Metronomic oral vinorelbine in a real-world population of advanced non-small cell lung cancer patients

被引:4
作者
Estevinho, Fernanda [1 ,6 ]
Gomes, Rita [2 ,3 ]
Hasmucrai, Direndra [4 ]
Barata, Fernando [5 ]
机构
[1] Hosp Pedro Hispano, Unidade Local Saude Matosinhos, Matosinhos, Portugal
[2] Hosp Sousa Martins, Unidade Local Saude Guarda, Guarda, Portugal
[3] Univ Beira Interior, Fac Ciencias Saude, Covilha, Portugal
[4] Ctr Hosp Lisboa Norte, Hosp Pulido Valente, Lisbon, Portugal
[5] Ctr Hosp & Univ Coimbra, Coimbra, Portugal
[6] Hosp Pedro Hispano, Unidade Local Saude Matosinhos, Matosinhos Rua Dr Eduardo Torres, P-4464513 Senhora Da Hora, Portugal
来源
PULMONOLOGY | 2022年 / 28卷 / 05期
关键词
Non-small cell lung cancer; Metronomic oral vinorelbine; Unfit patients; Elderly; QUALITY-OF-LIFE; ELDERLY-PATIENTS; PHASE-II; CHEMOTHERAPY; MULTICENTER; NSCLC;
D O I
10.1016/j.pulmoe.2020.09.003
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
Introduction: An increasing body of evidence from clinical trials and real-world studies suggests that metronomic oral vinorelbine (VNR) is a promising treatment option for elderly and unfit advanced non-small cell lung cancer (NSCLC) patients. The aim of this multicenter study was to present real-world data about the experience in treatment of NSCLC with metronomic VNR in Portugal. Material and methods: Retrospective data from NSCLC patients not eligible for conventional chemotherapy or tyrosine kinase inhibitors who received oral metronomic VNR irrespective of treatment line and dose was retrieved from 19 Portuguese Oncology Centers between 2016 and 2018. Results: A total of 293 patients were included, with a median of 76 (39 - 94) years; 71% were & GE;70 years old. Patients had a median of 3 comorbidities and predominantly (61%) ECOG PS 2. Most (42%) received metronomic oral VNR as first-line treatment. Overall response rate was 18%, with 42 (18%) partial and no (0%) complete responses. A total of 54% of patients experienced stable disease and 28% of patients, disease progression. Disease control rate was 72%. Patients were a median of 4 (1 - 40) months on treatment. Treatment discontinuation was observed in 90%, mostly (67%) due to disease progression, followed by death (16%). Adverse events leading to treatment discontinuation were only reported in 5% of patients. Female gender (HR 0.601, 95% CI 0.434 - 0.832; p = 0.002) and ECOG PS 1 (HR 0.625, 95% CI [0.443 - 0.881]; p = 0.007) were significantly associated with a lower risk of metronomic oral VNR discontinuation. Overall, 21% of patients experienced G3/4 toxicity.
引用
收藏
页码:368 / 375
页数:8
相关论文
共 37 条
[1]   Metronomics: towards personalized chemotherapy? [J].
Andre, Nicolas ;
Carre, Manon ;
Pasquier, Eddy .
NATURE REVIEWS CLINICAL ONCOLOGY, 2014, 11 (07) :413-431
[2]  
[Anonymous], INT AG RES CANC GLOB
[3]  
[Anonymous], 2010, Common Terminology Criteria for Adverse Events (CTCAE) Version 4.03
[4]   Oral Metronomic Vinorelbine in Advanced Non-small Cell Lung Cancer Patients Unfit for Chemotherapy [J].
Banna, Giuseppe L. ;
Camerini, Andrea ;
Bronte, Giuseppe ;
Anile, Giuseppe ;
Addeo, Alfredo ;
Rundo, Francesco ;
Zanghi, Guido ;
Lal, Rohit ;
Libra, Massimo .
ANTICANCER RESEARCH, 2018, 38 (06) :3689-3697
[5]   Histology-based Combination Induction Chemotherapy for Elderly Patients with Clinical Stage III Non-small Cell Lung Cancer [J].
Banna, Giuseppe L. ;
Parra, Hector Jose Soto ;
Castaing, Marine ;
Dieci, Maria Vittoria ;
Anile, Giuseppe ;
Nicolosi, Maurizio ;
Strano, Salvatore ;
Marletta, Francesco ;
Guarneri, Valentina ;
Conte, Pierfranco ;
Lal, Rohit .
ANTICANCER RESEARCH, 2017, 37 (07) :3723-3728
[6]   A three-drug induction chemotherapy with gemcitabine, carboplatin, and paclitaxel for stage III non-small cell lung cancer [J].
Banna, Giuseppe Luigi ;
Lipari, Helga ;
Nicolosi, Maurizio ;
Basile, Antonio ;
Fraggetta, Filippo ;
Vaglica, Marina ;
Marletta, Francesco ;
Urso, Orazio Ezio ;
Ippolito, Massimo ;
Terminella, Alberto ;
Saita, Salvatore .
MEDICAL ONCOLOGY, 2013, 30 (02)
[7]   Oral vinorelbine in the treatment of non-small-cell lung cancer [J].
Barletta, Giulia ;
Genova, Carlo ;
Rijavec, Erika ;
Burrafato, Giovanni ;
Biello, Federica ;
Sini, Claudio ;
Dal Bello, Maria Giovanna ;
Coco, Simona ;
Truini, Anna ;
Vanni, Irene ;
Alama, Angela ;
Beltramini, Sabrina ;
Grassi, Maria Attilia ;
Boccardo, Francesco ;
Grossi, Francesco .
EXPERT OPINION ON PHARMACOTHERAPY, 2014, 15 (11) :1585-1599
[8]   Efficacy of metronomic vinorelbine in elderly patients with advanced non-small-cell lung cancer and poor performance status [J].
Bilir, C. ;
Durak, S. ;
Kizilkaya, B. ;
Hacibekiroglu, I. ;
Nayir, E. ;
Engin, H. .
CURRENT ONCOLOGY, 2017, 24 (03) :E199-E204
[9]   Dose selection trial of metronomic oral vinorelbine monotherapy in patients with metastatic cancer: a hellenic cooperative oncology group clinical translational study [J].
Briasoulis, Evangelos ;
Aravantinos, Gerasimos ;
Kouvatseas, George ;
Pappas, Periklis ;
Biziota, Eirini ;
Sainis, Ioannis ;
Makatsoris, Thomas ;
Varthalitis, Ioannis ;
Xanthakis, Ioannis ;
Vassias, Antonios ;
Klouvas, George ;
Boukovinas, Ioannis ;
Fountzilas, George ;
Syrigos, Kostantinos N. ;
Kalofonos, Haralambos ;
Samantas, Epaminontas .
BMC CANCER, 2013, 13
[10]   Metronomic oral vinorelbine for the treatment of advanced non-small cell lung cancer: a multicenter international retrospective analysis [J].
Camerini, A. ;
Banna, G. L. ;
Cinieri, S. ;
Pezzuto, A. ;
Mencoboni, M. ;
Rosetti, F. ;
Figueiredo, A. ;
Rizzo, P. ;
Ricci, A. ;
Langenhoven, L. ;
Santo, A. ;
Addeo, A. ;
Amoroso, D. ;
Barata, F. .
CLINICAL & TRANSLATIONAL ONCOLOGY, 2019, 21 (06) :790-795