Abstract

BackgroundOlder patients are underrepresented in the clinical trials that determine the standards of care for oncological treatment. We conducted a review to identify whether there have been age-restrictive inclusion criteria in clinical trials over the last twenty five years, focusing on patients with metastatic gastroesophageal cancer.MethodsA search strategy was developed encompassing Embase, PubMed and The Cochrane Library databases. Completed phase III randomised controlled trials evaluating systemic anti-cancer therapies in metastatic gastroesophageal malignancies from 1st January 1995 to 18th November 2020 were identified. These were screened for eligibility using reference management software (Covidence; Veritas Health Innovation Ltd). Data including age inclusion/exclusion criteria and median age of participants were recorded. The percentage of patients ≥ 65 enrolled was collected where available. The change over time in the proportion of studies using an upper age exclusion was estimated using a linear probability model.ResultsThree hundred sixty-three phase III studies were identified and screened, with 66 trials remaining for final analysis. The majority of trials were Asian (48%; n = 32) and predominantly evaluated gastric malignancies, (86%; n = 56).The median age of participants was 62 (range 18–94). Thirty-two percent (n = 21) of studies specified an upper age limit for inclusion and over half of these were Asian studies. The median age of exclusion was 75 (range 65–80). All studies prior to 2003 used an upper age exclusion (n = 12); whereas only 9 that started in 2003 or later did (17%). Among later studies, there was a very modest downward yearly-trend in the proportion of studies using an upper age exclusion (-0.02 per year; 95%CI -0.05 to 0.01; p = 0.31). Fifty-two percent (n = 34) of studies specified the proportion of their study population who were ≥ 65 years. Older patients represented only 36% of the trial populations in these studies (range 7–60%).ConclusionsRecent years have seen improvements in clinical trial protocols, with many no longer specifying restrictive age criteria. Reasons for poor representation of older patients are complex and ongoing efforts are needed to broaden eligibility criteria and prioritise the inclusion of older adults in clinical trials.

Highlights

  • Older patients are underrepresented in the clinical trials that determine the standards of care for oncological treatment

  • Cancers of the upper gastrointestinal tract have the propensity for early dissemination, and the majority of older patients present with locally-advanced, unresectable or metastatic disease [5].In general, combination chemotherapy with platinum doublet regimens have been shown to improve overall survival and provide higher response rates than single agents in the treatment of advanced gastric and esophageal cancer [6]

  • The highest incidence rates of advanced gastroesophageal cancers are among older patients, they are often treated with less intensive chemotherapy regimens, due to concerns regarding toxicity and tolerability, and this is in part due to the lack of evidence from phase III trials [5]

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Summary

Introduction

Older patients are underrepresented in the clinical trials that determine the standards of care for oncological treatment. Gastroesophageal cancers remain one of the most lethal malignancies, with 5 year survival rates of approximately 20–30% [1]. Cancers of the upper gastrointestinal tract have the propensity for early dissemination, and the majority of older patients present with locally-advanced, unresectable or metastatic disease [5].In general, combination chemotherapy with platinum doublet regimens have been shown to improve overall survival and provide higher response rates than single agents in the treatment of advanced gastric and esophageal cancer [6]. The highest incidence rates of advanced gastroesophageal cancers are among older patients, they are often treated with less intensive chemotherapy regimens, due to concerns regarding toxicity and tolerability, and this is in part due to the lack of evidence from phase III trials [5]

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