AI Article Synopsis

  • This study examined how the histologic type of non-small cell lung cancer (NSCLC) affects survival and recurrence rates in stage II and III patients.
  • A total of 2155 patients were analyzed, revealing that those with squamous cell carcinoma (SqCC) had better rates of freedom from recurrence compared to those with adenocarcinoma (ADC).
  • Although ADC patients had a slightly better overall survival at the five-year mark, the difference was not statistically significant, and SqCC patients faced higher non-lung cancer mortality and shorter time from recurrence to death.

Article Abstract

Objectives: This study aimed to investigate the clinical impact of histologic type on the survival and recurrence outcomes of patients with stage II and III non-small cell lung cancer (NSCLC).

Materials And Methods: A total of 2155 consecutive adult patients who underwent complete resection of stage II and III NSCLC between 2008 and 2018 were enrolled. The primary endpoints were freedom from recurrence (FFR) and overall survival (OS). The secondary endpoint was the time to lung cancer or non-lung cancer death.

Results: Of the 2155 patients, 1436 (66.6 %) had adenocarcinoma (ADC) and 719 (33.4 %) had squamous cell carcinoma (SqCC). Patients with SqCC had better FFR than those with ADC (stage II, p < 0.001; stage III, p < 0.001). Although patients with ADC showed a slightly better OS until 5 years than those with SqCC, the difference was insignificant (stage II, p = 0.292; stage III, p = 0.196). Patients with SqCC had higher rates of non-lung cancer death than patients with ADC (stage II, p < 0.001; stage III, p = 0.039). The time from lung cancer recurrence to death was shorter in patients with SqCC than in those with ADC (stage II, median 13 vs 37 months, p < 0.001; stage III, median 11 vs 26 months, p < 0.001).

Conclusions: In stage II and III NSCLC, ADC had a higher risk of recurrence than SqCC, with no difference in OS. These results were related to significant differences in non-lung cancer mortality and recurrence-to-death time between the two histologic types.

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Source
http://dx.doi.org/10.1016/j.lungcan.2022.12.008DOI Listing

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