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Effects of capecitabine treatment on the uptake of thymidine analogs using exploratory PET imaging agents: 18F-FAU, 18F-FMAU, and 18F-FLT.
McHugh, Christopher I; Lawhorn-Crews, Jawana M; Modi, Dipenkumar; Douglas, Kirk A; Jones, Steven K; Mangner, Thomas J; Collins, Jerry M; Shields, Anthony F.
Afiliação
  • McHugh CI; Cancer Biology Graduate Program, Wayne State University, Detroit, MI, 48201, USA.
  • Lawhorn-Crews JM; Karmanos Cancer Institute and Oncology, Wayne State University, 4100 John R., HW04HO, Detroit, MI, 48201, USA.
  • Modi D; Karmanos Cancer Institute and Oncology, Wayne State University, 4100 John R., HW04HO, Detroit, MI, 48201, USA.
  • Douglas KA; Karmanos Cancer Institute and Oncology, Wayne State University, 4100 John R., HW04HO, Detroit, MI, 48201, USA.
  • Jones SK; Cancer Biology Graduate Program, Wayne State University, Detroit, MI, 48201, USA.
  • Mangner TJ; Radiology, Wayne State University, Detroit, MI, 48201, USA.
  • Collins JM; National Cancer Institute, Bethesda, MD, 20892, USA.
  • Shields AF; Karmanos Cancer Institute and Oncology, Wayne State University, 4100 John R., HW04HO, Detroit, MI, 48201, USA. shieldsa@karmanos.org.
Cancer Imaging ; 16(1): 34, 2016 Oct 17.
Article em En | MEDLINE | ID: mdl-27751167
ABSTRACT

BACKGROUND:

A principal goal for the use of positron emission tomography (PET) in oncology is for real-time evaluation of tumor response to chemotherapy. Given that many contemporary anti-neoplastic agents function by impairing cellular proliferation, it is of interest to develop imaging modalities to monitor these pathways. Here we examined the effect of capecitabine on the uptake of thymidine analogs used with PET 3'-deoxy-3'-[18F]fluorothymidine (18F-FLT), 1-(2'-deoxy-2'-[18F]fluoro-ß-D-arabinofuranosyl) thymidine (18F-FMAU), and 1-(2'-deoxy-2'-[18F]fluoro-ß-D-arabinofuranosyl) uracil (18F-FAU) in patients with advanced cancer.

METHODS:

Fifteen patients were imaged, five with each imaging agent. Patients had been previously diagnosed with breast, colorectal, gastric, and esophageal cancers and had not received therapy for at least 4 weeks prior to the first scan, and had not been treated with any prior fluoropyrimidines. Subjects were imaged within a week before the start of capecitabine and on the second day of treatment, after the third dose of capecitabine. Tracer uptake was quantified by mean standard uptake value (SUVmean) and using kinetic analysis.

RESULTS:

Patients imaged with 18F-FLT showed variable changes in retention and two patients exhibited an increase in SUVmean of 172.3 and 89.9 %, while the other patients had changes ranging from +19.4 to -25.4 %. The average change in 18F-FMAU retention was 0.2 % (range -24.4 to 23.1) and 18F-FAU was -10.2 % (range -40.3 to 19.2). Observed changes correlated strongly with SUVmax but not kinetic measurements.

CONCLUSIONS:

This pilot study demonstrates that patients treated with capecitabine can produce a marked increase in 18F-FLT retention in some patients, which will require further study to determine if this flare is predictive of therapeutic response. 18F-FAU and 18F-FMAU showed little change, on average, after treatment.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Arabinofuranosiluracila / Didesoxinucleosídeos / Compostos Radiofarmacêuticos / Tomografia por Emissão de Pósitrons / Capecitabina / Neoplasias / Antimetabólitos Antineoplásicos Idioma: En Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Arabinofuranosiluracila / Didesoxinucleosídeos / Compostos Radiofarmacêuticos / Tomografia por Emissão de Pósitrons / Capecitabina / Neoplasias / Antimetabólitos Antineoplásicos Idioma: En Ano de publicação: 2016 Tipo de documento: Article