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Impact of KRAS, BRAF and microsatellite instability status after cytoreductive surgery and HIPEC in a national cohort of colorectal peritoneal metastasis patients.
Larsen, S G; Goscinski, M A; Dueland, S; Steigen, S E; Hofsli, E; Torgunrud, A; Lund-Iversen, M; Dagenborg, V J; Flatmark, K; Sorbye, H.
Afiliação
  • Larsen SG; Section for Surgical Oncology, Norwegian Radium Hospital, Department of Gastroenterological Surgery, Oslo University Hospital, Oslo, Norway. stl@ous-hf.no.
  • Goscinski MA; Section for Surgical Oncology, Norwegian Radium Hospital, Department of Gastroenterological Surgery, Oslo University Hospital, Oslo, Norway.
  • Dueland S; Department of Oncology, Norwegian Radium Hospital, Oslo University Hospital, Oslo, Norway.
  • Steigen SE; Department of Clinical Pathology, University Hospital of North Norway, Tromsø, Norway.
  • Hofsli E; The Cancer Clinic, St. Olavs Hospital, Trondheim University Hospital, Trondheim, Norway.
  • Torgunrud A; Department of Clinical and Molecular Medicine, Norwegian University of Science and Technology, Trondheim, Norway.
  • Lund-Iversen M; Department of Clinical and Molecular Medicine, Norwegian University of Science and Technology, Trondheim, Norway.
  • Dagenborg VJ; Department of Clinical Pathology, University of Oslo, Oslo, Norway.
  • Flatmark K; Section for Surgical Oncology, Norwegian Radium Hospital, Department of Gastroenterological Surgery, Oslo University Hospital, Oslo, Norway.
  • Sorbye H; Section for Surgical Oncology, Norwegian Radium Hospital, Department of Gastroenterological Surgery, Oslo University Hospital, Oslo, Norway.
Br J Cancer ; 126(5): 726-735, 2022 03.
Article em En | MEDLINE | ID: mdl-34887523
ABSTRACT

BACKGROUND:

Patients with metastatic colorectal cancer (mCRC) carrying BRAF (mutBRAF) or KRAS mutation (mutKRAS) have an inferior prognosis after liver or lung surgery, whereas the prognostic role in the context of peritoneal metastasis (PM) after cytoreductive surgery (CRS) and hyperthermic intraperitoneal chemotherapy (HIPEC) has been less investigated.

METHODS:

In total, 257 patients with non-appendiceal PM-CRC were included from the Norwegian National Unit for CRS-HIPEC.

RESULTS:

In total, 180 patients received CRS-HIPEC with Mitomycin C, 77 patients received palliative surgery only. In the CRS-HIPEC group, mutBRAF was found in 24.7%, mutKRAS 33.9% and double wild-type 41.4% without differences in survival. MSI was found in 29.3% of mutBRAF cases. Patients with mutBRAF/MSI had superior 5-year survival compared to mutBRAF with MSS (58.3% vs 25.2%, P = 0.022), and better 3-year disease-free survival (DFS) compared to mutKRAS (48.6% vs 17.2%, P = 0.049). Peritoneal Cancer Index and the number of lymph node metastasis were prognostic for OS, and the same two, location and gender prognostic for DFS in multivariate analysis.

CONCLUSIONS:

PM-CRC with CRS-HIPEC patients has a surprisingly high proportion of mutBRAF (24.7%). Survival was similar comparing mutBRAF, mutKRAS and double wild-type cases, whereas a small subgroup with mutBRAF and MSI had better survival. Patients with mutBRAF tumours and limited PM should be considered for CRS-HIPEC.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Peritoneais / Neoplasias Colorretais / Proteínas Proto-Oncogênicas p21(ras) / Mitomicina / Proteínas Proto-Oncogênicas B-raf / Instabilidade de Microssatélites / Metástase Linfática Tipo de estudo: Observational_studies / Prognostic_studies Limite: Adult / Female / Humans / Male / Middle aged Idioma: En Revista: Br J Cancer Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Noruega

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Peritoneais / Neoplasias Colorretais / Proteínas Proto-Oncogênicas p21(ras) / Mitomicina / Proteínas Proto-Oncogênicas B-raf / Instabilidade de Microssatélites / Metástase Linfática Tipo de estudo: Observational_studies / Prognostic_studies Limite: Adult / Female / Humans / Male / Middle aged Idioma: En Revista: Br J Cancer Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Noruega