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Poster session 01

125P - Assessing the accuracy of multiple prognostic scores for immune checkpoint inhibitors (ICI) in patients with advanced solid tumors

Date

10 Sep 2022

Session

Poster session 01

Topics

Clinical Research;  Translational Research;  Immunotherapy

Tumour Site

Presenters

Javier Garcia-Corbacho

Citation

Annals of Oncology (2022) 33 (suppl_7): S27-S54. 10.1016/annonc/annonc1037

Authors

J. Garcia-Corbacho1, A. Indacochea2, A. Gonzalez3, I. Victoria Ruiz4, D. Moreno Fernández4, D.S. Pesantez Coronel4, L. Angelats4, A. Modrego5, E. Sanfeliu Torres6, O. Castillo7, P. Blasco7, L. Mezquita4, N. Vinolas Segarra4, M. Nogue Aliguer8, B. Adamo4, N. Baste Rotllan4, T. Sauri Nadal4, M. Juan3, A. Prat7, F. Schettini7

Author affiliations

  • 1 Ugci - Medical Oncology Department, Hospitales Universitarios Virgen de la Victoria y Regional, 29010 - Málaga/ES
  • 2 Medical Oncology Department, Hospital Clinic y Provincial de Barcelona / H Granollers, 08036 - Barcelona/ES
  • 3 Immunology Department, Hospital Clinic y Provincial de Barcelona, 08036 - Barcelona/ES
  • 4 Medical Oncology Department, Hospital Clinic y Provincial de Barcelona, 08036 - Barcelona/ES
  • 5 Medical Oncology Department, Hospital Universitario 12 de Octubre, 28041 - Madrid/ES
  • 6 Diagnostic Biomedical Center, Hospital Clinic y Provincial de Barcelona, 08036 - Barcelona/ES
  • 7 Medical Oncology Department, Hospital Clinic y Provincial de Barcelona / IDIBAPS, 08036 - Barcelona/ES
  • 8 Medical Oncology Department, Hospital General de Granollers, 08402 - Granollers/ES

Resources

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Abstract 125P

Background

Many patients fail to achieve a clinical benefit from ICI. Several scores have been developed to improve ICI candidates selection but it is uncertain which one better predicts patients’ outcome. Here, we performed a direct comparison of the most successful scores.

Methods

This is a sub-analysis of the immunoblood prospective observational study that enrolled patients diagnosed with advanced solid tumors treated with ICI. Main clinicopathological data were retrieved from medical records and responses assessed according to RECIST 1.1 criteria. LIPI, RMH, PMH, dNLR, NLR, PIPO and GRIm scores were calculated. Receiving operator characteristics (ROC) curves and their area under curve (AUC) were used to predict PFS and durable clinical benefit (DCB; stable disease≥6 months or better). Associations with PFS, OS and DCB, where assessed with Cox and logistic regressions. Scores’ correlation was assessed with Spearman rho. Significance was set at p<0.05.

Results

We recruited 155 patients (65% male, mean age 63). NSCLC (28%), colorectal (20%) breast (9%) H&N (6%) cancer and melanoma (6%) were the most frequent tumor types. Frequency of the high risk/bad outcome group of each score were: LIPI 13%, RMH 36%, PMH 54%, GRIm 14%, PIPO 6%, NLR 32% and dNRL 27%. Fair accuracy in identifying patients at higher risk of progression or mild accuracy in predicting DCB were observed for the RMH (AUC PFS: 0.7, 95%CI: 0.6-0.8; AUC DCB: 0.6, 0.5-0.8) and LIPI (AUC PFS: 0.7, 95%CI: 0.6-0.8; AUC: 0.6, 0.5-0.7) scores. All other scores provided poor/no accuracy. No significant difference was observed between RMH and LIPI AUC for PFS and DCB (both p>0.05). Additionally, only LIPI and RMH were associated with PFS (p=0.001; p<0.001), OS (p<0.001; p=0.001) and DCB (p=0.034; p=0.010) at univariate analyses. At multivariate analyses RMH and LIPI remained significantly associated with PFS (p=0.030; p=0.021) and OS (p=0.012; p<0.001). A strong correlation between both scores (rho=0.72, p<0.001) was observed.

Conclusions

RMH and LIPI scores were sufficiently reliable in assessing the prognosis of patients with advanced solid tumors treated with ICI. They were superior to other analyzed scores in our population and highly correlated.

Clinical trial identification

Editorial acknowledgement

Legal entity responsible for the study

Hospital Clinic y Provincial de Barcelona, Medical Oncology Department.

Funding

Has not received any funding.

Disclosure

J. Garcia-Corbacho: Financial Interests, Personal, Advisory Board, FGFR inhibitors implementation in clinical practice: Johnson & Johnson Pharmaceutical; Financial Interests, Institutional, Invited Speaker, Participation in clinical trials of the company as PI: Johnson and Johnson Pharmaceutical, Boehringer Ingelheim, Astellas, Cytomx, Incyte, Lilly, Menarini, Merck, Bayer, AstraZeneca, Amgen, Daiichi Sankyo. L. Mezquita: Financial Interests, Personal, Advisory Board: Takeda, AstraZeneca, Roche; Financial Interests, Personal, Invited Speaker: Roche, BMS, AstraZeneca, Takeda; Financial Interests, Personal, Research Grant, SEOM Beca Retorno 2019: BI; Financial Interests, Personal, Research Grant, ESMO TR Research Fellowship 2019: BMS; Financial Interests, Institutional, Research Grant, COVID research Grant: Amgen; Financial Interests, Institutional, Invited Speaker: Inivata, Stilla. N. Baste Rotllan: Non-Financial Interests, Advisory Role: Eisai, MSD, Merck Serono, BioNTech, Roche, BMS, Exelixis. A. Prat: Financial Interests, Personal, Invited Speaker: Roche; Financial Interests, Personal, Invited Speaker, Lecture fees: Novartis, Daiichi Sankyo; Financial Interests, Personal, Advisory Board, Advisory role/consultancy: Novartis, Pfizer, BMS, Puma, Oncolytics Biotech, MSD, Guardant Health, Peptomyc; Financial Interests, Institutional, Invited Speaker, Clinical trials: Daiichi Sankyo; Financial Interests, Institutional, Other, Contracted research: Boehringer, Medica Scientia Inno. Research; Financial Interests, Personal, Advisory Board: AstraZeneca; Financial Interests, Personal, Invited Speaker, Leadership role: Reveal Genomics, SL.; Financial Interests, Personal, Stocks/Shares: Reveal Genomics, Oncolytics Biotech; Financial Interests, Personal, Royalties: Reveal Genomics; Financial Interests, Institutional, Invited Speaker: Roche, AstraZeneca, Novartis; Financial Interests, Personal and Institutional, Invited Speaker: Daiichi Sankyo; Non-Financial Interests, Institutional, Other, Leadership roles: Patronage committee: SOLTI Foundation, Actitud Frente al Cáncer Foundation. All other authors have declared no conflicts of interest.

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