Baseline Quality of Life is a Strong and Independent Prognostic Factor for Overall Survival in Metastatic Colorectal Cancer

Author:

McGarrah Patrick1ORCID,Hubbard Joleen1,Novotny Paul J.2,Branda Megan E.2,Sargent Daniel S.2,Morton Roscoe F.3,Fuchs Charles S.4,Benson Al B.5,Williamson Stephen K.6,Findlay Brian P.7,Alberts Steven R.1,Goldberg Richard M.8,Sloan Jeff A.2

Affiliation:

1. Division of Medical Oncology, Mayo Clinic, Rochester, MN, USA

2. Alliance Statistics and Data Management Center, Mayo Clinic, Rochester, MN, USA

3. North Central Cancer Treatment Group, Iowa Oncology Research Association, Des Moines, IA, USA

4. Yale Cancer Center, New Haven, CT, USA

5. Division of Hematology and Medical Oncology, Northwestern University, Chicago, IL, USA; and ECOG-ACRIN Cancer Research Group, Philadelphia, PA, USA

6. SWOG Cancer Research Network, Division of Hematology and Oncology, University of Kansas Medical Center, Kansas City, KS, USA

7. Canadian Cancer Trials Group, St. Catharines, ON, Canada

8. The Ohio State University Medical Center, Columbus, OH, USA

Abstract

Background Previous studies have established that higher baseline quality of life (QOL) scores are associated with improved survival in patients with metastatic colorectal cancer (mCRC). We examined the relationship between overall survival (OS) and baseline QOL. Patients and Methods A total of 1 247 patients with mCRC participating in N9741 (comparing bolus 5-FU/LV, irinotecan [IFL] vs infusional 5-FU/leucovorin [LV]/oxaliplatin [FOLFOX] vs. irinotecan/oxaliplatin [IROX]) provided data at baseline on overall QOL using a single-item linear analogue self-assessment (LASA) 0–100 point scale. The association of OS according to clinically deficient (defined as CD-QOL, score 0–50) vs not clinically deficient (nCD-QOL, score 51–100) baseline QOL scores was tested. A multivariable analysis using Cox proportional hazards modeling was performed to adjust for the effects of multiple baseline factors. An exploratory analysis was performed evaluating OS according to baseline QOL status among patients who did or did not receive second-line therapy. Results Baseline QOL was a strong predictor of OS for the whole cohort (CD-QOL vs nCD-QOL: 11.2 months vs 18.4 months, P < .0001), and in each arm IFL 12.4 vs 15.1 months, FOLFOX 11.1 months vs 20.6 months, and IROX 8.9 months vs 18.1 months. Baseline QOL was associated with baseline performance status (PS) ( P < .0001). After adjusting for PS and treatment arm, baseline QOL was still associated with OS ( P = .017). Conclusions Baseline QOL is an independent prognostic factor for OS in patients with mCRC. The demonstration that patient-assessed QOL and PS are independent prognostic indicators suggests that these assessments provide important complementary prognostic information.

Funder

National Cancer Institute

Publisher

SAGE Publications

Subject

Oncology,Hematology,General Medicine

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