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Poster session 12

1884P - Development and validation of a prediction tool for severe treatment-related toxicities in older cancer patients on systemic treatment (TR-TRM)

Date

14 Sep 2024

Session

Poster session 12

Topics

Cancer in Older Adults;  Management of Systemic Therapy Toxicities

Tumour Site

Presenters

Wendy Chan

Citation

Annals of Oncology (2024) 35 (suppl_2): S1077-S1114. 10.1016/annonc/annonc1612

Authors

W.W.L. Chan1, H. Hou2, C.W.H. Choi3, S.L.T. Yik4, P.C.N. Tse4, H.F.M. Cheng5, W.L. Tsoi6, T.K. Wu4, L.S.J. Au5, R. Liu5, S. Siu5, E. Cheung1, C.L. Chiang7, A. El-Helali1, K.M. Cheung8, K.C.R. Ngan9, K.K. Yuen10, D.L.W. Kwong1, V.H.F. Lee7

Author affiliations

  • 1 Department Of Clinical Oncology, The University of Hong Kong - Li Ka Shing Faculty of Medicine, NA - Hong Kong/HK
  • 2 Department Of Clinical Oncology, The University of Hong Kong - Li Ka Shing Faculty of Medicine, Hong Kong/HK
  • 3 School Of Public Health, HKU - The University of Hong Kong, Hong Kong/HK
  • 4 School Of Clinical Medicine, The University of Hong Kong - Li Ka Shing Faculty of Medicine, Hong Kong/HK
  • 5 Clinical Oncology, Queen Mary Hospital, Hong Kong/HK
  • 6 School Of Nursing, The Hong Kong Polytechnic University, Hong Kong/HK
  • 7 Clinical Oncology, The University of Hong Kong - Li Ka Shing Faculty of Medicine, Hong Kong/HK
  • 8 Clinical Oncology, Queen Elizabeth Hospital, 0000 - Kowloon/HK
  • 9 Department Of Clinical Oncology, Gleneagles Hospital, Kowloon/HK
  • 10 Clinical Oncology Dept., Queen Mary Hospital, Hong Kong/HK

Resources

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Abstract 1884P

Background

Older cancer patients are at a higher risk of treatment-related toxicities (TRT) due to various reasons. Existing chemotherapy toxicity calculators have limitations. This study aimed to develop and validate a prediction tool for severe TRT in older cancer patients on systemic treatment.

Methods

Consecutive cancer patients aged ≥65 undergoing systemic anti-cancer treatment were recruited from three large oncology centers in Hong Kong (Queen Mary Hospital, Queen Elizabeth Hospital and Gleneagles Hospital) from March 2019 to May 2022. Pre-treatment assessments captured clinical, tumour/treatment, laboratory, and geriatric assessment variables. Patients were followed throughout treatment or 6 months for grade 3-5 TRT based on CTCAE version 5. Univariate and multivariable logistic regression identified predictive factors, and a weighted scoring system was used to develop the prediction model. Model performance was evaluated using area under the ROC curve (AUC) and goodness-of-fit statistics, with internal and external validation.

Results

Among the 500 patients (400 in development cohort, 100 in validation cohort) with median age 71, 304 (60.8%) developed grade 3-5 TRT. Ten independent predictors associated with TRT were identified. The predictive model categorized patients into low (0-3 points: incidence of TRT in development cohort: 35.3%, validation cohort: 29.0%), intermediate (4-8 points: 59.7% and 61.7%), and high-risk (9-26 points: 82.8% vs. 77.3%) groups. The AUC was 0.718 (95% CI: 0.667-0.769) in the development cohort and 0.717 (95% CI:0.616-0.818) in the validation cohort. Table: 1884P

Treatment-related toxicity risk model (TR-TRM)

Category Variable Score
1 Treatment factor No chemotherapy/ monotherapy Doublet or more chemotherapies 0 3
2 Current no use of immune checkpoint inhibitor Current use of immune checkpoint inhibitor 0 2
3 No history of chemotherapy use Previous use of chemotherapy 0 1
4 Patient factor Self rated health status: Better or similar to same age Worse than same age 0 1
5 Geriatric variable Clinical frailty scale 1-5 6-9 0 3
6 Charles comorbidity index 0-7 8-10 ≥11 0 1 3
7 Laboratory result Hemoglobin (g/dl) ≥10.0

Conclusions

This study developed and validated a prediction tool for severe TRT in older cancer patients receiving systemic treatment. The tool incorporates patient and treatment characteristics, geriatric assessment variables, and laboratory results. It helps clinicians assess TRT risk and guide treatment decisions in this population.

Clinical trial identification

Editorial acknowledgement

Legal entity responsible for the study

The authors.

Funding

Madam Tsoi Foundation for Geriatric Oncology Research.

Disclosure

All authors have declared no conflicts of interest.

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