Peeters Stephanie T H, Hoogeman Mischa S, Heemsbergen Wilma D, Hart Augustinus A M, Koper Peter C M, Lebesque Joos V
Department of Radiation Oncology, The Netherlands Cancer Institute-Antoni van Leeuwenhoek Hospital, Amsterdam, The Netherlands.
Int J Radiat Oncol Biol Phys. 2006 Sep 1;66(1):11-9. doi: 10.1016/j.ijrobp.2006.03.034. Epub 2006 Jun 6.
To analyze whether inclusion of predisposing clinical features in the Lyman-Kutcher-Burman (LKB) normal tissue complication probability (NTCP) model improves the estimation of late gastrointestinal toxicity.
This study includes 468 prostate cancer patients participating in a randomized trial comparing 68 with 78 Gy. We fitted the probability of developing late toxicity within 3 years (rectal bleeding, high stool frequency, and fecal incontinence) with the original, and a modified LKB model, in which a clinical feature (e.g., history of abdominal surgery) was taken into account by fitting subset specific TD50s. The ratio of these TD50s is the dose-modifying factor for that clinical feature. Dose distributions of anorectal (bleeding and frequency) and anal wall (fecal incontinence) were used.
The modified LKB model gave significantly better fits than the original LKB model. Patients with a history of abdominal surgery had a lower tolerance to radiation than did patients without previous surgery, with a dose-modifying factor of 1.1 for bleeding and of 2.5 for fecal incontinence. The dose-response curve for bleeding was approximately two times steeper than that for frequency and three times steeper than that for fecal incontinence.
Inclusion of predisposing clinical features significantly improved the estimation of the NTCP. For patients with a history of abdominal surgery, more severe dose constraints should therefore be used during treatment plan optimization.
分析在莱曼 - 库彻 - 伯曼(LKB)正常组织并发症概率(NTCP)模型中纳入易感临床特征是否能改善对晚期胃肠道毒性的估计。
本研究纳入了468例参与比较68 Gy与78 Gy的随机试验的前列腺癌患者。我们用原始的和改良的LKB模型拟合了3年内发生晚期毒性(直肠出血、高排便频率和大便失禁)的概率,在改良的LKB模型中,通过拟合特定亚组的TD50来考虑临床特征(如腹部手术史)。这些TD50的比值就是该临床特征的剂量修正因子。使用了直肠肛门(出血和频率)以及肛管壁(大便失禁)的剂量分布。
改良的LKB模型比原始的LKB模型拟合效果显著更好。有腹部手术史的患者对放疗的耐受性低于无手术史的患者,出血的剂量修正因子为1.1,大便失禁的剂量修正因子为2.5。出血的剂量反应曲线比频率的曲线陡约两倍,比大便失禁的曲线陡三倍。
纳入易感临床特征显著改善了NTCP的估计。因此,对于有腹部手术史的患者,在治疗计划优化过程中应使用更严格的剂量限制。