J Garde-Noguera1, P Martin-Martorell2, M De Julián3, J Perez-Altozano4, C Salvador-Coloma5, J García-Sanchez6, A Insa-Molla2, M Martín7, X Mielgo-Rubio8, S Marin-Liebana9, A Blasco-Cordellat10, S Blasco-Molla11, R Gironés12, D Marquez-Medina13, F Aparisi14, M C Bas Cerda15, S Macia-Escalante16, A Sánchez3, O Juan-Vidal5. 1. Hospital Arnau de Vilanova, C/Sant Climent, 12, 46015, Valencia, Spain. javiergardenoguera1@gmail.com. 2. University Hospital Clínic de Valencia, Valencia, Spain. 3. Hospital Provincial de Castellón, Castellón, Spain. 4. Hospital General de Elche, Elche, Spain. 5. Hospital Universitari I Politècnic La Fe, Valencia, Spain. 6. Hospital Arnau de Vilanova, C/Sant Climent, 12, 46015, Valencia, Spain. 7. Hospital Dr Peset, Valencia, Spain. 8. Hospital Universitario Fundación Alcorcón, Alcorcón, Spain. 9. Hospital de Manises, Manises, Spain. 10. Hospital General Universitario de Valencia, Valencia, Spain. 11. Hospital de Sagunto, Sagunto, Spain. 12. Hospital Lluis Alcanyís, Xátiva, Spain. 13. Hospital Arnau de Vilanova, Lleida, Spain. 14. Hospital Virgen de los Lirios, Alcoy, Spain. 15. Universidad Politecnica de Valencia, Valencia, Spain. 16. Pivotal CRO, Madrid, Spain.
Abstract
BACKGROUND: Immunotherapy increases overall response rate (ORR) and overall survival (OS) in patients with non-small-cell lung cancer (NSCLC). Prognostic and predictive factors are a high need. PATIENTS AND METHODS: Retrospective review of NSCLC patients treated with nivolumab was performed. Analyzed variables included age, sex, stage, performance status (PS), location of metastases, presence of tumour-related symptoms and comorbidities, number of metastasis locations, previous chemotherapy, anti-angiogenic and radiotherapy treatments, and analytical data from the standard blood count and biochemistry. RESULTS: A total of 175 patients were included. Median age was 61.5 years, 73.1% were men, 77.7% were ECOG-PS 0-1, and 86.7% were included with stage IV disease. Histology was non-squamous in 77.1%. Sixty-five received nivolumab in second line (37.1%). Thirty-eight patients had brain metastasis (22%), and 39 (22.3%) liver metastasis and 126 (72%) had more than one metastatic location. The ORR was 15.7% with median Progression free survival (PFS) 2.8 months and median OS 5.81 months. Stage III vs IV and time since the beginning of the previous line of treatment ≥ 6 vs < 6 months were associated with better response. PS 2, time since the previous line of treatment < 6 vs ≥ 6 months, and more than one metastatic location were independently associated with shorter OS in multivariable analysis (7.8 vs 2.7 months, 11.2 vs 4.6 months, and 9.4 vs 5.1 month). Finally, time since the previous treatment < 6 vs ≥ 6 months and more than one metastatic location were independently associated with shorter PFS in multivariable analysis (4.3 vs 2.3 months and 4.7 vs 2.3 months). CONCLUSION: Poor PS, short period of time since the previous treatment, and more than one metastatic location were associated with poorer prognostic.
BACKGROUND: Immunotherapy increases overall response rate (ORR) and overall survival (OS) in patients with non-small-cell lung cancer (NSCLC). Prognostic and predictive factors are a high need. PATIENTS AND METHODS: Retrospective review of NSCLCpatients treated with nivolumab was performed. Analyzed variables included age, sex, stage, performance status (PS), location of metastases, presence of tumour-related symptoms and comorbidities, number of metastasis locations, previous chemotherapy, anti-angiogenic and radiotherapy treatments, and analytical data from the standard blood count and biochemistry. RESULTS: A total of 175 patients were included. Median age was 61.5 years, 73.1% were men, 77.7% were ECOG-PS 0-1, and 86.7% were included with stage IV disease. Histology was non-squamous in 77.1%. Sixty-five received nivolumab in second line (37.1%). Thirty-eight patients had brain metastasis (22%), and 39 (22.3%) liver metastasis and 126 (72%) had more than one metastatic location. The ORR was 15.7% with median Progression free survival (PFS) 2.8 months and median OS 5.81 months. Stage III vs IV and time since the beginning of the previous line of treatment ≥ 6 vs < 6 months were associated with better response. PS 2, time since the previous line of treatment < 6 vs ≥ 6 months, and more than one metastatic location were independently associated with shorter OS in multivariable analysis (7.8 vs 2.7 months, 11.2 vs 4.6 months, and 9.4 vs 5.1 month). Finally, time since the previous treatment < 6 vs ≥ 6 months and more than one metastatic location were independently associated with shorter PFS in multivariable analysis (4.3 vs 2.3 months and 4.7 vs 2.3 months). CONCLUSION: Poor PS, short period of time since the previous treatment, and more than one metastatic location were associated with poorer prognostic.
Entities:
Keywords:
GIDO; Immunotherapy; Nivolumab; Non-small-cell lung cancer
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