Neutrophil-platelet score (NPS), a predictive systemic inflammation score for PD-1 immune checkpoint inhibitors (ICI) in pretreated advanced non-small cell lung cancer (NSCLC) patients

Xabier Mielgo-Rubio,M. Sereno Moyano, L.E. Chara,Rafael López-Castro, Jaime Rubio-Martínez, A. Velástegui, Clara Olier Gárate,Sandra Falagan, I. Gómez-Barreda,Alejandro Riquelme, J. Silva-Ruiz,Juan Moreno-Rubio,C. López,Coralia Bueno,Ana Cardeña, Elia Pérez‐Fernández, M.P. Martí-Castelló, M.J. Sotelo-Lezama

Annals of Oncology(2018)

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Abstract
Background: Systemic inflammation response can be characterized by changes of peripheral blood cell amounts. Several blood cell-based scores have been found to have prognostic value in some tumors treated with ICI. Neutrophil-platelet score (NPS) is a systemic inflammation-based score characterizing 3 prognostic groups: good (0), neutrophils < =7500 and platelets < =400000; intermediate (1), neutrophils >7500 or platelets >400000; poor (2), neutrophils >7500 and platelets >400000). It has never been evaluated as prognostic biomarker in NSCLC patients treated with ICI. Methods: This is a multicenter retrospective study with the aim to evaluate prognostic value of NPS in patients with pretreated advanced NSCLC treated with PD-1 ICI between March 2015 and April 2018. Clinical data were contributed by 7 medical centers in Spain. Primary endpoint was association of NPS with overall survival (OS). Results: 168 patients were included. Median age 65 years (39-85). 134(79,8%) were male and 121(72%) were PS > =1. Predominant histologies were adenocarcinoma (50%) and squamous-cell carcinoma (42,9%). 92,3% received nivolumab and 7,7% pembrolizumab. 2,3% had EGFR mutations, and 0,6% ALK rearrangement. PD-L1 IHC was available in 25% (<1%: 36,6%; 1-49%: 39%; > =50%: 24,4%). Median number of prior lines was 1 (1-5). Median number of cycles 11 (1-68). Median follow-up time 6,3m. Response rate (RR) was 30,4% and disease control rate (DCR) 52%. Median PFS and OS were 5,6 months (m) (3,9-7,3) and 11,4 m (9,4-13,5). According to NPS, median OS for good, intermediate, and poor prognostic groups was 11,9m (9,4-14,4), 6,8m (3,3-10,2), and 3m (1,4-4,6), respectively (p = 0,003). Higher NPS was associated with poor OS: NPS1 HR 1,73 (95%CI,1,13-2,65),p=0,01; NPS2 HR 2,89 (95%CI,1,31-6,39), p = 0,009). No significant association between NPS and PFS was found. NPS was associated with DCR, NPS2 had more patients with progression disease as best response to ICI than NPS1 and 0 (86 vs 57 vs 42%, p = 0,039). Conclusions: NPS predicted OS and DCR in pretreated advanced NSCLC patients who received treatment with PD-1 ICI nivolumab or pembrolizumab. These results need to be validated in prospective studies. Legal entity responsible for the study: Xabier Mielgo Rubio. Funding: Has not received any funding. Disclosure: All authors have declared no conflicts of interest.
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Key words
predictive systemic inflammation score,immune checkpoint inhibitors,lung cancer,neutrophil-platelet,non-small
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