Patient-reported outcomes (PROs) in locally advanced cervical cancer (LACC): Insights from the OUTBACK trial.

R Rebecca Mercieca-Bebber E Elizabeth H. Barnes (NHMRC Clinical Trials Centre, The University of Sydney, Sydney, NSW, Australia) K Kathleen N. Moore (Division of Gynecologic Oncology Stephenson Cancer Center University of Oklahoma Oklahoma City Oklahoma USA) Y Yeh Chen Lee K Kailash Narayan (Peter MacCallum Cancer Centre and University of Melbourne, Melbourne, Australia) P Pearly Khaw (Department of Radiation Oncology, Peter MacCallum Cancer Centre, Melbourne, Australia) M Martin Buck (Department of Life Sciences, Imperial College London) A Anthony Fyles (National Cancer Institute of Canada Clinical Trial Group, Radiation Medicine Program, Princess Margaret Cancer Centre, Toronto, ON, Canada) S Susan Brooks (Department of Radiation Oncology, Auckland City Hospital, Auckland, New Zealand) J Jayanthi Sivasothy Lea (UT Southwestern Medical Center, Dallas, TX) A Ashley Stuckey (Women and Infants Hospital of Rhode Island, Providence, RI) T Thomas E. Lad (Cook County Health and Hospital System, Chicago, IL) C Christine Holschneider (David Geffen School of Medicine at UCLA, Department of Obstetrics and Gynecology, Olive View UCLA Medical Center, Los Angeles, CA) N Nicola M. Spirtos (Women's Cancer Center of Nevada, Las Vegas, NV) L Leslie R. Boyd (Division of Gynecologic Oncology, Department of Obstetrics and Gynecology, NYU Grossman School of Medicine, New York University Langone Medical Center, New York, NY) W William Small B Bradley J. Monk M Martin R. Stockler M Madeleine T. King L Linda R. Mileshkin (Department of Medical Oncology, Peter MacCallum Cancer Centre and; Sir Peter MacCallum Department of Oncology, the University of Melbourne, Melbourne, VIC, Australia)

Abstract

5503 Background: OUTBACK (ACTRN12610000732088), an open-label, international, randomized phase 3 trial of 919 participants (pts) with LACC, showed that adding adjuvant chemotherapy (ACT) after chemoradiotherapy (CRT) increased adverse events without improving overall survival compared to CRT alone. PRO objectives of OUTBACK were to determine the: 1) prevalence of patient-reported moderate-severe symptom issues at years 1-3 post-randomisation 2) duration of common issues; 3) long-term psycho-sexual health. Methods: Pts completed the EORTC core questionnaire QLQ-C30; cervical cancer module QLQ-CX24 (questions 50-54 only for sexually active pts); EORTC Item Library questions on abdominal, urinary, bowel and chemotherapy side-effects; & FACT-GOG-NTX4 neurotoxicity over 36 months. A moderate-severe long-term symptom issue was defined as a score in the worst 2 response categories (EORTC items), a total score ≤8/16 on FACT-GOG-NTX4 at years 1, 2 or 3 for Objectives 1-2, or equivalent subscale score for Objective 3. The availability of PROs for analysis was not related to 11 pre-specified demographic/clinical variables so no imputation for missing data was performed. Results: PRO completion rates were 94% at baseline, 64% at year 1 & 37% by year 3. Table 1 shows the 10 top-ranked issues at year 1 & their persistence or resolution by years 2-3. These may be underestimates, due to lower PRO completion rates at years 2-3. Issues and frequencies were similar across treatment arms by year 1. Moderate-severe peripheral neuropathy affected 24% post CRT+ACT & 18% post CRT (year 1); 19% post CRT+ACT & 12% post CRT (year 3). At baseline, 77% reported no sexual activity in the past 4 weeks. Overall, 92% of pts reported low sexual activity at years 1, 2 or 3; 68% reported low enjoyment, 40% moderate-severe vaginal tightness, 37% vaginal dryness during sex and 32% were moderately-severely worried sex would be painful. Conclusions: Long-term symptom issues & sexual health concerns are common & persistent following CRT +/-ACT for LACC and need dedicated survivorship care. Clinical trial information: 12610000732088 . Frequency and duration of top-ranked moderate-severe symptoms. Item CRT + ACTn (%) CRT alonen (%) All participants n (%) Issue rated moderate-severe at Year 1 Issue rated moderate-severe at Year 1 Issue rated moderate-severe at Year 1 Issue from Year 1 resolved by Year 2 or 3 Issue from Year 1 persistent at Year 2 or 3 Worried future health 76 (50) 59 (38) 135 (44) 14 (10) 49 (36) Hot flushes/ sweats 68 (39) 64 (35) 132 (37) 24 (18) 49 (37) Frequent urination 67 (38) 59 (32) 126 (35) 24 (19) 45 (36) Sexual activity (not) enjoyable 59 (63) 66 (65) 125 (64) 11 (9) 43 (34) Trouble sleeping 62 (35) 55 (30) 117 (32) 19 (16) 37 (32) Tired 53 (30) 51 (28) 104 (29) 22 (21) 33 (32) Changed bowel habit 56 (32) 46 (25) 102 (28) 22 (22) 41 (40) Financial difficulties 51 (27) 50 (28) 101 (28) 17 (17) 32 (32) Pain 54 (29) 42 (24) 96 (27) 21 (22) 23 (24) Dissatisfied with body 48 (26) 47 (27) 95 (26) 21 (22) 27 (28)

Article Details

Volume / Issue Vol. 43, Issue 16_suppl
Published June 01, 2025
Pages 5503-5503
ISSN 0732-183X
Publisher Lippincott Williams & Wilkins

Journal Info

Journal of Clinical Oncology

Lippincott Williams & Wilkins

ISSN: 0732-183X Health Sciences

Authors (20)

R

Rebecca Mercieca-Bebber

E

Elizabeth H. Barnes

NHMRC Clinical Trials Centre, The University of Sydney, Sydney, NSW, Australia

K

Kathleen N. Moore

Division of Gynecologic Oncology Stephenson Cancer Center University of Oklahoma Oklahoma City Oklahoma USA

Y

Yeh Chen Lee

K

Kailash Narayan

Peter MacCallum Cancer Centre and University of Melbourne, Melbourne, Australia

P

Pearly Khaw

Department of Radiation Oncology, Peter MacCallum Cancer Centre, Melbourne, Australia

M

Martin Buck

Department of Life Sciences, Imperial College London

A

Anthony Fyles

National Cancer Institute of Canada Clinical Trial Group, Radiation Medicine Program, Princess Margaret Cancer Centre, Toronto, ON, Canada

S

Susan Brooks

Department of Radiation Oncology, Auckland City Hospital, Auckland, New Zealand

J

Jayanthi Sivasothy Lea

UT Southwestern Medical Center, Dallas, TX

A

Ashley Stuckey

Women and Infants Hospital of Rhode Island, Providence, RI

T

Thomas E. Lad

Cook County Health and Hospital System, Chicago, IL

C

Christine Holschneider

David Geffen School of Medicine at UCLA, Department of Obstetrics and Gynecology, Olive View UCLA Medical Center, Los Angeles, CA

N

Nicola M. Spirtos

Women's Cancer Center of Nevada, Las Vegas, NV

L

Leslie R. Boyd

Division of Gynecologic Oncology, Department of Obstetrics and Gynecology, NYU Grossman School of Medicine, New York University Langone Medical Center, New York, NY

W

William Small

B

Bradley J. Monk

M

Martin R. Stockler

M

Madeleine T. King

L

Linda R. Mileshkin

Department of Medical Oncology, Peter MacCallum Cancer Centre and; Sir Peter MacCallum Department of Oncology, the University of Melbourne, Melbourne, VIC, Australia