Peptide Receptor Radionuclide Therapy Outcomes in a North American Cohort With Metastatic Well-Differentiated Neuroendocrine Tumors.

Pancreas

From the *Division of Hematology, Oncology, and Bone and Marrow Transplantation and the Holden Comprehensive Cancer Center, University of Iowa Hospitals and Clinics, Iowa City, IA; †Banner MD Anderson Cancer Center, Gilbert, AZ; ‡Medical Associates Clinic, Dubuque; and §Department of Biostatistics, College of Public Health, University of Iowa; ∥Department of Radiology, University of Iowa Hospitals and Clinics; ¶Iowa City Veterans Administration Medical Center; #Division of Endocrinology and Metabolism and the Holden Comprehensive Cancer Center, University of Iowa Hospitals and Clinics; and **Department of Pediatrics, University of Iowa Hospitals and Clinics, Iowa City, IA; ††Institute of Nuclear Medicine, University Hospital Basel, Basel, Switzerland; ‡‡Division of Surgical Oncology, University of Iowa Hospitals and Clinics, Iowa City, IA; and §§Division of Medical Oncology, Mayo Clinic Rochester, Rochester, MN.

Published: February 2017

AI Article Synopsis

  • The study aimed to evaluate the outcomes of patients from the University of Iowa undergoing peptide receptor radionuclide therapy (PRRT) for neuroendocrine tumors (NETs).
  • A total of 135 patients were analyzed, revealing a median diagnosis age of 51 years, with common tumor locations including the small bowel (37.8%) and pancreas (26.0%).
  • Results showed that 65.8% of patients had a positive radiographic response, with an overall survival of 40 months, while higher levels of chromogranin A and pancreastatin indicated poorer survival outcomes.

Article Abstract

Objectives: The objective of this study was to describe the outcomes of patients in the University of Iowa Neuroendocrine Tumor (NET) Database treated with peptide receptor radionuclide therapy (PRRT).

Methods: One hundred thirty-five patients from the University of Iowa NET Database who received PRRT were analyzed, their characteristics were described, and survival was calculated.

Results: The median age at diagnosis was 51 years, and 64% were men. The primary tumor was located in the small bowel (SBNET) in 37.8%, in the pancreas (PNET) in 26.0%, in the lung in 13.3%, in unknown primary in 9.6%, and in other sites in 13.3%. A radiographic response of any magnitude was observed in 65.8%, 11.1% had a mixed response, and 15.4% showed progression. The overall survival (OS) from the first PRRT was 40 months, and the median time to progression was 23.9 months. Higher pretreatment chromogranin A and pancreastatin levels predicted inferior OS.

Conclusions: Peptide receptor radionuclide therapy resulted in a relatively long OS and time to progression in heavily pretreated North American patients with advanced NETs. Elevated pretreatment chromogranin A and pancreastatin predicted shorter OS after therapy. Peptide receptor radionuclide therapy is a valuable treatment option in patients with advanced NETs, especially SBNETS.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5595066PMC
http://dx.doi.org/10.1097/MPA.0000000000000734DOI Listing

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