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Phase III trial comparing 3-6months of adjuvant FOLFOX4/XELOX in stage II-III colon cancer: Safety and compliance in the TOSCA trial

Articolo
Data di Pubblicazione:
2016
Abstract:
BACKGROUND: Six months of oxaliplatin-based adjuvant chemotherapy is standard of care for radically resected stage III colon cancer and an accepted option for high-risk stage II. A shorter duration of therapy, if equally efficacious, would be advantageous for patients and Health-Care Systems. PATIENTS AND METHODS: TOSCA ['Randomized trial investigating the role of FOLFOX-4 or XELOX (3 versus 6 months) regimen duration and bevacizumab as adjuvant therapy for patients with stage II/III colon cancer] is an open-label, phase III, multicenter, noninferiority trial randomizing patients with high-risk stage II or stage III radically resected colon cancer to receive 3 months (arm 3 m) versus 6 months (arm 6 m) of FOLFOX4/XELOX. Primary end-point was relapse-free survival. We present here safety and compliance data. RESULTS: From June 2007 to March 2013, 3759 patients were accrued from 130 Italian sites, 64% receiving FOLFOX4 and 36% XELOX in either arm. Treatment completion rate without any modification was 35% versus 12% and with delays or dose reduction 52% versus 44% in arm 3 and 6 m. Treatment was permanently discontinued in 8% (arm 3 m) and 33% (arm 6 m). In arm 6 m, 50% of patients discontinuing treatment did so after completing 80% of planned program. Grade 3+ toxicities were higher in arm 6 m than that in 3 m. Grade 2+ neuropathy was 31.2% versus 8.8% (P < 0.0001) while grade 3+ was 8.4 versus 1.3 (P < 0.0001), in arm 3 and 6 m. Seven deaths within 30 days from last treatment administration in arm 6 m and three deaths in arm 3 m were observed (0.3% versus 0.1%, P = 0.34). CONCLUSIONS: TOSCA is the first trial comparing 3 versus 6 months of adjuvant chemotherapy completing accrual within the international initiative of treatment duration evaluation (International Duration Evaluation of Adjuvant, IDEA). High compliance to treatment in control arm will allow a correct assessment of potential differences between the two treatment durations.
Tipologia CRIS:
14.a.1 Articolo su rivista
Keywords:
Adjuvant chemotherapy, Colon cancer, Duration, Hematology, Oncology
Elenco autori:
Lonardi, S.; Sobrero, A.; Rosati, G.; Di Bartolomeo, M.; Ronzoni, M.; Aprile, G.; Scartozzi, M.; Banzi, M.; Zampino, M. G.; Pasini, F.; Marchetti, P.; Cantore, M.; Zaniboni, A.; Rimassa, L.; Ciuffreda, L.; Ferrari, D.; Barni, S.; Zagonel, V.; Maiello, E.; Rulli, E.; Labianca, R.; Adamo, Vincenzo
Link alla scheda completa:
https://iris.unime.it/handle/11570/3107446
Link al Full Text:
https://iris.unime.it//retrieve/handle/11570/3107446/347026/3107446.pdf
Pubblicato in:
ANNALS OF ONCOLOGY
Journal
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URL

https://www.annalsofoncology.org/article/S0923-7534(19)35844-2/fulltext; https://www.sciencedirect.com/science/article/pii/S0923753419358442?via=ihub
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