BPB Reports

Paper Details

BPB Reports
Vol. 6 No. 5 p.172-174 2023
Report
Thyroid Transcription Factor-1 as a Potential Hematologic Toxicity Indicator for the Three-Drug Combination Regimen of Carboplatin, Pemetrexed, and Pembrolizumab in Patients with Advanced Recurrent Non-Squamous Non-Small Cell Lung Cancer
  • Takayoshi Maiguma (Graduate school of Clinical Pharmacy, Shujitsu University / Department of Pharmaceutical Care and Health Sciences, School of Pharmacy, Shujitsu University / maiguma@shujitsu.ac.jp)
Shoma Mori 1) 2) , Takayoshi Maiguma 2) 3) , Keisuke Yoshii 3) , Hikari Hashimoto 3) , Atsushi Komoto 3) , Yuto Haruki 1) , Tetsuhiro Sugiyama 1) , Kenichi Shimada 2) 3)
1) Department of Pharmacy, Tsuyama Chuo Hospital , 2) Graduate school of Clinical Pharmacy, Shujitsu University , 3) Department of Pharmaceutical Care and Health Sciences, School of Pharmacy, Shujitsu University
Received: July 27, 2023;   Accepted: October 16, 2023;   Released: October 26, 2023
Keywords: thyroid transcription factor-1, immune checkpoint inhibitors, adverse events
Abstracts

Thyroid transcription factor-1 (TTF-1) expression in patients with non-squamous non-small cell lung cancer (NS-NSCLC) is reportedly useful in selecting treatment regimens and predicting life expectancy. However, only a few studies have reported the association between TTF-1 expression and the efficacy of the current first-line regimens containing immune checkpoint inhibitors. It is unclear whether TTF-1 can be a hematologic toxicity indicator in patients receiving these treatment regimens. Patients who received the three-drug combination regimen of carboplatin, pemetrexed, and pembrolizumab, i.e., KEYNOTE-189, between April 2019 and December 2021 at Tsuyama Chuo Hospital and who had known TTF-1 expression were retrospectively studied using electronic medical records. Among the seven patients included, four patients were TTF-1 positive, while three were TTF-1 negative. TTF-1-positive patients showed a trend toward improved progression-free survival and were more likely to experience thrombocytopenia than the TTF-1-negative patients. These results suggest that TTF-1 expression in patients with NS-NSCLC could play a role in determining both treatment efficiency and hematologic toxicity.