4.7 Article

Long-Term Toxicity and Health-Related Quality of Life After Adjuvant Chemoradiation Therapy or Radiation Therapy Alone for High-Risk Endometrial Cancer in the Randomized PORTEC-3 Trial

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ELSEVIER SCIENCE INC
DOI: 10.1016/j.ijrobp.2020.10.030

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Funding

  1. Dutch Cancer Society, the Netherlands [UL2006-4168/CKTO 2006-04]
  2. United Kingdom by Cancer Research UK [C7925/A8659]
  3. NHMRC Project [570894]
  4. Cancer Australia Grant (2011 round of the priority-driven Collaborative Cancer Research Scheme)
  5. Cancer Australia Grant (Cancer Australia)
  6. Italian Medicines Agency AIFA [FARM84BCX2]
  7. Canadian Cancer Society Research Institute [015469, 021039]

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The study compared long-term adverse events and health-related quality of life between chemoradiation therapy and radiation therapy alone in high-risk endometrial cancer patients. Results showed that the chemoradiation therapy group had more patients with grade ≥ 2 adverse events at 5 years, and persistent sensory neuropathy toxicity led to more patients reporting significant tingling or numbness in HRQOL. Physical and role functioning impairments were seen up to 3 years in the chemoradiation therapy group.
Purpose: The survival results of the PORTEC-3 trial showed a significant improvement in both overall and failure-free survival with chemoradiation therapy versus pelvic radiation therapy alone. The present analysis was performed to compare long-term adverse events (AE) and health-related quality of life (HRQOL). Methods and Materials: In the study, 660 women with high-risk endometrial cancer were randomly assigned to receive chemoradiation therapy (2 concurrent cycles of cisplatin followed by 4 cycles of carboplatin/paclitaxel) or radiation therapy alone. Toxicity was graded using Common Terminology Criteria for Adverse Events, version 3.0. HRQOL was measured using EORTC QLQ-C30 and CX24/OV28 subscales and compared with normative data. An as-treated analysis was performed. Results: Median follow-up was 74.6 months; 574 (87%) patients were evaluable for HRQOL. At 5 years, grade >= 2 AE were scored for 78 (38%) patients who had received chemoradiation therapy versus 46 (24%) who had received radiation therapy alone (P = .008). Grade 3 AE did not differ significantly between the groups (8% vs 5%, P = .18) at 5 years, and only one new late grade 4 toxicity had been reported. At 3 and 5 years, sensory neuropathy toxicity grade >= 2 persisted after chemoradiation therapy in 6% (vs 0% after radiation therapy, P < .001) and more patients reported significant tingling or numbness at HRQOL (27% vs 8%, P < .001 at 3 years; 24% vs 9%, P = .002 at 5 years). Up to 3 years, more patients who had chemoradiation therapy reported limb weakness (21% vs 5%, P < .001) and lower physical (79 vs 87, P < .001) and role functioning (78 vs 88, P < .001) scores. Both treatment groups reported similar long-term global health/quality of life scores, which were better than those of the normative population. Conclusions: This study shows a long-lasting, clinically relevant, negative impact of chemoradiation therapy on toxicity and HRQOL, most importantly persistent peripheral sensory neuropathy. Physical and role functioning impairments were seen until 3 years. These long-term data are essential for patient information and shared decision-making regarding adjuvant chemotherapy for high-risk endometrial cancer. (C) 2020 The Author(s). Published by Elsevier Inc.

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