapy and radiotherapy can involve immunologic processes. Unfortunately, no reliable biomarkers are available so far that are suited to predict the unique normal tissue sensitivity of a given patient to a given treatment. Consequently, clinical trials combining radiotherapy and immunotherapy are attracting major attention, not only regarding efficacy, but also with regard to safety. In the present review, we summarize the current knowledge of radiation-induced and immunotherapy-induced effects in tumor and normal tissue of the lung, and discuss the potential limitations of combined radio-immunotherapy in lung cancer with a focus on the suspected risk for enhanced acute and chronic normal tissue toxicity.

Relationship between pneumonitis induced by immune checkpoint inhibitors and the underlying parenchymal status: a retrospective study

“…However, the first clinical data suggest that a safe and tolerable profile is maintained [2,6,23,26]. Nevertheless, it has been recently described that immunotherapy may cause an inflammatory reaction in previously irradiated area as a RP or even years after irradiation, owing to the known "recall effect" [5,[14][15][16][27][28][29]. These biological effects reinforce the interest of combined radiotherapy and immunotherapy, and could partly explain the predominant location of IP abnormalities within RT fields [2][3][4]19].…”

Vinte anos de avanços na Radioterapia Torácica

“…Ao actuar com a imunoterapia, a RT potencia alterações no microambiente tumoral, tornando -o menos imunossupressor, permitindo uma resposta mais eficaz. Pode ainda induzir o chamado efeito abscopal, que não é mais do que uma resposta sistémica (imuno--mediada) à RT 89 .…”

Evolution of the Supermodel: Progress in Modelling Radiotherapy Response in Mice

“…Humanised xenograft models involving implantation of human tissue into NODscid-g mice with injection of peripheral blood or bone marrow cells, allow for an almost complete reconstitution of the immune response, which is also a major evolution in trying to accurately recapitulate aspects of patient immune response during treatment [83]. These models are also important in the context of immune checkpoint therapies and may play a central role in optimising radioimmunotherapy combinations, an area of intense experimental and clinical research [84].…”