Second-line treatment and prognostic factors in neuroendocrine carcinoma: the RBNEC study

Author:

Hadoux Julien1ORCID,Walter Thomas2,Kanaan Christina3ORCID,Hescot Ségolène4ORCID,Hautefeuille Vincent5,Perrier Marine6,Tauveron Igor78,Laboureau Sandrine9,Do Cao Christine10,Petorin Caroline11,Blanchet Odile12,Faron Matthieu13,Leteurtre Emmanuelle14,Rousselet Marie-Christine15,Joubert Zakeyh Juliette16,Marchal Aude17,Chatelain Denis18,Beaulaton Clément19ORCID,Hervieu Valérie20,Lombard-Bohas Catherine2,Ducreux Michel2122,Scoazec Jean-Yves322,Baudin Eric1,_ _,_ _

Affiliation:

1. Oncologie Endocrinienne, Département d’Imagerie, Gustave Roussy, Villejuif, France

2. Service d’Oncologie, ENETS Centre of Excellence, Hospices Civils de Lyon et Université de Lyon, Lyon, France

3. Service de Pathologie, Département de Biologie et Pathologie Médicale, Gustave Roussy, Villejuif, France

4. Département d’Oncologie, Institut Curie, Paris, France

5. Service d’Hépato-gastro-entérologie et Cancérologie Digestive, CHU Amiens Picardie, Amiens, France

6. Département d’Hépato-gastro-entérologie, CHU de Reims, Reims, France

7. Service d'Endocrinologie, Diabétologie et Maladies Métaboliques, CHU Clermont-Ferrand, Clermont-Ferrand, France

8. Laboratoire GReD, Université Clermont Auvergne, Clermont-Ferrand, France

9. Département d’Endocrinologie-Diabétologie-Nutrition, CHU d’Angers, Angers Cedex 9, France

10. CHU de Lille, Service d’Endocrinologie, Lille, France

11. CHU Clermont-Ferrand, Service de Chirurgie Digestive et Hépatobiliaire, Clermont-Ferrand, France

12. CRB, CHU d’Angers, Angers Cedex 9, France

13. Département de Chirurgie, Gustave Roussy, Villejuif, France

14. CANTHER - Cancer Heterogeneity Plasticity and Resistance to Therapies, Université de Lille, CNRS, Inserm, CHU Lille, UMR9020-U1277, Lille, France

15. Département de Pathologie, CHU d’Angers, Angers Cedex 9, France

16. Laboratoire d’Anatomie Pathologique, CHU Clermont-Ferrand, Clermont-Ferrand, France

17. Service d’Anatomo-Pathologie, CHU Reims, Reims, France

18. Service d’Anatomo-Pathologie, CHU Amiens, Amiens, France

19. Service d’Anatomo-Pathologie, Institut Curie, Paris, France

20. Service d’Anatomo-Pathologie, ENETS Centre of Excellence, Hospices Civils de Lyon et Université de Lyon, Lyon, France

21. Service d’Oncologie Digestive, Département de Médecine, Gustave Roussy, Villejuif, France

22. Faculté de Médecine, Université Paris Saclay, Le Kremlin-Bicêtre, France

Abstract

Neuroendocrine carcinomas (NEC) are aggressive malignant diseases. Etoposide-based rechallenge (EBR) and the prognostic role of RB transcriptional corepressor 1 (RB1) status in second-line chemotherapy (2L) have not been studied. The objectives of this study were to report the results of 2L including EBR as well as prognostic factors in a national retrospective multicentre study. NEC patients treated with 2L and further, with tissue samples available, were included. RB1 status and morphological classification were reviewed centrally. Among the 121 NEC patients (40% female, median age 61 years) included, there were 73 small-cell NEC (60%), 34 large-cell NEC (28%) and 14 NEC (not otherwise specified, 12%). Primary sites were lung (39%), gastroenteropancreatic (36%), other (13%) and unknown (12%). Median Ki-67 index was 80%. Median progression-free survival (PFS) and overall survival (OS) under 2L were 2.1 and 6.2 months, respectively. No difference was observed between patients who received an ‘adenocarcinoma-like’ or a ‘neuroendocrine-like’ 2L or according to the RB1 status. Thoracic NEC primary was the only adverse prognostic factor for OS. EBR, administered to 31 patients, resulted in a 62% disease control rate with a median PFS and OS of 3.2 and 11.7 months, respectively. In the 94 patients with a relapse-free interval of ≥3 months after first-line platinum–etoposide chemotherapy, the median OS was 12 months in patients who received EBR as compared to 5.9 months in patients who did not (P = 0.043). EBR could be the best 2L option for patient with initial response to first-line platinum–etoposide lasting at least 3 months. RB1 status does not provide prognostic information in this setting.

Publisher

Bioscientifica

Subject

Cancer Research,Endocrinology,Oncology,Endocrinology, Diabetes and Metabolism

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