Kwa S L, Lebesque J V, Theuws J C, Marks L B, Munley M T, Bentel G, Oetzel D, Spahn U, Graham M V, Drzymala R E, Purdy J A, Lichter A S, Martel M K, Ten Haken R K
Department of Radiotherapy, The Netherlands Cancer Institute/Antoni van Leeuwenhoek Huis, Amsterdam.
Int J Radiat Oncol Biol Phys. 1998 Aug 1;42(1):1-9. doi: 10.1016/s0360-3016(98)00196-5.
To determine the relation between the incidence of radiation pneumonitis and the three-dimensional dose distribution in the lung.
In five institutions, the incidence of radiation pneumonitis was evaluated in 540 patients. The patients were divided into two groups: a Lung group, consisting of 399 patients with lung cancer and 1 esophagus cancer patient and a Lymph./Breast group with 78 patients treated for malignant lymphoma, 59 for breast cancer, and 3 for other tumor types. The dose per fraction varied between 1.0 and 2.7 Gy and the prescribed total dose between 20 and 92 Gy. Three-dimensional dose calculations were performed with tissue density inhomogeneity correction. The physical dose distribution was converted into the biologically equivalent dose distribution given in fractions of 2 Gy, the normalized total dose (NTD) distribution, by using the linear quadratic model with an alpha/beta ratio of 2.5 and 3.0 Gy. Dose-volume histograms (DVHs) were calculated considering both lungs as one organ and from these DVHs the mean (biological) lung dose, NTDmean, was obtained. Radiation pneumonitis was scored as a complication when the pneumonitis grade was grade 2 (steroids needed for medical treatment) or higher. For statistical analysis the conventional normal tissue complication probability (NTCP) model of Lyman (with n=1) was applied along with an institutional-dependent offset parameter to account for systematic differences in scoring patients at different institutions.
The mean lung dose, NTDmean, ranged from 0 to 34 Gy and 73 of the 540 patients experienced pneumonitis, grade 2 or higher. In all centers, an increasing pneumonitis rate was observed with increasing NTDmean. The data were fitted to the Lyman model with NTD50=31.8 Gy and m=0.43, assuming that for all patients the same parameter values could be used. However, in the low dose range at an NTDmean between 4 and 16 Gy, the observed pneumonitis incidence in the Lung group (10%) was significantly (p=0.02) higher than in the Lymph./Breast group (1.4%). Moreover, between the Lung groups of different institutions, also significant (p=0.04) differences were present: for centers 2, 3, and 4, the pneumonitis incidence was about 13%, whereas for center 5 only 3%. Explicitly accounting for these differences by adding center-dependent offset values for the Lung group, improved the data fit significantly (p < 10(-5)) with NTD50=30.5+/-1.4 Gy and m=0.30+/-0.02 (+/-1 SE) for all patients, and an offset of 0-11% for the Lung group, depending on the center.
The mean lung dose, NTDmean, is relatively easy to calculate, and is a useful predictor of the risk of radiation pneumonitis. The observed dose-effect relation between the NTDmean and the incidence of radiation pneumonitis, based on a large clinical data set, might be of value in dose-escalating studies for lung cancer. The validity of the obtained dose-effect relation will have to be tested in future studies, regarding the influence of confounding factors and dose distributions different from the ones in this study.
确定放射性肺炎的发生率与肺内三维剂量分布之间的关系。
在五家机构中,对540例患者的放射性肺炎发生率进行了评估。患者被分为两组:肺部组,包括399例肺癌患者和1例食管癌患者;淋巴/乳腺组,有78例接受恶性淋巴瘤治疗的患者、59例乳腺癌患者和3例其他肿瘤类型的患者。每次分割剂量在1.0至2.7 Gy之间,处方总剂量在20至92 Gy之间。采用组织密度不均匀性校正进行三维剂量计算。通过使用α/β比值为2.5和3.0 Gy的线性二次模型,将物理剂量分布转换为以2 Gy分割给出的生物等效剂量分布,即归一化总剂量(NTD)分布。将双肺视为一个器官计算剂量体积直方图(DVH),并从这些DVH中得出平均(生物)肺剂量NTDmean。当肺炎分级为2级(需要药物治疗的类固醇)或更高时,将放射性肺炎作为一种并发症进行评分。为了进行统计分析,应用了Lyman的传统正常组织并发症概率(NTCP)模型(n = 1)以及一个与机构相关的偏移参数,以考虑不同机构在对患者评分方面的系统差异。
平均肺剂量NTDmean范围为0至34 Gy,540例患者中有73例发生2级或更高等级的肺炎。在所有中心,随着NTDmean的增加,观察到肺炎发生率上升。假设所有患者都可以使用相同的参数值,数据拟合Lyman模型,NTD50 = 31.8 Gy,m = 0.43。然而,在NTDmean为4至16 Gy的低剂量范围内,肺部组观察到的肺炎发生率(10%)显著高于淋巴/乳腺组(1.4%)(p = 0.02)。此外,在不同机构的肺部组之间也存在显著差异(p = 0.04):对于中心2、3和4,肺炎发生率约为13%,而中心5仅为3%。通过为肺部组添加与中心相关的偏移值来明确考虑这些差异,显著改善了数据拟合(p < 10^(-5)),所有患者的NTD50 = 30.5 ± 1.4 Gy,m = 0.30 ± 0.02(±1标准误),肺部组的偏移为0 - 11%,具体取决于中心。
平均肺剂量NTDmean相对容易计算,是放射性肺炎风险的有用预测指标。基于大量临床数据集观察到的NTDmean与放射性肺炎发生率之间的剂量 - 效应关系,可能在肺癌剂量递增研究中具有价值。关于混杂因素的影响以及与本研究不同的剂量分布,所获得的剂量 - 效应关系的有效性将需要在未来的研究中进行检验。