Department of Radiation Oncology (MAASTRO), University Medical Centre Maastricht, Maastricht, The Netherlands.
Radiother Oncol. 2010 Feb;94(2):151-5. doi: 10.1016/j.radonc.2009.12.033. Epub 2010 Jan 29.
The purpose of this study was to prospectively investigate metabolic changes of rectal tumors after 1 week of treatment of either radiochemotherapy (28 x 1.8 Gy+Capecitabine) (RCT) or hypofractionated radiotherapy (5 x 5 Gy) alone (RT).
Fourty-six rectal cancer patients, 25 RCT- and 21 RT-patients, were included in this study. Sequential FDG-PET-CT scans were performed for each of the included patients both prior to treatment and after the first week of treatment. Consecutively, the metabolic treatment response of the tumor was evaluated.
For the patients referred for pre-operative RCT, significant reductions of SUV(mean) (p<0.001) and SUV(max) (p<0.001) within the tumor were found already after the first week of treatment (8 Gy biological equivalent dose (BED). In contrast, 1 week of treatment with RT alone did not result in significant changes in the metabolic activity of the tumor (p=0.767, p=0.434), despite the higher applied RT dose of 38.7 Gy BED.
Radiochemotherapy of rectal cancer leads to significant early changes in the metabolic activity of the tumor, which was not the case early after hypofractionated radiotherapy alone, despite the higher radiotherapy dose given. Thus, the chemotherapeutic agent Capecitabine might be responsible for the early metabolic treatment responses during radiochemotherapy in rectal cancer.
本研究旨在前瞻性地观察直肠癌患者接受 1 周放化疗(28 次 x 1.8 Gy+卡培他滨)(RCT)或单纯低分割放疗(5 次 x 5 Gy)(RT)治疗后直肠肿瘤的代谢变化。
本研究共纳入 46 例直肠癌患者,其中 25 例接受 RCT,21 例接受 RT。所有患者均在治疗前和治疗第 1 周后分别进行连续 FDG-PET-CT 扫描,随后评估肿瘤的代谢治疗反应。
对于接受术前 RCT 的患者,在治疗的第 1 周(8 Gy 生物等效剂量(BED)),肿瘤的 SUV(mean)(p<0.001)和 SUV(max)(p<0.001)均显著降低。相比之下,单纯 RT 治疗 1 周后,肿瘤的代谢活性并未发生显著变化(p=0.767,p=0.434),尽管给予的 RT 剂量较高(38.7 Gy BED)。
直肠癌放化疗可导致肿瘤代谢活性的早期显著变化,而单纯低分割放疗早期则无此变化,尽管给予的放疗剂量较高。因此,卡培他滨化疗药物可能是直肠癌放化疗中早期代谢治疗反应的原因。