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Automated Preparation of [68Ga]Ga-3BP-3940 on a Synthesis Module for PET Imaging of the Tumor Microenvironment
Published on: April 25, 2025
Nuclear Medicine Application of Pentixafor/Pentixather Targeting CXCR4 for Imaging and Therapy in Related Disease
Zhenying Chen1, Qianqian Xue1, Shaobo Yao1
1Department of Nuclear Medicine, The First Affiliated Hospital of Fujian Medical University, Fuzhou, 35005, Fujian, P.R. China.
Abstract:
C-X-C-motif chemokine receptor 4 (CXCR4) is a novel predictive biomarker for metastasis and poor prognosis in individuals with malignancies. CXCL12 is the only cognate ligand of CXCR4. CXCL12/CXCR4 signaling pathways are involved in the cross-talk among cancer cells, T cells, stromal cells, and their microenvironments, including the regulation and direction of T cell migration (chemotaxis), proliferation, and differentiation of immature progenitor stem cells. As CXCR4 overexpression is related to tumor prognosis, it is essential to quantitatively evaluate CXCR4 expression levels in vivo. 68Ga-Pentixafor, as a radiolabeled tracer, shows high specificity and affinity for CXCR4 in tumors. Thus, CXCR4-directed imaging with 68Ga-Pentixafor has been investigated to evaluate CXCR4 expression in patients non-invasively. In recent years, many small cohorts, including those of individuals with hematologic malignancies, solid tumors, and cardiovascular and infectious diseases, have been reported. So far, 68Ga-Pentixafor has been used successfully in individuals with hematologic malignancies. In addition, Lutetium-177 (177Lu) or Yttrium-90 (90Y)-labeled Pentixather (an analog of Pentixafor) suggested high potential applicability in tumor endoradiotherapy (ERT) with CXCR4 overexpression. Patients with advanced-stage multiple myeloma, refractory acute leukemia, and diffuse large B-cell lymphoma received a certain amount of 177Lu-Pentixather or 90Y-Pentixather. This review aimed to overview the current CXCR4-directed positron emission computed tomography (PET) molecular imaging based on Pentixafor in several diseases and ERT.
Insights
C-X-C-motif chemokine receptor 4 (CXCR4) imaging with 68Ga-Pentixafor shows promise for diagnosing malignancies. CXCR4-targeted radiotracers like 177Lu-Pentixather also hold potential for effective tumor endoradiotherapy.
Area of Science:
- Oncology and Nuclear Medicine
- Molecular Imaging and Targeted Therapy
Background:
- C-X-C-motif chemokine receptor 4 (CXCR4) is a biomarker for metastasis and poor prognosis in malignancies.
- CXCR4 overexpression correlates with tumor progression, necessitating in vivo expression evaluation.
- CXCL12/CXCR4 signaling influences cancer cell and immune cell interactions within the tumor microenvironment.
Approach:
- Utilizing 68Ga-Pentixafor, a radiolabeled tracer with high specificity and affinity for CXCR4, for non-invasive in vivo imaging.
- Investigating CXCR4-directed positron emission computed tomography (PET) molecular imaging with Pentixafor across various diseases.
- Exploring the therapeutic potential of Lutetium-177 (177Lu) or Yttrium-90 (90Y)-labeled Pentixather (an analog of Pentixafor) for endoradiotherapy (ERT).
Key Points:
- 68Ga-Pentixafor enables quantitative CXCR4 expression assessment in vivo, crucial for prognosis.
- Successful applications of 68Ga-Pentixafor imaging reported in hematologic malignancies and other diseases.
- 177Lu-Pentixather and 90Y-Pentixather demonstrate significant potential for CXCR4-targeted tumor endoradiotherapy.
Conclusions:
- CXCR4-directed PET imaging with 68Ga-Pentixafor is a valuable tool for evaluating CXCR4 expression in diverse malignancies.
- Pentixafor-based molecular imaging and Pentixather-based endoradiotherapy represent promising advancements in cancer management.
- Further research and clinical application of these CXCR4-targeted strategies are warranted for improved patient outcomes.
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