TY - JOUR
T1 - Risk factors for metachronous isolated peritoneal metastasis after preoperative chemotherapy and potentially curative gastric cancer resection
T2 - Results from the CRITICS trial
AU - Caspers, Irene A.
AU - Sikorska, Karolina
AU - Slagter, Astrid E.
AU - van Amelsfoort, Romy M.
AU - Kranenbarg, Elma Meershoek Klein
AU - van de Velde, Cornelis J.H.
AU - Lind, Pehr
AU - Nordsmark, Marianne
AU - Jansen, Edwin P.M.
AU - Verheij, Marcel
AU - van Sandick, Johanna W.
AU - Cats, Annemieke
AU - van Grieken, Nicole C.T.
N1 - Funding Information:
Conflicts of Interest: M.V. and A.C. have received grants from the Dutch Cancer Society, the Dutch Colorectal Cancer Group and Hoffmann La Roche. N.C.T.v.G. has received grants from the Dutch Cancer Society and The Netherlands Organization for Health Research and Development.
Publisher Copyright:
© 2021 by the authors. Licensee MDPI, Basel, Switzerland.
PY - 2021/9
Y1 - 2021/9
N2 - Gastric cancer (GC) patients at high risk of developing peritoneal metastasis (PM) as a single site of metastasis after curative treatment may be candidates for adjuvant prophylactic strategies. Here we investigated risk factors for metachronous isolated PM in patients who were treated in the CRITICS trial (NCT00407186). Univariable and multivariable analyses on both metachronous isolated PM and ‘other events’, i.e., (concurrent) distant metastasis, locoregional recurrence or death, were performed using a competing risk model and summarized by cumulative incidences. Isolated PM occurred in 64 of the 606 (11%) included patients. Diffuse or mixed histological subtype, ypT4 tumor stage and LNhigh (ypN3 lymph node stage or a lymph node ratio >20%) were independent risk factors for isolated PM in both univariable and multivariable analyses. Likewise, LNhigh was an independent risk factor for ‘other events’. Patients with tumors who were positive for all three independent risk factors had the highest two-year cumulative incidence of 43% for isolated PM development. In conclusion, diffuse or mixed histological subtype, ypT4 and LNhigh were identified as independent risk factors for isolated PM in patients treated with preoperative chemotherapy followed by surgical resection. The combination of these factors may identify a subgroup that may benefit from PM-preventing treatment strategies.
AB - Gastric cancer (GC) patients at high risk of developing peritoneal metastasis (PM) as a single site of metastasis after curative treatment may be candidates for adjuvant prophylactic strategies. Here we investigated risk factors for metachronous isolated PM in patients who were treated in the CRITICS trial (NCT00407186). Univariable and multivariable analyses on both metachronous isolated PM and ‘other events’, i.e., (concurrent) distant metastasis, locoregional recurrence or death, were performed using a competing risk model and summarized by cumulative incidences. Isolated PM occurred in 64 of the 606 (11%) included patients. Diffuse or mixed histological subtype, ypT4 tumor stage and LNhigh (ypN3 lymph node stage or a lymph node ratio >20%) were independent risk factors for isolated PM in both univariable and multivariable analyses. Likewise, LNhigh was an independent risk factor for ‘other events’. Patients with tumors who were positive for all three independent risk factors had the highest two-year cumulative incidence of 43% for isolated PM development. In conclusion, diffuse or mixed histological subtype, ypT4 and LNhigh were identified as independent risk factors for isolated PM in patients treated with preoperative chemotherapy followed by surgical resection. The combination of these factors may identify a subgroup that may benefit from PM-preventing treatment strategies.
KW - Gastric cancer
KW - Metachronous
KW - Multimodality treatment
KW - Peritoneal metastasis
KW - Risk factors
UR - http://www.scopus.com/inward/record.url?scp=85114879414&partnerID=8YFLogxK
U2 - 10.3390/cancers13184626
DO - 10.3390/cancers13184626
M3 - Article
C2 - 34572852
AN - SCOPUS:85114879414
VL - 13
JO - Cancers (Basel)
JF - Cancers (Basel)
SN - 2072-6694
IS - 18
M1 - 4626
ER -