Name | No. | For Patients with | Purpose |
---|---|---|---|
Vulval Cancer: A Focus on Survivorship | 25-40 | Vulvar Cancer |
This research aims to understand the long-term impact of vulvar cancer and its treatments on various aspects of a woman’s life, including physical health, emotional well-being, and sexual functioning. |
DSSG Group: Gynaecological
AFG Post-RT
Name | No. | For Patients with | Purpose |
---|---|---|---|
AFG Post-RT | 24-117 | Vulvar Cancer |
To examine the feasibility, safety and effect of autologous fat grafting (AFG) in the treatment of chronic vulval symptoms following radiotherapy. |
IMGN-858-0424
Name | No. | For Patients with | Purpose |
---|---|---|---|
IMGN-858-0424 | 24-116 | Recurrent Ovarian Cancer with High Folate Receptor-Alpha Expression |
The purpose of this study is to evaluate the incidence rate and severity of prespecified mirvetuximab soravtansine (MIRV)-related ocular treatment-emergent adverse events (TEAEs) and assess prophylaxis strategies in all participants (symptomatic and asymptomatic) undergoing prospective ophthalmic evaluation with recurrent ovarian cancer (participants with either platinum-sensitive ovarian cancer or platinum-resistant ovarian cancer with high folate receptor alpha (FRα) expression. |
RAMP-301 (ENGOT ov81)
Name | No. | For Patients with | Purpose |
---|---|---|---|
RAMP-301 (ENGOT ov81) | 25-16 | Recurrent (previously treated) low grade serous ovarian cancer (LGSOC) who have progressed on a prior platinum-based therapy |
The purpose of the study is to assess how avutometinib plus defactinib compares to the standard |
GLORIOSA
Name | No. | For Patients with | Purpose |
---|---|---|---|
GLORIOSA | 22-18 | FRα-HIGH Platinum Sensitive Ovarian Cancer |
To compare progression-free survival (PFS) after patient receives platinum-based chemotherapy (doublet) plus bevacizumab and subsequently is randomised to maintenance mirvetuximab soravtansine (MIRV) plus bevacizumab versus bevacizumab alone. |
ENGOT cx20
Name | No. | For Patients with | Purpose |
---|---|---|---|
ENGOT cx20 | 24-10 | Second-line or third-line Patients with Recurrent or Metastatic Cervical Cancer |
To compare Sacituzumab Tirumotecan (MK-2870) Monotherapy to Treatment of Physician’s Choice (TPC) with respect to overall survival (OS) in patients with recurrent or metastatic cervical cancer. |
ENGOT-en23 / PREVENTER
Name | No. | For Patients with | Purpose |
---|---|---|---|
ENGOT-en23 / PREVENTER | 23-04 | Endometrial Cancer |
The goal of the study is to learn if people who receive MK-2870 (sacituzumab tirumotecan) live longer overall and without the cancer getting worse compared to people who receive chemotherapy. |
“XPORT” – ENGOT-EN20/GOG-3083/XPORT-EC-042
Name | No. | For Patients with | Purpose |
---|---|---|---|
“XPORT” – ENGOT-EN20/GOG-3083/XPORT-EC-042 | 22-08 | p53 Wild-Type, Advanced or Recurrent Endometrial Carcinoma. When we say someone has p53 wildtype cancer, it means their guardian (p53) is working as it should. It’s like having a strong and reliable guardian who can keep an eye on things and prevent trouble (like stopping cells from growing out of control). So, in simple terms, p53 wildtype cancer means the guardian in the body is doing its job properly, but still, cancer has somehow developed. |
The purpose of this study is to evaluate the efficacy and safety of Selinexor as a maintenance treatment in patients with p53 wildtype endometrial carcinoma (EC), who have achieved a partial response (PR) or complete response (CR) (per Response Evaluation Criteria in Solid Tumours version 1.1 [RECIST v 1.1]) after completing at least 12 weeks of platinum-based therapy. A total of 220 participants will be enrolled in the study and randomised in a 1:1 ratio to maintenance therapy with either Selinexor or placebo. |
HELP-ER
Name | No. | For Patients with | Purpose |
---|---|---|---|
HELP-ER | 22-05 | First platinum sensitive relapsed ovarian cancer |
Prospective Study of HE4 serum Level in Patients with First Relapsed Ovarian Cancer. Improving the prediction of surgical outcome at secondary cytoreduction in patients with ovarian cancer. This study aims to improve upon the contemporary AGO score by including additional clinical variables like circulating HE4 and CA125 levels to predict surgical outcome at secondary cytoreduction. |
OVHIPEC-2
Name | No. | For Patients with | Purpose |
---|---|---|---|
OVHIPEC-2 | 20-07 | Stage III Epithelial Ovarian Cancer |
The objective of this study is to prove that treatment with primary cytoreductive surgery in combination with HIPEC (treatment arm) improves outcome compared to primary cytoreductive surgery without HIPEC (standard arm) |