Patients who have had chemotherapy or radiotherapy within weeks prior to starting radiation treatment Participants who have received thoracic radiotherapy to lung fields =< weeks prior to starting the study treatment or patients who have not recovered from radiotherapy-related toxicities; for all other anatomic sites (including radiotherapy to thoracic vertebrae and ribs) radiotherapy =< weeks prior to starting the study treatment or has not recovered from radiotherapy-related toxicities; palliative radiotherapy for bone lesions =< weeks prior to starting study treatment is allowed Participants who have received radiotherapy =< weeks prior to starting study drug, and who have not recovered to grade or better from related side effects of such therapy (except alopecia and neuropathy) and/or in whom >= % of the bone marrow was irradiated Patient who has received radiotherapy =< weeks prior to starting study drug, and who has not recovered to grade or better from related side effects of such therapy (exceptions include alopecia), and/or in whom >= % of the bone marrow was irradiated Radiotherapy within one week prior to starting study treatment. Prior radiotherapy is acceptable provided the patient has recovered from any radiotherapy related acute toxicities. Prior radiotherapy is acceptable provided it was applied within four weeks before starting of this trial and the patient recovered from any radiotherapy related acute toxicities. Prior radiotherapy or radiosurgery < weeks prior to starting study treatment Thoracic radiotherapy to lung fields =< weeks prior to starting INC or patients who have not recovered from radiotherapy-related toxicities; for all other anatomic sites (including radiotherapy to thoracic vertebrae and ribs), radiotherapy =< weeks prior to starting INC or patients who have not recovered from radiotherapy-related toxicities; palliative radiotherapy for bone lesions =< weeks prior to starting INC is allowed Patients who have received radiotherapy =< weeks prior to starting study drugs, with exception of palliative radiotherapy, who have not recovered from side effects of such therapy to baseline or grade =< and/or from whom >= % of the bone marrow was irradiated Radiotherapy =< days prior to enrollment; patients must have recovered from all radiotherapy-related toxicities Patients who have had radiotherapy =< weeks prior to starting study drug, or who have not recovered from radiotherapy toxicities Patient who has received thoracic radiotherapy to lung fields =< weeks prior to starting the study treatment or patients who have not recovered from radiotherapyrelated toxicities; for all other anatomic sites (including radiotherapy to thoracic vertebrae and ribs) radiotherapy =< weeks prior to starting the study treatment or has not recovered from radiotherapyrelated toxicities; palliative radiotherapy for bone lesions =< weeks prior to starting study treatment is allowed Patients who have had radiotherapy ? weeks prior to starting study drug, or who have not recovered from radiotherapy toxicities CAPMATINIB EXCLUSION CRITERIA: Prior treatment with the following antineoplastic therapies within the following time frame:\r\n* Any prior treatment with capmatinib, crizotinib, or any other cMET or HGF inhibitor\r\n* Thoracic radiotherapy to lung fields =< weeks prior to starting capmatinib; for all other anatomic sites (including radiotherapy to thoracic vertebrae and ribs), radiotherapy =< weeks prior to starting capmatinib; palliative radiotherapy for bone lesions =< weeks prior to starting capmatinib is allowed\r\n* Receipt of any anticancer or investigational agent within weeks or =< half-lives of the agent (whichever is longer) prior to the first dose of capmatinib; if previous treatment is a monoclonal antibody, then the treatment must be discontinued at least weeks before the first dose of capmatinib CERITINIB EXCLUSION CRITERIA: Prior treatment with the following antineoplastic therapies within the following time frame:\r\n* Any prior treatment with ceritinib\r\n* Radiotherapy to lung fields =< weeks prior to starting ceritinib; for all other anatomic sites (including radiotherapy to thoracic vertebrae and ribs), radiotherapy =< weeks prior to starting ceritinib; palliative radiotherapy for bone lesions =< weeks prior to starting ceritinib is allowed\r\n* Receipt of any cytotoxic chemotherapy, biologic agent, or investigational agent within weeks prior to the first dose of study drug (within weeks for nitrosoureas, mitomycin C or liposomal doxorubicin) Patient who has received thoracic radiotherapy to lung fields =< weeks prior to starting the study treatment or patients who have not recovered from radiotherapy-related toxicities; for all other anatomic sites (including radiotherapy to thoracic vertebrae and ribs) radiotherapy =< weeks prior to starting the study treatment or has not recovered from radiotherapy-related toxicities; palliative radiotherapy for bone lesions =< weeks prior to starting study treatment is allowed Patient who has received thoracic radiotherapy to lung fields =< weeks prior to starting the study treatment or patients who have not recovered from radiotherapy-related toxicities; for all other anatomic sites (including radiotherapy to thoracic vertebrae and ribs) radiotherapy =< weeks prior to starting the study treatment or has not recovered from radiotherapy-related toxicities; palliative radiotherapy for bone lesions =< weeks prior to starting study treatment is allowed Patients who have had radiotherapy =< weeks prior to starting study drug, or =< weeks prior to starting study drug in the case of localized radiotherapy (e.g., for analgesic purpose or for lytic lesions at risk of fracture) Thoracic radiotherapy to lung fields ? weeks prior to starting INC or patients who have not recovered from radiotherapy-related toxicities Radiotherapy ? weeks prior to randomization. Patients must have recovered from all radiotherapy-related toxicities. Patients who have received radiotherapy =< weeks prior to starting study drugs, with exception of palliative radiotherapy, who have not recovered from side effects of such therapy to baseline or grade =< and/or from whom >= % of the bone marrow was irradiated Patients who have received radiotherapy =< weeks prior to starting study treatment and/or from whom >= % of the bone marrow was irradiated as determined by the investigator Patients must be >= weeks beyond treatment with any chemotherapy or radiotherapy, and must have recovered to =< grade toxicity for any treatment-limiting toxicity of prior therapy; (exception: patients may have received palliative low dose radiotherapy to the limbs - weeks before this therapy provided pelvis, ribs, sternum, scapulae, vertebrae or skull were not included in the radiotherapy field); also, patients who have received non-chemotherapeutic biologic agents will need to wait at least five half-lives or four weeks, whichever is shorter, from the last day of treatment; exception: no washout of cetuximab or regorafenib is required for patients who have received prior cetuximab or regorafenib and have recovered from any treatment-related toxicities to grade =< Patients who have received radiotherapy =< weeks prior to registration, with the exception of palliative radiotherapy, who have not recovered from side effects of such therapy to baseline or grade =< and/or from whom >= % of the bone marrow was irradiated are not eligible for participation Last radiotherapy treatment >= weeks prior to starting treatment with this protocol and there must be sites of measurable disease that did not receive radiation Patients who have received radiotherapy =< weeks prior to starting treatment Radiotherapy within days before the first dose of study treatment (within weeks if given as palliation to bone metastases, if recovered from all toxicities) Radiotherapy prior to initiation of therapy is allowed to a limited area (e.g., palliative treatment for painful bone metastases), if it is not the sole site of disease; subjects must have completed treatment at least one week prior to starting study drugs, and must have recovered from all treatment-related toxicities Any radiotherapy within week of starting treatment on protocol Radiotherapy within weeks prior to study registration. Subjects must have recovered from all therapy-related toxicities. Patients who have received definitive radiotherapy ? weeks prior to starting study drug, who have not recovered from side effects of such therapy and/or from whom ? % of the bone marrow was irradiated. Patients who have had radiotherapy =< weeks prior to starting study drug, or =< weeks prior to starting study drug in the case of localized radiotherapy (e.g. for analgesic purpose or for lytic lesions at risk of fracture), or who have not recovered from radiotherapy toxicities Last radiotherapy treatment weeks prior to starting treatment with this protocol with the exception of palliative radiotherapy and there must be sites of measurable disease that did not receive radiation Patient who has received thoracic radiotherapy to lung fields =< weeks prior to starting the study treatment or patients who have not recovered from radiotherapy-related toxicities; for all other anatomic sites (including radiotherapy to thoracic vertebrae and ribs) radiotherapy =< weeks prior to starting the study treatment or has not recovered from radiotherapy-related toxicities; palliative radiotherapy for bone lesions =< weeks prior to starting study treatment is allowed Radiotherapy (external beam or CyberKnife) =< days prior to starting study drug, or =< days prior to study registration in the case of localized radiotherapy (e.g. for analgesic purpose or for lytic lesions at risk of fracture), or who have not recovered from radiotherapy toxicities