Cihoric Nikola, Tapia Coya, Krüger Kamilla, Aebersold Daniel M, Klaeser Bernd, Lössl Kristina
Department of Radiation Oncology, Bern University Hospital, and University of Bern, Freiburgstrasse, 3010 Bern, Switzerland.
Radiat Oncol. 2014 Mar 25;9:83. doi: 10.1186/1748-717X-9-83.
To evaluate toxicity and outcome of intensity modulated radiotherapy (IMRT) with simultaneous integrated boost (SIB) to the positive lymph nodes in patients with loco-regional advanced cervical cancer (LRACC).
The study population comprised ten patients with 18FDG-PET\CT positive lymph nodes (LNs), who underwent chemoradiation with IMRT and SIB. A dose of 50.4 Gy, in daily fractions of 1.8 Gy, was delivered to primary tumor and draining LNs. Primary tumor received an additional external beam boost to a total dose of 55.8 Gy. A SIB of 62 Gy, in daily fractions of 2 Gy, was delivered to the 18FDG-PET\CT positive LNs. Finally, a high dose rate brachytherapy (HDRB) boost (15 - 18 Gy) was administered to the primary tumor. The primary goal of this study was to evaluate acute and early late toxicity and loco-regional control.
The median number of irradiated LNs per patient was 3 (range: 1-6) with a median middle nodal SIB-volume of 26.10 cm3 (range, 11.9-82.50 cm3). Median follow-up was 20 months (range, 12 to 30 months). Acute and late grade 3 toxicity was observed in 1 patient. Three of the patients developed a recurrence, one in the form of a local tumor relapse, one had a paraaortic LN metastasis outside the treated volume and the last one developed a distant metastasis.
IMRT with SIB in the region of 18FDG-PET positive lymph nodes appears to be an effective therapy with acceptable toxicity and might be useful in the treatment of patients with locally advanced cervical cancer.
评估调强放疗(IMRT)同步整合加量(SIB)治疗局部区域晚期宫颈癌(LRACC)患者阳性淋巴结的毒性和疗效。
研究人群包括10例18FDG-PET\CT显示阳性淋巴结(LNs)的患者,这些患者接受了IMRT和SIB的放化疗。原发肿瘤和引流淋巴结接受50.4 Gy的剂量,每日分次剂量为1.8 Gy。原发肿瘤额外接受外照射加量至总剂量55.8 Gy。18FDG-PET\CT显示阳性的淋巴结接受62 Gy的SIB,每日分次剂量为2 Gy。最后,对原发肿瘤进行高剂量率近距离放疗(HDRB)加量(15 - 18 Gy)。本研究的主要目的是评估急性和早期晚期毒性以及局部区域控制情况。
每位患者接受照射的淋巴结中位数为3个(范围:1 - 6个),淋巴结SIB体积中位数为26.10 cm³(范围,11.9 - 82.50 cm³)。中位随访时间为20个月(范围,12至30个月)。1例患者出现急性和晚期3级毒性。3例患者出现复发,1例为局部肿瘤复发,1例在治疗区域外出现腹主动脉旁淋巴结转移,最后1例发生远处转移。
对18FDG-PET阳性淋巴结区域进行IMRT同步整合加量似乎是一种有效的治疗方法,毒性可接受,可能对局部晚期宫颈癌患者的治疗有用。