Oehler-Jänne Christoph, Seifert Burkhardt, Lütolf Urs M, Studer Gabriela, Glanzmann Christoph, Ciernik I Frank
Radiation Oncology, Zurich University Hospital, Zurich, Switzerland.
Brachytherapy. 2007 Jul-Sep;6(3):218-26. doi: 10.1016/j.brachy.2007.02.152.
To evaluate the outcome after definitive whole pelvis external beam radiotherapy (EBRT) followed by brachytherapy (BT) boost after treatment break vs. external beam boost without break in the treatment of anal carcinoma.
Eighty-one consecutive patients with invasive anal carcinoma were analyzed retrospectively. Patients treated with an interstitial (192)Ir high-dose-rate (HDR) implant boost of 14Gy/7 fractions/3d given 3 weeks after completion of whole pelvis 45Gy EBRT were compared with those treated with external beam boost of 14.4Gy, started immediately after completion of whole pelvis 45Gy EBRT. Concomitant chemotherapy (CT) with mitomycin C was applied during whole pelvis EBRT depending on tumor stage. Pattern of care, local disease control (LC), cancer-specific survival (CSS), overall survival (OS), toxicity, and quality of life (QOL) were assessed.
Radiotherapy with or without concomitant CT achieved clinical complete response in 93.4% of patients. In early stage tumors, (192)Ir-HDR BT boost with CT resulted in a 5-year LC and CSS of 100%. In all patients, BT boost did not result in improved LC, OS, and CSS compared with EBRT boost, despite stage and treatment bias favoring small tumors to be treated with BT. The 5-year and 10-year OS were 66% and 44% (BT boost) and 66% and 52% (EBRT boost), respectively. Subgroup analysis of Stages I and II disease revealed no significant improvement after BT boost compared with EBRT boost. Acute skin toxicity was less common in the BT boost group (whole cohort: p=0.14; Stages I-IIIa: p=0.05), but long-term morbidity and QOL were similar. No local necrosis was seen after BT boost and the 10-year sphincter preservation rate was 87% in these patients.
Interstitial (192)Ir-HDR implant boost with break and EBRT boost without break yield similar results. Acute skin toxicity is reduced with BT boost but long-term morbidity and QOL are identical. BT boost is most beneficial in early stage tumors but the advantage of BT seems to be limited due to its invasiveness, doctor dependence, and logistic circumstances.
评估在治疗中断后进行全盆腔外照射放疗(EBRT)继以近距离放疗(BT)推量与不间断进行外照射推量治疗肛管癌后的疗效。
回顾性分析81例连续的浸润性肛管癌患者。将在全盆腔45Gy EBRT完成后3周给予14Gy/7次/3天的组织间(192)铱高剂量率(HDR)植入推量治疗的患者与在全盆腔45Gy EBRT完成后立即开始给予14.4Gy外照射推量治疗的患者进行比较。根据肿瘤分期,在全盆腔EBRT期间应用丝裂霉素C同步化疗(CT)。评估治疗模式、局部疾病控制(LC)、癌症特异性生存(CSS)、总生存(OS)、毒性和生活质量(QOL)。
无论是否同步CT,放疗使93.4%的患者达到临床完全缓解。在早期肿瘤中,(192)铱-HDR BT推量联合CT治疗的5年LC和CSS为100%。在所有患者中,与EBRT推量相比,BT推量并未改善LC、OS和CSS,尽管分期和治疗倾向于使小肿瘤接受BT治疗。5年和10年OS分别为66%和44%(BT推量)以及66%和52%(EBRT推量)。I期和II期疾病的亚组分析显示,与EBRT推量相比,BT推量后无显著改善。BT推量组急性皮肤毒性较少见(全队列:p = 0.14;I - IIIa期:p = 0.05),但长期发病率和QOL相似。BT推量后未见局部坏死,这些患者的10年括约肌保留率为87%。
有治疗中断的组织间(192)铱-HDR植入推量与无治疗中断的EBRT推量产生相似的结果。BT推量可降低急性皮肤毒性,但长期发病率和QOL相同。BT推量对早期肿瘤最有益,但由于其侵入性、对医生的依赖性和后勤情况,BT的优势似乎有限。