A nomogram to predict radiation pneumonitis, derived from a combined analysis of rtog 9311 and institutional data

被引:133
作者
Bradley, Jeffrey D.
Hope, Andrew
El Naqa, Issam
Apte, Aditya
Lindsay, Patricia E.
Bosch, Walter
Matthews, John
Sause, Wrlliam
Graham, Mary V.
Deasy, Joseph O.
机构
[1] Washington Univ, Sch Med, Dept Radiat Oncol, St Louis, MO 63110 USA
[2] Washington Univ, Sch Med, Image Guided Therapy QA Ctr, St Louis, MO 63110 USA
[3] Alvin J Siteman Canc Ctr, St Louis, MO USA
[4] Univ Texas, MD Anderson Canc Ctr, Dept Radiat Phys, Houston, TX 77030 USA
[5] LDS Hosp, Dept Radiat Oncol, Salt Lake City, UT USA
[6] Phelps Cty Reg Hosp, Dept Radiat Oncol, Rolla, MO USA
来源
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS | 2007年 / 69卷 / 04期
关键词
radiation pneumonitis; RTOG; 9311; nomogram;
D O I
10.1016/j.ijrobp.2007.04.077
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: To test the Washington University (WU) patient dataset, analysis of which suggested that superior-to-inferior tumor position, maximum dose, and D35 (minimum dose to the hottest 35% of the lung volume) were valuable to predict radiation pneumonitis (PP), against the patient database from Radiation Therapy Oncology Group (RTOG) trial 9311. Methods and Materials: The entire dataset consisted of 324 patients receiving definitive conformal radiotherapy for non-small-cell lung cancer (WU = 219, RTOG 9311 = 129). Clinical, dosimetric, and tumor location parameters were modeled to predict RP in the individual datasets and in a combined dataset. Association quality with RP was assessed using Spearman's rank correlation (r) for univariate analysis and multivariate analysis; comparison between subgroups was tested using the Wilcoxon rank sum test. Results: The WU model to predict RP performed poorly for the RTOG 9311 data. The most predictive model in the RTOG 9311 dataset was a single-parameter model, D15 (r = 0.28). Combining the datasets, the best derived model was a two-parameter model consisting of mean lung dose and superior-to-inferior gross tumor volume position (r = 0.303). An equation and nomogram to predict the probability of RP was derived using the combined patient population. Conclusions: Statistical models derived from a large pool of candidate models resulted in well-tuned models for each subset (WU or RTOG 9311), which did not perform well when applied to the other dataset. However, when the data were combined, a model was generated that performed well on each data subset. The final model incorporates two effects: greater risk due to inferior lung irradiation, and greater risk for increasing normal lung mean dose. This formula and nomogram may aid clinicians during radiation treatment planning for lung cancer. (c) 2007 Elsevier Inc.
引用
收藏
页码:985 / 992
页数:8
相关论文
共 15 条
  • [1] Toxicity and outcome results of RTOG 9311: A phase I-II dose-escalation study using three-dimensional conformal radiotherapy in patients with inoperable non-small-cell lung carcinoma
    Bradley, J
    Graham, MV
    Winter, K
    Purdy, JA
    Komaki, R
    Roa, WH
    Ryu, JK
    Bosch, W
    Emami, B
    [J]. INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 2005, 61 (02): : 318 - 328
  • [2] CERR: A computational environment for radiotherapy research
    Deasy, JO
    Blanco, AI
    Clark, VH
    [J]. MEDICAL PHYSICS, 2003, 30 (05) : 979 - 985
  • [3] Multivariable modeling of radiotherapy outcomes, including dose-volume and clinical factors
    El Naqa, I
    Bradley, J
    Blanco, AI
    Lindsay, PE
    Vicic, M
    Hope, A
    Deasy, JO
    [J]. INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 2006, 64 (04): : 1275 - 1286
  • [4] Dose-volume histogram analysis as predictor of radiation pneumonitis in primary lung cancer patients treated with radiotherapy
    Fay, M
    Tan, A
    Fisher, R
    Mac Manus, M
    Wirth, A
    Ball, D
    [J]. INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 2005, 61 (05): : 1355 - 1363
  • [5] Clinical dose-volume histogram analysis for pneumonitis after 3D treatment for non-small cell lung cancer (NSCLC)
    Graham, MV
    Purdy, JA
    Emami, B
    Harms, W
    Bosch, W
    Lockett, MA
    Perez, CA
    [J]. INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 1999, 45 (02): : 323 - 329
  • [6] SOUTHWEST-ONCOLOGY-GROUP STANDARD RESPONSE CRITERIA, END-POINT DEFINITIONS AND TOXICITY CRITERIA
    GREEN, S
    WEISS, GR
    [J]. INVESTIGATIONAL NEW DRUGS, 1992, 10 (04) : 239 - 253
  • [7] Radiation-induced pulmonary toxicity: A dose-volume histogram analysis in 201 patients with lung cancer
    Hernando, ML
    Marks, LB
    Bentel, GC
    Zhou, SM
    Hollis, D
    Das, SK
    Fan, M
    Munley, MT
    Shafman, TD
    Anscher, MS
    Lind, PA
    [J]. INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 2001, 51 (03): : 650 - 659
  • [8] Modeling radiation pneumonitis risk with clinical, dosimetric, and spatial parameters
    Hope, Andrew J.
    Lindsay, Patricia E.
    El Naqa, Issam
    Alaly, James R.
    Vicic, Milos
    Bradley, Jeffrey D.
    Deasy, Joseph O.
    [J]. INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 2006, 65 (01): : 112 - 124
  • [9] Final toxicity results of a radiation-dose escalation study in patients with non-small-cell lung cancer (NSCLC): Predictors for radiation pneumonitis and fibrosis
    Kong, Feng-Ming
    Hayman, James A.
    Griffith, Kent A.
    Kalemkerian, Gregory P.
    Arenberg, Douglas
    Lyons, Susan
    Turrisi, Andrew
    Lichter, Allen
    Fraass, Benedick
    Eisbruch, Avraham
    Lawrence, Theodore S.
    Ten Haken, Randall K.
    [J]. INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 2006, 65 (04): : 1075 - 1086
  • [10] Radiation pneumonitis as a function of mean lung dose: An analysis of pooled data of 540 patients
    Kwa, SLS
    Lebesque, JV
    Theuws, JCM
    Marks, LB
    Munley, MT
    Bentel, G
    Oetzel, D
    Spahn, U
    Ten Haken, RK
    Drzymala, RE
    Purdy, JA
    Lichter, AS
    Martel, MK
    TEN Haken, RK
    [J]. INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 1998, 42 (01): : 1 - 9