Izquierdo M A, Degen D, Raymond E, Caron D, Ortiz V, Banks P, Von Hoff D D
Cancer Therapy and Research Center of South Texas, Institute for Drug Development, San Antonio, Texas 78229, USA.
Clin Cancer Res. 1996 Oct;2(10):1713-6.
PIXY321, a granulocyte-macrophage colony-stimulating factor/interleukin 3 (GM-CSF/IL-3) genetically engineered hybrid, has shown greater biological activity in stimulating committed myeloid progenitors than either GM-CSF or IL-3 in vitro, in vivo, and in patients treated with high-dose chemotherapy. However, one concern is that PIXY321 may stimulate the proliferation of malignant cells which have functional GM-CSF or IL-3 receptors. Therefore, using a human tumor cloning assay, we have tested the effects of several concentrations of PIXY321 ranging from 0.1 to 100 ng/ml on tumor cells taken directly from 98 patients with solid tumors and Hodgkin's or non-Hodgkin's lymphomas. Of the 34 evaluable specimens, including 15 breast cancers, 5 ovarian cancers, 5 lung cancers, and 9 lymphomas, none showed stimulation of tumor growth. Interestingly, a significant inhibition of the tumor proliferation was seen in one breast cancer and in one large cell immunoblastic non-Hodgkin's lymphoma after continuous exposure of PIXY321. In conclusion, the use of PIXY321 to reduce myelosuppression after high-dose chemotherapy appears unlikely to result in stimulation of the growth of malignant cells in patients with lymphoma or cancers of the breast, lung, and ovary.
PIXY321是一种粒细胞-巨噬细胞集落刺激因子/白细胞介素3(GM-CSF/IL-3)基因工程杂交体,在体外、体内以及接受大剂量化疗的患者中,它在刺激定向髓系祖细胞方面表现出比GM-CSF或IL-3更强的生物学活性。然而,一个担忧是PIXY321可能刺激具有功能性GM-CSF或IL-3受体的恶性细胞增殖。因此,我们使用人肿瘤克隆试验,测试了浓度范围为0.1至100 ng/ml的几种PIXY321对直接取自98例实体瘤患者以及霍奇金淋巴瘤或非霍奇金淋巴瘤患者的肿瘤细胞的影响。在34份可评估标本中,包括15例乳腺癌、5例卵巢癌、5例肺癌和9例淋巴瘤,均未显示出肿瘤生长受到刺激。有趣的是,在持续暴露于PIXY321后,在1例乳腺癌和1例大细胞免疫母细胞性非霍奇金淋巴瘤中观察到肿瘤增殖受到显著抑制。总之,在淋巴瘤或乳腺癌、肺癌和卵巢癌患者中,使用PIXY321减轻大剂量化疗后的骨髓抑制似乎不太可能导致恶性细胞生长受到刺激。