Elgqvist Jörgen, Andersson Håkan, Bäck Tom, Claesson Ingela, Hultborn Ragnar, Jensen Holger, Johansson Bengt R, Lindegren Sture, Olsson Marita, Palm Stig, Warnhammar Elisabet, Jacobsson Lars
Department of Radiation Physics, The Sahlgrenska Academy at Göteborg University, Göteborg, Sweden.
J Nucl Med. 2006 Aug;47(8):1342-50.
The purpose of this work was to (a) investigate the efficacy of radioimmunotherapy using 211At-MX35 F(ab')2 or 211At-Rituximab F(ab')2 (nonspecific antibody) against differently advanced ovarian cancer in mice; (b) image the tumor growth on the peritoneum; and (c) calculate the specific energy and mean absorbed dose to tumors and critical organs.
Two experiments with 5-wk-old nude mice (n = 100 + 93), intraperitoneally inoculated with approximately 1 x 10(7) NIH:OVCAR-3 cells, were done. At either 1, 3, 4, 5, or 7 wk after inoculation animals were intraperitoneally treated with approximately 400 kBq 211At-MX35 F(ab')2 (n = 50 + 45), approximately 400 kBq 211At-Rituximab F(ab')2 (n = 25 + 24), or unlabeled Rituximab F(ab')2 (n = 25 + 24). At the time of treatment 29 animals were sacrificed and biopsies were taken for determination of tumor sizes using scanning electron microscopy (SEM). Eight weeks after each treatment the animals were sacrificed and the presence of macro- and microscopic tumors and ascites was determined. The specific energy and mean absorbed dose to tumors were calculated. The activity concentration was measured in critical organs and abdominal fluid.
When given treatment 1, 3, 4, 5, or 7 wk after cell inoculation the tumor-free fraction (TFF) was 95%, 68%, 58%, 47%, 26%, and 100%, 80%, 20%, 20%, and 0% when treated with 211At-MX35 F(ab')2 or 211At-Rituximab F(ab')2, respectively. The SEM images revealed maximum tumor radius of approximately 30 mum 1 wk after cell inoculation, increasing to approximately 340 mum at 7 wk. Specific energy to cell nuclei varied between 0 and approximately 540 Gy, depending on assumptions regarding activity distribution and tumor size. The mean absorbed dose to thyroid, kidneys, and bone marrow was approximately 35, approximately 4, and approximately 0.3 Gy, respectively.
Treatment with 211At-MX35 F(ab')2 or 211At-Rituximab F(ab')2 resulted in a TFF of 95%-100% when the tumor radius was < or =30 microm. The TFF was decreased (TFF < or = 20%) for 211At-Rituximab F(ab')2 when the tumor radius exceeded the range of the alpha-particles. The specific antibody gave for these tumor sizes a significantly better TFF, explained by a high mean absorbed dose (>22 Gy) from the activity bound to the tumor surface and probably some contribution from penetrating activity.
本研究的目的是:(a) 研究使用211At-MX35 F(ab')2或211At-利妥昔单抗F(ab')2(非特异性抗体)对不同进展期小鼠卵巢癌进行放射免疫治疗的疗效;(b) 对腹膜上的肿瘤生长进行成像;(c) 计算肿瘤和关键器官的比能及平均吸收剂量。
进行了两项实验,将5周龄的裸鼠(n = 100 + 93)腹腔内接种约1×10(7)个NIH:OVCAR-3细胞。接种后1、3、4、5或7周,分别用约400 kBq的211At-MX35 F(ab')2(n = 50 + 45)、约400 kBq的211At-利妥昔单抗F(ab')2(n = 25 + 24)或未标记的利妥昔单抗F(ab')2(n = 25 + 24)对动物进行腹腔内治疗。治疗时处死29只动物,取活检组织,用扫描电子显微镜(SEM)测定肿瘤大小。每次治疗8周后处死动物,确定有无宏观和微观肿瘤及腹水。计算肿瘤的比能和平均吸收剂量。测量关键器官和腹腔液中的活度浓度。
细胞接种后1、3、4、5或7周进行治疗时,用211At-MX35 F(ab')2或211At-利妥昔单抗F(ab')2治疗的无瘤率(TFF)分别为95%、68%、58%、47%、26%和100%、80%、20%、20%、0%。SEM图像显示,细胞接种后1周肿瘤最大半径约为30μm,7周时增至约340μm。细胞核的比能在0至约540 Gy之间变化,具体取决于关于活度分布和肿瘤大小的假设。甲状腺、肾脏和骨髓的平均吸收剂量分别约为35、约4和约0.3 Gy。
当肿瘤半径≤30μm时,用211At-MX35 F(ab')2或211At-利妥昔单抗F(ab')2治疗的无瘤率为95% - 100%。当肿瘤半径超过α粒子射程范围时,211At-利妥昔单抗F(ab')2的无瘤率降低(TFF≤20%)。对于这些肿瘤大小,特异性抗体的无瘤率明显更好,这可以通过与肿瘤表面结合的活度产生的高平均吸收剂量(>22 Gy)以及穿透活度的可能贡献来解释。