Radiotherapy Strategies for Use in Combined Treatment of Small-cell Lung Cancer

Inclusion criteria

• Histopathological confirmation of small cell lung cancer based on histological or cytological examination.
• Primary clinical stage: Extensive stage of the disease according to VASLG classification or stage IV according to TNM classification.
• Eastern Cooperative Oncology Group (ECOG) performance status 0-2 prior to randomization.
• Partial response (PR) or stable disease (SD) to platinum-based doublet chemotherapy with durvalumab or atezolizumab based on restaging (positron emission tomography [PET]/computed tomography [CT] or CT or magnetic resonance imaging [MRI]).
• Ability to undergo radiotherapy at a total dose of 45 Gy in 15 daily fractions of 3 Gy to the chest area and a total dose of 24 Gy administered in single fractions every 2-3 days of 8 Gy to the metastatic lesions.
• Clinical control of brain metastases (prior whole-brain irradiation at any stage is acceptable before study entry).
• Measurable residual disease after chemioimmunotherapy (according to RECIST 1.1 solid tumor response assessment criteria) or in case of CR/PR presence of tumor lesions not classified as measurable.
• Volume and number (up to 10) of metastatic lesions allowing for radiotherapy in doses according to the study protocol.
• Absence of clinically significant and uncontrolled co-morbidities with pharmacological treatment.
• Absence of active autoimmune diseases except for diabetes, hypothyroidism, psoriasis, eczema, lichen planus, and vitiligo.
• Adequate hematopoietic function allowing treatment with atezolizumab or durvalumab, according to the current SmPC (Summary of Product Characteristics).
• Renal and hepatic function allowing treatment according to the current SmPC for atezolizumab or durvalumab.

Exclusion criteria

• Age under 18 years old.
• Premenopausal women who do not accept the need for effective contraception during radiotherapy and/or chemotherapy/immunotherapy.
• Individuals excluded from participation in a medical experiment based on Article 23A(1) of the Act on the Profession of Physician and Pharmacist.
• Coexistence of other uncontrolled malignant neoplasms.
• Contraindications to the use of atezolizumab or durvalumab as specified in the SmPC.
• Grade 2 or greater CTCAE v.5 pneumonitis secondary to immunotherapy.
• Participation in another clinical trial during the study.
• Prior chest radiotherapy that precludes safe administration of radiotherapy according to the study protocol. Prior palliative radiotherapy to metastatic sites is acceptable before study entry if clinically indicated as determined by the physician.
• Contraindications to radiotherapy according to the approved protocol.