Literature DB >> 34524205

Prediction Model for Tumor Volume Nadir in EGFR-mutant NSCLC Patients Treated With EGFR Tyrosine Kinase Inhibitors.

Mizuki Nishino1, Junwei Lu, Takuya Hino, Natalie I Vokes, Pasi A Jänne, Hiroto Hatabu, Bruce E Johnson.   

Abstract

PURPOSE: In patients with advanced non-small cell lung cancer (NSCLC) and oncogenic driver mutations treated with effective targeted therapy, a characteristic pattern of tumor volume dynamics with an initial regression, nadir, and subsequent regrowth is observed on serial computed tomography (CT) scans. We developed and validated a linear model to predict the tumor volume nadir in EGFR-mutant advanced NSCLC patients treated with EGFR tyrosine kinase inhibitors (TKI).
MATERIALS AND METHODS: Patients with EGFR-mutant advanced NSCLC treated with EGFR-TKI as their first EGFR-directed therapy were studied for CT tumor volume kinetics during therapy, using a previously validated CT tumor measurement technique. A linear regression model was built to predict tumor volume nadir in a training cohort of 34 patients, and then was validated in an independent cohort of 84 patients.
RESULTS: The linear model for tumor nadir prediction was obtained in the training cohort of 34 patients, which utilizes the baseline tumor volume before initiating therapy (V0) to predict the volume decrease (mm3) when the nadir volume (Vp) was reached: V0-Vp=0.717×V0-1347 (P=2×10-16; R2=0.916). The model was tested in the validation cohort, resulting in the R2 value of 0.953, indicating that the prediction model generalizes well to another cohort of EGFR-mutant patients treated with EGFR-TKI. Clinical variables were not significant predictors of tumor volume nadir.
CONCLUSION: The linear model was built to predict the tumor volume nadir in EGFR-mutant advanced NSCLC patients treated with EGFR-TKIs, which provide an important metrics in treatment monitoring and therapeutic decisions at nadir such as additional local abrasive therapy.
Copyright © 2021 Wolters Kluwer Health, Inc. All rights reserved.

Entities:  

Year:  2021        PMID: 34524205      PMCID: PMC8920948          DOI: 10.1097/RTI.0000000000000615

Source DB:  PubMed          Journal:  J Thorac Imaging        ISSN: 0883-5993            Impact factor:   3.000


  34 in total

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Authors:  Kathryn A Gold; Edward S Kim; J Jack Lee; Ignacio I Wistuba; Carol J Farhangfar; Waun Ki Hong
Journal:  Cancer Prev Res (Phila)       Date:  2011-07

Review 2.  SBRT for oligoprogressive oncogene addicted NSCLC.

Authors:  L Basler; S G C Kroeze; M Guckenberger
Journal:  Lung Cancer       Date:  2017-02-06       Impact factor: 5.705

3.  Erlotinib versus chemotherapy as first-line treatment for patients with advanced EGFR mutation-positive non-small-cell lung cancer (OPTIMAL, CTONG-0802): a multicentre, open-label, randomised, phase 3 study.

Authors:  Caicun Zhou; Yi-Long Wu; Gongyan Chen; Jifeng Feng; Xiao-Qing Liu; Changli Wang; Shucai Zhang; Jie Wang; Songwen Zhou; Shengxiang Ren; Shun Lu; Li Zhang; Chengping Hu; Chunhong Hu; Yi Luo; Lei Chen; Ming Ye; Jianan Huang; Xiuyi Zhi; Yiping Zhang; Qingyu Xiu; Jun Ma; Li Zhang; Changxuan You
Journal:  Lancet Oncol       Date:  2011-07-23       Impact factor: 41.316

4.  Volumetric Tumor Response and Progression in EGFR-mutant NSCLC Patients Treated with Erlotinib or Gefitinib.

Authors:  Mizuki Nishino; Suzanne E Dahlberg; Linnea E Fulton; Subba R Digumarthy; Hiroto Hatabu; Bruce E Johnson; Lecia V Sequist
Journal:  Acad Radiol       Date:  2016-01-08       Impact factor: 3.173

Review 5.  Optimal management of EGFR-mutant non-small cell lung cancer with disease progression on first-line tyrosine kinase inhibitor therapy.

Authors:  Bin-Chi Liao; Chia-Chi Lin; Jih-Hsiang Lee; James Chih-Hsin Yang
Journal:  Lung Cancer       Date:  2017-05-11       Impact factor: 5.705

Review 6.  State of the art: Response assessment in lung cancer in the era of genomic medicine.

Authors:  Mizuki Nishino; Hiroto Hatabu; Bruce E Johnson; Theresa C McLoud
Journal:  Radiology       Date:  2014-04       Impact factor: 11.105

7.  Osimertinib Plus Durvalumab versus Osimertinib Monotherapy in EGFR T790M-Positive NSCLC following Previous EGFR TKI Therapy: CAURAL Brief Report.

Authors:  James Chih-Hsin Yang; Frances A Shepherd; Dong-Wan Kim; Gyeong-Won Lee; Jong Seok Lee; Gee-Chen Chang; Sung Sook Lee; Yu-Feng Wei; Yun Gyoo Lee; Gianluca Laus; Barbara Collins; Francesca Pisetzky; Leora Horn
Journal:  J Thorac Oncol       Date:  2019-02-11       Impact factor: 15.609

8.  Osimertinib in Untreated EGFR-Mutated Advanced Non-Small-Cell Lung Cancer.

Authors:  Jean-Charles Soria; Yuichiro Ohe; Johan Vansteenkiste; Thanyanan Reungwetwattana; Busyamas Chewaskulyong; Ki Hyeong Lee; Arunee Dechaphunkul; Fumio Imamura; Naoyuki Nogami; Takayasu Kurata; Isamu Okamoto; Caicun Zhou; Byoung Chul Cho; Ying Cheng; Eun Kyung Cho; Pei Jye Voon; David Planchard; Wu-Chou Su; Jhanelle E Gray; Siow-Ming Lee; Rachel Hodge; Marcelo Marotti; Yuri Rukazenkov; Suresh S Ramalingam
Journal:  N Engl J Med       Date:  2017-11-18       Impact factor: 91.245

9.  Osimertinib or Platinum-Pemetrexed in EGFR T790M-Positive Lung Cancer.

Authors:  Tony S Mok; Yi-Long Wu; Myung-Ju Ahn; Marina C Garassino; Hye R Kim; Suresh S Ramalingam; Frances A Shepherd; Yong He; Hiroaki Akamatsu; Willemijn S M E Theelen; Chee K Lee; Martin Sebastian; Alison Templeton; Helen Mann; Marcelo Marotti; Serban Ghiorghiu; Vassiliki A Papadimitrakopoulou
Journal:  N Engl J Med       Date:  2016-12-06       Impact factor: 91.245

10.  Diffuse Lung Metastases in EGFR-Mutant Non-Small Cell Lung Cancer.

Authors:  Subba R Digumarthy; Dexter P Mendoza; Atul Padole; Tianqi Chen; P Gabriel Peterson; Zofia Piotrowska; Lecia V Sequist
Journal:  Cancers (Basel)       Date:  2019-09-13       Impact factor: 6.639

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