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ePoster Display

1463P - Improvement of the Barretos Prognostic Nomogram (BPN): New prognostic models for advanced cancer outpatients

Date

16 Sep 2021

Session

ePoster Display

Topics

Supportive Care and Symptom Management;  End-of-Life Care

Tumour Site

Presenters

Daniel Preto

Citation

Annals of Oncology (2021) 32 (suppl_5): S1076-S1083. 10.1016/annonc/annonc679

Authors

D.D. Preto1, B.S.R. Paiva2, D. Hui3, E. Bruera3, C.E. Paiva1

Author affiliations

  • 1 Clinical Oncology Department / Palliative Care And Quality Of Life Research Group (gpqual), Barretos Cancer Hospital, 14784-400 - Barretos/BR
  • 2 Palliative Care And Quality Of Life Research Group (gpqual), Barretos Cancer Hospital, 14784-400 - Barretos/BR
  • 3 Department Of Palliative Care And Rehabilitation Medicine, Division Of Cancer Medicine, The University of Texas MD Anderson Cancer Center, Houston/US

Resources

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Abstract 1463P

Background

Prognostic tools have been used in clinical practice helping to estimate survival in advanced cancer patients. The Barretos Prognostic Nomogram (BPN) is an instrument composed of 5 variables: sex, metastasis, leukocytes, KPS and albumin. Although accurate, it has some limitations such as the variable ‘metastasis’ as dichotomous and KPS as functionality evaluation, less used in the oncologist's clinical routine. We aimed at improving the BPN by reclassifying the variable ‘metastasis’ and assessing functional performance by ECOG-PS (BPN v2.0 model) and developing an alternative version without laboratorial varibles (BPN vClin model).

Methods

This was a reanalysis of the data from the BPN's 497 advanced cancer patients when referred to Palliative Care (development sample n=221; validation sample n=276). Site-volume combinations were tested for the ‘metastasis’ variable and KPS was replaced by ECOG-PS to assess functional performance. Prognostic variables were selected for multivariable Cox regression analyses; the most accurate final models were identified by backward variable elimination. Calibration and discrimination properties of the new models for BPN were evaluated in the validation sample.

Results

BPN v2.0 model was composed of 6 parameters: sex, locoregional disease present, metastasis sites (liver; bone; CNS; peritoneum; adrenal and/or spleen and/or kidney; muscle and/or subcutaneous), ECOG-PS, white blood cell (WBC), and albumin. The C-index was 0.78. The values of the area under the curve (AUC) of the receiver operating characteristic (ROC) curve were 0.79, 0.74, and 0.73 at 30, 90, and 180 days, respectively. The BPN vClin model was composed of 5 parameters: as compared with the v2.0 model there was the inclusion of ‘antineoplastic treatment’ and exclusion of laboratorial variables. The C-index was 0.74. The values of the AUC of the ROC curve were 0.77, 0.74, and 0.71 at 30, 90, and 180 days, respectively. Both versions presented good calibration results according to the Hosmer-Lemeshow test.

Conclusions

The new models are refined prognostic tools with adequate calibration and discrimination properties. It could be used to assist health professionals in estimating the survival of advanced cancer outpatients.

Clinical trial identification

Editorial acknowledgement

Legal entity responsible for the study

Barretos Cancer Hospital.

Funding

Has not received any funding.

Disclosure

All authors have declared no conflicts of interest.

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