Ueno N T, Rizzo J D, Demirer T, Cheng Y C, Hegenbart U, Zhang M-J, Bregni M, Carella A, Blaise D, Bashey A, Bitran J D, Bolwell B J, Elfenbein G J, Fields K K, Freytes C O, Gale R P, Lazarus H M, Champlin R E, Stiff P J, Niederwieser D
The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Bone Marrow Transplant. 2008 Mar;41(6):537-45. doi: 10.1038/sj.bmt.1705940. Epub 2007 Dec 17.
We reviewed 66 women with poor-risk metastatic breast cancer from 15 centers to describe the efficacy of allogeneic hematopoietic cell transplantation (HCT). Median follow-up for survivors was 40 months (range, 3-64). A total of 39 patients (59%) received myeloablative and 27 (41%) reduced-intensity conditioning (RIC) regimens. More patients in the RIC group had poor pretransplant performance status (63 vs 26%, P=0.002). RIC group developed less chronic GVHD (8 vs 36% at 1 year, P=0.003). Treatment-related mortality rates were lower with RIC (7 vs 29% at 100 days, P=0.03). A total of 9 of 33 patients (27%) who underwent immune manipulation for persistent or progressive disease had disease control, suggesting a graft-vs-tumor (GVT) effect. Progression-free survival (PFS) at 1 year was 23% with myeloablative conditioning and 8% with RIC (P=0.09). Women who developed acute GVHD after an RIC regimen had lower risks of relapse or progression than those who did not (relative risk, 3.05: P=0.03), consistent with a GVT effect, but this did not affect PFS. These findings support the need for preclinical and clinical studies that facilitate targeted adoptive immunotherapy for breast cancer to explore the benefit of a GVT effect in breast cancer.
我们回顾了来自15个中心的66例高危转移性乳腺癌女性患者,以描述异基因造血细胞移植(HCT)的疗效。幸存者的中位随访时间为40个月(范围3 - 64个月)。共有39例患者(59%)接受了清髓性预处理方案,27例(41%)接受了减低强度预处理(RIC)方案。RIC组中更多患者移植前的体能状态较差(63%对26%,P = 0.002)。RIC组发生慢性移植物抗宿主病(GVHD)的比例较低(1年时为8%对36%,P = 0.003)。RIC方案的治疗相关死亡率较低(100天时为7%对29%,P = 0.03)。在33例因疾病持续或进展而接受免疫干预的患者中,共有9例(27%)病情得到控制,提示存在移植物抗肿瘤(GVT)效应。清髓性预处理方案组1年时的无进展生存期(PFS)为23%,RIC组为8%(P = 0.09)。接受RIC方案后发生急性GVHD的女性患者复发或进展风险低于未发生者(相对风险为3.05:P = 0.03),这与GVT效应一致,但这并未影响PFS。这些发现支持开展临床前和临床研究,以促进针对乳腺癌的靶向过继性免疫治疗,探索GVT效应在乳腺癌中的益处。