Efficacy of ramucirumab combination chemotherapy as second‐line treatment in patients with advanced adenocarcinoma of the stomach or gastroesophageal junction after exposure to checkpoint inhibitors and chemotherapy as first‐line therapy

Author:

Masetti Michael1ORCID,Al‐Batran Salah‐Eddin2,Goetze Thorsten O.2,Thuss‐Patience Peter3,Knorrenschild Jorge Riera4,Goekkurt Eray5,Folprecht Gunnar6,Ettrich Thomas Jens7ORCID,Lindig Udo8,Luley Kim Barbara9,Pink Daniel10,Dechow Tobias11,Sookthai Disorn12,Junge Sabine12,Loose Maria12ORCID,Pauligk Claudia12,Lorenzen Sylvie1ORCID

Affiliation:

1. Klinikum rechts der Isar Technische Universität München, Klinik für Innere Medizin III Munich Germany

2. Institut für Klinische Krebsforschung IKF am Krankenhaus Nordwest, Frankfurt, Germany and Krankenhaus Nordwest University Cancer Center Frankfurt Frankfurt Germany

3. Medizinische Klinik mit Schwerpunkt Hämatologie, Onkologie und Tumorimmunologie Charité–Universitätsmedizin Berlin Berlin Germany

4. Klinik für Innere Medizin Universitätsklinikum Marburg Marburg Germany

5. Haematologisch‐Onkologische Praxis Eppendorf Universitäres Cancer Center Hamburg (UCCH) Hamburg Germany

6. Medizinische Klinik I Universitätsklinikum Carl Gustav Carus Dresden Germany

7. Department of Internal Medicine I Ulm University Hospital Ulm Germany

8. Klinik für Innere Medizin II Universitätsklinikum Jena Jena Germany

9. UKSH Campus Lübeck Klinik für Hämatologie und Onkologie Lübeck Germany

10. Klinik und Poliklinik für Innere Medizin C, Hämatologie und Onkologie, Transplantationszentrum, Palliativmedizin Universität Greifswald and Klinik für Hämatologie, Onkologie und Palliativmedizin‐Sarkomzentrum, HELIOS Klinikum Bad Saarow Bad Saarow Germany

11. Onkologie Ravensburg Ravensburg Germany

12. Institut für Klinische Krebsforschung IKF am Krankenhaus Nordwest Frankfurt Germany

Abstract

AbstractFOLFOX plus nivolumab represents a standard of care for first‐line therapy of advanced gastroesophageal cancer (aGEC) with positive PD‐L1 expression. The efficacy of second‐line VEGFR‐2 inhibition with ramucirumab (RAM) plus chemotherapy after progression to immunochemotherapy remains unclear. Medical records of patients with aGEC enrolled in the randomized phase II AIO‐STO‐0417 trial after treatment failure to first‐line FOLFOX plus nivolumab and ipilimumab were retrospectively analyzed. Patients were divided into two groups based on second‐line therapy: RAM plus chemotherapy (RAM group) or treatment without RAM (control group). Eighty three patients were included. In the overall population, progression‐free survival (PFS) in the RAM group was superior to the control (4.5 vs 2.9 months). Responders (CR/PR) to first‐line immunochemotherapy receiving RAM containing second‐line therapy had prolonged OS from start of first‐line therapy (28.9 vs 16.5 months), as well as second‐line OS (9.6 vs 7.5 months), PFS (5.6 vs 2.9 months) and DCR (53% vs 29%) compared to the control. PD‐L1 CPS ≥1 was 42% and 44% for the RAM and the control, respectively. Patients with CPS ≥1 in the RAM group showed better tumor control (ORR 25% vs 10%) and improved survival (total OS 11.5 vs 8.0 months; second‐line OS 6.5 vs 3.9 months; PFS 4.5 vs 1.6 months) compared to the control. Prior exposure to first‐line FOLFOX plus dual checkpoint inhibition followed by RAM plus chemotherapy shows favorable response and survival rates especially in patients with initial response and positive PD‐L1 expression and has the potential to advance the treatment paradigm in aGEC.

Funder

Eli Lilly and Company

Publisher

Wiley

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