Zimmermann Michel, Beer Jürgen, Bodis Stefan, von Moos Roger, Vlachopoulou Vasiliki, Zwahlen Daniel R, Oehler Christoph
a Department of Radiation Oncology , Kantonsspital Graubünden , Chur , Switzerland.
b Center for Radiation Oncology KSA-KSB , Aarau , Switzerland.
Acta Oncol. 2017 Dec;56(12):1734-1740. doi: 10.1080/0284186X.2017.1325003. Epub 2017 May 30.
To evaluate local control (LC), survival and toxicity in anal cancer patients treated with intensity-modulated radiation therapy (IMRT) and concurrent chemotherapy at a single institution.
From August 2010 to May 2015, 26 patients were treated at our institution with IMRT and concurrent 5-fluorouracil/mitomycin-C (5-FU/MMC) for localized squamous cell carcinoma of the anal canal (SCCAC). Radiotherapy (RT) with 50.4-60 Gy was delivered with a sequential boost in 31%, and a simultaneous-integrated boost (SIB-IMRT) in 69% of cases. Initial staging was based on PET-CT and MRI. Clinical measures of interest were the influence of PET-CT on staging and treatment planning, LC, disease free survival (DFS), overall survival (OS), colostomy free survival (CFS) and toxicities.
Median age was 61 years, 22 patients (85%) were female, and no patient was HIV-positive. The proportion of patients with stage I, II, IIIA and IIIB disease was 15%, 35%, 23% and 27%, respectively. PET-CT modified the extent of nodal disease in 9/23 cases (39%) and lead to major changes in treatment planning in 4/23 patients (17%). MRI was more accurate at identifying T4 disease. RT was delivered at full dose in 26 patients (100%) and chemotherapy in 22/26 patients (85%). Two patients (7.7%) required RT breaks. Median follow-up was 35 months [IQR: 19-52]. The 2-year LC, DFS, OS and CFS were 100%, 100%, 100% and 92%. Acute grade ≥3 dermatitis and diarrhea occurred in 73% and 8% of cases, respectively. Grade 3-4 neutropenia was seen in 10/23 patients (43%). Four patients (15%) developed chronic grade 2 GI toxicity.
PET-CT provided additional information leading to major changes in treatment planning for 17% of patients. Considering our excellent outcomes, routine use of PET-CT as standard staging modality and IMRT planning procedure appears justified for patients with SCCAC.
评估在单一机构接受调强放射治疗(IMRT)及同步化疗的肛管癌患者的局部控制率(LC)、生存率和毒性反应。
2010年8月至2015年5月,26例患者在我院接受IMRT及同步5-氟尿嘧啶/丝裂霉素-C(5-FU/MMC)治疗局部肛管鳞状细胞癌(SCCAC)。50.4 - 60 Gy的放射治疗(RT)中,31%采用序贯推量,69%采用同步整合推量(SIB-IMRT)。初始分期基于PET-CT和MRI。感兴趣的临床指标包括PET-CT对分期和治疗计划的影响、LC、无病生存期(DFS)、总生存期(OS)、无结肠造口生存期(CFS)和毒性反应。
中位年龄为61岁,22例患者(85%)为女性,无患者HIV阳性。I期、II期、IIIA期和IIIB期疾病患者的比例分别为15%、35%、23%和27%。PET-CT在9/23例(39%)患者中改变了淋巴结疾病的范围,在4/23例(17%)患者中导致治疗计划发生重大改变。MRI在识别T4期疾病方面更准确。26例患者(100%)接受了全量RT,22/26例患者(85%)接受了化疗。2例患者(7.7%)需要中断RT。中位随访时间为35个月[四分位间距:19 - 52]。2年的LC、DFS、OS和CFS分别为100%、100%、100%和92%。急性3级及以上皮炎和腹泻分别发生在73%和8%的病例中。10/23例患者(43%)出现3 - 4级中性粒细胞减少。4例患者(15%)出现慢性2级胃肠道毒性反应。
PET-CT为17%的患者提供了额外信息,导致治疗计划发生重大改变。鉴于我们出色的治疗结果,对于SCCAC患者,将PET-CT作为标准分期方式和IMRT计划程序的常规应用似乎是合理的。