Table 2. Eligibility criteria for study selection process according to PICOS guidelines.
| PICOS guidelines | Eligibility criteria | Exclusion criteria |
|---|---|---|
| Patients | Patients that underwent curative-intent lung surgery for NSCLC. Patients with theoretical indication of AC or patients who received AC | Patients with advanced or metastatic NSCLC were excluded |
| Articles that enrolled only patients with stage I NSCLC disease were excluded | ||
| Patients with other histologic sub-types (i.e., small-cell lung cancer, large cell neuroendocrine lung carcinoma, carcinoid tumours, malignant pleural mesothelioma and other cancers) were excluded | ||
| Intervention | AC in real-life practice | Neoadjuvant strategies and other adjuvant strategies (i.e., targeted therapies, immunotherapy, other chemotherapy regimens) were excluded |
| Other studies dealing with treatments part of the multimodal strategy (i.e., surgery, radiotherapy, concomitant or sequential chemotherapy) were excluded | ||
| Comparison | No control group defined for intervention | – |
| Outcomes | No primary or secondary endpoints were defined | – |
| Study design | Prospective or retrospective observational studies on AC use in real-life practice for resected NSCLC. As the first randomized clinical trial on AC was published in 2004, study eligibility criteria also included period of publications from 2004 to 2021 | Randomized clinical trials and sub-group analysis on AC out of the context of real-life practice were excluded |
| Reviews and meta-analysis about lung cancer and AC out of the context of real-life practice were excluded | ||
| Articles dealing with predictive and prognostic markers in lung cancer, pre-clinical studies, guidelines and case report on lung cancer were excluded |
NSCLC, non-small cell lung cancer; AC, adjuvant chemotherapy.