Prognostic Impact of Early Treatment and Oxaliplatin Discontinuation in Patients With Stage III Colon Cancer: An ACCENT/IDEA Pooled Analysis of 11 Adjuvant Trials

Author:

Gallois Claire1ORCID,Shi Qian2ORCID,Meyers Jeffrey P.2,Iveson Timothy3ORCID,Alberts Steven R.4ORCID,de Gramont Aimery5ORCID,Sobrero Alberto F.6ORCID,Haller Daniel G.7ORCID,Oki Eiji8ORCID,Shields Anthony Frank9ORCID,Goldberg Richard M.10ORCID,Kerr Rachel11,Lonardi Sara12ORCID,Yothers Greg13ORCID,Kelly Caroline14,Boukovinas Ioannis15ORCID,Labianca Roberto16,Sinicrope Frank A.4ORCID,Souglakos Ioannis17,Yoshino Takayuki18ORCID,Meyerhardt Jeffrey A.19ORCID,André Thierry20ORCID,Papamichael Demetris21,Taieb Julien1ORCID

Affiliation:

1. Paris‐Cité University, Department of Gastroenterology and Digestive Oncology, Georges Pompidou European Hospital, SIRIC CARPEM, Paris, France

2. Department of Health Science Research, Mayo Clinic, Rochester, MN

3. Department of Medical Oncology, University of Southampton, Southampton, United Kingdom

4. Department of Oncology, Mayo Clinic, Rochester, MN

5. Department of Medical Oncology, Franco-British Institute, Levallois-Perret, France

6. Medical Oncology, IRCCS San Martino IST, Genoa, Italy

7. Division of Hematology/Oncology, University of Pennsylvania, Philadelphia, PA

8. Department of Surgery and Science, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan

9. Karmanos Cancer Institute, Wayne State University, Detroit, MI

10. West Virginia University Cancer Institute and the Mary Babb Randolph Cancer Center, Morgantown, WV

11. Department of Oncology, Oxford University, Oxford, United Kingdom

12. Medical Oncology Unit 1, Clinical and Experimental Oncology Department, Veneto Institute of Oncology IRCCS, Padua, Italy

13. Department of Biostatistics, University of Pittsburgh, Pittsburgh, PA

14. Cancer Research UK Clinical Trials Unit, Institute of Cancer Sciences, University of Glasgow, Glasgow, United Kingdom

15. Bioclinic Thessaloniki Medical Oncology Unit, Thessaloniki, Greece

16. Ospdale Papa Giovanni XXIII, Bergamo, Italy

17. Department of Medical Oncology, University Hospital of Heraklion, Heraklion, Greece

18. Department of Gastrointestinal Oncology, National Cancer Center Hospital East, Kashiwa, Japan

19. Dana-Farber Cancer Institute, Boston, MA

20. Sorbonne Université, Department of Medical Oncology, Hôpital Saint-Antoine, Paris, France

21. Division of Medical Oncology, Bank Of Cyprus Oncology Centre, Nicosia, Cyprus

Abstract

PURPOSE Oxaliplatin-based adjuvant chemotherapy in patients with stage III colon cancer (CC) for 6 months remains a standard in high-risk stage III patients. Data are lacking as to whether early discontinuation of all treatment (ETD) or early discontinuation of oxaliplatin (EOD) could worsen the prognosis. MATERIALS AND METHODS We studied the prognostic impact of ETD and EOD in patients with stage III CC from the ACCENT/IDEA databases, where patients were planned to receive 6 months of infusional fluorouracil, leucovorin, and oxaliplatin or capecitabine plus oxaliplatin. ETD was defined as discontinuation of treatment and EOD as discontinuation of oxaliplatin only before patients had received a maximum of 75% of planned cycles. Association between ETD/EOD and overall survival and disease-free survival (DFS) were assessed by Cox models adjusted for established prognostic factors. RESULTS Analysis of ETD and EOD included 10,447 (20.9% with ETD) and 7,243 (18.8% with EOD) patients, respectively. Compared with patients without ETD or EOD, patients with ETD or EOD were statistically more likely to be women, with Eastern Cooperative Oncology Group performance status ≥ 1, and for ETD, older with a lower body mass index. In multivariable analyses, ETD was associated with a decrease in disease-free survival and overall survival (hazard ratio [HR], 1.61, P < .001 and HR, 1.73, P < .001), which was not the case for EOD (HR, 1.07, P = .3 and HR, 1.13, P = .1). However, patients who received < 50% of the planned cycles of oxaliplatin had poorer outcomes. CONCLUSION In patients treated with 6 months of oxaliplatin-based chemotherapy for stage III CC, ETD was associated with poorer oncologic outcomes. However, this was not the case for EOD. These data favor discontinuing oxaliplatin while continuing fluoropyrimidine in individuals with significant neurotoxicity having received > 50% of the planned 6-month chemotherapy.

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Cancer Research,Oncology

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