TY - JOUR
T1 - Gastrointestinal metastases in renal cell carcinoma
T2 - A retrospective multicenter GETUG (Groupe d′Étude des Tumeurs Uro-Génitales) study
AU - Carneiro, F.
AU - Vinceneux, A.
AU - Larroquette, M.
AU - Rony, M.
AU - Carril, L.
AU - Laguerre, B.
AU - Blazevic, I.
AU - Bartelemy, P.
AU - Teyssonneau, D.
AU - Goujon, M.
AU - Linassier, C.
AU - Thiery-Vuillemin, A.
AU - Roubaud, G.
AU - Mourey, L.
AU - Albiges, L.
AU - Gravis, G.
AU - Gross-Goupil, M.
AU - Cancel, M.
N1 - Publisher Copyright:
© 2024
PY - 2024/3/1
Y1 - 2024/3/1
N2 - Background: Among patients with renal cell carcinoma (RCC), bone and visceral metastases have a poor prognosis, while endocrine gland metastases have a more favorable prognosis. Gastrointestinal metastases (GIMs) are rare, and their prognosis is still poorly understood. Objectives: To report clinical presentations, patient characteristics, therapeutic strategies, and prognosis of GIMs from RCC. Methods: We retrospectively collected data from RCC patients presenting GIMs, in 10 French GETUG centers, between 2000 and 2021. Results: We identified 74 patients with 87 GIMs, mostly gastric or duodenal. The median age at GIM diagnosis was 69 years and 76% of patients already had other metastases. GIMs occurred after a median duration of 5.4 years (IC95%=[4.2–7.1]) and 1.9 years (IC95%=[1.2–3.8]) from RCC diagnosis and first metastasis, respectively. GIMs were symptomatic in 52 patients (70%), with anemia in 41 patients (55%) and/or gastrointestinal bleeding in 31 patients (42%). Only 22 asymptomatic patients (30%) were fortuitously diagnosed. GIM management consisted of systemic treatment only in 29 GIMs (33%), local treatment only in 23 GIMs (26%), and both local and systemic treatment in 18 GIMs (21%). For 17 GIMs (20%), there was no therapeutic modification. After diagnosis of GIM, median overall survival was 19 months. Conclusion: We report the largest retrospective cohort of GIMs in RCC patients. They should be suspected in case of anemia or gastrointestinal bleeding in any patient with a history of RCC. Their management varies widely depending on their location in the digestive tract and whether or not they are symptomatic.
AB - Background: Among patients with renal cell carcinoma (RCC), bone and visceral metastases have a poor prognosis, while endocrine gland metastases have a more favorable prognosis. Gastrointestinal metastases (GIMs) are rare, and their prognosis is still poorly understood. Objectives: To report clinical presentations, patient characteristics, therapeutic strategies, and prognosis of GIMs from RCC. Methods: We retrospectively collected data from RCC patients presenting GIMs, in 10 French GETUG centers, between 2000 and 2021. Results: We identified 74 patients with 87 GIMs, mostly gastric or duodenal. The median age at GIM diagnosis was 69 years and 76% of patients already had other metastases. GIMs occurred after a median duration of 5.4 years (IC95%=[4.2–7.1]) and 1.9 years (IC95%=[1.2–3.8]) from RCC diagnosis and first metastasis, respectively. GIMs were symptomatic in 52 patients (70%), with anemia in 41 patients (55%) and/or gastrointestinal bleeding in 31 patients (42%). Only 22 asymptomatic patients (30%) were fortuitously diagnosed. GIM management consisted of systemic treatment only in 29 GIMs (33%), local treatment only in 23 GIMs (26%), and both local and systemic treatment in 18 GIMs (21%). For 17 GIMs (20%), there was no therapeutic modification. After diagnosis of GIM, median overall survival was 19 months. Conclusion: We report the largest retrospective cohort of GIMs in RCC patients. They should be suspected in case of anemia or gastrointestinal bleeding in any patient with a history of RCC. Their management varies widely depending on their location in the digestive tract and whether or not they are symptomatic.
KW - Gastrointestinal Hemorrhage
KW - Gastrointestinal Tract
KW - Metastasis
KW - Renal Cell Carcinoma
UR - http://www.scopus.com/inward/record.url?scp=85182875770&partnerID=8YFLogxK
U2 - 10.1016/j.ejca.2024.113534
DO - 10.1016/j.ejca.2024.113534
M3 - Article
C2 - 38241819
AN - SCOPUS:85182875770
SN - 0959-8049
VL - 199
JO - European Journal of Cancer
JF - European Journal of Cancer
M1 - 113534
ER -