Kehrl Wolfgang, Sagowski Christoph, Wenzel Sören, Zywietz Friedrich
Department of Oto-Rhino-Laryngology, Marienkrankenhaus Hamburg, Germany.
Strahlenther Onkol. 2004 Jun;180(6):383-90. doi: 10.1007/s00066-004-1224-3.
Tumor oxygenation is well recognized as a major factor of tumor response to radiotherapy. In this respect, a number of studies have examined the response of primary tumors, whereas little is known about the oxygenation of tumor recurrences after radiotherapy. It was the aim of this study to investigate the oxygenation of tumor recurrences after preceding irradiation of the primary tumor.
Tumor oxygenation in primary tumors and recurrences of rat rhabdomyosarcomas R1H was measured by using pO(2) probes and Eppendorf pO(2) histography. Primary tumors were irradiated at a (60)Co radiotherapy facility with a total dose of 75 Gy, given in 30 fractions over 6 weeks. Oxygenation was measured in R1H tumors before and directly after completion of irradiation. In R1H recurrences oxygenation was determined, when they reached the same size as the previously treated primary tumors (V(o) = 3.1 +/- 0.5 cm(3)). Additionally, tumor microvessel density and the intercapillary distance of tumor blood vessels were determined on histological sections using a counting grid.
Tumor oxygenation in R1H recurrences was significantly lower when compared to primary R1H tumors. In primary tumors a median pO(2) of 17 +/- 7 mmHg was measured. By contrast, the median pO(2) in R1H recurrences was only 5 +/- 5 mmHg (p < 0.05). The high frequency of pO(2) values < 5 mmHg indicated that R1H recurrences were significantly more hypoxic (58 +/- 5%) in comparison to primary tumors (22 +/- 4%). The histological sections of the R1H recurrences showed a higher heterogeneity in their tissue structure than primary nonirradiated tumors. The morphometric studies demonstrated a reduced microvessel density (91 +/- 21/9.04 mm(2) in the tumor periphery; p = 0.0001) compared with recurrent tumors (68 +/- 26) and an enhanced mean distance of tumor blood vessels, especially in the center of the R1H recurrences (184 +/- 20 vs. 243 +/- 70 mm; p = 0.0001).
In R1H rhabdomyosarcomas tumor oxygenation in recurrent tumors following radiation therapy is significantly lower than in primary tumors. This observation has to be taken into account in cases of tumor recurrences where repeated radiotherapy, chemotherapy or combined treatment modalities are used.
肿瘤氧合作用是肿瘤对放疗反应的一个主要因素,这一点已得到广泛认可。在这方面,许多研究已经探讨了原发性肿瘤的反应,而对于放疗后肿瘤复发的氧合情况却知之甚少。本研究的目的是调查原发性肿瘤先行照射后肿瘤复发的氧合情况。
使用pO₂探针和Eppendorf pO₂组织血氧定量法测量大鼠横纹肌肉瘤R1H原发性肿瘤及复发肿瘤的氧合情况。原发性肿瘤在⁶⁰Co放疗设备上进行照射,总剂量为75 Gy,分30次在6周内给予。在照射完成前及完成后直接测量R1H肿瘤的氧合情况。当R1H复发肿瘤达到与先前治疗的原发性肿瘤相同大小时(V₀ = 3.1 ± 0.5 cm³),测定其氧合情况。此外,使用计数网格在组织切片上测定肿瘤微血管密度和肿瘤血管的毛细血管间距。
与原发性R1H肿瘤相比,R1H复发肿瘤的氧合情况显著降低。原发性肿瘤的pO₂中位数为17 ± 7 mmHg。相比之下,R1H复发肿瘤的pO₂中位数仅为5 ± 5 mmHg(p < 0.05)。pO₂值< 5 mmHg的高频率表明,与原发性肿瘤(22 ± 4%)相比,R1H复发肿瘤的缺氧情况显著更严重(58 ± 5%)。R1H复发肿瘤的组织切片显示,其组织结构的异质性高于未照射的原发性肿瘤。形态计量学研究表明,与原发性肿瘤(91 ± 21/9.04 mm²)相比,R1H复发肿瘤的微血管密度降低(肿瘤周边为68 ± 26;p = 0.0001),且肿瘤血管的平均间距增大,尤其是在R1H复发肿瘤的中心(184 ± 20对243 ± 70 mm;p = 0.0001)。
在R1H横纹肌肉瘤中,放疗后复发肿瘤的氧合情况显著低于原发性肿瘤。在肿瘤复发且采用重复放疗、化疗或联合治疗方案的情况下,必须考虑这一观察结果。