@article{1453b4f6d6e34e6ab8f14e077cb096d0,
title = "Pathologic Assessment After Neoadjuvant Chemotherapy for NSCLC: Importance and Implications of Distinguishing Adenocarcinoma From Squamous Cell Carcinoma",
abstract = "Introduction: Major pathologic response after neoadjuvant chemotherapy (NAC) for NSCLC has been defined as 10% or less residual viable tumor without distinguishing between histologic types. We sought to investigate whether the optimal cutoff percentage of residual viable tumor for predicting survival differs between lung adenocarcinoma (ADC) and squamous cell carcinoma (SCC). Methods: Tumor slides from 272 patients treated with NAC and surgery for clinical stage II-III NSCLC (ADC, n = 192; SCC, n = 80) were reviewed. The optimal cutoff percentage of viable tumor for predicting lung cancer–specific cumulative incidence of death (LC-CID) was determined using maximally selected rank statistics. LC-CID was analyzed using a competing-risks approach. Overall survival was evaluated using Kaplan-Meier methods and Cox proportional hazard analysis. Results: Patients with SCC had a better response to NAC (median percentage of viable tumor: SCC versus ADC, 40% versus 60%; p = 0.027). Major pathologic response (≤10% viable tumor) was observed in 26% of SCC cases versus 12% of ADC cases (p = 0.004). The optimal cutoff percentage of viable tumor for LC-CID was 10% for SCC and 65% for ADC. On multivariable analysis, viable tumor 10% or less was an independent factor for better LC-CID (p = 0.035) in patients with SCC; in patients with ADC, viable tumor 65% or less was a factor for better LC-CID (p = 0.033) and overall survival (p = 0.050). Conclusions: In response to NAC, the optimal cutoff percentage of viable tumor for predicting survival differs between ADC and SCC. Our findings have implications for the pathologic assessment of resected specimens, especially in upcoming clinical trials design.",
keywords = "NSCLC, Neoadjuvant chemotherapy, Pathologic response, Prognosis, Viable tumor",
author = "Yang Qu and Katsura Emoto and Takashi Eguchi and Aly, {Rania G.} and Hua Zheng and Chaft, {Jamie E.} and Tan, {Kay See} and Jones, {David R.} and Kris, {Mark G.} and Adusumilli, {Prasad S.} and Travis, {William D.}",
note = "Funding Information: R01 CA217169, NIH, National Institutes of Health, 100000002, R01CA236615, NIH, National Institutes of Health, 100000002, P30 CA008748, NIH, National Institutes of Health, 100000002, BC132124, NIH, National Institutes of Health, 100000002, LC160212, NIH, National Institutes of Health, 100000002, CA170630, NIH, National Institutes of Health, 100000002, Dr. Adusumilli's laboratory work is supported by grants from the National Institutes of Health (R01 CA217169, R01CA236615, and P30 CA008748), the U.S. Department of Defense (BC132124, LC160212, and CA170630), the Joanne and John DallePezze Foundation, the Derfner Foundation, and the Mr. William H. Goodwin and Alice Goodwin, the Commonwealth Foundation for Cancer Research, and the Experimental Therapeutics Center of Memorial Sloan Kettering Cancer Center. The authors thank Joe Dycoco of the MSK Thoracic Surgery Service for his help with the Thoracic Service lung cancer database and David Sewell of the Memorial Sloan Kettering Thoracic Surgery Service for editorial assistance., Disclosure: Dr. Chaft has received grants from Astra Zeneca, Genentech, and Bristol-Myers Squibb; and had received personal fees from Astra Zeneca, Merck, Genentech, and Bristol-Myers Squibb. Dr. Kris has received personal fees from Astra Zeneca, Pfizer, and Regeneron. Dr. Adusumilli has received grants from the National Institutes of Health the U.S. Department of Defense, the Joanne and John DallePezze Foundation, the Derfner Foundation, and the Mr. William H. Goodwin and Alice Goodwin, the Commonwealth Foundation for Cancer Research, and the Experimental Therapeutics Center of Memorial Sloan Kettering Cancer Center. Dr. Travis has been a nonpaid consultant for Genentech. The remaining authors declare no conflict of interest. Funding Information: Dr. Adusumilli{\textquoteright}s laboratory work is supported by grants from the National Institutes of Health ( R01 CA217169 , R01CA236615 , and P30 CA008748 ), the U.S. Department of Defense ( BC132124 , LC160212 , and CA170630 ), the Joanne and John DallePezze Foundation, the Derfner Foundation, and the Mr. William H. Goodwin and Alice Goodwin, the Commonwealth Foundation for Cancer Research, and the Experimental Therapeutics Center of Memorial Sloan Kettering Cancer Center. The authors thank Joe Dycoco of the MSK Thoracic Surgery Service for his help with the Thoracic Service lung cancer database and David Sewell of the Memorial Sloan Kettering Thoracic Surgery Service for editorial assistance. Publisher Copyright: {\textcopyright} 2018 International Association for the Study of Lung Cancer",
year = "2019",
month = mar,
doi = "10.1016/j.jtho.2018.11.017",
language = "English",
volume = "14",
pages = "482--493",
journal = "Journal of Thoracic Oncology",
issn = "1556-0864",
publisher = "International Association for the Study of Lung Cancer",
number = "3",
}