REGYNERA(dia)TION is an international, multicenter, ambispective observational patient registry of adults with recurrent gynecologic malignancies after prior radiotherapy who are treated or planned for reirradiation and/or total ablative strategies as part of routine clinical care. The registry does not assign treatment. Radiotherapy technique, dose, systemic therapy, surgery, metastasis-directed therapy, imaging, and follow-up are selected by the treating multidisciplinary team according to local standards and patient-specific factors. The registry will collect harmonized retrospective and prospective data on disease characteristics, prior radiotherapy, recurrence pattern, reirradiation or ablative treatment exposure, response, progression, survival, severe treatment-related morbidity, fistula events, and patient-reported outcomes where available.
Study Comparing the Standard Administration of IO Versus the Same IO Administered Each 3 Months in Patients in Response After 6 Months of Standard IO
This is not medical advice. AI-assisted translation — inaccuracies may occur. Always verify the original and consult your oncologist before taking any steps.
This trial is no longer recruiting — here are similar active trials
Matched by cancer type/biomarker, currently recruiting.
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The primary objective of this study is to measure efficacy of saruparib + physician's choice of ARPI compared with placebo + ARPI in men with metastatic hormone-sensitive prostate cancer (mHSPC) who have previously received docetaxel chemotherapy or a prostate-specific membrane antigen (PSMA)-directed lutetium-177 radioligand therapy with no evidence of disease progression and PSA ≥ 0.2 ng/mL.
The purpose of this study is to compare the efficacy of zipalertinib versus placebo in participants with early stage resected non-small cell lung cancer (NSCLC) harboring uncommon epidermal growth factor receptor mutation (EGFRmt).
About the trial
Immunotherapy (IO), such as treatment with anti-PD-1, PD-L1, or CTLA-4 inhibitors, is a rapidly expanding treatment for multiple metastatic cancers with improved survival for certain cancers. However, the optimal duration of immunotherapies is currently unknown. Our hypothesis is that a reduced dose intensity of IO could be as effective as the current standard treatment in term of prevention of the disease progression. If proved right, this study will have a positive medico-economic impact by reduction of the costs associated with the treatment and the toxicity, and an increase of the patients' quality of life.
Original English text from ClinicalTrials.gov
Who can (and can't) join
✓ Qualifies
- •Podpisana zgoda na uczestnictwo w badaniu
- •Wiek 18 lat lub więcej
- •Zaawansowany nowotwór (potwierdzony badaniem histologicznym) - m.in. rak płuca, nerki, głowy i szyi, pęcherza moczowego, piersi, czerniak
- •Odpowiedź na leczenie immunologiczne (zmniejszenie guza o co najmniej 30% lub całkowite zniknięcie) utrzymywana przez co najmniej 6 miesięcy
- •Zdolność do kontynuacji tego samego leczenia immunologicznego
- •Ogólny stan zdrowia pozwalający na aktywne życie z minimalnymi ograniczeniami (ECOG ≤1)
- •Przystosowanie metod antykoncepcji dla kobiet w wieku rozrodczym i mężczyzn przez cały czas badania
- •Gotowość do uczestnictwa w badaniu i wykonywania wizyt kontrolnych
✗ Disqualifies
- •Czerniak z całkowitym zniknięciem guza
- •Rak nerki w dobrej prognozie leczony kombinacją leków celowanych i immunoterapii
- •Nowotwory krwi (białaczka, szpiczak, chłoniak)
- •Aktywna infekcja wymagająca leczenia
- •Uczestnictwo w innym badaniu klinicznym w ciągu ostatnich 30 dni
Simplified criteria — AI translation
Trial details
- Minimum age
- 18 Years
- Last updated (source)
- July 17, 2026
- Sex
- No restrictions
Therapies / drugs in trial
Locations (33)
Institut de cancérologie de l'Ouest
Angers, France
Clinique Sainte Catherine
Avignon, France
Centre Hospitalier de la Côte Basque
Bayonne, France
CHU Bordeaux - Hôpial Saint André
Bordeaux, France
CH Boulogne sur Mer
Boulogne-sur-Mer, France
Centre François Baclesse
Caen, France
Centre Jean Perrin
Clermont-Ferrand, France
Centre Hospitalier Intercommunal
Créteil, France
CHU Henri Mondor
Créteil, France
Centre Georges François Leclerc
Dijon, France
GH Mutualiste de Grenoble
Grenoble, France
CHD Vendée
La Roche-sur-Yon, France
Centre Oscar Lambret
Lille, France
Clinique Chenieux
Limoges, France
Hospices Civils de Lyon
Lyon, France
Centre Léon Bérard
Lyon, France
Centre Antoine Lacassagne
Nice, France
CHU Nîmes/Institut de cancérologie du Gard
Nîmes, France
Hôpital Saint Louis
Paris, France
Hôpital Cochin APHP
Paris, France
Hôpital Saint Antoine APHP
Paris, France
CHU Poitiers
Poitiers, France
Centre Eugene Marquis
Rennes, France
CHI Elbeuf
Saint-Aubin-lès-Elbeuf, France
Institut de cancérologie de l'Ouest
Saint-Herblain, France
Centre Hospitalier Mémorial de Saint-Lô
Saint-Lô, France
Clinique Mutualiste de l'Estuaire
Saint-Nazaire, France
ICANS
Strasbourg, France
Hôpital Foch
Suresnes, France
HIA Sainte Anne
Toulon, France
IUCT
Toulouse, France
CHU Bretonneau
Tours, France
Centre Gustave Roussy
Villejuif, France
Share this trial
Data from ClinicalTrials.gov. AI-assisted translation, last sync: 7/1/2026.
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