Rastogi Madhup, Nanda Sambit Swarup, Gandhi Ajeet Kumar, Dalela Divakar, Khurana Rohini, Mishra Surendra Prasad, Srivastava Anoop, Farzana S, Bhatt Madan Lal Brahma, Husain Nuzhat
Department of Radiation Oncology, Dr. Ram Manohar Lohia Institute of Medical Sciences, Vibhutikhand, Gomtinagar, Lucknow 226010, India.
Department of Radiation Oncology, Dr. Ram Manohar Lohia Institute of Medical Sciences, Vibhutikhand, Gomtinagar, Lucknow 226010, India.
J Egypt Natl Canc Inst. 2017 Dec;29(4):185-190. doi: 10.1016/j.jnci.2017.08.003. Epub 2017 Nov 9.
We compared the prostate motion variability and toxicities between patients treated with gold marker registration based IG-IMRT (IG-IMRT-M) and bony landmark registration based IG-IMRT (IG-IMRT-B).
T1c-T3b (node negative), intermediate and high risk (non-metastatic) adenocarcinoma of prostate, age ≥18years, Karnofsky Performance Status of ≥70 were included in this retrospective study. The prostate motion variability, acute and late radiation toxicities between the two treatment arms (IG-IMRT-M versus IG-IMRT-B) were compared.
Total of 35 patients (17 for IG-IMRT-M and 18 for IG-IMRT-B) were treated with a median radiotherapy dose of 76 Gray. The prostate variability observed with and without markers in millimeter was 4.1±2.3 vs 3.7±2.1 [Antero-Posterior (A-P); p=0.001], 2.3±1.5 vs 2.1±1.2 [Superior-Inferior (S-I); p=0.095] and 1.1±1.7 vs 0.4±1.4 [Left-Right (L-R); p=0.003]. There was higher acute toxicity in IG-IMRT-B arm compared to IG-IMRT-M arm in terms of grade ≥2 diarrhea [50% vs 11% OR=7.5 (1.3-42.7); p=0.02] and grade ≥2 proctitis [38% vs 5.8%, OR=10.1 (1.09-94.1); p=0.04]. At a median follow up of 36months, the late genitourinary toxicities grade ≥2 [27% vs 0%; p=0.04] were higher in the IG-IMRT-B arm compared to IG-IMRT-M arm.
IG-IMRT-M detects higher prostate motion variability as compared to IG-IMRT-B, inferring a significant prostate motion inside fixed pelvic bony cavity. The addition of marker based image guidance results in higher precision of prostate localization and lesser acute and late toxicities.
我们比较了接受基于金标注册的影像引导调强放疗(IG-IMRT-M)和基于骨性标志注册的影像引导调强放疗(IG-IMRT-B)的患者之间前列腺运动变异性和毒性反应。
本回顾性研究纳入了年龄≥18岁、卡氏评分≥70分的T1c-T3b期(无淋巴结转移)、中高危(非转移性)前列腺腺癌患者。比较了两个治疗组(IG-IMRT-M与IG-IMRT-B)之间的前列腺运动变异性、急性和晚期放射毒性反应。
共35例患者接受治疗(IG-IMRT-M组17例,IG-IMRT-B组18例),中位放疗剂量为76格雷。有标记和无标记时观察到的前列腺在毫米水平的变异性为:前后径(A-P)4.1±2.3对3.7±2.1 [p = 0.001],上下径(S-I)2.3±1.5对2.1±1.2 [p = 0.095],左右径(L-R)1.1±1.7对0.4±1.4 [p = 0.003]。在≥2级腹泻方面,IG-IMRT-B组的急性毒性反应高于IG-IMRT-M组[50%对11%,OR = 7.5(1.3 - 42.7);p = 0.02],在≥2级直肠炎方面也是如此[38%对5.8%,OR = 10.1(1.09 - 94.1);p = 0.04]。中位随访36个月时,IG-IMRT-B组≥2级晚期泌尿生殖系统毒性反应高于IG-IMRT-M组[27%对0%;p = 0.04]。
与IG-IMRT-B相比,IG-IMRT-M检测到更高的前列腺运动变异性,提示在固定的盆腔骨腔内前列腺有显著运动。基于标记的图像引导可提高前列腺定位的精度,并减少急性和晚期毒性反应。