Clinical data included sex, age, marital status, smoking status, type of medical insurance, pathological type, clinical stage, metastatic sites, distal metastasis, performance status (PS) score, first-line chemotherapy drugs, antiangiogenic drugs, therapeutic effects evaluated after first-line chemotherapy, MT regimen (targeted and anti-angiogenic drugs, chemotherapy with one drug), complications during chemotherapy, and follow-up information. Patients with stable or responsive stage IIIB/IV NSCLC were also classified into the MT and non-MT groups according to whether they received MT or not after 4–6 cycles of first-line chemotherapy.
By reviewing the hospital clinical records, as well as messages and telephone follow-up, tumor response and complications were analyzed until the end of December 31, 2019. The endpoints comprised the PFS calculated from the first dose until disease progression, and OS calculated from the initial diagnosis to death or the end of follow-up, which are expressed on a monthly basis.
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