Vulval Cancer: A Focus on Survivorship

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.


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
treatments for LGSOC. The study will measure effectiveness, including overall response rate (how well the
combination reduces tumor size) and safety. The study will also include quality of life assessments by the
patient.


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)