Identifying Early-Phase Clinical Trial Participants at Risk for Experiencing Worse Clinical Outcomes

Author:

Lundquist Debra M.1ORCID,Jimenez Rachel2ORCID,Durbin Sienna3ORCID,Horick Nora4,Healy Megan1,Johnson Andrew1ORCID,Bame Viola1,Capasso Virginia5ORCID,McIntyre Casandra5ORCID,Cashavelly Barbara5,Juric Dejan3ORCID,Nipp Ryan D.6ORCID

Affiliation:

1. Cancer Center Protocol Office, Massachusetts General Hospital, Boston, MA

2. Department of Radiation Oncology, Massachusetts General Hospital, Boston, MA

3. Department of Medicine, Division of Hematology and Oncology, Massachusetts General Hospital and Harvard Medical School, Boston, MA

4. Biostats Center, Massachusetts General Hospital, Boston, MA

5. Department of Nursing & Patient Care Services, Massachusetts General Hospital, Boston, MA

6. University of Oklahoma Stephenson Cancer Center, Oklahoma City, OK

Abstract

PURPOSE: To identify early-phase clinical trial (EP-CT) participants at risk for experiencing worse clinical outcomes and describe receipt of supportive care services. METHODS: A retrospective review of the electronic health records of consecutive patients enrolled in EP-CTs from 2017 to 2019 examined baseline characteristics, clinical outcomes, and receipt of supportive care services. The validated Royal Marsden Hospital (RMH) prognosis score was calculated using data at the time of EP-CT enrollment (scores range from 0 to 3; scores ≥ 2 indicate poor prognosis). Differences in patient characteristics, clinical outcomes, and receipt of supportive care services were compared on the basis of RMH scores. RESULTS: Among 350 patients (median age = 63.2 years [range, 23.0-84.3 years], 57.1% female, 98.0% metastatic cancer), 31.7% had an RMH score indicating a poor prognosis. Those with poor prognosis RMH scores had worse overall survival (hazard ratio [HR], 2.00; P < .001), shorter time on trial (HR, 1.53; P < .001), and lower likelihood of completing the dose-limiting toxicity period (odds ratio, 0.42; P = .006) versus those with good prognosis scores. Patients with poor prognosis scores had greater risk of emergency room visits (HR, 1.66; P = .037) and hospitalizations (HR, 1.69; P = .016) while on trial, and earlier hospice enrollment (HR, 2.22; P = .006). Patients with poor prognosis scores were significantly more likely to receive palliative care consultation (46.8% v 27.6%; P < .001), but not other supportive care services. CONCLUSION: This study found that RMH prognosis score could identify patients at risk for decreased survival, shorter time on trial, and greater use of health care services. The findings underscore the need to develop supportive care interventions targeting EP-CT participants' distinct needs.

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Oncology (nursing),Health Policy,Oncology

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