In this editorial we will discuss several interesting and timely topics which are relevant for current thoracic oncological practice. First, we will address epidermal growth factor receptor (EGFR) mutations and resistance, followed by ground glass opacities (GGO), current diagnostic assessment tools including patient derived organoids (PDO), assessment of circulating tumour DNA (ctDNA) and circulation tumour cells (CTC). Finally, we will also address a complex case of delayed extensive chest wall infection following a lobectomy via thoracotomy.The treatment of advanced non-small cell lung cancer (NSCLC) has traditionally been via the systemic administration of platinum-based chemotherapy. Overall survival (OS) is poor with only 33% at 1 year and 11% at 2 years (1). With the discovery of EGFR mutations, new treatment pathways emerged. These mutations are primarily found in lung cancer with an adenocarcinoma component, non-squamous NSCLC, young Asian women (<50 years) and non or light smokers (2). In these patients, if systemic treatment is considered, molecular testing including EGFR mutations need to be assessed. Selective tyrosine kinase inhibitors (TKI) of EGFR (EGFR-TKI) were developed to target EGFR mutation harbouring NCSLC. Via EGFR stimulation, the tyrosine kinase (TK) pathway has a role in cell proliferation and migration, apoptosis evasion, and angiogenesis pathways. In case of EGFR mutated NSCLC activation, this will lead to overstimulation of the EGFR and cause tumour growth.Initial first generation inhibitors of the EGFR-TK pathway, in the form of gefitinib, erlotinib and icotinib were promising. Monotherapy with gefitinib showed an overall response rate (ORR) of 71.2% vs. 47.3% when compared to platinum-based chemotherapy as demonstrated in the IPASS trial (3). Yet the ORR in the population lacking an EGFR mutation was a mere 1.1% (gefinitib group) vs. 23.5% (carboplatin-paclitaxel group). In the WJTOG345 trial, gefitinib was compared to docetaxel and cisplatin in patients with EGFR mutated NSCLC, demonstrating an ORR of 62.1% vs. 32.2% (4). Erlotinib, another first generation EGFR-TKI has been used in the first-line treatment for EGFR mutated NSCLC patients. It showed a progressionfree survival (PFS) of 8.0-13.1 months compared to 4.6-6.9 months in the platinum-based chemotherapy (5).