Positron emitting 18F-2-deoxy-2-fluoro-D-glucose: potential 'hot' new therapy
Breast Cancer Research volume 5, Article number: 329 (2003)
Preclinical studies suggest that 18F-2-deoxy-2-fluoro-D-glucose (18F-FDG) kills breast cancer cells without significant marrow toxicity or parenchymal toxicity. Radiation dose calculations estimated from fluorodeoxyglucose positron emission tomography images in women with metastatic disease indicate that 18F-FDG should be a feasible and safe option in humans. Because the available radiotherapeutic agents, strontium 89 and samarium 153 provide palliation to a limited population of women with bony metastases, new radiopharmaceutical agents with broader applicability are needed. The development of 18F-FDG as the first positron-emitting radiotherapeutic has the potential to be an innovative treatment, not only in osteoblastic disease, but also in osteolytic disease and in soft tissue metastases.
Moadel and colleagues have explored the potential use of 18F-2-deoxy-2-fluoro-D-glucose (18F-FDG), a positron-emitting agent, as a radiomolecular therapy in the management of advanced breast cancer. In two separate transgenic mouse models of breast cancer, they demonstrated the feasibility and the efficacy of 18F-FDG as a treatment for metastatic disease. After 18F-FDG treatment, the mammary glands were removed from the mice and were examined for evidence of tumor cell kill. Apoptotic changes were observed in small tumors (< 1 cm) and necrosis was observed in larger lesions. To determine what the radiation dose would be in patients with breast cancer, the authors extrapolated the preclinical information to the fluorodeoxyglucose positron emission tomography (FDG PET) images from five women with widely disseminated breast cancer. The dose of radiation delivered was calculated according to the standard uptake value at the site of disease. Moadel and colleagues conclude that 18F-FDG therapy could be safely administered to these individuals without the risk of significant red marrow toxicity .
Samarium 153 and strontium 89 are the only radiopharmaceutical agents to date that are used to treat women with breast cancer. Both are approved for the management of bone metastases, which develop in more than 70% of women with advanced breast cancer and are the source of significant morbidity. Both agents are most effective in patients who have diffuse osteoblastic disease and who are also treated with external beam radiation to areas of significant tumor burden. These two available agents appear to be equivalent in efficacy, although samarium 153 may produce less myelosuppression [2, 3]. Samarium 153 and strontium 89 may also provide meaningful but short-lived palliation of bone pain. However, bone metastases are rarely the sole site of metastatic disease. An obvious advantage of 18F-FDG is that it could be used to treat both skeletal disease and extra-skeletal disease.
Presumably if a lesion can be imaged by FDG PET then it can also be treated with 18F-FDG. Because FDG PET has been shown to be superior to conventional radiography, the Food and Drugs Administration has approved FDG PET imaging in the staging of advanced breast cancer and in the assessment of response to treatment [4–8]. In women with locally advanced breast cancers, FDG PET may be more accurate than computerized tomography in identifying internal mammary and mediastinal nodes .
Similar to multiple myeloma, the bone lesions produced by breast cancer may be purely osteolytic. In such instances the serum alkaline phosphatase and bone scintigraphy may be entirely normal. FDG PET may be more effective than conventional radiography and bone scintigraphy in identifying osteolytic disease . If this is the case 18F-FDG may prove superior to samarium 153 and strontium 89. If FDG PET identifies disease with greater resolution than conventional radiography, then presumably 18F-FDG may also be able to control more disease.
With our present resolution capabilities, FDG PET is unlikely to supplant surgery for staging newly diagnosed breast cancers. Sentinel node mapping appears to be superior to FDG PET staging of the axilla as FDG PET is unable to identify micrometastatic disease and small amounts of macrometastatic disease in the axilla. It seems unlikely at this time that 18F-FDG will have a role in the treatment of early stage disease .
The uptake of 18F-FDG varies according to the tumor histology, the microvasculature, the proliferative rate, the tumor cell density and the degree of necrosis. 18F-FDG uptake requires the tumor to have the ability both to incorporate glucose into the cell and to phosphorylate glucose to glucose-6-phosphate [12, 13]. Breast cancer is a heterogeneous disease with distinct natural histories defined by histologic type, by tumor grade, by the presence or absence of hormone receptors and by the her-2 expression. Recognizing the variability of the disease, it is not surprising that 18F-FDG uptake varies from patient to patient and may even vary from metastasis to metastasis in the same patient [12, 14]. Because the delivered dose of radiation is calculated by the standard uptake value, the differences in FDG PET uptake have implications for determining the radiation dose at different sites following 18F-FDG therapy.
Even in the palliative setting, the toxicity of treatment must be minimized. At present, most of the women who receive strontium 89 or samarium 153 already have some degree of marrow compromise as a result of prior cytotoxic therapy, external beam irradiation and tumor infiltration. Even small doses of radiation to the red marrow may impact blood counts.
Moadel and colleagues acknowledge that uptake of 18F-FDG by the brain is "impossible to avoid" and provides a dose of 570 cGy . Similarly muscle, both skeletal muscle and cardiac muscle, may incorporate 18F-FDG. The muscle uptake of 18F-FDG may be decreased by the patient fasting or by administering benzodiazepines. Whether corticosteroids will decrease edema and inflammation in the brain will need to be determined.
More than 80,000 women each year are diagnosed with metastatic breast cancer. In this setting the goal of intervention with chemotherapy and hormonal therapies is to provide palliation. After hormonal therapies have been exhausted, sequential single-agent chemotherapy is advocated. Even combinations of cytotoxic chemotherapy do not appear to alter patient survival. The addition of the humanized antibody to the her-2 protein Herceptin has recently been shown to improve survival when it is co-administered with first-line chemotherapy .
Newer agents that are targeted at unique aspects of tumor biology are the hope for the future. These targeted agents are often used in conjunction with conventional agents. 18F-FDG will possibly be used in combination with other systemic therapies. The refinement of ways to target radiation therapy to the tumor is an important avenue to pursue. Moadel and colleagues are to be congratulated for taking the steps to develop a positron-emitting agent for use in the breast cancer arsenal.
- FDG PET:
= fluorodeoxyglucose positron emission tomography.
Moadel RM, Nguyen AV, Lin EY, Lu P, Mani J, Blaufox MD, Pollard JW, Dadachova E: Positron emission tomography agent 2-deoxy-2-18F-fluoro-D-glucose as a therapeutic potential in breast cancer. Breast Cancer Res. 2003, 5: R199-R205. 10.1186/bcr643.
Silberstein EB: Systemic radiopharmaceutical therapy of painful osteoblastic metastases. Semin Radiat Oncol. 2000, 10: 240-249. 10.1053/srao.2000.6592.
Serafini AN, Houston SJ, Resche I, Quick DP, Grund FM, Ell PJ, Bertrand A, Ahmann FR, Orihuela E, Reid RH, Lerski RA, Collier BD, McKillop JH, Purnell GL, Pecking AP, Thomas FD, Harrison KA: Palliation of pain associated with metastatic bone cancer using samarium-153 lexidonam: a double-blind placebo-controlled clinical trial. J Clin Oncol. 1998, 16: 1574-1581.
Hoh CK, Hawkins RA, Glaspy JA, Dahlbom M, Tse NY, Hoffman EJ, Schiepers C, Choi Y, Rege S, Nitzsche E, et al: Cancer detection with whole-body PET using 2-[18F]fluoro-2-deoxy-D-glucose. J Comput Assist Tomogr. 1993, 17: 582-589.
Moon DH, Maddahi J, Silverman DH, Glaspy JA, Phelps ME, Hoh CK.: Accuracy of whole-body fluorine-18-FDG PET for the detection of recurrent or metastatic breast carcinoma. J Nucl Med. 1998, 39: 431-435.
Smith IC, Welch AE, Hutcheon AW, Miller ID, Payne S, Chilcott F, Waikar S, Whitaker T, Ah-See AK, Eremin O, Heys SD, Gilbert FJ, Sharp PF: Positron emission tomography using [18F]fluorodeoxyglucose for monitoring primary chemotherapy in breast cancer. J Clin Oncol. 2000, 18: 1676-1688.
Schelling M, Avril N, Nahrig J, Kuhn W, Romer W, Sattler D, Werner M, Dose J, Janicke F, Graeff H, Schwaiger M: Positron emission tomography using [18F]-fluorodeoxy-D-glucose to predict the pathologic response of breast cancer to primary chemotherapy. J Clin Oncol. 2000, 18: 1689-1695.
Mortimer JE, Dehdashti F, Siegel BA, Trinkaus K, Katzenellenbogen JA, Welch MJ: Metabolic flare: indicator of hormone responsiveness in advanced breast cancer. J Clin Oncol. 2001, 19: 2797-2803.
Eubank WB, Mankoff DA, Takasugi J, Vesselle H, Eary JF, Shanley TJ, Gralow JR, Charlop A, Ellis GK, Lindsley KL, Austin-Seymour MM, Funkhouser CP, Livingston RB: 18Fluorodeoxyglucose positron emission tomography to detect mediastinal or internal mammary metastases in breast cancer. J Clin Oncol. 2001, 19: 3516-3523.
Cook GJ, Houston S, Rubens R, Maisey MN, Fogelman I: Detection of bone metastases in breast cancer by 18FDG PET: differing metabolic activity in osteoblastic and osteolytic lesions. J Clin Oncol. 1998, 16: 3375-3379.
Guller U, Nitzsche E, Moch H, Zuber M: Is positron emission tomography an accurate non-invasive alternative to sentinel lymph node biopsy in breast cancer patients?. J Natl Cancer Inst. 2003, 95: 1040-1043. 10.1093/jnci/95.14.1040.
Bos R, van Der Hoeven JJ, van Der Wall E, van Der Groep P, van Diest PJ, Comans EF, Joshi U, Semenza GL, Hoekstra OS, Lammertsma AA, Molthoff CF: Biologic correlates of 18fluorodeoxyglucose uptake in human breast cancer measured by positron emission tomography. J Clin Oncol. 2002, 20: 379-387. 10.1200/JCO.20.2.379.
Avril N, Rose CA, Schelling M, Dose J, Kuhn W, Bense S, Weber W, Ziegler S, Graeff H, Schwaiger M: Breast imaging with positron emission tomography and fluorine-18 fluorodeoxyglucose: use and limitations. J Clin Oncol. 2000, 18: 3495-3502.
Mortimer JE, Dehdashti F, Siegel BA, Katzenellenbogen JA, Fracasso P, Welch MJ: Positron emission tomography with 2-[18F] fluoro-2-deoxy-D-glucose and 16α-[18F] fluoro-17β-estradiol in breast cancer: correlation with estrogen receptor status and response to systemic therapy. Clin Cancer Res. 1996, 2: 933-939.
Slamon DJ, Leyland-Jones B, Shak S, Fuchs H, Paton V, Bajamonde A, Fleming T, Eiermann W, Wolter J, Pegram M, Baselga J, Norton L: Use of chemotherapy plus a monoclonal antibody against HER2 for metastatic breast cancer that overexpressed HER2. New Engl J Med. 2001, 344: 783-792. 10.1056/NEJM200103153441101.
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Mortimer, J.E., Taylor, M.E. Positron emitting 18F-2-deoxy-2-fluoro-D-glucose: potential 'hot' new therapy. Breast Cancer Res 5, 329 (2003). https://doi.org/10.1186/bcr725
- breast cancer