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[¹²³I]Iodometomidate imaging in adrenocortical carcinoma.

AbstractCONTEXT:
Imaging with [¹²³I]iodometomidate ([¹²³I]IMTO) has been shown to diagnose adrenocortical lesions with high sensitivity and specificity.
OBJECTIVE:
Our objective was to evaluate the clinical utility of [¹²³I]IMTO imaging in adrenocortical carcinoma (ACC).
DESIGN:
We conducted a prospective monocentric diagnostic study and a prospective case series at a single tertiary referral center.
PATIENTS AND INTERVENTIONS:
Fifty-eight patients with histologically confirmed ACC, all European Network for the Study of Adrenal Tumors stage IV (with distant metastases), received 185 MBq [¹²³I]IMTO. Sequential planar whole-body scans until 24 hours post injection and single photon emission computed tomography/computed tomography (SPECT/CT) hybrid imaging 4 to 6 hours post injection were performed.
MAIN OUTCOME MEASURES:
Outcome measures included uptake of [¹²³I]IMTO in ACC lesions, sensitivity and specificity of [¹²³I]IMTO imaging compared with conventional imaging, and number of patients eligible for [¹³¹I]IMTO therapy.
RESULTS:
Of 430 lesions detected by conventional imaging, 30% showed strong, 8% moderate, and 62% no tracer accumulation. [¹²³I]IMTO detected both primary and metastatic lesions of ACC. However, a substantial percentage of lesions failed to show [¹²³I]IMTO uptake. The overall sensitivity and specificity values were 38% and 100%, respectively. Thirty-four patients (59%) had at least 1 [¹²³I]IMTO-positive lesion. Cortisol and aldosterone secretion by ACC was positively correlated to [¹²³I]IMTO uptake (P = .01); cytotoxic chemotherapy and mitotane treatment presumably did not influence tracer uptake. Twenty-one patients (36.2%) had radiotracer uptake in all lesions ≥ 2 cm and therefore were potential candidates for targeted systemic radiotherapy with [¹³¹I]IMTO.
CONCLUSION:
About one-third of patients with ACC show specific retention of [¹²³I]IMTO in metastatic lesions. This study provides support for the conduct of a prospective trial to determine whether the first molecular informed therapy using [¹³¹I]IMTO will be of value to patients with metastatic ACC.
AuthorsMichael C Kreissl, Andreas Schirbel, Martin Fassnacht, Heribert Haenscheid, Frederik A Verburg, Stefanie Bock, Wolfgang Saeger, Pascal Knoedler, Christoph Reiners, Andreas K Buck, Bruno Allolio, Stefanie Hahner
JournalThe Journal of clinical endocrinology and metabolism (J Clin Endocrinol Metab) Vol. 98 Issue 7 Pg. 2755-64 (Jul 2013) ISSN: 1945-7197 [Electronic] United States
PMID23609836 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Iodine Radioisotopes
  • Radiopharmaceuticals
  • iodophenyl metomidate
  • Aldosterone
  • Hydrocortisone
  • Etomidate
Topics
  • Adrenal Cortex (diagnostic imaging, metabolism, pathology)
  • Adrenal Cortex Neoplasms (blood, diagnostic imaging, metabolism, pathology)
  • Adrenocortical Carcinoma (diagnostic imaging, metabolism, pathology, secondary)
  • Adult
  • Aged
  • Aldosterone (blood, metabolism)
  • Cohort Studies
  • Etomidate (analogs & derivatives, pharmacokinetics)
  • Female
  • Humans
  • Hydrocortisone (blood, metabolism)
  • Iodine Radioisotopes (pharmacokinetics)
  • Male
  • Middle Aged
  • Neoplasm Recurrence, Local (diagnostic imaging, metabolism, pathology)
  • Neoplasm Staging
  • Pilot Projects
  • Prospective Studies
  • Radiopharmaceuticals (pharmacokinetics)
  • Sensitivity and Specificity
  • Tomography, Emission-Computed, Single-Photon
  • Tomography, X-Ray Computed
  • Whole Body Imaging

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