Role of MPR as an Early Signal for Efficacy in Neoadjuvant Studies

Clin Cancer Res. 2020 Jul 15;26(14):3499-3500. doi: 10.1158/1078-0432.CCR-20-1129. Epub 2020 May 4.

Abstract

Overall survival and disease-free survival have been the gold standard primary endpoints for neoadjuvant clinical trials. Major pathologic response is a clinically proven surrogate of efficacy and when used as the primary endpoint, can allow for more efficient evaluation of drugs in the neoadjuvant setting.See related article by Cascone et al., p. 3525.

Publication types

  • Research Support, Non-U.S. Gov't
  • Comment

MeSH terms

  • Carcinoma, Non-Small-Cell Lung*
  • Cisplatin
  • Docetaxel
  • Humans
  • Indoles
  • Lung Neoplasms*
  • Neoadjuvant Therapy

Substances

  • Indoles
  • Docetaxel
  • nintedanib
  • Cisplatin