Center for Molecular Imaging, The Brown Foundation Institute of Molecular Medicine, Houston, Texas.
Center for Laboratory Animal Medicine and Care, University of Texas Health Science, Houston, Texas.
Int J Radiat Oncol Biol Phys. 2019 Nov 15;105(4):852-860. doi: 10.1016/j.ijrobp.2019.07.054. Epub 2019 Aug 5.
Postoperative radiation therapy (RT) delivered to lymphatics is associated with an increased risk of developing lymphedema. Reported effects of RT on lymphatic vessels have varied, however, possibly because of the use of different animal models with varying surgery and radiation schedules and the inability to directly and longitudinally image lymphatics in vivo. Here we report, using noninvasive imaging, changes in lymphatic remodeling and function in response to surgery and RT in a mouse model.
Popliteal lymphadenectomy in mice preceded single-dose gamma irradiation of the lower extremity at a single dose of 0, 20, or 40 Gy. The right hind limb of intact mice was also radiated with 4 fractions (4 × 5 Gy). Near-infrared fluorescence lymphatic imaging with indocyanine green was performed over 6 months to monitor lymphatic vessel remodeling.
Postoperative mice treated with 20 Gy showed transient changes in lymphatic drainage, exacerbated vessel remodeling including qualitative vessel dilation and abnormal indocyanine green pooling from week 1 to 2, and initiation of restoration of lymphatic vessels, although dermal backflow was occasionally observed. Mice treated with 40 Gy showed steadily increasing lymphatic impairment until week 3 and extravasation of dye and dermal backflow in weeks 4 to 25. The ankles of mice treated with 40 Gy were significantly swollen from weeks 2 to 4 as compared with mice treated with 0 Gy or 20 Gy. Mice that received fractionated RT exhibited lymphatic vessel remodeling similar to remodeling that occurred when a single 20 Gy dose was given; however, dermal backflow did not resolve as it did in the case of a single 20 Gy dose.
The degree of nonreversing lymphatic damage seen in our mouse model was dependent on RT dose. Our results suggest that near-infrared fluorescence lymphatic imaging detection of early lymphatic changes can be used to predict development of lymphedema in patients with cancer.
术后给予淋巴管的放射治疗(RT)会增加发生淋巴水肿的风险。然而,RT 对淋巴管的影响报道各异,这可能是由于使用了不同的动物模型,手术和放射方案不同,以及无法直接和纵向地对体内淋巴管进行成像。在此,我们通过非侵入性成像报告了在一种小鼠模型中,手术和 RT 对淋巴管重塑和功能的影响。
在接受单剂量 γ 射线照射下肢之前,先对小鼠行腘窝淋巴结切除术,剂量为 0、20 或 40Gy。还对完整小鼠的右后肢进行 4 个部分(4×5Gy)的放射。在 6 个月的时间内,使用近红外荧光淋巴成像技术进行吲哚菁绿(ICG)检测,以监测淋巴管重塑。
20Gy 术后治疗的小鼠表现出短暂的淋巴引流改变,从第 1 周到第 2 周,血管重塑加剧,包括定性的血管扩张和异常的 ICG 积聚,并且开始恢复淋巴管,尽管偶尔会观察到皮肤反流。40Gy 治疗的小鼠从第 3 周开始,淋巴管损伤逐渐加重,第 4 周到第 25 周出现染料外渗和皮肤反流。与 0Gy 或 20Gy 治疗的小鼠相比,40Gy 治疗的小鼠从第 2 周到第 4 周踝关节明显肿胀。接受分次 RT 的小鼠的淋巴管重塑类似于单次 20Gy 剂量时发生的重塑;然而,与单次 20Gy 剂量时的情况不同,皮肤反流并未解决。
我们的小鼠模型中观察到的非逆转性淋巴损伤程度取决于 RT 剂量。我们的结果表明,近红外荧光淋巴成像检测早期的淋巴变化可以用于预测癌症患者发生淋巴水肿的情况。