阿仑单抗联合氟达拉滨和美法仑联合或不联合环孢素、吗替麦考酚酯及低剂量全身照射后行供者外周血干细胞移植治疗血液系统恶性肿瘤

该数据集来自 clinicaltrials.gov,聚焦于血液系统恶性肿瘤患者接受阿仑单抗、氟达拉滨和美法仑组成的减低强度预处理方案,联合或不联合环孢素、吗替麦考酚酯及低剂量全身放疗,随后进行单倍型错配、KIR I 类表位错配的 CD34 阳性异基因外周血干细胞移植

Alliance for Clinical Trials in OncologyAlliance for Clinical Trials in Oncology
clinicaltrials
浏览 9
基因组预测LeukemiaLymphomaMyelodysplastic Syndromes
Alemtuzumab Plus Fludarabine and Melphalan With or Without Cyclosporine, Mycophenolate Mofetil, and Low-Dose Total-Body Irradiation Therapy Followed by Donor Peripheral Stem Cell Transplant in Treating Patients With Hematologic Cancer

基本信息

模态
基因组
任务类型
预测
创建/更新时间
2026-10-12

资源简介

阿仑单抗联合氟达拉滨和美法仑联合或不联合环孢素、吗替麦考酚酯及低剂量全身照射后行供者外周血干细胞移植治疗血液系统恶性肿瘤

该数据集来自 clinicaltrials.gov,聚焦于血液系统恶性肿瘤患者接受阿仑单抗、氟达拉滨和美法仑组成的减低强度预处理方案,联合或不联合环孢素、吗替麦考酚酯及低剂量全身放疗,随后进行单倍型错配、KIR I 类表位错配的 CD34 阳性异基因外周血干细胞移植。覆盖白血病、淋巴瘤、多发性骨髓瘤和浆细胞肿瘤、骨髓增生异常综合征及骨髓增生异常/骨髓增殖性肿瘤。可用于评估移植后第 35 天植入成功率、移植物抗宿主病风险及无进展生存期等结局(来源 clinicaltrials.gov)。

【数据内容】

源站描述(机器翻译,仅供参考):条件:白血病、淋巴瘤、多发性骨髓瘤和浆细胞肿瘤、骨髓增生异常综合征、骨髓增生异常/骨髓增殖性肿瘤。目的: 确定由阿仑单抗、氟达拉滨和美法仑组成的减低强度预处理方案,联合或不联合环孢素、吗替麦考酚酯和低剂量全身放疗,随后进行单倍型错配、KIR I 类表位错配的 CD34 阳性异基因外周血干细胞移植,能否促进至少 85% 的复发性、难治性或高危血液系统恶性肿瘤患者在移植后第 35 天实现植入。 确定接受这些方案治疗的患者发生移植物抗宿主病的风险。 初步确定这些方案在这些患者中基于无进展生存期的疗效。 将结局、植入情况、a

【主题与分类】

主题标签:Leukemia、Lymphoma、Myelodysplastic Syndromes。本站分类:肿瘤/白血病。

【获取与许可】

源站页面:https://clinicaltrials.gov/study/NCT00085449

官方服务

专家保障全链路合规授权与标注交付

陕川双基地 × 超十家三甲医院直连

从合规授权、采集治理、专业标注到数据集交付,我们提供全链路闭环服务,让高质量临床数据即拿即用。

⚡️ 需要原始数据或标注支持?联系我们获取定制方案。

帮我联系

下载信息

注册下载

需要注册 Kaggle 账号并登录后下载,适合需要跟踪下载记录和使用 API 的用户。

暂未开放

公开下载

无需注册即可直接获取公开样本或文档,适合快速预览和评估数据集质量。

免登录

有偿下载

公开数据集受托下载与技术交付服务。

提供高速下载与技术交付服务(收技术服务费,非数据销售)

暂未开放

当前数据集主要来源为 Kaggle 公开托管,完整影像包建议通过原始链接或 Kaggle API 获取。

使用方式

数据集获取

源站:https://clinicaltrials.gov/study/NCT00085449

标准获取流程:

  1. 访问源站链接,注册/登录账号;
  2. 进入数据集详情页,按页面指引申请权限或直接下载;
  3. 部分平台提供 SDK,例如:
    • OpenDataLab: pip install openxlab 后 openxlab.dataset.get(...)
    • ModelScope: pip install modelscope 后 modelscope download
    • 天池: 登录后页面提供直链下载
      以源站「数据下载/使用文档」页面为准。

数据说明

Conditions: Leukemia, Lymphoma, Multiple Myeloma and Plasma Cell Neoplasm, Myelodysplastic Syndromes, Myelodysplastic/Myeloproliferative Neoplasms. OBJECTIVES: * Determine the ability of a reduced-intensity conditioning regimen comprising alemtuzumab, fludarabine, and melphalan with or without cyclosporine, mycophenolate mofetil, and low-dose total body radiotherapy followed by haplotype-mismatched, KIR class I epitope-mismatched CD34-positive allogeneic peripheral blood stem cell transplantation to facilitate engraftment by day 35 post-transplantation in at least 85% of patients with relapsed, refractory, or poor-risk hematological malignancies. * Determine the risk of graft-versus-host-disease in patients treated with these regimens. * Determine, preliminarily, the efficacy of these regimens, in terms of progression-free survival, in these patients. * Correlate outcomes, engraftment, and progression-free survival with the number of detectable alloreactive natural killer cell clones before transplantation and after engraftment in patients treated with these regimens. * Determine immune reconstitution in patients treated with these regimens. OUTLINE: This is a multicenter, pilot study. Patients are initially treated with conditioning regimen A. If adequate donor engraftment is not achieved, subsequent patients are treated with conditioning regimen B. * Conditioning regimen A: Patients receive alemtuzumab IV over 2 hours on days -14 to -12; fludarabine IV over 30 minutes on days -7 to -3; and melphalan IV over 20-30 minutes on day -2. * Conditioning regimen B: Patients receive oral or IV cyclosporine twice daily and oral or IV mycophenolate mofetil twice daily on days -15 to 0. Patients also receive alemtuzumab, fludarabine, and melphalan as in conditioning regimen A. Patients undergo low-dose total body irradiation twice daily on days -2 and -1. All patients undergo allogeneic, T-cell-depleted, CD34-positive peripheral blood stem cell transplantation on day 0. Patients receive sargramostim (GM-CSF) subcutaneously beginning on day 1 and continuing until blood counts recover. Patients are followed every 3 months

数据加载示例(图像类)

from PIL import Image
import glob, os

files = (glob.glob(os.path.join(path, "**", "*.png"), recursive=True)
       + glob.glob(os.path.join(path, "**", "*.jpg"), recursive=True)
       + glob.glob(os.path.join(path, "**", "*.tif"), recursive=True))
print("图像文件数:", len(files))
img = Image.open(files[0]); print("尺寸/模式:", img.size, img.mode)

# torchvision Dataset 方式:
# from torchvision import datasets
# ds = datasets.ImageFolder(path)  # 要求 子目录=类别

目录组织与标注格式以源站说明和下载后实际文件为准。

数据缺失?

依托陕西、四川两大基地,我们与超过十家三甲医院建立直接合作关系,覆盖合规授权、采集治理、专业标注、数据交付的全流程,为AI医疗团队提供即拿即用的高质量临床数据。

⚡️ 需要数据支持或标注服务?立即联系我们获取专业方案。

获取专属数据定制方案