Roeder Falk, Nicolay Nils H, Nguyen Tam, Saleh-Ebrahimi Ladan, Askoxylakis Vasilis, Bostel Tilman, Zwicker Felix, Debus Juergen, Timke Carmen, Huber Peter E
CCU Radiation Oncology, German Cancer Research Center (DKFZ), Heidelberg, Germany.
Radiat Oncol. 2014 Aug 29;9:191. doi: 10.1186/1748-717X-9-191.
To report our experience with increased dose intensity-modulated radiation and concurrent systemic chemotherapy as definitive treatment of locally advanced esophageal cancer.
We analyzed 27 consecutive patients with histologically proven esophageal cancer, who were treated with increased-dose IMRT as part of their definitive therapy. The majority of patients had T3/4 and/or N1 disease (93%). Squamous cell carcinoma was the dominating histology (81%). IMRT was delivered in step-and-shoot technique in all patients using an integrated boost concept. The boost volume was covered with total doses of 56-60 Gy (single dose 2-2.14 Gy), while regional nodal regions received 50.4 Gy (single dose 1.8 Gy) in 28 fractions. Concurrent systemic therapy was scheduled in all patients and administered in 26 (96%). 17 patients received additional adjuvant systemic therapy. Loco-regional control, progression-free and overall survival as well as acute and late toxicities were retrospectively analyzed. In addition, quality of life was prospectively assessed according to the EORTC QLQs (QLQ-OG25, QLQ-H&N35 and QLQ-C30).
Radiotherapy was completed as planned in all but one patient (96%), and 21 patients received more than 80% of the planned concurrent systemic therapy. We observed ten locoregional failures, transferring into actuarial 1-, 2- and 3-year-locoregional control rates of 77%, 65% and 48%. Seven patients developed distant metastases, mainly to the lung (71%). The actuarial 1-, 2- and 3-year-disease free survival rates were 58%, 48% and 36%, and overall survival rates were 82%, 61% and 56%. The concept was well tolerated, both in the clinical objective examination and also according to the subjective answers to the QLQ questionnaire. 14 patients (52%) suffered from at least one acute CTC grade 3/4 toxicity, mostly hematological side effects or dysphagia. Severe late toxicities were reported in 6 patients (22%), mostly esophageal strictures and ulcerations. Severe side effects to skin, lung and heart were rare.
IMRT with concurrent systemic therapy in the definitive treatment of esophageal cancer using an integrated boost concept with doses up to 60 Gy is feasible and yields good results with acceptable acute and late overall toxicity and low side effects to skin, lung and heart.
报告我们使用增加剂量的调强放疗及同步全身化疗作为局部晚期食管癌确定性治疗的经验。
我们分析了27例经组织学证实的食管癌连续患者,他们接受了增加剂量的调强放疗作为其确定性治疗的一部分。大多数患者患有T3/4和/或N1期疾病(93%)。鳞状细胞癌是主要的组织学类型(81%)。所有患者均采用步进式调强放疗技术,并采用整合加量概念。加量体积接受56 - 60 Gy的总剂量(单次剂量2 - 2.14 Gy),而区域淋巴结区域接受50.4 Gy(单次剂量1.8 Gy),分28次照射。所有患者均安排了同步全身治疗,26例(96%)接受了治疗。17例患者接受了额外的辅助全身治疗。对局部区域控制、无进展生存期和总生存期以及急性和晚期毒性进行了回顾性分析。此外,根据欧洲癌症研究与治疗组织的QLQ问卷(QLQ - OG25、QLQ - H&N35和QLQ - C30)对生活质量进行了前瞻性评估。
除1例患者(96%)外,所有患者均按计划完成了放疗,21例患者接受了超过80%的计划同步全身治疗。我们观察到10例局部区域复发,1年、2年和3年的精算局部区域控制率分别为77%、65%和48%。7例患者发生远处转移,主要转移至肺部(71%)。1年、2年和3年的精算无病生存率分别为58%、48%和36%,总生存率分别为82%、61%和56%。无论是临床客观检查还是根据QLQ问卷的主观回答,该方案耐受性良好。14例患者(52%)至少发生1次急性CTC 3/4级毒性反应,主要为血液学副作用或吞咽困难。6例患者(22%)报告有严重的晚期毒性反应,主要为食管狭窄和溃疡。皮肤、肺部和心脏的严重副作用很少见。
在食管癌的确定性治疗中,采用整合加量概念、剂量高达60 Gy的调强放疗同步全身治疗是可行的,能取得良好效果,急性和晚期总体毒性可接受,对皮肤、肺部和心脏的副作用低。