Safety and Efficacy of Neoadjuvant Durvalumab Plus Gemcitabine/Cisplatin or Carboplatin in Patients With Operable High-Risk Upper Tract Urothelial Carcinoma: The iNDUCT-GETUG V08 Trial
Abstract
PURPOSE After radical nephroureterectomy (RNU) for upper tract urothelial carcinoma (UTUC), prognosis is poor for high-risk patients. This study evaluated safety and efficacy of neoadjuvant chemotherapy (cisplatin or carboplatin + gemcitabine) in combination with durvalumab in these patients. PATIENTS AND METHODS This phase II trial (ClinicalTrials.gov identifier: NCT04617756 ) included patients with nonmetastatic, high-grade UTUC, on the basis of the ureteroscopic biopsy or urine cytology, and/or infiltrative aspect of the renal pelvis/ureteral wall by computed tomography imaging. Before RNU, patients received durvalumab plus gemcitabine/cisplatin (cohort 1) or durvalumab plus gemcitabine/carboplatin (cohort 2) once every 3 weeks for a total of four cycles (cohort choice on the basis of the glomerular filtration rate). The primary objective was the pathologic complete response (ypT0) rate in each cohort. RESULTS Fifty patients were enrolled between 2021 and 2024 (31 in cohort 1; 19 in cohort 2). Median age was 68 years (range, 38-79), and 59% were men. Forty-five patients received four cycles of treatment, three patients three cycles, and one patient two cycles. Five patients switched to carboplatin during treatment. At surgery (N = 45 patients), rates of pT0 were 13% (4/29) in cohort 1 and 5% (1/19) in cohort 2. Fifty percent (15/29) of patients were pTa/pT1 in cohort 1, and 42% (8/19) in cohort 2. No severe immunotherapy-mediated toxicity was observed. Four patients had chemotherapy-related grade 3 neutropenia, one grade 4; one patient had grade 3 thrombopenia, one grade 4; and four patients had grade 3 anemia. CONCLUSION Although our negative study did not meet its primary end point in either cohort, the combination of durvalumab and platin-based chemotherapy, especially cisplatin, showed promising results in terms of downstaging. The safety profile was good and the surgical risk was not increased.
Article Details
Journal Info
Journal of Clinical Oncology
Lippincott Williams & Wilkins
Authors (21)
Nadine Houede
Medical Oncology Department, Institut de Cancérologie du Gard - CHU Caremeau, Nimes, France
Thierry Chevallier
CHU Nîmes, Department of Biostatistics, Epidemiology, Public Health and Innovation in Methodology, Nîmes, France
François Audenet
Institut du Cancer Paris CARPEM, AP-HP Centre, Paris Cité University, Paris, France
Constance Thibault
Department of Medical Oncology, Hôpital Européen Georges Pompidou, AP-HP, Paris Cité University, Paris, France
Yann Neuzillet
Department of Urology, Foch Hospital, Paris-Saclay University, Paris, France
Christine Abraham
Hopital Foch, Suresnes, France
Alexandra Masson-Lecomte
Paris Cité University, U976 HIPI, Saint-Louis Research Institute, Paris, France
Hélène Gauthier
Department of Medical Oncology, Saint Louis Hospital, Paris, France
Gwenaelle Gravis
Department of Medical Oncology, Institut Paoli-Calmettes, Aix-Marseille Univ, INSERM, CNRS, CRCM, Immunity and Cancer Team, Marseille, France
Geraldine Pignot
Institut Paoli-Calmettes, Department of Surgical Oncology, Marseille, France
Sophie Tartas
Medical Oncology, Lyon Sud Hospital, Hospices Civils De Lyon, Lyon, France
Alain Ruffion
Urology Department, Lyon Sud Hospital, Hospices Civils de Lyon, Lyon Cancer Innovation Center (EA 3738 CICLY), Lyon Sud Medical School, University of Lyon 1, Lyon, France
Damien Pouessel
Medical Oncology Department, Oncopole Claudius Regaud, IUCT-Oncopole, Toulouse, France
Mathieu Roumiguié
Institut Universitaire du Cancer Toulouse Oncopole CHU, Toulouse, France
Brigitte Laguerre
Department of Medical Oncology, Centre Eugene—Marquis, Rennes, France
Karim Bensalah
Department of Urology, Rennes University, Rennes, France
Evanguelos Xylinas
Department of Urology, Bichat-Claude Bernard Hospital, Assistance Publique-Hôpitaux de Paris, Université de Paris Cité, Paris, France
Loic Jaffrelot
Department of Medical Oncology Pitié Salpêtrière Hospital, AP-HP, Paris, France
Stephane Droupy
Guillaume Luquiens
CHU Nîmes, Department of Biostatistics, Epidemiology, Public Health and Innovation in Methodology, Nîmes, France
Morgan Roupret
Sorbonne Université, Pitié-Salpêtrière Hospital, AP-HP, Paris, France