The impact of inter-cycle treatment delays on overall survival in patients with advanced-stage ovarian cancer

Author:

Steventon Luke12ORCID,Man Kenneth K C12ORCID,Nicum Shibani13ORCID,Miller Rowan E1ORCID,Peleg Hasson Shira45ORCID,Shah Samixa1,Baser Michael6,Kipps Emma5ORCID,Forster Martin D13,Almossawi Ofran7,Chambers Pinkie12ORCID

Affiliation:

1. Medical Oncology Department and Centre of Medicines Optimization Research and Education (CMORE), University College Hospitals NHS Foundation Trust , 235 Euston rd, London NW1 2PP , United Kingdom

2. Department of Practice and Policy, UCL School of Pharmacy , London WC1H 9JP , United Kingdom

3. UCL Cancer Institute, Department of Oncology , London WC1 6DD , United Kingdom

4. School of Medicine, Tel Aviv University , Tel Aviv , Israel

5. The Royal Marsden NHS Trust , London SW3 6JJ , United Kingdom

6. National Disease Registration Service (NDRS) , NHS England, London E14 4PU , United Kingdom

7. Great Ormond Street Hospital for Children NHS Foundation Trust, Population, Policy & Practice Department , London WC1N 1LE , United Kingdom

Abstract

Abstract Introduction Chemotherapy forms the cornerstone of systemic treatment for advanced ovarian cancer, extending overall survival; however, drug-related toxicity can lead to treatment delays, potentially diminishing treatment efficacy. This study evaluated the impact of treatment delays on all-cause mortality of patients with ovarian cancer, to better inform decisions on patient management. Methods This retrospective, population-based cohort study included 1517 women with advanced-stage ovarian cancer, receiving first-line adjuvant or neoadjuvant chemotherapy in 2014 and 2015. The frequency of inter-cycle delays >7 days was calculated using drug administration dates. Kaplan-Meier estimates were used to compare 2-year overall survival (OS) between patients who were delayed and those treated to schedule. Cox proportional hazards regression was used to investigate the impact of treatment delay on all-cause mortality. Inverse probability of treatment weighting propensity scores were used to adjust for confounding variables. Results Delays >7 days occurred in 35.3% of patients. Two-year OS probability was 62.7% in patients who experienced treatment delays >7 days (95% CI, 58.7-66.9) compared to 69.1% in those treated to schedule (95% CI, 66.2-72.0). Delays were not significantly associated with all-cause mortality when adjusted for confounders (HR 1.00 95% CI, 0.83-1.20, P = .9). Conclusions Delays to chemotherapy treatment were not significantly associated with worsened survival in patients with advanced-stage ovarian cancer. These results can inform clinical decision making that prioritize toxicity management and quality of life for those treated with chemotherapy.

Funder

National Institute for Health and Care Research

Research for Patient Benefit

Publisher

Oxford University Press (OUP)

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