Drug Holidays and Overall Survival of Patients with Metastatic Colorectal Cancer

Author:

Garattini Silvio KenORCID,Basile Debora,Bonotto Marta,Ongaro Elena,Porcu Luca,Corvaja Carla,Cattaneo Monica,Andreotti Victoria Josephine,Lisanti Camilla,Bertoli Elisa,Pelizzari GiacomoORCID,Iacono Donatella,Miolo GianmariaORCID,Cardellino Giovanni Gerardo,Buonadonna Angela,Aprile Giuseppe,Fasola Gianpiero,Puglisi FabioORCID,Pella Nicoletta

Abstract

Different de-escalation strategies have been proposed to limit the risk of cumulative toxicity and guarantee quality of life during the treatment trajectory of patients with metastatic colorectal cancer (mCRC). Programmed treatment interruptions, defined as drug holidays (DHs), have been implemented in clinical practice. We evaluated the association between DHs and overall survival (OS). This was a retrospective study, conducted at the University Hospital of Udine and the IRCCS CRO of Aviano. We retrieved records of 608 consecutive patients treated for mCRC from 1 January 2005 to 15 March 2017 and evaluated the impact of different de-escalation strategies (maintenance, DHs, or both) on OS through uni- and multivariate Cox regression analyses. We also looked at attrition rates across treatment lines according to the chosen strategy. In our study, 19.24% of patients received maintenance therapy, 16.12% DHs, and 9.87% both, while 32.07% continued full-intensity first-line treatment up to progression or death. In uni- and multivariate analyses first-line continuous treatment and early discontinuation (treatment for less than 3 months) were associated to worse OS compared to non-continuous strategies (HR, 1.68; 95% CI, 1.22–2.32; p = 0.002 and HR,4.89; 95% CI, 3.33–7.19; p < 0.001, respectively). Attrition rates were 22.8%, 20.61%, and 19.64% for maintenance, DHs, or both, respectively. For continuous therapy and for treatment of less than 3 months it was 21.57% and 49%. De-escalation strategies are safe and effective options. DHs after initial induction chemotherapy may be considered in clinically selected patients with metastatic colorectal cancer.

Publisher

MDPI AG

Subject

Cancer Research,Oncology

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