Early metabolic response using FDG PET/CT and molecular phenotypes of breast cancer treated with neoadjuvant chemotherapy
Creators
- 1. Cancer Research Institute, Seoul National University College of Medicine, Seoul (Korea, Republic of)
- 2. Department of Internal Medicine, Seoul National University College of Medicine, Seoul (Korea, Republic of)
- 3. Department of Radiology, Seoul National University College of Medicine, Seoul (Korea, Republic of)
- 4. Department of Pathology, Seoul National University College of Medicine, Seoul (Korea, Republic of)
- 5. Department of Surgery, Seoul National University College of Medicine, Seoul (Korea, Republic of)
- 6. Department Nuclear Medicine, Seoul National University College of Medicine, Seoul (Korea, Republic of)
Description
This study was aimed 1) to investigate the predictive value of FDG PET/CT (fluorine-18 fluorodeoxyglucose positron emission tomography/computed tomography) for histopathologic response and 2) to explore the results of FDG PET/CT by molecular phenotypes of breast cancer patients who received neoadjuvant chemotherapy. Seventy-eight stage II or III breast cancer patients who received neoadjuvant docetaxel/doxorubicin chemotherapy were enrolled in this study. FDG PET/CTs were acquired before chemotherapy and after the first cycle of chemotherapy for evaluating early metabolic response. The mean pre- and post-chemotherapy standard uptake value (SUV) were 7.5 and 3.9, respectively. The early metabolic response provided by FDG PET/CT after one cycle of neoadjuvant chemotherapy was correlated with the histopathologic response after completion of neoadjuvant chemotherapy (P = 0.002). Sensitivity and negative predictive value were 85.7% and 95.1%, respectively. The estrogen receptor negative phenotype had a higher pre-chemotherapy SUV (8.6 vs. 6.4, P = 0.047) and percent change in SUV (48% vs. 30%, P = 0.038). In triple negative breast cancer (TNBC), the pre-chemotherapy SUV was higher than in non-TNBC (9.8 vs. 6.4, P = 0.008). The early metabolic response using FDG PET/CT could have a predictive value for the assessment of histopathologic non-response of stage II/III breast cancer treated with neoadjuvant chemotherapy. Our findings suggest that the initial SUV and the decline in SUV differed based on the molecular phenotype. ClinicalTrials.gov: http://www.clinicaltrials.gov/ct2/show/NCT01396655
Availability note (English)
Available from http://dx.doi.org/10.1186/1471-2407-11-452; Available from http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3224348Additional details
Identifiers
Publishing Information
- Journal Title
- BMC cancer (Online)
- Journal Volume
- 11
- Journal Page Range
- p. 452
- ISSN
- 1471-2407
INIS
- Country of Publication
- United Kingdom
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 46102650
- Subject category
- S62: RADIOLOGY AND NUCLEAR MEDICINE;
- Descriptors DEI
- CHARGES; CHEMOTHERAPY; DOXORUBICIN; ESTROGENS; FLUORINE 18; FLUORODEOXYGLUCOSE; MAMMARY GLANDS; NEOPLASMS; PATIENTS; PHENOTYPE; RECEPTORS; SENSITIVITY; UPTAKE
- Descriptors DEC
- ANTIBIOTICS; ANTI-INFECTIVE AGENTS; ANTIMETABOLITES; ANTINEOPLASTIC DRUGS; BETA DECAY RADIOISOTOPES; BETA-PLUS DECAY RADIOISOTOPES; BODY; DISEASES; DRUGS; FLUORINE ISOTOPES; GLANDS; HORMONES; HOURS LIVING RADIOISOTOPES; ISOMERIC TRANSITION ISOTOPES; ISOTOPES; LIGHT NUCLEI; MEDICINE; MEMBRANE PROTEINS; NANOSECONDS LIVING RADIOISOTOPES; NUCLEI; ODD-ODD NUCLEI; ORGANIC COMPOUNDS; ORGANS; PROTEINS; RADIOISOTOPES; STEROID HORMONES; THERAPY
Optional Information
- Copyright
- Copyright (c)2011 Keam et al
- Notes
- PMCID: PMC3224348; PUBLISHER-ID: 1471-2407-11-452; PMID: 22011459; OAI: oai:pubmedcentral.nih.gov:3224348; licensee BioMed Central Ltd.