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First-line pembrolizumab in advanced non-small cell lung cancer patients with poor performance status
被引:102
|作者:
Facchinetti, Francesco
[1
,2
]
Mazzaschi, Giulia
[1
]
Barbieri, Fausto
[3
]
Passiglia, Francesco
[4
]
Mazzoni, Francesca
[5
]
Berardi, Rossana
[6
]
Proto, Claudia
[7
]
Cecere, Fabiana Letizia
[8
]
Pilotto, Sara
[9
]
Scotti, Vieri
[10
]
Rossi, Sabrina
[11
]
Del Conte, Alessandro
[12
]
Vita, Emanuele
[13
]
Bennati, Chiara
[14
]
Ardizzoni, Andrea
[15
]
Cerea, Giulio
[16
]
Migliorino, Maria Rita
[17
]
Sala, Elisa
[18
]
Camerini, Andrea
[19
]
Bearz, Alessandra
[12
]
De Carlo, Elisa
[12
]
Zanelli, Francesca
[20
]
Guaitoli, Giorgia
[3
]
Garassino, Marina Chiara
[7
]
Ciccone, Lucia Pia
[10
]
Sartori, Giulia
[9
]
Toschi, Luca
[11
]
Dall'Olio, Filippo Gustavo
[15
]
Landi, Lorenza
[14
]
Pizzutilo, Elio Gregory
[16
,21
]
Bartoli, Gabriele
[17
]
Baldessari, Cinzia
[3
]
Novello, Silvia
[4
]
Bria, Emilio
[13
]
Cortinovis, Diego Luigi
[18
]
Rossi, Giulio
[22
]
Rossi, Antonio
[23
]
Banna, Giuseppe Luigi
[24
]
Camisa, Roberta
[17
]
Di Maio, Massimo
[25
]
Tiseo, Marcello
[1
,26
]
机构:
[1] Univ Hosp Parma, Med Oncol Unit, Parma, Italy
[2] Univ Paris Saclay, Inst Gustave Roussy, Biomarqueurs Predictifs & Nouvelles Strategies Th, INSERM, F-94800 Villejuif, France
[3] Azienda Osped Univ Policlin, Div Med Oncol, Modena, Italy
[4] Univ Turin, San Luigi Hosp, Dept Oncol, Orbassano, Italy
[5] Careggi Univ Hosp, Dept Oncol, Med Oncol Unit, Florence, Italy
[6] Univ Politecn Marche, Osped Riuniti Ancona, Oncol Clin, Ancona, Italy
[7] Fdn IRCCS Ist Nazl Tumori, Dept Med Oncol, Milan, Italy
[8] IRCCS Regina Elena Natl Canc Inst, Rome, Italy
[9] Univ Verona, Dept Med, Sect Med Oncol, Verona, Italy
[10] Careggi Univ Hosp, Dept Oncol, Radiat Therapy Unit, Florence, Italy
[11] Humanitas Clin & Res Ctr, Dept Oncol & Hematol, Milan, Italy
[12] Ctr Riferimento Oncol Aviano CRO IRCCS, Med Oncol & Immunorelated Tumors, Aviano, Italy
[13] Univ Cattolica Sacro Cuore, Fdn Policlin Univ Agostino Gemelli, Comprehens Canc Ctr, IRCCS, Rome, Italy
[14] S Maria Delle Croci Hosp Ravenna, Oncohematol Dept, Ravenna, Italy
[15] Univ Bologna, Dept Oncol, Policlin S Orsola Malpighi, Bologna, Italy
[16] Grande Osped Metropolitano Niguarda, Niguarda Canc Ctr, Milan, Italy
[17] Azienda Osped San Camillo Forlanini, Pneumol Oncol, Rome, Italy
[18] Osped San Gerardo, Oncol Unit, Monza, Italy
[19] Osped Versilia, Med Oncol, Azienda USL Toscana Nord Ovest, Toscana, Italy
[20] Azienda Unita Sanit Locale IRCCS Reggio Emilia, Oncol Unit, Reggio Emilia, Italy
[21] Univ Milan, Dept Oncol & Hematooncol, Milan, Italy
[22] S Maria Delle Croci Hosp, Pathol Unit, Ravenna, Italy
[23] Fdn IRCCS Casa Sollievo Sofferenza, Div Med Oncol, San Giovanni Rotondo, FG, Italy
[24] United Lincolnshire Hosp NHS Trust, Lincoln, England
[25] Univ Turin, Ordine Mauriziano Hosp, Dept Oncol, Turin, Italy
[26] Univ Parma, Dept Med & Surg, Parma, Italy
关键词:
NSCLC;
Immunotherapy;
Immune checkpoint inhibitors;
PD-1;
ECOG PS 2;
ELDERLY-PATIENTS;
NIVOLUMAB;
CHEMOTHERAPY;
RADIOTHERAPY;
ASSOCIATION;
PHASE-1;
D O I:
10.1016/j.ejca.2020.02.023
中图分类号:
R73 [肿瘤学];
学科分类号:
100214 ;
摘要:
Background: Pembrolizumab is the first-line standard of care for advanced non-small cell lung cancer (NSCLC) with a PD-L1 tumour proportion score (TPS) >= 50%. Eastern Cooperative Oncology Group performance status (PS) 2 patients may receive pembrolizumab, despite the absence of sustaining evidence. Patients and methods: GOIRC-2018-01 is a multicentre, retrospective, observational study. PS 2 NSCLC patients with a PD-L1 TPS >= 50% receiving first-line pembrolizumab from June 2017 to December 2018 at 21 Italian institutions were included. Clinical-pathological characteristics were correlated with disease response and survival outcomes; adverse events were recorded. The primary objective was 6-months progression-free rate (6-months PFR). Results: One hundred fifty-three patients (median age 70 years) were enrolled. At a median follow-up of 18.2 months, median progression-free survival (PFS) and overall survival (OS) were 2.4 (95% confidence interval, 95% CI, 1.6-2.5) and 3.0 months (95% CI 2.4-3.5), respectively. 6-months PFR was 27% (95% CI 21-35%). Patients with a PS 2 determined by comorbidities (n = 41) had significantly better outcomes compared with disease burden-induced PS 2 (n = 112). Indeed, 6-months PFR was 49% versus 19%, median PFS 5.6 versus 1.8 months and OS 11.8 versus 2.8 months, respectively. Additional potential prognostic factors (radiotherapy, antibiotics, steroids received before pembrolizumab) correlated with clinical outcomes. The determinant of PS 2 resulted the only factor independently impacting on both PFS and OS. No toxicity issues emerged. Conclusions: Outcomes of PS 2 NSCLC patients with PD-L1 TPS >= 50% receiving first-line pembrolizumab were globally dismal but strongly dependent on the reason conditioning the poor PS itself. (C) 2020 Elsevier Ltd. All rights reserved.
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页码:155 / 167
页数:13
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