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Immune checkpoint blockers in solid organ transplant recipients and cancer: the INNOVATED cohort.
Remon, J; Auclin, E; Zubiri, L; Schneider, S; Rodriguez-Abreu, D; Minatta, N; Gautschi, O; Aboubakar, F; Muñoz-Couselo, E; Pierret, T; Rothschild, S I; Cortiula, F; Reynolds, K L; Thibault, C; Gavralidis, A; Blais, N; Barlesi, F; Planchard, D; Besse, B M D.
Affiliation
  • Remon J; Paris-Saclay University, Department of Cancer Medicine, Gustave Roussy, Villejuif. Electronic address: JORDI.REMON-MASIP@gustaveroussy.fr.
  • Auclin E; Department of Cancer Medicine, Hôpital Européen Georges-Pompidou, Paris, France.
  • Zubiri L; Massachusetts General Hospital Cancer Center, Division of Hematology/Oncology, Department of Medicine, Massachusetts General Hospital, Boston, USA.
  • Schneider S; Department Pneumology, Hôpital de Bayonne, Bayonne, France.
  • Rodriguez-Abreu D; Medical Oncology Department, Complejo Hospitalario Universitario Insular-Materno Infantil de Gran Canaria, Universidad de Las Palmas de Gran Canaria, Las Palmas de Gran Canaria, Spain.
  • Minatta N; Department of Oncology Hospital Italiano Buenos Aires, Buenos Aires, Argentina.
  • Gautschi O; Department of Cancer Medicine, University of Berne and Cantonal Hospital of Lucerne, Lucerne, Switzerland.
  • Aboubakar F; Department of Pneumology, Cliniques Universitaires Saint Luc, Brussels, Belgium.
  • Muñoz-Couselo E; Department of Oncology, Hospital Vall d'Hebron de Barcelona, VHIO Vall d'Hebron Institute of Oncology, Barcelona, Spain.
  • Pierret T; Department of Pneumology, CHU Grenoble Alpes, Grenoble, France.
  • Rothschild SI; Medical Oncology Department, University Hospital Basel, Basel; Division Oncology/Hematology, Department of Medicine, Cantonal Hospital Baden, Baden, Switzerland.
  • Cortiula F; Department of Oncology, University Hospital of Udine, Udine, Italy.
  • Reynolds KL; Massachusetts General Hospital Cancer Center, Division of Hematology/Oncology, Department of Medicine, Massachusetts General Hospital, Boston, USA.
  • Thibault C; Department of Cancer Medicine, Hôpital Européen Georges-Pompidou, Paris, France.
  • Gavralidis A; Massachusetts General Hospital Cancer Center, Division of Hematology/Oncology, Department of Medicine, Massachusetts General Hospital, Boston, USA; Division of Hematology/Oncology, Department of Medicine, Massachusetts General Hospital, Boston; Salem Hospital, Salem, USA.
  • Blais N; Centre Hospitalier de l'Université de Montréal (CHUM), Montreal, Canada.
  • Barlesi F; Paris-Saclay University, Department of Cancer Medicine, Gustave Roussy, Villejuif.
  • Planchard D; Paris-Saclay University, Department of Cancer Medicine, Gustave Roussy, Villejuif.
  • Besse BMD; Paris-Saclay University, Department of Cancer Medicine, Gustave Roussy, Villejuif.
ESMO Open ; 9(5): 103004, 2024 May.
Article in En | MEDLINE | ID: mdl-38653155
ABSTRACT

BACKGROUND:

Patients with solid organ transplant (SOT) and solid tumors are usually excluded from clinical trials testing immune checkpoint blockers (ICB). As transplant rates are increasing, we aimed to evaluate ICB outcomes in this population, with a special focus on lung cancer.

METHODS:

We conducted a multicenter retrospective cohort study collecting real data of ICB use in patients with SOT and solid tumors. Clinical data and treatment outcomes were assessed by using retrospective medical chart reviews in every participating center. Study endpoints were overall response rate (ORR), 6-month progression-free survival (PFS), and grade ≥3 immune-related adverse events.

RESULTS:

From August 2016 to October 2022, 31 patients with SOT (98% kidney) and solid tumors were identified (36.0% lung cancer, 19.4% melanoma, 13.0% genitourinary cancer, 6.5% gastrointestinal cancer). Programmed death-ligand 1 expression was positive in 29% of tumors. Median age was 61 years, 69% were males, and 71% received ICB as first-line treatment. In the whole cohort the ORR was 45.2%, with a 6-month PFS of 56.8%. In the lung cancer cohort, the ORR was 45.5%, with a 6-month PFS of 32.7%, and median overall survival of 4.6 months. The grade 3 immune-related adverse events rate leading to ICB discontinuation was 12.9%. Allograft rejection rate was 25.8%, and risk of rejection was similar regardless of the type of ICB strategy (monotherapy or combination, 28% versus 33%, P = 1.0) or response to ICB treatment.

CONCLUSIONS:

ICB could be considered a feasible option for SOT recipients with some advanced solid malignancies and no alternative therapeutic options. Due to the risk of allograft rejection, multidisciplinary teams should be involved before ICB therapy.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Organ Transplantation / Immune Checkpoint Inhibitors Limits: Adult / Aged / Female / Humans / Male / Middle aged Language: En Journal: ESMO Open Year: 2024 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Organ Transplantation / Immune Checkpoint Inhibitors Limits: Adult / Aged / Female / Humans / Male / Middle aged Language: En Journal: ESMO Open Year: 2024 Document type: Article