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




TekijätJoensuu, 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

KustantajaSpringer Nature

Julkaisuvuosi2024

JournalBritish Journal of Cancer

Tietokannassa oleva lehden nimiBritish journal of cancer

Lehden akronyymiBr J Cancer

Vuosikerta131

Numero2

Aloitussivu299

Lopetussivu302

ISSN0007-0920

eISSN1532-1827

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

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

Rinnakkaistallenteen osoitehttps://research.utu.fi/converis/portal/detail/Publication/456849576


Tiivistelmä

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.


Ladattava julkaisu

This is an electronic reprint of the original article.
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Julkaisussa olevat rahoitustiedot
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 2025-27-01 at 19:29