- ICH GCP
- Registre américain des essais cliniques
- Essai clinique NCT07586449
A Prospective Observational Study of Senaparib in the Treatment of Epithelial Ovarian Cancer (RESO)
Evaluation of Safety and Effectiveness of Senaparib in Epithelial Ovarian Cancer, Primary Peritoneal Cancer, or Fallopian Tube Cancer: A Prospective Observational Real-World Study
Ovarian cancer is one of the most fatal malignant tumors that threaten women's health. The incidence rate is the third place among the female reproductive system malignant tumors, and the mortality rate ranks the first in gynecologic malignancies, the majority of patients have advanced diseases at the time of diagnosis.
This observational study is to evaluate the safety and efficacy of senaparib in ovarian cancer patients under real conditions, especially in various subgroups of ovarian cancer patients, in order to provide information about treatment modes for ovarian cancer patients in real-world diagnosis and treatment。
Aperçu de l'étude
Statut
Les conditions
Intervention / Traitement
Description détaillée
Ovarian cancer is one of the most serious malignant tumors that threaten women's health. The incidence rate is third place in the female reproductive system malignant tumors. The mortality rate ranks the first in gynecologic malignancies, and most of them are advanced at the time of diagnosis. The initial treatment of ovarian cancer is mainly surgery and adjuvant chemotherapy. Although most patients can obtain clinical remission after initial treatment, 70% of patients still relapse within 3 years. Therefore, finding effective drugs to prolong the chemotherapy-free interval and exploring comprehensive treatment schemes to prolong survival is the key to treatment.
In recent years, the advent of poly adenosine diphosphate ribose polymerase inhibitors has brought significant changes to the treatment of ovarian cancer. A series of high-level evidence-based medical evidence shows that the application of PARP inhibitors after complete and partial remission of initial treatment or platinum-sensitive recurrence treatment can significantly prolong the progression-free survival time of ovarian cancer patients, Maintenance therapy has become a new model for the treatment of ovarian cancer. At the same time, PARP inhibitors have been approved for posterior line treatment of ovarian cancer. At present, PARP inhibitors have been widely used in clinics and become an important cornerstone of the comprehensive treatment of ovarian cancer.
FLAMES study is a multicenter, randomized, double-blind, placebo-controlled phase III clinical study of senaparib in the maintenance treatment of advanced ovarian cancer. The preliminary results were published on the American Society of Gynecological Oncology (SGO) in 2023. A total of 404 patients were included in the study and were treated with senaparib (n =271 ) or placebo (n =133 ). The median follow-up time was 22.3months. The population-wide data assessed by BIRC showed that the median PFS data were not reached. According to the Kaplan Meier curve, senaparib could significantly prolong the PFS (NR vs 13.6 months) and reduce the risk of disease progression or death by 57%.
Senaparib was approved for the maintenance treatment of advanced ovarian cancer in January 2025 . A number of studies on senaparib in the field of ovarian cancer are also underway. It is urgent to obtain the real-world data of senaparib in the field of ovarian cancer in China. This study will collect information on the baseline characteristics, treatment, and management of ovarian cancer provided in the real world to illustrate the safety and effectiveness of senaparib in the treatment of ovarian cancer under the conditions of real clinical practice. It may also include various subgroups of patients with ovarian cancer, which are not involved in the existing phase III registered studies, In order to better understand and explore the use of PARP inhibitors in some patient subgroups and the treatment mode and effect of PARP inhibitors in the treatment of this disease.
Type d'étude
Inscription (Estimé)
Contacts et emplacements
Coordonnées de l'étude
- Nom: Tao Zhu
- Numéro de téléphone: +86 138 5806 5156
- E-mail: zhutao@zjcc.org.cn
Sauvegarde des contacts de l'étude
- Nom: Ying Li Zhang
- Numéro de téléphone: +86152 6853 0651
Lieux d'étude
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Zhejiang
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Hangzhou, Zhejiang, Chine
- Zhejiang Cancer Hospital
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Critères de participation
Critère d'éligibilité
Âges éligibles pour étudier
- Adulte
- Adulte plus âgé
Accepte les volontaires sains
Méthode d'échantillonnage
Population étudiée
La description
Inclusion Criteria:
- Sign informed consent and voluntarily join the study;
Epithelial ovarian cancer, fallopian tube cancer, or primary peritoneal cancer diagnosed by histology or cytology;
-≥ 18 years old;
- The investigator determined that the patient could receive senaparib monotherapy or combination therapy;
- For patients with fertility, effective contraceptive methods should be used during the study period and within 90 days after the last administration of senaparib
Exclusion Criteria:
- There is evidence that the patient is a pregnant or lactating woman;
- Participating in any research with intervention measures other than routine -clinical practice;
- The researcher judges other situations that are not suitable for inclusion in the study;
Plan d'étude
Comment l'étude est-elle conçue ?
Détails de conception
Que mesure l'étude ?
Principaux critères de jugement
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
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Incidence and severity of Treatment-Related Adverse Events (TRAEs) according to NCI CTCAE v5.0
Délai: 30 days after the last dose of fluzoparib
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Incidence and severity of Treatment-Related Adverse Events (TRAEs) as assessed by the investigator.
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30 days after the last dose of fluzoparib
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Mesures de résultats secondaires
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
|
treatment patterns of senaparib
Délai: 2 years
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the initial dose of senaprib 、incidence of dose reduction of senaparib 、treatment discontinuaiton of senaparib
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2 years
|
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Progression free survival (PFS)
Délai: 6 years
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Progression-free survival, defined as time from first administration senaparib to documented disease progression or death from any cause after baseline, whichever occurs first;.
To assess clinical effectiveness of senaparib monotherapy or combination therapy involved in this study by assessment of progression free survival (PFS) in patients with Ovarian Cancer.
Patients will be followed up once 3-6 months at least.
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6 years
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overall survival (OS)
Délai: 6 years
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Overall survival, defined as time from first administration senaparib to documented death.
To assess clinical effectiveness of senaprib monotherapy or combination therapy involved in this study by assessment of overall survival (OS) in patients with Ovarian Cancer.
Patients will be followed up once 3-6 months at least.
|
6 years
|
Collaborateurs et enquêteurs
Parrainer
Dates d'enregistrement des études
Dates principales de l'étude
Début de l'étude (Estimé)
Achèvement primaire (Estimé)
Achèvement de l'étude (Estimé)
Dates d'inscription aux études
Première soumission
Première soumission répondant aux critères de contrôle qualité
Première publication (Réel)
Mises à jour des dossiers d'étude
Dernière mise à jour publiée (Réel)
Dernière mise à jour soumise répondant aux critères de contrôle qualité
Dernière vérification
Plus d'information
Termes liés à cette étude
Mots clés
Termes MeSH pertinents supplémentaires
- Maladies urogénitales
- Maladies génitales
- Maladies du système endocrinien
- Tumeurs urogénitales
- Tumeurs par site
- Tumeurs
- Maladies urogénitales féminines
- Maladies urogénitales féminines et complications de la grossesse
- Maladies génitales, femme
- Tumeurs des glandes endocrines
- Maladies ovariennes
- Maladies annexielles
- Tumeurs génitales, femme
- Troubles gonadiques
- Tumeurs ovariennes
- séaparib
Autres numéros d'identification d'étude
- IRB-2026-348 (IIT)
Plan pour les données individuelles des participants (IPD)
Prévoyez-vous de partager les données individuelles des participants (DPI) ?
Informations sur les médicaments et les dispositifs, documents d'étude
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