Different pathologic responses to neoadjuvant anti-PD-1 in primary squamous lung cancer and regional lymph nodes.
Yun LingNing LiLin LiChangyuan GuoJiacong WeiPei YuanFengwei TanXiuli TaoShuhang WangZhijie WangNing WuJie WangJian-Ming YingShugeng GaoJie HePublished in: NPJ precision oncology (2020)
Neoadjuvant immunotherapy provides a unique opportunity for understanding therapeutic responses. We analyzed pathologic responses in surgical specimens obtained from 31 squamous non-small cell lung cancer (NSCLC) patients receiving neoadjuvant anti-PD-1 treatment. Fifteen (48.4%) patients achieved pathologic complete response (pCR) or major pathologic response (MPR). Among them, seven (46.7%) were assessed as radiological partial response and eight (53.3%) as stable disease. Among 20 patients with pathologically identified tumor beds in lymph nodes (LNs), 10 and six patients achieved pCR/MPR in primary tumors and paired LNs, respectively. pCR was achieved in 6/19 N1 nodes and 1/7 N2 nodes. Residual viable tumor (RVT) cells in 8/9 MPR specimens had 100% immune-activated phenotype, while a median of 80% of RVT cells in pathologic nonresponse specimens presented immune-excluded/desert phenotype. These findings demonstrated that assessment of pathologic responses in both primary tumor and LNs may be important as a surrogate for assessing neoadjuvant immunotherapeutic efficacy.
Keyphrases
- lymph node
- locally advanced
- neoadjuvant chemotherapy
- rectal cancer
- sentinel lymph node
- end stage renal disease
- ejection fraction
- newly diagnosed
- induced apoptosis
- radiation therapy
- chronic kidney disease
- small cell lung cancer
- peritoneal dialysis
- cell cycle arrest
- high grade
- oxidative stress
- patient reported outcomes
- early stage
- endoplasmic reticulum stress
- patient reported
- ultrasound guided
- pi k akt
- epidermal growth factor receptor