Improvement in Patient-Reported Outcomes With Intensity-Modulated Radiotherapy (RT) Compared With Standard RT: A Report From the NRG Oncology RTOG 1203 Study

Author:

Yeung Anamaria R.1,Pugh Stephanie L.2,Klopp Ann H.3,Gil Karen M.4,Wenzel Lari5,Westin Shannon N.3,Gaffney David K.6,Small William7,Thompson Spencer8,Doncals Desiree E.9,Cantuaria Guilherme H.C.10,Yaremko Brian P.11,Chang Amy12,Kundapur Vijayananda13,Mohan Dasarahally S.14,Haas Michael L.15,Kim Yong Bae16,Ferguson Catherine L.17,Deshmukh Snehal2,Bruner Deborah W.18,Kachnic Lisa A.19

Affiliation:

1. University of Florida, Gainesville, FL

2. NRG Oncology Statistics and Data Management Center, Philadelphia, PA

3. MD Anderson Cancer Center, Houston, TX

4. Summa Health System, Akron, OH

5. University of California Irvine, Irvine, CA

6. Huntsman Cancer Institute, University of Utah, Salt Lake City, UT

7. Loyola University Chicago, Chicago, IL

8. University of Oklahoma Health Sciences Center, Oklahoma City, OK

9. Cooper Cancer Center, Summa Akron City Hospital, Akron, OH

10. Northside Hospital, Atlanta, GA

11. London Regional Cancer Program, London, United Kingdom

12. Pamela Youde Nethersole Eastern Hospital, Hong Kong, Special Administrative Region, People’s Republic of China

13. Saskatoon Cancer Centre, Saskatoon, Saskatchewan, Canada

14. Kaiser Permanente Cancer Treatment Center, South San Francisco, CA

15. Reading Hospital, Reading, PA

16. Severance Hospital, Yonsei University Health System, Seoul, South Korea

17. Georgia Regents University, Augusta, GA

18. Emory University, Atlanta, GA

19. Vanderbilt University School of Medicine, Nashville, TN

Abstract

PURPOSE In oncology trials, the National Cancer Institute Common Terminology Criteria for Adverse Events (CTCAE) is the standard tool for reporting adverse events (AEs), but it may underreport symptoms experienced by patients. This analysis of the NRG Oncology RTOG 1203 compared symptom reporting by patients and clinicians during radiotherapy (RT). PATIENTS AND METHODS Patients with cervical or endometrial cancer requiring postoperative RT were randomly assigned to standard 4-field RT or intensity-modulated RT (IMRT). Patients completed the 6-item patient-reported outcomes version of the CTCAE (PRO-CTCAE) for GI toxicity assessing abdominal pain, diarrhea, and fecal incontinence at various time points. Patients reported symptoms on a 5-point scale. Clinicians recorded these AEs as CTCAE grades 1 to 5. Clinician- and patient-reported AEs were compared using McNemar’s test for rates > 0%. RESULTS Of 278 eligible patients, 234 consented and completed the PRO-CTCAE. Patients reported high-grade abdominal pain 19.1% ( P < .0001), high-grade diarrhea 38.5% ( P < .0001), and fecal incontinence 6.8% more frequently than clinicians. Similar effects were seen between grade ≥ 1 CTCAE toxicity and any-grade patient-reported toxicity. Between-arm comparison of patient-reported high-grade AEs revealed that at 5 weeks of RT, patients who received IMRT experienced fewer GI AEs than patients who received 4-field pelvic RT with regard to frequency of diarrhea (18.2% difference; P = .01), frequency of fecal incontinence (8.2% difference; P = .01), and interference of fecal incontinence (8.5% difference; P = .04). CONCLUSION Patient-reported AEs showed a reduction in symptoms with IMRT compared with standard RT, whereas clinician-reported AEs revealed no difference. Clinicians also underreported symptomatic GI AEs compared with patients. This suggests that patient-reported symptomatic AEs are important to assess in this disease setting.

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Cancer Research,Oncology

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