89Zr-Trastuzumab PET/CT Imaging of HER2-Positive Breast Cancer for Predicting Pathological Complete Response after Neoadjuvant Systemic Therapy: A Feasibility Study

Author:

Linders D. G. J.1ORCID,Deken M. M.1,van Dam M. A.1ORCID,Wasser M. N. J. M.2ORCID,Voormolen E. M. C.2,Kroep J. R.3ORCID,van Dongen G. A. M. S.4,Vugts D.4,Oosterkamp H. M.5,Straver M. E.6,van de Velde C. J. H.1,Cohen D.7,Dibbets-Schneider P.8ORCID,van Velden F. H. P.8ORCID,Pereira Arias-Bouda L. M.89,Vahrmeijer A. L.1,Liefers G. J.1,de Geus-Oei L. F.81011ORCID,Hilling D. E.112ORCID

Affiliation:

1. Department of Surgery, Leiden University Medical Center, 2333 ZA Leiden, The Netherlands

2. Department of Radiology, Leiden University Medical Center, 2333 ZA Leiden, The Netherlands

3. Department of Medical Oncology, Leiden University Medical Center, 2333 ZA Leiden, The Netherlands

4. Department of Radiology and Nuclear Medicine, Amsterdam University Medical Center, 1081 HV Amsterdam, The Netherlands

5. Department of Internal Medicine, Haaglanden Medical Center, 2512 VA The Hague, The Netherlands

6. Department of Surgery, Haaglanden Medical Center, 2512 VA The Hague, The Netherlands

7. Department of Pathology, Leiden University Medical Center, 2333 ZA Leiden, The Netherlands

8. Department of Radiology, Section of Nuclear Medicine, Leiden University Medical Center, 2333 ZA Leiden, The Netherlands

9. Department of Nuclear Medicine, Alrijne Hospital, 2353 GA Leiderdorp, The Netherlands

10. Biomedical Photonic Imaging Group, University of Twente, 7522 NB Enschede, The Netherlands

11. Department of Radiation Science and Technology, Delft University of Technology, 2628 CD Delft, The Netherlands

12. Department of Surgical Oncology and Gastrointestinal Surgery, Erasmus MC Cancer Institute, University Medical Center Rotterdam, 3015 GD Rotterdam, The Netherlands

Abstract

Background: Approximately 20% of invasive ductal breast malignancies are human epidermal growth factor receptor 2 (HER2)-positive. These patients receive neoadjuvant systemic therapy (NAT) including HER2-targeting therapies. Up to 65% of patients achieve a pathological complete response (pCR). These patients might not have needed surgery. However, accurate preoperative identification of a pCR remains challenging. A radiologic complete response (rCR) on MRI corresponds to a pCR in only 73% of patients. The current feasibility study investigates if HER2-targeted PET/CT-imaging using Zirconium-89 (89Zr)-radiolabeled trastuzumab can be used for more accurate NAT response evaluation. Methods: HER2-positive breast cancer patients scheduled to undergo NAT and subsequent surgery received a 89Zr-trastuzumab PET/CT both before (PET/CT-1) and after (PET/CT-2) NAT. Qualitative and quantitative response evaluation was performed. Results: Six patients were enrolled. All primary tumors could be identified on PET/CT-1. Four patients had a pCR and two a pathological partial response (pPR) in the primary tumor. Qualitative assessment of PET/CT resulted in an accuracy of 66.7%, compared to 83.3% of the standard-of-care MRI. Quantitative assessment showed a difference between the SUVR on PET/CT-1 and PET/CT-2 (ΔSUVR) in patients with a pPR and pCR of −48% and −90% (p = 0.133), respectively. The difference in tumor-to-blood ratio on PET/CT-1 and PET/CT-2 (ΔTBR) in patients with pPR and pCR was −79% and −94% (p = 0.133), respectively. Three patients had metastatic lymph nodes at diagnosis that were all identified on PET/CT-1. All three patients achieved a nodal pCR. Qualitative assessment of the lymph nodes with PET/CT resulted in an accuracy of 66.7%, compared to 50% of the MRI. Conclusions: NAT response evaluation using 89Zr-trastuzumab PET/CT is feasible. In the current study, qualitative assessment of the PET/CT images is not superior to standard-of-care MRI. Our results suggest that quantitative assessment of 89Zr-trastuzumab PET/CT has potential for a more accurate response evaluation of the primary tumor after NAT in HER2-positive breast cancer.

Funder

European Research Council Advanced Grant

Publisher

MDPI AG

Subject

Cancer Research,Oncology

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