TY - JOUR
T1 - What is the Risk for Peritoneal Metastases and Survival Afterwards in T4 Colon Cancers?
AU - Uppal, Abhineet
AU - Helmink, Beth
AU - Grotz, Travis E.
AU - Konishi, Tsuyoshi
AU - Fournier, Keith F.
AU - Nguyen, Sa
AU - Taggart, Melissa W.
AU - Shen, John Paul
AU - Bednarski, Brian K.
AU - You, Yi Qian N.
AU - Chang, George J.
N1 - Publisher Copyright:
© 2022, Society of Surgical Oncology.
PY - 2022/7
Y1 - 2022/7
N2 - Background: Patients with T4 colon adenocarcinomas have an increased risk of peritoneal metastases (PM) but the histopathologic risk factors for its development are not well-described. Objective: The purpose of this study was to determine factors associated with PM, time to recurrence, and survival after recurrence among patients with T4 colon cancer. Patients and Methods: Patients with pathologic T4 colon cancer who underwent curative resection from 2005 to 2017 were identified from a prospectively maintained institutional database and classified by recurrence pattern: (a) none – 68.8%; (b) peritoneal only – 7.9%; (c) peritoneal and extraperitoneal – 9.9%; and (d) extraperitoneal only – 13.2%. Associations between PM development and patient, primary tumor, and treatment factors were assessed. Results: Overall, 151 patients were analyzed, with a median follow-up of 66.2 months; 27 patients (18%) developed PM (Groups B and C) and 20 (13%) patients recurred at non-peritoneal sites only (Group D). Median time to developing metastases was shorter for Groups B and C compared with Group D (B and C: 13.7 months; D: 46.7 months; p = 0.022). Tumor deposits (TDs) and nodal stage were associated with PM (p < 0.05), and TDs (p = 0.048) and LVI (p = 0.015) were associated with additional extraperitoneal recurrence. Eleven (41%) patients with PM underwent salvage surgery, and median survival after recurrence was associated with the ability to undergo cytoreduction (risk ratio 0.20, confidence interval 0.06–0.70). Conclusion: PM risk after resection of T4 colon cancer is independently associated with factors related to lymphatic spread, such as N stage and TDs. Well-selected patients can undergo cytoreduction with long-term survival. These findings support frequent postoperative surveillance and aggressive early intervention, including cytoreduction.
AB - Background: Patients with T4 colon adenocarcinomas have an increased risk of peritoneal metastases (PM) but the histopathologic risk factors for its development are not well-described. Objective: The purpose of this study was to determine factors associated with PM, time to recurrence, and survival after recurrence among patients with T4 colon cancer. Patients and Methods: Patients with pathologic T4 colon cancer who underwent curative resection from 2005 to 2017 were identified from a prospectively maintained institutional database and classified by recurrence pattern: (a) none – 68.8%; (b) peritoneal only – 7.9%; (c) peritoneal and extraperitoneal – 9.9%; and (d) extraperitoneal only – 13.2%. Associations between PM development and patient, primary tumor, and treatment factors were assessed. Results: Overall, 151 patients were analyzed, with a median follow-up of 66.2 months; 27 patients (18%) developed PM (Groups B and C) and 20 (13%) patients recurred at non-peritoneal sites only (Group D). Median time to developing metastases was shorter for Groups B and C compared with Group D (B and C: 13.7 months; D: 46.7 months; p = 0.022). Tumor deposits (TDs) and nodal stage were associated with PM (p < 0.05), and TDs (p = 0.048) and LVI (p = 0.015) were associated with additional extraperitoneal recurrence. Eleven (41%) patients with PM underwent salvage surgery, and median survival after recurrence was associated with the ability to undergo cytoreduction (risk ratio 0.20, confidence interval 0.06–0.70). Conclusion: PM risk after resection of T4 colon cancer is independently associated with factors related to lymphatic spread, such as N stage and TDs. Well-selected patients can undergo cytoreduction with long-term survival. These findings support frequent postoperative surveillance and aggressive early intervention, including cytoreduction.
UR - http://www.scopus.com/inward/record.url?scp=85126764735&partnerID=8YFLogxK
U2 - 10.1245/s10434-022-11472-w
DO - 10.1245/s10434-022-11472-w
M3 - Article
C2 - 35298760
AN - SCOPUS:85126764735
SN - 1068-9265
VL - 29
SP - 4224
EP - 4233
JO - Annals of Surgical Oncology
JF - Annals of Surgical Oncology
IS - 7
ER -