TY - JOUR
T1 - A new prognostic and predictive tool for shared decision making in stage III colon cancer
AU - Sobrero, Alberto F.
AU - Puccini, Alberto
AU - Shi, Qian
AU - Grothey, Axel
AU - Andrè, Thierry
AU - Shields, Anthony F.
AU - Souglakos, Ioannis
AU - Yoshino, Takayuki
AU - Iveson, Timothy
AU - Ceppi, Marcello
AU - Bruzzi, Paolo
N1 - Funding Information:
This manuscript was partly supported by Associazione Italiana per la Ricerca sul Cancro (AIRC) IG 2018; by the National Cancer Institute at the National Institutes of Health [grant number: U10CA180882 ]; NCA ( Institut National du Cancer ) and PHRC2009 ( Institut National du Cancer, Programme Hospitalier de Recherche Clinique en Cancérologie ).
Funding Information:
This manuscript was partly supported by Associazione Italiana per la Ricerca sul Cancro (AIRC) IG 2018; by the National Cancer Institute at the National Institutes of Health [grant number: U10CA180882]; NCA (Institut National du Cancer) and PHRC2009 (Institut National du Cancer, Programme Hospitalier de Recherche Clinique en Canc?rologie). The authors would like to thank coordinators and investigators of all IDEA trials TOSCA, SCOT, HORG, C80702, IDEA France and ACHIEVE to have the authorisation to use IDEA data.
Publisher Copyright:
© 2020 Elsevier Ltd
PY - 2020/10
Y1 - 2020/10
N2 - Background: Survival of patients with stage III colon cancer varies widely according to T-N sub-stages. Estimating the benefit of each therapeutic option in each T-N subgroup may provide more accurate information helping doctors and patients in the complex shared decision-making process surrounding adjuvant therapy. Methods: The outcomes data of 12,834 patients with stage III colon cancer enrolled in the IDEA trial served as our database. Patients were categorised in 16 sub-stages, based on T-N categories. We created a meta-regression model to predict the expected 5-year DFS within each T-N sub-stage. We then evaluated the efficacy of each therapeutic option in every sub-stage, working backward by subtraction, using an average of the HRs reported in pertinent trial publications as a conversion factor. Results: Large differences in 5-year DFS rate were observed among the subgroups, ranging from 89% (T1N1a) to 31% (T4N2b) in the overall population. The contribution to the outcome of each therapeutic option in this setting varied widely across sub-stages. According to our model, patients with T1N1a cancers have a projected 5-year DFS of 79.6% with surgery alone. Adjuvant fluoropyrimidine alone results in 5.6% absolute DFS gain; an additional 2.3% and 0.8% gain is seen with oxaliplatin for 3 and 6 months, respectively. Patients with T4N2b cancers show a 13.9% 5-year DFS with surgery alone, and an 11.2%, 6.4%, 2.5% increase with the aforementioned adjuvant options, respectively. Conclusion: The resulting overlay bar graph gives patients and doctors the projected relative benefit of each treatment option and may substantially help the shared decision-making process, although caution must be exercised in using this model due to the significant variance of the estimates.
AB - Background: Survival of patients with stage III colon cancer varies widely according to T-N sub-stages. Estimating the benefit of each therapeutic option in each T-N subgroup may provide more accurate information helping doctors and patients in the complex shared decision-making process surrounding adjuvant therapy. Methods: The outcomes data of 12,834 patients with stage III colon cancer enrolled in the IDEA trial served as our database. Patients were categorised in 16 sub-stages, based on T-N categories. We created a meta-regression model to predict the expected 5-year DFS within each T-N sub-stage. We then evaluated the efficacy of each therapeutic option in every sub-stage, working backward by subtraction, using an average of the HRs reported in pertinent trial publications as a conversion factor. Results: Large differences in 5-year DFS rate were observed among the subgroups, ranging from 89% (T1N1a) to 31% (T4N2b) in the overall population. The contribution to the outcome of each therapeutic option in this setting varied widely across sub-stages. According to our model, patients with T1N1a cancers have a projected 5-year DFS of 79.6% with surgery alone. Adjuvant fluoropyrimidine alone results in 5.6% absolute DFS gain; an additional 2.3% and 0.8% gain is seen with oxaliplatin for 3 and 6 months, respectively. Patients with T4N2b cancers show a 13.9% 5-year DFS with surgery alone, and an 11.2%, 6.4%, 2.5% increase with the aforementioned adjuvant options, respectively. Conclusion: The resulting overlay bar graph gives patients and doctors the projected relative benefit of each treatment option and may substantially help the shared decision-making process, although caution must be exercised in using this model due to the significant variance of the estimates.
KW - Adjuvant
KW - Colon cancer
KW - Shared decision making
KW - Stage III
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U2 - 10.1016/j.ejca.2020.07.031
DO - 10.1016/j.ejca.2020.07.031
M3 - Article
C2 - 32892120
AN - SCOPUS:85090156430
SN - 0959-8049
VL - 138
SP - 182
EP - 188
JO - European Journal of Cancer
JF - European Journal of Cancer
ER -