Effect of Hyperthermic Intraperitoneal Chemotherapy on Cytoreductive Surgery in Gastric Cancer With Synchronous Peritoneal Metastases: The Phase III GASTRIPEC-I Trial

Author:

Rau Beate1ORCID,Lang Hauke2,Koenigsrainer Alfred3,Gockel Ines4ORCID,Rau Horst-Guenter5ORCID,Seeliger Hendrik6ORCID,Lerchenmueller Christian7,Reim Daniel8,Wahba Roger9ORCID,Angele Martin10,Heeg Steffen11ORCID,Keck Tobias12,Weimann Arved13ORCID,Topp Stefan14,Piso Pompiliu15,Brandl Andreas1ORCID,Schuele Silke16ORCID,Jo Peter17,Pratschke Johann1,Wegel Sandra1,Rehders Alexander18,Moosmann Nicolas19,Gaedcke Jochen17ORCID,Heinemann Volker20ORCID,Trips Evelyn2122ORCID,Loeffler Markus23,Schlag Peter Michael24,Thuss-Patience Peter25ORCID

Affiliation:

1. Department of Surgery, Charité—Universitätsmedizin Berlin, Corporate Member of Freie Universität, Berlin, Germany

2. Department of Surgery, Johannes Gutenberg Universität Mainz Klinikum, Mainz, Germany

3. Department of Surgery, Universitätsklinikum Tübingen, Tübingen, Germany

4. Department of Surgery, Universitätsklinikum Leipzig, Leipzig, Germany

5. Emeritus Department of Surgery, Amper Kliniken AG, Dachau, Germany

6. Department of Surgery, Charité—Universitätsmedizin Berlin, Berlin, Germany

7. Department of Medical Oncology, Gemeinschaftspraxis für Hämatologie und Onkologie—Münster, Münster, Germany

8. Department of Surgery, Klinikum rechts der Isar, Technische Universität München, München, Germany

9. Department of General, Visceral, Cancer and Transplantation Surgery, Faculty of Medicine and University Hospital of Cologne, University of Cologne, Cologne, Germany

10. Department of Surgery, Klinikum der Universität München—Großhadern, München, Germany

11. Department of Medicine II, Medical Center—University of Freiburg, Faculty of Medicine, University of Freiburg, Germany

12. Department of Surgery, Campus Lübeck, Universitätsklinikum Schleswig-Holstein, Lübeck, Germany

13. Department of Surgery, St Georg-Krankenhaus Leipzig, Leipzig, Germany

14. Department of Surgery, Bonifatius Hospital Lingen (für Düsseldorf), Lingen, Germany

15. Department of Surgery, Krankenhaus Barmherzige Brüder Regensburg, Regensburg, Germany

16. Department of Surgery, Universitätsklinikum Jena, Jena, Germany

17. Department of Surgery, Universitätsmedizin Göttingen, Göttingen, Germany

18. Department of Surgery, Universitätsklinikum Düsseldorf, Düsseldorf, Germany

19. Department of Medical Oncology, Krankenhaus Barmherzige Brüder Regensburg, Regensburg, Germany

20. Department of Medical Oncology, Klinikum der Universität München—Großhadern, München, Germany

21. Zentrum für Klinische Studien (ZKS) Leipzig, Medizinische Fakultät, Universität Leipzig, Leipzig, Germany

22. Coordination Centre for Clinical Trials Dresden, Carl Gustav Carus Medical Faculty, Technische Universität Dresden, Dresden, Germany

23. Institut für Medizinische Informatik, Statistik und Epidemiologie (IMISE), Medizinische Fakultät, Universität Leipzig, Leipzig, Germany

24. Department of Surgery and Surgical Oncology, Charité—Universitätsmedizin Berlin, Berlin, Germany

25. Department of Hematology, Oncology and Cancer Immunology, Charité—Universitätsmedizin Berlin, Berlin, Germany

Abstract

PURPOSE In patients with peritoneal metastasis (PM) from gastric cancer (GC), chemotherapy is the treatment of choice. Cytoreductive surgery (CRS) and hyperthermic intraperitoneal chemotherapy (HIPEC) are still being debated. This randomized, controlled, open-label, multicenter phase III trial (EudraCT 2006-006088-22; ClinicalTrials.gov identifier: NCT02158988 ) explored the impact on overall survival (OS) of HIPEC after CRS. PATIENTS AND METHODS Adult patients with GC and histologically proven PM were randomly assigned (1:1) to perioperative chemotherapy and CRS alone (CRS-A) or CRS plus HIPEC (CRS + H). HIPEC comprised mitomycin C 15 mg/m2 and cisplatin 75 mg/m2 in 5 L of saline perfused for 60 minutes at 42°C. The primary end point was OS; secondary endpoints included progression-free survival (PFS), other distant metastasis-free survival (MFS), and safety. Analyses followed the intention-to-treat principle. RESULTS Between March 2014 and June 2018, 105 patients were randomly assigned (53 patients to CRS-A and 52 patients to CRS + H). The trial stopped prematurely because of slow recruitment. In 55 patients, treatment stopped before CRS mainly due to disease progression/death. Median OS was the same for both groups (CRS + H, 14.9 [97.2% CI, 8.7 to 17.7] months v CRS-A, 14.9 [97.2% CI, 7.0 to 19.4] months; P = .1647). The PFS was 3.5 months (95% CI, 3.0 to 7.0) in the CRS-A group and 7.1 months (95% CI, 3.7 to 10.5; P = .047) in the CRS + H group. The CRS + H group showed better MFS (10.2 months [95% CI, 7.7 to 14.7] v CRS-A, 9.2 months [95% CI, 6.8 to 11.5]; P = .0286). The incidence of grade ≥3 adverse events (AEs) was similar between groups (CRS-A, 38.1% v CRS + H, 43.6%; P = .79). CONCLUSION This study showed no OS difference between CRS + H and CRS-A. PFS and MFS were significantly better in the CRS + H group, which needs further exploration. HIPEC did not increase AEs.

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Cancer Research,Oncology

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