- ICH GCP
- Amerikanska kliniska prövningsregistret
- Klinisk prövning NCT06238232
68Ga-Pentixafor PET/CT Versus Adrenal Vein Sampling in Primary Aldosteronism: The GAPA Randomized Clinical Trial (GAPA)
To compare the 68Ga-Pentixafor PET/CT and adrenal vein sampling on the long-term outcomes of primary aldosteronism (PA) patients with adrenal nodule (≥1cm)
Studieöversikt
Status
Betingelser
Intervention / Behandling
Detaljerad beskrivning
This is a multicenter randomized noninferiority clinical trial involving patients with primary aldosteronism (PA) patients with adrenal nodule (≥1cm) who completed AVS or 68Ga-Pentixafor PET/CT.We will enroll 320 PA patients with adrenal nodule (≥1cm) .All paticipants will be randomized into 68Ga-Pentixafor PET/CT group(Intervention group) and AVS group(Control group) to compare the long-term outcomes of patients with PA.
Studietyp
Inskrivning (Faktisk)
Fas
- Inte tillämpbar
Kontakter och platser
Studieorter
-
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Chongqing Municipality
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Chongqing, Chongqing Municipality, Kina, 400016
- The First Affilated Hospital of Chongqing Medical University
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Deltagandekriterier
Urvalskriterier
Åldrar som är berättigade till studier
Tar emot friska volontärer
Kön som är behöriga för studier
Beskrivning
1 Inclusion Criteria
Participants must meet all of the following criteria:
- .Ability to understand the trial procedures and provide written informed consent.
- .Age 18 to 70 years.
- .Hypertension with a confirmed diagnosis of primary aldosteronism.
- .Adrenal gland CT or MRI scan showing an adrenal nodule of 1 cm or larger.
- .Willingness to undergo adrenalectomy if lateralizing primary aldosteronism is identified.
A confirmed diagnosis of primary aldosteronism will be defined as a positive screening result and at least one positive aldosterone suppression test. A positive screening result will be defined as an aldosterone-to-renin ratio of ≥20(pg/mL)/(mIU/L) or≥30 (ng/dL)/(ng/mL/hr). A positive aldosterone suppression test will be defined as a plasma aldosterone concentration of≥110 pg/mL after the captopril challenge test or ≥80pg/mL after the seated saline infusion test.
2 Exclusion Criteria
Participants will be excluded if any of the following criteria are met:
- .Autonomous cortisol secretion,defined as a serum cortisol levels ≥ 50 nmol/L after a 1-mg overnight dexamethasone suppression test.
- .Fulfillment of prespecified criteria for bypassing AVS, defined as age younger than 35 years, typical features of aldosterone-producing adenoma, plasma aldosterone concentration >300 pg/mL, spontaneous hypokalemia, and a unilateral low-density adrenal nodule >1 cm on CT.
- .Compliacted with other secondary hypertension (such as Cushing's syndrome, renal artery stenosis, but not including obstructive sleep apnea syndrome).
- .Onset of hypertension before 20 years of age with hypokalemia and a family history suggestive of familial hyperaldosteronism, Liddle syndrome, or another hereditary form of hypertension.
- . Adrenal nodules with imaging characteristics suggestive of pheochromocytoma, adrenocortical carcinoma, adrenal cysts, adrenal hematomas, or adrenal myelolipomas.
- .Active malignant disease.
- .Previous adrenal surgery.
- .Adrenal insufficiency requiring glucocorticoid replacement therapy.
- .Long-term glucocorticoid therapy that cannot be discontinued.
- .Allergy or intolerance to contrast media or contraindication to AVS.
- .Pregnancy or lactation.
- .Alcohol or drug abuse, or psychiatric illness that would interfere with trial participation.
- .New York Heart Association class III or IV heart failure.
- .Hospitalization for worsening chronic heart failure within the previous 3 months.
- .Stroke or acute coronary syndrome within the previous 3 months.
- .Severe anemia, defined as hemoglobin <6 g/dl.
- .Severe liver disease, defined as alanine aminotransferase ≥3 times the upper limit of the normal range.
- .Severe kidney disease, defined as dialysis treatment or an estimated glomerular filtration rate <30 mL/min/1.73 m².
- .Systemic inflammatory response syndrome.
- .Uncontrolled diabetes, defined as fasting blood glucose ≥13.3 mmol/L.
- .Severe obesity, defined as a body-mass index ≥35 kg/m², or underweight status, defined as a body-mass index ≤18 kg/m².
- .Untreated aneurysm or any other condition that, in the investigator's judgment, would interfere with safe participation or continued treatment for primary aldosteronism.
Studieplan
Hur är studien utformad?
Designdetaljer
- Primärt syfte: Diagnostisk
- Tilldelning: Randomiserad
- Interventionsmodell: Parallellt uppdrag
- Maskning: Enda
Vapen och interventioner
Deltagargrupp / Arm |
Intervention / Behandling |
|---|---|
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Experimentell: 68Ga-Pentixafor PET/CT group
Patients divided into 68Ga-Pentixafor PET/CT group need to undergo 68Ga-Pentixafor PET/CT examination and guide subsequent treatment based on the results |
The patients had a normal diet with no special preparation before 68Ga-Pentixafor PET/CT imaging. The dosage of intravenously injected 68Ga-Pentixafor was calculated based on the patient's weight (1.85 MBq [0.05mCi]/kg). Local PET/CT scanning of the upper abdomen was performed on a hybrid PET/CT scanner at 10 minutes after the injection of the intravenous tracer, respectively. |
|
Inget ingripande: AVS group
Patients divided into AVS group need to undergo AVS to guide subsequent treatment based on the results |
Vad mäter studien?
Primära resultatmått
Resultatmått |
Åtgärdsbeskrivning |
Tidsram |
|---|---|---|
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The proportion of complete biochemical rsuccess
Tidsram: At 6 months of follow-up.
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Blood was drawn to measure aldosterone, renin and potassium.According to PASO criteria, outcomes of adrenalectomy for unilateral primary aldosteronism were classified into complete, partial, and absent success, for both clinical and biochemical outcomes.The proportion of complete biochemical remission according to PASO consensus criteria. |
At 6 months of follow-up.
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Sekundära resultatmått
Resultatmått |
Åtgärdsbeskrivning |
Tidsram |
|---|---|---|
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The proportion of complete clinical success
Tidsram: At 6 months of follow-up.
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Complete clinical success was assessed according to PASO criteria based on blood pressure and antihypertensive medication use. The outcome was the proportion of participants with complete clinical success at 6-month follow-up after treatment. |
At 6 months of follow-up.
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The change in the Defined Daily Dose (DDD) of antihypertensive medications
Tidsram: At 6 months of follow-up.
|
Prescribed The change in the Defined Daily Dose (DDD) of antihypertensive medications from baseline to 6-month after treatment. |
At 6 months of follow-up.
|
Andra resultatmått
Resultatmått |
Åtgärdsbeskrivning |
Tidsram |
|---|---|---|
|
Adverse events
Tidsram: At 6 month of follow-up.
|
Adverse events were assessed throughout the study, including any adverse events, serious adverse events, adverse events leading to study discontinuation, adverse events of special interest, and diagnostic procedure-related adverse events. Prespecified adverse events of special interest included adrenal vein rupture, femoral vein hematoma, deep vein thrombosis, post-procedure infection, hypertensive emergency or urgency, and contrast-media or tracer hypersensitivity. |
At 6 month of follow-up.
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Health Economics Outcomes
Tidsram: At 6 months of follow-up.
|
Health economic outcomes included: 1) medical costs; 2) cost-effectiveness ratio (CER), calculated using medical costs and the complete biochemical success rate; and 3) incremental cost-effectiveness ratio (ICER), calculated using the between-group differences in medical costs and complete biochemical success rates. |
At 6 months of follow-up.
|
Samarbetspartners och utredare
Sponsor
Samarbetspartners
Utredare
- Huvudutredare: Qifu Li, MD, PhD, First Affiliated Hospital of Chongqing Medical University
- Studiestol: Shumin Yang, MD, PhD, First Affiliated Hospital of Chongqing Medical University
Publikationer och användbara länkar
Allmänna publikationer
- Funder JW, Carey RM, Mantero F, Murad MH, Reincke M, Shibata H, Stowasser M, Young WF Jr. The Management of Primary Aldosteronism: Case Detection, Diagnosis, and Treatment: An Endocrine Society Clinical Practice Guideline. J Clin Endocrinol Metab. 2016 May;101(5):1889-916. doi: 10.1210/jc.2015-4061. Epub 2016 Mar 2.
- Rossi GP, Bernini G, Caliumi C, Desideri G, Fabris B, Ferri C, Ganzaroli C, Giacchetti G, Letizia C, Maccario M, Mallamaci F, Mannelli M, Mattarello MJ, Moretti A, Palumbo G, Parenti G, Porteri E, Semplicini A, Rizzoni D, Rossi E, Boscaro M, Pessina AC, Mantero F; PAPY Study Investigators. A prospective study of the prevalence of primary aldosteronism in 1,125 hypertensive patients. J Am Coll Cardiol. 2006 Dec 5;48(11):2293-300. doi: 10.1016/j.jacc.2006.07.059. Epub 2006 Nov 13.
- Nishikawa T, Omura M, Satoh F, Shibata H, Takahashi K, Tamura N, Tanabe A; Task Force Committee on Primary Aldosteronism, The Japan Endocrine Society. Guidelines for the diagnosis and treatment of primary aldosteronism--the Japan Endocrine Society 2009. Endocr J. 2011;58(9):711-21. doi: 10.1507/endocrj.ej11-0133. Epub 2011 Aug 9.
- Young WF, Stanson AW, Thompson GB, Grant CS, Farley DR, van Heerden JA. Role for adrenal venous sampling in primary aldosteronism. Surgery. 2004 Dec;136(6):1227-35. doi: 10.1016/j.surg.2004.06.051.
- Xu Z, Yang J, Hu J, Song Y, He W, Luo T, Cheng Q, Ma L, Luo R, Fuller PJ, Cai J, Li Q, Yang S; Chongqing Primary Aldosteronism Study (CONPASS) Group. Primary Aldosteronism in Patients in China With Recently Detected Hypertension. J Am Coll Cardiol. 2020 Apr 28;75(16):1913-1922. doi: 10.1016/j.jacc.2020.02.052.
- Mulatero P, Sechi LA, Williams TA, Lenders JWM, Reincke M, Satoh F, Januszewicz A, Naruse M, Doumas M, Veglio F, Wu VC, Widimsky J. Subtype diagnosis, treatment, complications and outcomes of primary aldosteronism and future direction of research: a position statement and consensus of the Working Group on Endocrine Hypertension of the European Society of Hypertension. J Hypertens. 2020 Oct;38(10):1929-1936. doi: 10.1097/HJH.0000000000002520.
- Amar L, Baguet JP, Bardet S, Chaffanjon P, Chamontin B, Douillard C, Durieux P, Girerd X, Gosse P, Hernigou A, Herpin D, Houillier P, Jeunemaitre X, Joffre F, Kraimps JL, Lefebvre H, Menegaux F, Mounier-Vehier C, Nussberger J, Pagny JY, Pechere A, Plouin PF, Reznik Y, Steichen O, Tabarin A, Zennaro MC, Zinzindohoue F, Chabre O. SFE/SFHTA/AFCE primary aldosteronism consensus: Introduction and handbook. Ann Endocrinol (Paris). 2016 Jul;77(3):179-86. doi: 10.1016/j.ando.2016.05.001. Epub 2016 Jun 15.
- Heinze B, Fuss CT, Mulatero P, Beuschlein F, Reincke M, Mustafa M, Schirbel A, Deutschbein T, Williams TA, Rhayem Y, Quinkler M, Rayes N, Monticone S, Wild V, Gomez-Sanchez CE, Reis AC, Petersenn S, Wester HJ, Kropf S, Fassnacht M, Lang K, Herrmann K, Buck AK, Bluemel C, Hahner S. Targeting CXCR4 (CXC Chemokine Receptor Type 4) for Molecular Imaging of Aldosterone-Producing Adenoma. Hypertension. 2018 Feb;71(2):317-325. doi: 10.1161/HYPERTENSIONAHA.117.09975. Epub 2017 Dec 26.
- Ding J, Zhang Y, Wen J, Zhang H, Wang H, Luo Y, Pan Q, Zhu W, Wang X, Yao S, Kreissl MC, Hacker M, Tong A, Huo L, Li X. Imaging CXCR4 expression in patients with suspected primary hyperaldosteronism. Eur J Nucl Med Mol Imaging. 2020 Oct;47(11):2656-2665. doi: 10.1007/s00259-020-04722-0. Epub 2020 Mar 23.
- Monticone S, D'Ascenzo F, Moretti C, Williams TA, Veglio F, Gaita F, Mulatero P. Cardiovascular events and target organ damage in primary aldosteronism compared with essential hypertension: a systematic review and meta-analysis. Lancet Diabetes Endocrinol. 2018 Jan;6(1):41-50. doi: 10.1016/S2213-8587(17)30319-4. Epub 2017 Nov 9.
- Hundemer GL, Curhan GC, Yozamp N, Wang M, Vaidya A. Renal Outcomes in Medically and Surgically Treated Primary Aldosteronism. Hypertension. 2018 Sep;72(3):658-666. doi: 10.1161/HYPERTENSIONAHA.118.11568.
- Scala S. Molecular Pathways: Targeting the CXCR4-CXCL12 Axis--Untapped Potential in the Tumor Microenvironment. Clin Cancer Res. 2015 Oct 1;21(19):4278-85. doi: 10.1158/1078-0432.CCR-14-0914. Epub 2015 Jul 21.
- Hu J, Xu T, Shen H, Song Y, Yang J, Zhang A, Ding H, Xing N, Li Z, Qiu L, Ma L, Yang Y, Feng Z, Du Z, He W, Sun Y, Cai J, Li Q, Chen Y, Yang S; Chongqing Primary Aldosteronism Study (CONPASS) Group. Accuracy of Gallium-68 Pentixafor Positron Emission Tomography-Computed Tomography for Subtyping Diagnosis of Primary Aldosteronism. JAMA Netw Open. 2023 Feb 1;6(2):e2255609. doi: 10.1001/jamanetworkopen.2022.55609.
- Zhang X, Song Y, Jing Y, Hu J, Shen H, Zhang A, He W, Feng Z, Yang Y, Pang H, Li Q, Yang S; Chongqing Primary Aldosteronism Study (CONPASS) Group; the. Comparison of Different Diagnostic Criteria of 68Ga-Pentixafor PET/CT for the Classification of Primary Aldosteronism. J Clin Endocrinol Metab. 2025 Jul 15;110(8):e2583-e2590. doi: 10.1210/clinem/dgae747.
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Studiestart (Faktisk)
Primärt slutförande (Faktisk)
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Först inskickad
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Uppdateringar av studier
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