TY - JOUR
T1 - Impact of age on the efficacy of newer adjuvant therapies in patients with stage II/III colon cancer
T2 - Findings from the ACCENT database
AU - McCleary, Nadine J.
AU - Meyerhardt, Jeffrey A.
AU - Green, Erin
AU - Yothers, Greg
AU - De Gramont, Aimery
AU - Van Cutsem, Eric
AU - O’Connell, Michael
AU - Twelves, Christopher J.
AU - Saltz, Leonard B.
AU - Haller, Daniel G.
AU - Sargent, Daniel J.
N1 - Funding Information:
The ACCENT (Adjuvant Colon Cancer End Points) Collaborative Group includes: D.J. Sargent, E. Green, A. Grothey, S.R. Alberts, Q. Shi, L. Renfro (Mayo Clinic, Rochester, MN); G. Yothers, M.J. O’Connell, N. Wolmark (National Surgical Adjuvant Breast and Bowel Project Biostatistical and Operations Centers, Pittsburgh, PA); A. de Gramont (Hôpital Saint Antoine, Paris, France); R. Gray, D. Kerr (Quasar Collaborative Group, Birmingham and Oxford, United Kingdom); D.G. Haller (Abramson Cancer Center, University of Pennsylvania, Philadelphia, PA); J. Benedetti (Southwest Oncology Group Statistical Center, Seattle, WA); M. Buyse (International Drug Development Institute, Louvain-la-Neuve, Belgium); R. Labianca (Ospedali Riuniti, Bergamo, Italy); J.F. Seitz (University of the Mediterranean, Marseilles, France); C.J. O’Callaghan (National Cancer Institute of Canada Clinical Trials Group, Queens University, Kingston, Ontario, Canada); G. Francini (University of Siena, Siena, Italy); P.J. Catalano (Eastern Cooperative Oncology Group Statistical Center, Boston, MA); C.D. Blanke (British Columbia Cancer Agency, Vancouver, British Columbia, Canada); T. Andre (Groupe Hospitalier Piti e-Salpetriere, Paris, France); R.M. Goldberg (University of North Carolina, Chapel Hill, NC); A. Benson (Northwestern University, Chicago, IL); C. Twelves (University of Leeds, Leeds, United Kingdom); J. Cassidy (Genentech/Roche, Glasgow, United Kingdom); F. Sirzen (Roche, Basel, Switzerland); L. Cisar (Pfizer, New York, NY); E. Van Cutsem (University Hospital Gasthuisberg, Leuven, Belgium); L. Saltz (Memorial Sloan-Kettering Cancer Center, New York, NY); J. Meyerhardt, N.J. McCleary (Dana-Farber Cancer Center, Boston, MA).
Funding Information:
Supported in part by the American Society of Clinical Oncology Young Investigator Award cosponsored by the Hartford Foundation, North Central Cancer Treatment Group (National Cancer Institute [NCI] Grant No. CA25224), and Dana-Farber Cancer Institute/Harvard Cancer Center SPORE (Specialized Programs of Research Excellence; NCI Grant No. P50 CA127003).
Funding Information:
Supported in part by the American Soci ety of Clinical Oncology Young Investi gator Award cosponsored by the Hartford Foundation, North Central Cancer Treatment Group (National Cancer Institute [NCI] Grant No. CA25224), and Dana-Farber Cancer Institute/Harvard Cancer Center SPORE (Specialized Programs of Research Excellence; NCI Grant No. P50 CA127003).
Publisher Copyright:
© 2013 by American Society of Clinical Oncology.
PY - 2013/7/10
Y1 - 2013/7/10
N2 - Purpose: Prior studies have suggested that patients with stage II/III colon cancer receive similar benefit from intravenous (IV) fluoropyrimidine adjuvant therapy regardless of age. Combination regimens and oral fluorouracil (FU) therapy are now standard. We examined the impact of age on colon cancer recurrence and mortality after adjuvant therapy with these newer options. Patients and Methods: We analyzed 11,953 patients age < 70 and 2,575 age ≥ 70 years from seven adjuvant therapy trials comparing IV FU with oral fluoropyrimidines (capecitabine, uracil, or tegafur) or combinations of fluoropyrimidines with oxaliplatin or irinotecan in stage II/III colon cancer. End points were disease-free survival (DFS), overall survival (OS), and time to recurrence (TTR). Results: In three studies comparing oxaliplatin-based chemotherapy with IV FU, statistically significant interactions were not observed between treatment arm and age (P interaction = .09 for DFS, .05 for OS, and .36 for TTR), although the stratified point estimates suggested limited benefit from the addition of oxaliplatin in elderly patients (DFS hazard ratio [HR], 0.94; 95% CI, 0.78 to 1.13; OS HR, 1.04; 95% CI, 0.85 to 1.27). No significant interactions by age were detected with oral fluoropyrimidine therapy compared with IV FU; noninferiority was supported in both age populations. Conclusion: Patients age ≥ 70 years seemed to experience reduced benefit from adding oxaliplatin to fluoropyrimidines in the adjuvant setting, although statistically, there was not a significant effect modification by age, whereas oral fluoropyrimidines retained their efficacy.
AB - Purpose: Prior studies have suggested that patients with stage II/III colon cancer receive similar benefit from intravenous (IV) fluoropyrimidine adjuvant therapy regardless of age. Combination regimens and oral fluorouracil (FU) therapy are now standard. We examined the impact of age on colon cancer recurrence and mortality after adjuvant therapy with these newer options. Patients and Methods: We analyzed 11,953 patients age < 70 and 2,575 age ≥ 70 years from seven adjuvant therapy trials comparing IV FU with oral fluoropyrimidines (capecitabine, uracil, or tegafur) or combinations of fluoropyrimidines with oxaliplatin or irinotecan in stage II/III colon cancer. End points were disease-free survival (DFS), overall survival (OS), and time to recurrence (TTR). Results: In three studies comparing oxaliplatin-based chemotherapy with IV FU, statistically significant interactions were not observed between treatment arm and age (P interaction = .09 for DFS, .05 for OS, and .36 for TTR), although the stratified point estimates suggested limited benefit from the addition of oxaliplatin in elderly patients (DFS hazard ratio [HR], 0.94; 95% CI, 0.78 to 1.13; OS HR, 1.04; 95% CI, 0.85 to 1.27). No significant interactions by age were detected with oral fluoropyrimidine therapy compared with IV FU; noninferiority was supported in both age populations. Conclusion: Patients age ≥ 70 years seemed to experience reduced benefit from adding oxaliplatin to fluoropyrimidines in the adjuvant setting, although statistically, there was not a significant effect modification by age, whereas oral fluoropyrimidines retained their efficacy.
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U2 - 10.1200/JCO.2013.49.6638
DO - 10.1200/JCO.2013.49.6638
M3 - Article
C2 - 23733765
AN - SCOPUS:84883893403
SN - 0732-183X
VL - 31
SP - 2600
EP - 2606
JO - Journal of Clinical Oncology
JF - Journal of Clinical Oncology
IS - 20
ER -