非小细胞肺癌和乳腺癌患者晚期立体定向放疗后的并发症增加

A. Belikova, V. Gerasimov, A. Kaprin, P. Datsenko
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引用次数: 0

摘要

这项工作的目的是评估延迟增强后的功能状态和主要并发症,这取决于所使用的剂量水平和放射转移的数量。在WBRT结束后,30例非小细胞肺癌(n=11)和乳腺癌(n=19)伴有转移性脑病变的患者进行了长期增强(SRS)。规定的晚期增强剂量范围从10到22戈瑞,中位数为15戈瑞。26例患者(86.7%),2例患者(6.7%),3例患者(6.7%)分别接受了单段放疗。截至2021年12月,30例患者中有26例(86.7%)死亡,仅53.3%死于中枢神经系统进展,0%死于并发症。7例(23.3%)患者出现局部进展(增强区生长),56.7%的患者出现远处进展(出现新的转移或癌变)。通常,患者有合并病变。在WBRT后12个月(p=0.767)、24个月(p=0.820)和36个月(p=1.0)后,延迟增加剂量≥15 Gy对患者的功能状态没有影响。尽管与标准强化相比,后期强化有更多的放射外科靶点和高剂量水平,但并未导致认知障碍的显著增加(p=0.437)。增强剂量≥15 Gy和<15 Gy组放射性坏死发生频率差异无统计学意义(p=0.935);24例患者中有6例(23.1%)和4例患者中有1例(25%)出现这种并发症。在平均剂量水平≥20 Gy时,发生放射性坏死的概率较高(p=0.002)。肿瘤体积(Vbust)对未来放射性坏死的形成没有影响(p=0.213),转移的最大横向大小(p=0.991)、转移数(p=0.224)和靶向(免疫)治疗(p=0.289)等预测因子无显著性意义。放射性坏死患者的中位总生存期为38.6个月(95% Cl: 25.5-51.7),无放射性坏死患者的中位总生存期仅为21.5个月(p=0.015)。晚期强化可用于多发(从4到10)转移性脑病变或大小不符合放射外科治疗标准的寡转移灶。总的来说,这种治疗方案是安全的,患者的功能状态保持在相当高的水平。即使随着放射性坏死的发展,生活质量和总体存活率也不会下降。
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Complications after late (delayed) stereotactic radiosurgery boost in patients with non-small cell lung and breast cancer
The purpose of the work is the assessment of the functional state and the main complications af-ter the delayed boost, depending on the level of doses used and the number of irradiated metastases. In 30 patients with non-small cell lung cancer (n=11) and breast cancer (n=19) with metastatic brain lesion after the end of WBRT, in the long term a boost (SRS) was performed. The prescribed dose for the late boost ranged from 10 to 22 Gy with a median of 15 Gy. Irradiation for single-fraction was performed in 26 patients (86.7%), for 2 fractions – in 2 patients (6.7%), for 3 fractions – in 2 patients (6.7%), respectively. As of December 2021, 26 of 30 patients (86.7%) died, only 53.3% from progression in the central nervous system, from complications 0%. Local progression (growth in the boost zone) was noted in 7 patients (23.3%), distant progression (the appearance of new metastasis or carcinomatosis) – in 56.7%. Often, patients had a combined lesion. Increasing the dose with a delayed boost of ≥15 Gy did not affect the functional state of patients after 12 (p=0.767), 24 (p=0.820), and 36 months (p=1.0) after WBRT. The late boost did not lead to a significant increase in cognitive impairment (p=0.437), despite the larger number of ra-diosurgical targets and the high dose level compared to the standard boost. There were no significant differences (p=0.935) in the frequency of radionecrosis in groups with a boost dose of ≥15 Gy and <15 Gy (p=0.935); this complication was recorded in 6 out of 24 (23.1%) and 1 out of 4 (25%) patients. At an average dose level ≥20 Gy, the probability of developing radionecrosis was higher (p=0.002). The volume of the tumor mass (Vbust) did not affect the formation of radionecrosis in the future (p=0.213), there was no significance for such predictors as the maximum transverse size of metastasis (p=0.991), the number of metastases (p=0.224) and target (im-mune) therapy (p=0.289). The median overall survival in patients with developed radionecrosis was 38.6 months (95% Cl: 25.5-51.7), in its absence – only 21.5 months (p=0.015). Late boost can be used for multiple (from 4 to 10) metastatic brain lesions or oligometastases that do not meet the criteria for radiosurgical treatment in size. In general, this treatment program is safe, the functional status of patients remains at a fairly high level. Even with the development of radionecrosis, the quality of life and overall survival rates do not decrease.
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