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NCT06127446Toboroz

The Registry of Genetic Alterations of Taiwan Ovarian Cancer

Forrás: ClinicalTrials.gov · Utoljára frissítve: 2026. ápr. 9.

Következő lépések

Rövid összefoglaló (regiszter, angolul)

Despite recent progress in chemotherapy and targeted therapy for ovarian cancer, the 5-year survival rate remains around 40% because of rapid development of treatment resistance and recurrence. The sensitivity to platinum agents or BRCA genes mutation has been the prerequisite for improved survival using PARP inhibitors, though only 15-20% ovarian cancer patients harbor BRCA mutations through germline or somatic variants. Bevacizumab can only delayed disease recurrence but failed to improve overall survival. Several approved cancer therapeutics with established safety and toxicity profiles should be assessed in the immediate future based on biomarkers of platinum resistant, BRCA wild type recurrent ovarian cancer. Furthermore, the proportion high grade serous and clear cell adenocarcinoma of ovary cancer in Taiwan increased substantially in recent 10 years. Genetic factors (such as homologous recombination deficiency, mismatch repair genes mutation), environmental factors (such as oral contraceptives, nulliparity/low parity) as well as comorbidity including endometriosis may be associated with the changing pattern and clinical outcomes of ovarian cancer in Taiwan. Next-generation sequencing technology has enabled cancer genome sequencing in screening and searching for new cancer genes in an efficient manner. This massive sequencing technique not only help to identify new altered genes for novel biomarker development, but also reveal gene alterations sensitive or resistant to specific therapies. The specific aims of this project are (1) to systemically explore genomic profiling of Taiwanese primary or platinum-resistant or -sensitive recurrent (or recurrent) ovarian cancer focusing on high grade serous and clear cell adenocarcinoma; (2) to collect clinical data regarding comorbidity, survival time and responses to major types of anticancer therapy; and (3) to establish a comprehensive ovarian cancer cohort for additional translational studies. The long-term goals of this study are to help implement personalized therapy, to develop novel therapy, and to improve outcomes of patients with ovarian cancer.

Állapot (regiszter)
Toboroz
Vizsgálattípus
Megfigyeléses
Résztvevők száma
300 (tervezett)
Első benyújtás
2023. okt. 25.
Kezdés
2023. dec. 13.
Elsődleges befejezés
2031. dec. 31.
Fő szponzor
National Health Research Institutes, Taiwan
Betegségek
Petefészekrák
NCT-szám
NCT06127446

Mit vállalsz

  • Vizsgálat típusa: Megfigyeléses
  • Tervezett résztvevők: 300
  • 2023. dec. 13. és az elsődleges befejezés (2031. dec. 31.) között
  • 8 helyszín, 1 országban
  • Vizitek és vizsgálatok: kérdezd a vizsgálat csapatát, a regiszter nem sorolja fel őket

A(z) ClinicalTrials.gov regisztermezőiből összeállítva. A vizsgálat felépítését írja le.

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Korábbi kezelés

  • Concomitant ovarian and endometrial cancer
  • Tumor specimen of primary surgery or recurrent biopsy/surgery are not qualified for genetic testing.
  • Concomitant malignancy under surveillance or treatment in the past three years (excluding curatively treated basal or squamous cell skin carcinoma or carcinoma in situ)

Életkor

  • Paraffin tissue tumor block older than five years.

Egyéb

  • Inability to cooperate or undesirable compliance to the study.

Kiket keres a vizsgálat

  • Age 18 and above.
  • Stage I to IV high grade serous or clear cell carcinoma of ovary, peritoneal and fallopian tube.
  • Patients with primary ovarian cancer had undergone primary surgery. Patients with recurrent ovarian cancer had undergone primary surgery (and biopsy/surgery for recurrent tumors).
  • Tumor tissues before neoadjuvant therapy will be collected for patients receiving surgery after any neoadjuvant treatment.
  • Willingness to provide the surgical tissues of primary tumors, non-tumor part normal tissue (and paired recurrent tumors in 80 patients).
  • Willingness to provide blood sample of 20ml within four weeks after registration (in at least 72 patients of primary ovarian cancer and 72 patients of recurrent ovarian cancer).
  • Patient fully understand the protocol with the willingness to have regular follow-up.
  • Life expectancy more than 3 months.

Életkor a regiszterben: 18 év – - · Nem: csak nők · Egészséges önkénteseket nem fogad

A teljes feltétellista: ClinicalTrials.gov

Helyszínek (8)

Helyszínek a regiszter sorrendjében. Ha a profilodba mented a városodat, távolság szerint rendeződnek.

HelyszínVárosOrszágHelyszín állapota
Kaohsiung Veterans General HospitalKaohsiung CityTajvanToboroz
Chang Gung Medical FoundationKaohsiung CityTajvanToboroz
Taichung Veterans General HospitalTaichungTajvanToboroz
China Medical University HospitalTaichungTajvanToboroz
National Cheng Kung University HospitalTainanTajvanToboroz
MacKay Memorial HospitalTaipeiTajvanToboroz
National Taiwan University HospitalTaipeiTajvanToboroz
Cathay General HospitalTaipeiTajvanToboroz

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