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YF-H-2015005, a CXCR4 Antagonist, for the Mobilization of Hematopoietic Stem Cells in Non-Hodgkin Lymphoma Patients: A Randomized, Controlled, Phase 3 Clinical Trial.
Liu, Weiping; Li, Yufu; Wang, Quanshun; Su, Hang; Ding, Kaiyang; Shuang, Yuerong; Gao, Sujun; Zou, Dehui; Jing, Hongmei; Chai, Ye; Zhang, Yicheng; Liu, Lihong; Wang, Chunling; Liu, Hui; Lin, Jinying; Zhu, Haiyan; Yao, Chen; Yan, Xiaoyan; Shang, Meixia; Wang, Shufang; Chang, Fengyuan; Wang, Xiaopei; Zhu, Jun; Song, Yuqin.
Afiliação
  • Liu W; Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education), Department of Lymphoma, Peking University Cancer Hospital & Institute, Beijing, China.
  • Li Y; Department of Hematology, Henan Cancer Hospital, Zhengzhou, China.
  • Wang Q; Department of Hematology, The First Medical Center, Chinese PLA General Hospital, Beijing, China.
  • Su H; Department of Lymphoma, The Fifth Medical Center, Chinese PLA General Hospital, Beijing, China.
  • Ding K; Department of Hematology, Anhui Provincial Cancer Hospital, Hefei, China.
  • Shuang Y; Department of Lymphoma & Hematology, Jiangxi Cancer Hospital, Nanchang, China.
  • Gao S; Department of Hematology, First Affiliated Hospital of Jilin University, Changchun, China.
  • Zou D; Department of Hematology, Chinese Academy of Medical Sciences & Peking Union Medical College, Tianjin, China.
  • Jing H; Department of Hematology, Peking University Third Hospital, Beijing, China.
  • Chai Y; Department of Hematology, Lanzhou University Second Hospital, Lanzhou, China.
  • Zhang Y; Department of Hematology, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.
  • Liu L; Department of Hematology, The Fourth Hospital of Hebei Medical University, Shijiazhuang, China.
  • Wang C; Department of Hematology, Huai'an First People's Hospital, Nanjing Medical University, Huai'an, China.
  • Liu H; Department of Hematology, Beijing Hospital, Beijing, China.
  • Lin J; Department of Hematology, People's Hospital of Guangxi Zhuang Autonomous Region, Nanning, China.
  • Zhu H; Department of Hematology, The First Medical Center, Chinese PLA General Hospital, Beijing, China.
  • Yao C; Department of Medical Statistics, Peking University First Hospital, Beijing, China.
  • Yan X; Peking University Clinical Research Institute, Beijing, China.
  • Shang M; Department of Medical Statistics, Peking University First Hospital, Beijing, China.
  • Wang S; Hefei Yifan Biopharmaceuticals Inc., Economic Development Zone, Hefei, China.
  • Chang F; Hefei Yifan Biopharmaceuticals Inc., Economic Development Zone, Hefei, China.
  • Wang X; Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education), Department of Lymphoma, Peking University Cancer Hospital & Institute, Beijing, China.
  • Zhu J; Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education), Department of Lymphoma, Peking University Cancer Hospital & Institute, Beijing, China.
  • Song Y; Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education), Department of Lymphoma, Peking University Cancer Hospital & Institute, Beijing, China.
Front Med (Lausanne) ; 8: 609116, 2021.
Article em En | MEDLINE | ID: mdl-33604348
ABSTRACT

Background:

YF-H-2015005, a novel CXCR4 antagonist, has been proven to increase the quantities of circulating hematopoietic stem cells (HSCs), which results in an adequate collection of HSCs in non-Hodgkin lymphoma (NHL) patients.

Methods:

This was a multicenter, double-blind, randomized (11), placebo-controlled phase III clinical trial. All patients received granulocyte colony-stimulating factor (G-CSF) for up to 8 consecutive days. YF-H-2015005 or placebo was administrated on the evening of day 4 and continued daily for up to 4 days. Apheresis was conducted 9-10 h after each dose of YF-H-2015005 or placebo. The primary endpoint was the proportion of NHL patients procuring ≥5 × 106/kg CD34+ HSCs within ≤4 apheresis sessions.

Results:

In total, 101 patients with NHL were enrolled. The proportions of patients achieving primary endpoint were 57 and 12% in YF-H-2015005 and placebo groups, respectively (P < 0.001). Moreover, a higher proportion of YF-H-2015005-treated patients reached a minimum target collection of ≥2 × 106/kg CD34+ HSCs in ≤4 apheresis days compared to placebo-treated patients (86 vs. 38%, P < 0.001). Furthermore, the median time to collect ≥2 or 5 × 106/kg CD34+ HSCs were 1 and 3 days in YF-H-2015005-treated patients, but 4 days and not reached in placebo-treated patients, respectively. No severe treatment emergent adverse events were observed in both YF-H-2015005 treatment and placebo groups.

Conclusions:

YF-H-2015005 plus G-CSF regimen was a tolerable combination with high efficacy, which might be used to rapidly mobilize and collect HSCs in NHL patients.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Clinical_trials Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Clinical_trials Idioma: En Ano de publicação: 2021 Tipo de documento: Article