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A Prospective Interventional Study of Temozolomide in Refractory Parathyroid Carcinoma

A Prospective Interventional Study of Temozolomide in Refractory Parathyroid Carcinoma

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600120647
Enrollment
Unknown
Registered
2026-03-18
Start date
2026-03-25
Completion date
Unknown
Last updated
2026-03-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Refractory Parathyroid Carcinoma

Interventions

Experimental Group:Temozolomide

Sponsors

Chinese Academy of Medical Sciences, Peking Union Medical College Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1.Patients with parathyroid carcinoma jointly assessed by the teams from the Department of Endocrinology and the Department of General Surgery, Peking Union Medical College Hospital, as being unsuitable for repeat surgery, or those who explicitly refuse surgical treatment; 2.At least one month since the last treatment (e.g., surgery), with documented non-response (disease not in remission); 3.Age > 18 years and = 3 × 10^9/L, NEUT >= 1.5 × 10^9/L, PLT >= 100 × 10^9/L, HGB >= 85 g/L), and normal cardiac and pulmonary function;^95.Patients of childbearing potential agree to use contraception; 6.Patients provide written informed consent to participate in the study.

Exclusion criteria

Exclusion criteria: 1.Presence of other malignant tumors, excluding carcinoma in situ and basal cell carcinoma; 2.Currently receiving other anti-tumor drug therapy; 3.Pregnant or breastfeeding women; 4.History of allergy to temozolomide, dacarbazine, or related drugs; 5.Severe bone marrow suppression; 6.Severe hepatic or renal insufficiency; 7.Presence of the following cardiovascular conditions: 1) QTc prolongation or other clinically significant ECG abnormalities; 2) Current or prior cardiac insufficiency, NYHA Class III or IV; 3) Myocardial infarction, arrhythmias other than sinus tachycardia, stable or unstable angina, symptomatic congestive heart failure, or coronary/peripheral artery bypass graft surgery or stent implantation within the past 12 months; 8.Intestinal obstruction or other conditions affecting drug administration.

Design outcomes

Primary

MeasureTime frame
Disease Control Rate (DCR);

Secondary

MeasureTime frame
Progression-free survival (PFS);Biochemical remission rate;

Countries

China

Contacts

Public ContactSong An

Chinese Academy of Medical Sciences, Peking Union Medical College Hospital

songan4720@126.com+86 10 69155073

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Apr 3, 2026