Shpall E J, Stemmer S M, Bearman S I, Myers S, Purdy M, Jones R B
University of Colorado Bone Marrow Transplant Program, University of Colorado Health Sciences Center, Denver 80262.
Breast Cancer Res Treat. 1993;26 Suppl:S19-23. doi: 10.1007/BF00668356.
High-dose chemotherapy and autologous bone marrow transplantation (ABMT) are commonly used to treat selected patients with high-risk breast cancer. A limitation of ABMT is that clonogenic cancer cells could be collected with the bone marrow and produce a relapse of diseases when reinfused into patients. Purging the marrow ex vivo may eliminate the tumor cells, but it can also delay engraftment. We employed two different purging methods whereby breast cancer cells were depleted without delaying engraftment. The addition of WR-2721 (amifostine) to 4-hydroperoxycyclophosphamide (4-HC) reduced the time to engraftment by 10 days compared with marrow purged with 4-HC alone (26 versus 37 days, respectively). The positive selection of CD34+ hematopoietic progenitors produced engraftment within 21 days. The use of granulocyte colony-stimulating factor (G-CSF) accelerated the engraftment time of CD34+ hematopoietic progenitors to 11 days.
大剂量化疗和自体骨髓移植(ABMT)常用于治疗部分高危乳腺癌患者。ABMT的一个局限性在于,克隆形成癌细胞可能随骨髓一同采集,并在回输至患者体内时导致疾病复发。体外净化骨髓或许能清除肿瘤细胞,但也可能延迟植入。我们采用了两种不同的净化方法,在不延迟植入的情况下耗尽乳腺癌细胞。与单独使用4-氢过氧环磷酰胺(4-HC)净化的骨髓相比,在4-氢过氧环磷酰胺(4-HC)中添加WR-2721(氨磷汀)可将植入时间缩短10天(分别为26天和37天)。对CD34+造血祖细胞进行阳性选择可在21天内实现植入。使用粒细胞集落刺激因子(G-CSF)可将CD34+造血祖细胞的植入时间加速至11天。