Human gastrin- releasing peptide receptor expression in women with uterine cervix cancer

Pb-DOTAM-GRPR1 is a pharmaceutical radioimmunoconjugate consisiting of an α-particle-emitting radionuclide lead-212 ( Pb), a metal chelator DOTAM (1,4,7,10-tetrakis(carbamoylmethyl)-1,4,7,10-tetraazacyclododecane), and a gastrin-releasing peptide receptor (GRPR)-targeted antagonist currently being e...

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Published in:Frontiers in oncology Vol. 13; p. 1126426
Main Authors: Kunos, Charles A, Fabian, Denise, Napier, Dana, Stonecypher, Mark S, Duncan, Ravyn M, Hurt, Jason
Format: Journal Article
Language:English
Published: Switzerland Frontiers Media S.A 25-01-2023
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Summary:Pb-DOTAM-GRPR1 is a pharmaceutical radioimmunoconjugate consisiting of an α-particle-emitting radionuclide lead-212 ( Pb), a metal chelator DOTAM (1,4,7,10-tetrakis(carbamoylmethyl)-1,4,7,10-tetraazacyclododecane), and a gastrin-releasing peptide receptor (GRPR)-targeted antagonist currently being evaluated as therapy in uterine cervix and other cancer types. Previous studies have revealed that a variable proportion of uterine cervix cancer tumors overexpress the radiopharmaceutical target GRPR when assessed by cell proportion and staining intensity immunoreactive scores (IRS). Tumor response to Pb-DOTAM-GRPR1 strongly associates with GRPR overexpression, and therefore, it seems reasonable to assess uterine cervix cancer GRPR immunoreactivity for greater insight into the feasibility of using Pb-DOTAM-GRPR1 as a radiopharmaceutical treatment. We examined a series of 33 uterine cervix cancer paraffin-embedded tumors in order to establish whether this tumor type overexpresses GRPR at an IRS score of 6 or higher, as Pb-DOTAM-GRPR1 is currently being evaluated in clinical trials against tumors showing such a level of expression. The results show that five of five (100%) primary adenocarcinomas and 10 of 16 (63%) primary squamous cell tumors overexpress GRPR at an IRS score of 6 or higher. The frequency of overexpression in this study suggests that Pb-DOTAM-GRPR1 radiopharmaceutical treatment may be useful in the management of persistent, recurrent, or metastatic uterine cervix cancer patients. A phase I clinical trial involving patients with metastatic uterine cervix cancer is currently underway (NCT05283330).
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This article was submitted to Radiation Oncology, a section of the journal Frontiers in Oncology
Edited by: Mark Trombetta, Allegheny Health Network, United States
Reviewed by: Filipa Mendes, University of Lisbon, Portugal; Marcelo Mamede, Federal University of Minas Gerais, Brazil
ISSN:2234-943X
2234-943X
DOI:10.3389/fonc.2023.1126426