Survival of patients with ruptured gastrointestinal stromal tumour treated with adjuvant imatinib in a randomised trial




Joensuu, Heikki; Reichardt, Annette; Eriksson, Mikael; Hohenberger, Peter; Boye, Kjetil; Cameron, Silke; Lindner, Lars H.; Jost, Philipp J.; Bauer, Sebastian; Schütte, Jochen; Lindskog, Stefan; Kallio, Raija; Jaakkola, Panu M.; Goplen, Dorota; Wardelmann, Eva; Reichardt, Peter

PublisherSpringer Nature

2024

British Journal of Cancer

British journal of cancer

Br J Cancer

131

2

299

302

0007-0920

1532-1827

DOIhttps://doi.org/10.1038/s41416-024-02738-z

https://www.nature.com/articles/s41416-024-02738-z

https://research.utu.fi/converis/portal/detail/Publication/456849576



Background: Patients with ruptured gastrointestinal stromal tumour (GIST) have poor prognosis. Little information is available about how adjuvant imatinib influences survival.

Methods: We explored recurrence-free survival (RFS) and overall survival (OS) of patients with ruptured GIST who participated in a randomised trial (SSG XVIII/AIO), where 400 patients with high-risk GIST were allocated to adjuvant imatinib for either 1 year or 3 years after surgery. Of the 358 patients with confirmed localised GIST, 73 (20%) had rupture reported. The ruptures were classified retrospectively using the Oslo criteria.

Results: Most ruptures were major, four reported ruptures were reclassified unruptured. The 69 patients with rupture had inferior RFS and OS compared with 289 patients with unruptured GIST (10-year RFS 21% vs. 55%, OS 59% vs. 78%, respectively). Three-year adjuvant imatinib did not significantly improve RFS or OS of the patients with rupture compared with 1-year treatment, but in the largest mutational subset with KIT exon 11 deletion/indel mutation OS was higher in the 3-year group than in the 1-year group (10-year OS 94% vs. 54%).

Conclusions: About one-fifth of ruptured GISTs treated with adjuvant imatinib did not recur during the first decade of follow-up. Relatively high OS rates were achieved despite rupture.


The study was supported financially in part by Sigrid Juselius Foundation and Louise and Henrik Kuningas Foundation (Dr. Joensuu). Novartis Oncology supported the SSG XVIII/AIO trial. Open Access funding provided by University of Helsinki (including Helsinki University Central Hospital).


Last updated on 2025-15-08 at 15:10