Impact of the IDEA collaboration study results on clinical practice in France for patients with stage III colon cancer: A national GERCOR - PRODIGE survey Journal Article


Authors: Ouali, K.; Turpin, A.; Neuzillet, C.; Rousseau, B.; Garcia-Larnicol, M. L.; Tournigand, C.; Samalin, E.; Taieb, J.; André, T.; Cohen, R.
Article Title: Impact of the IDEA collaboration study results on clinical practice in France for patients with stage III colon cancer: A national GERCOR - PRODIGE survey
Abstract: Background: The IDEA collaboration showed that the type and duration of adjuvant chemotherapy in stage III colon cancer (CC) could be adjusted according to the schedule of chemotherapy and the level of risk. We aimed at evaluating the implementation of IDEA's results in real-life practice for stage III CC. Material and Methods: All clinicians registered in the French oncology cooperative groups GERCOR, FFCD, and UNICANCER GI mailing lists were invited to participate to an online anonymized nationwide survey from January 30, 2019 to March 31, 2019. Proportions were compared using the χ2 test. Results: A total of 213 physicians answered the survey. Of these, 173 (81%) considered that 3 months of adjuvant chemotherapy was the new standard of care for low-risk (pT1-3/N1) stage III CC, and 99% considered that 6 months remained the standard of care for high-risk (pT4 and/or pN2) stage III CC. In patients under 70 years, capecitabine and oxaliplatin (CAPOX) for 3 months was prescribed by 74% of the participants in low-risk CC, whereas 6 months of 5-fluorouracil, leucovorin, and oxaliplatin (FOLFOX) was preferred for high-risk CC in 94% of cases. For patients over 70 years with good performance status and no comorbidities, 172 (81%) physicians prescribed oxaliplatin-based chemotherapy for low-risk CC (3 months, 144 of 172%; 88%), and 200 (94%) physicians prescribed oxaliplatin-based adjuvant chemotherapy for high-risk CC (6 months, 199 of 200%; 99.5%). Conclusions: The IDEA results have been practice-changing as French physicians have implemented 3 months of CAPOX for patients with low-risk stage III CC, substituting from 6 months of FOLFOX, which remains the preferred regimen for high-risk patients. © 2020 Elsevier Inc. The IDEA study showed that the type and duration of adjuvant chemotherapy might be adjusted according to the schedule of chemotherapy (5-fluorouracil, leucovorin, and oxaliplatin [FOLFOX] or capecitabine and oxaliplatin [CAPOX]) and the level of risk in stage III colon cancer. Hereby, we show that it has been mainly integrated in routine practice in France with a switch from 6 to 3 months and from the FOLFOX to the CAPOX regimen in patients with low-risk stage III colon cancer. © 2020 Elsevier Inc.
Keywords: aged; major clinical study; fluorouracil; treatment duration; capecitabine; cancer adjuvant therapy; cancer patient; cancer staging; clinical practice; high risk patient; colorectal neoplasms; folinic acid; colon cancer; adjuvant chemotherapy; comorbidity; physician; oxaliplatin; guidelines; france; folfox; vascular access; low risk patient; capox; human; article
Journal Title: Clinical Colorectal Cancer
Volume: 20
Issue: 1
ISSN: 1533-0028
Publisher: Elsevier Inc.  
Date Published: 2021-03-01
Start Page: 79
End Page: 83.e4
Language: English
DOI: 10.1016/j.clcc.2020.11.004
PUBMED: 33281064
PROVIDER: scopus
DOI/URL:
Notes: Article -- Export Date: 1 April 2021 -- Source: Scopus
Altmetric
Citation Impact
BMJ Impact Analytics
MSK Authors