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Patient-Reported Outcomes during and after Treatment for Locally Advanced Rectal Cancer in the PROSPECT Trial (Alliance N1048)

  • Ethan Basch
  • , Amylou C. Dueck
  • , Sandra A. Mitchell
  • , Harvey Mamon
  • , Martin Weiser
  • , Leonard Saltz
  • , Marc Gollub
  • , Lauren Rogak
  • , Brenda Ginos
  • , Gina L. Mazza
  • , Brian Colgrove
  • , George Chang
  • , Lori Minasian
  • , Andrea Denicoff
  • , Gita Thanarajasingam
  • , Benjamin Musher
  • , Thomas George
  • , Alan Venook
  • , Jeffrey Farma
  • , Eileen O'Reilly
  • Jeffrey A. Meyerhardt, Qian Shi, Deborah Schrag
  • University of North Carolina at Chapel Hill
  • Mayo Clinic Arizona
  • National Institutes of Health
  • Brigham and Women's Hospital
  • Memorial Sloan-Kettering Cancer Center
  • Mayo Clinic
  • University of Texas MD Anderson Cancer Center
  • Baylor College of Medicine
  • University of Florida
  • University of California at San Francisco
  • Dana-Farber Cancer Institute

Research output: Contribution to journalArticlepeer-review

135 Scopus citations

Abstract

PURPOSE: The standard of care for locally advanced rectal cancer in North America is neoadjuvant pelvic chemoradiation with fluorouracil (5FUCRT). Neoadjuvant chemotherapy with fluorouracil and oxaliplatin (FOLFOX) is an alternative that may spare patients the morbidity of radiation. Understanding the relative patient experiences with these options is necessary to inform treatment decisions.

METHODS: PROSPECT was a multicenter, unblinded, noninferiority, randomized trial of neoadjuvant FOLFOX versus 5FUCRT, which enrolled adults with rectal cancer clinically staged as T2N+, cT3N-, or cT3N+ who were candidates for sphincter-sparing surgery. Neoadjuvant FOLFOX was given in six cycles over 12 weeks, followed by surgery. Neoadjuvant 5FUCRT was delivered in 28 fractions over 5.5 weeks, followed by surgery. Adjuvant chemotherapy was suggested but not mandated in both groups. Enrolled patients were asked to provide patient-reported outcomes (PROs) at baseline, during neoadjuvant treatment, and at 12 months after surgery. PROs included 14 symptoms from the National Cancer Institute's Patient-Reported Outcomes version of the Common Terminology Criteria for Adverse Events (PRO-CTCAE). Additional PRO instruments measured bowel, bladder, sexual function, and health-related quality of life (HRQL).

RESULTS: From June 2012 to December 2018, 1,194 patients were randomly assigned, 1,128 initiated treatment, and 940 contributed PRO-CTCAE data (493 FOLFOX; 447 5FUCRT). During neoadjuvant treatment, patients reported significantly lower rates of diarrhea and better overall bowel function with FOLFOX while anxiety, appetite loss, constipation, depression, dysphagia, dyspnea, edema, fatigue, mucositis, nausea, neuropathy, and vomiting were lower with 5FUCRT (all multiplicity adjusted P < .05). At 12 months after surgery, patients randomly assigned to FOLFOX reported significantly lower rates of fatigue and neuropathy and better sexual function versus 5FUCRT (all multiplicity adjusted P < .05). Neither bladder function nor HRQL differed between groups at any time point.

CONCLUSION: For patients with locally advanced rectal cancer choosing between neoadjuvant FOLFOX and 5FUCRT, the distinctive PRO profiles inform treatment selection and shared decision making.

Original languageEnglish
Pages (from-to)3724-3734
Number of pages11
JournalJournal of Clinical Oncology
Volume41
Issue number21
DOIs
StatePublished - Jul 20 2023

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • Adult
  • Anal Canal/pathology
  • Antineoplastic Combined Chemotherapy Protocols/adverse effects
  • Fluorouracil
  • Humans
  • Leucovorin
  • Neoadjuvant Therapy/adverse effects
  • Neoplasm Staging
  • Organ Sparing Treatments
  • Patient Reported Outcome Measures
  • Quality of Life
  • Rectal Neoplasms/drug therapy
  • Treatment Outcome

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