1.Eruption of Metastatic Paraganglioma After Successful Therapy with ¹â·â·Lu/â¹â°Y-DOTATOC and ¹â·â·Lu-DOTATATE
Katherine I WOLF ; Abhishek JHA ; Anouk VAN BERKEL ; Damian WILD ; Ingo JANSSEN ; Corina M MILLO ; M J R JANSSEN ; Melissa K GONZALES ; Henri J K M TIMMERS ; Karel PACAK
Nuclear Medicine and Molecular Imaging 2019;53(3):223-230
Metastatic paraganglioma treatment options are limited. Peptide receptor radionuclide therapy (PRRT) has been introduced as a novel management option for metastatic neuroendocrine tumors demonstrating safety, efficacy, and increased quality of life.We present two cases of marked progression of metastatic paraganglioma following initial partial response to PRRT. Given their positivity on â¶â¸Ga-DOTATATE PET/CT and ¹¹¹In-octreotide SPECT, they underwent PRRT. Imaging following treatment revealed significant improvement in size and intensity, with some foci nearly completely resolved in one patient, and disease regression with a decrease in the number and size of bone and liver lesions in the second patient.Within months, repeat imaging in both patients revealed extensive metastatic disease with new lesions, which eventually lead to their deaths. The mechanism for rapid disease progression after partial response is not well understood, although it could be related to initially high Ki-67 levels or ¹â¸F-FDG PET/CT SUV(max) values. However, naturally rapid disease progression despite PRRT response cannot be excluded. This finding warrants the importance of proper patient counseling along with early and accurate pre-PRRT assessment, taking into consideration the above potential risk factors for therapy response in order to personalize treatment regimens and achieve maximum patient benefit.
2.Role of 68Ga-DOTATATE PET/CT in a Case of SDHB-Related Pterygopalatine Fossa Paraganglioma Successfully Controlled with Octreotide
Abhishek JHA ; Mayank PATEL ; Eva BAKER ; Melissa K. GONZALES ; Alexander LING ; Corina MILLO ; Marianne KNUE ; Ali Cahid CIVELEK ; Karel PACAK
Nuclear Medicine and Molecular Imaging 2020;54(1):48-52
We describe an unusual case of a 42-year-old female with an unresectable succinate dehydrogenase subunit B (SDHB)-related pterygopalatine fossa paraganglioma. She underwent somatostatin receptor imaging with 68Ga-DOTA(0)-Tyr(3)-octreotate (68Ga-DOTATATE) positron emission tomography/computed tomography (PET/CT), which showed uptake in the above mentioned tumor. Hence, the patient was started on octreotide, a cold somatostatin analog, and responded with tumor stabilization and improvement of clinical symptoms for 36 months since initiation of octreotide therapy. This case demonstrates the role of 68Ga-DOTATATE PET/CT in diagnostic localization and its subsequent role in treatment using cold somatostatin analog as a potential choice of therapy in the management of paraganglioma in an unusual location with limited therapeutic options.
3.Eruption of Metastatic Paraganglioma After Successful Therapy with ¹⁷⁷Lu/⁹⁰Y-DOTATOC and ¹⁷⁷Lu-DOTATATE
Katherine I WOLF ; Abhishek JHA ; Anouk VAN BERKEL ; Damian WILD ; Ingo JANSSEN ; Corina M MILLO ; M J R JANSSEN ; Melissa K GONZALES ; Henri J K M TIMMERS ; Karel PACAK
Nuclear Medicine and Molecular Imaging 2019;53(3):223-230
Metastatic paraganglioma treatment options are limited. Peptide receptor radionuclide therapy (PRRT) has been introduced as a novel management option for metastatic neuroendocrine tumors demonstrating safety, efficacy, and increased quality of life.We present two cases of marked progression of metastatic paraganglioma following initial partial response to PRRT. Given their positivity on ⁶⁸Ga-DOTATATE PET/CT and ¹¹¹In-octreotide SPECT, they underwent PRRT. Imaging following treatment revealed significant improvement in size and intensity, with some foci nearly completely resolved in one patient, and disease regression with a decrease in the number and size of bone and liver lesions in the second patient.Within months, repeat imaging in both patients revealed extensive metastatic disease with new lesions, which eventually lead to their deaths. The mechanism for rapid disease progression after partial response is not well understood, although it could be related to initially high Ki-67 levels or ¹⁸F-FDG PET/CT SUV(max) values. However, naturally rapid disease progression despite PRRT response cannot be excluded. This finding warrants the importance of proper patient counseling along with early and accurate pre-PRRT assessment, taking into consideration the above potential risk factors for therapy response in order to personalize treatment regimens and achieve maximum patient benefit.
Counseling
;
Disease Progression
;
Humans
;
Liver
;
Neuroendocrine Tumors
;
Paraganglioma
;
Positron-Emission Tomography and Computed Tomography
;
Receptors, Peptide
;
Risk Factors
;
Tomography, Emission-Computed, Single-Photon