Adeberg Sebastian, Windisch Paul, Ehret Felix, Baur Melissa, Akbaba Sati, Held Thomas, Bernhardt Denise, Haefner Matthias F, Krauss Juergen, Kargus Steffen, Freudlsperger Christian, Plinkert Peter, Flechtenmacher Christa, Herfarth Klaus, Debus Juergen, Rieken Stefan
Department of Radiation Oncology, Heidelberg University Hospital, Heidelberg, Germany.
Heidelberg Institute for Radiation Oncology, Heidelberg, Germany.
Front Oncol. 2019 Dec 20;9:1420. doi: 10.3389/fonc.2019.01420. eCollection 2019.
To assess outcomes and treatment related toxicity following intensity-modulated radiotherapy (IMRT) and a Carbon Ion Radiotherapy (CIRT) boost for salivary duct carcinoma (SDC). Twenty-eight consecutive patients with SDC who underwent a postoperative (82%) or definitive (18%) radiation therapy between 2010 and 2017 were assessed in this retrospective single-center analysis. CIRT boost was delivered with median 18 Gy(RBE) in 6 daily fractions, followed by an TomoTherapy-based IMRT (median 54 Gy in 27 daily fractions). Treatment-related acute toxicity was assessed according to CTCAE Version 4. Tumors were most commonly located in the major salivary glands ( = 25; 89%); 23 patients (82%) received previous surgery (R0: 30%; R1: 57%; R2: 4%; RX: 19%). Median follow-up was 30 months. Four patients (14%) experienced a local relapse and 3 (11%) developed locoregional recurrence. The two-year local control (LC) and locoregional control (LRC) was 96 and 93%, respectively. Median disease-free survival (DFS) was 27 months, metastasis-free survival (MFS) was 69 months, and overall survival (OS) was 93 months. Acute grade 3 toxicity occurred in 11 patients (mucositis, dermatitis, xerostomia; = 2 each (7%) were the most common) and 2 osteonecroses of the mandibular (grade 3) occurred. No patients experienced grade ≥4 toxicities. Multimodal therapy approaches with surgery followed by IMRT and CIRT boost for SDC leads to good local and locoregional disease control. However, the frequent occurrence of distant metastases limits the prognosis and requires optimization of adjuvant systemic therapies.
评估调强放射治疗(IMRT)联合碳离子放射治疗(CIRT)增敏对涎腺导管癌(SDC)的疗效及治疗相关毒性。在这项回顾性单中心分析中,评估了2010年至2017年间连续28例接受术后(82%)或根治性(18%)放射治疗的SDC患者。CIRT增敏采用中位剂量18 Gy(相对生物效应),分6次每日照射,随后进行基于螺旋断层放疗(TomoTherapy)的IMRT(中位剂量54 Gy,分27次每日照射)。根据美国国立癌症研究所常见不良反应事件评价标准(CTCAE)第4版评估治疗相关急性毒性。肿瘤最常见于大涎腺(n = 25;89%);23例患者(82%)曾接受手术(R0:30%;R1:57%;R2:4%;RX:19%)。中位随访时间为30个月。4例患者(14%)出现局部复发,3例(11%)发生区域复发。两年局部控制率(LC)和区域控制率(LRC)分别为96%和93%。中位无病生存期(DFS)为27个月,无转移生存期(MFS)为69个月,总生存期(OS)为93个月。11例患者发生3级急性毒性(口腔黏膜炎、皮炎、口干症;各2例(7%)最为常见),发生2例下颌骨3级骨坏死。无患者出现≥4级毒性。对于SDC,采用手术联合IMRT及CIRT增敏的多模式治疗方法可实现良好的局部和区域疾病控制。然而,远处转移的频繁发生限制了预后,需要优化辅助全身治疗。