Efficacy of second-line chemotherapy or immune checkpoint inhibitors for patients with a prolonged objective response (≥ 6 months) after first-line therapy for recurrent or metastatic head and neck squamous cell carcinoma: a retrospective study

被引:2
作者
Vienne, Agathe [1 ]
Collet, Laetitia [2 ,3 ]
Chevalier, Thomas [4 ]
Borel, Christian [5 ]
Tardy, Magalie [6 ]
Huguet, Florence [7 ]
Richard, Sandrine [8 ]
Salas, Sebastien [4 ]
Saada-Bouzid, Esma [6 ]
Fayette, Jerome [2 ]
Daste, Amaury [1 ]
机构
[1] Univ Bordeaux, Hop St Andre, Dept Med Oncol, CHU Bordeaux, 1 Rue Jean Burguet, F-33000 Bordeaux, France
[2] Univ Lyon, Leon Berard Ctr, Dept Med Oncol, Lyon, France
[3] Inst Jules Bordet, Breast Canc Translat Res Lab, Brussels, Belgium
[4] CHU Timone, AP HM, Dept Med Oncol, Marseille, France
[5] Inst Cancerol Strasbourg Europe, Dept Med Oncol, Strasbourg, France
[6] Univ Cote dAzur, Ctr Antoine Lacassagne, Dept Med Oncol, Nice, France
[7] Sorbonne Univ, Tenon Hosp, AP HP, Dept Radiat Oncol, Paris, France
[8] Sorbonne Univ, Tenon Hosp, AP HP, Dept Med Oncol, Paris, France
关键词
Platinum chemotherapy; Head and neck; Immune checkpoint inhibitors; Diseases free interval; OPEN-LABEL; CETUXIMAB; PLATINUM; PROGRESSION;
D O I
10.1186/s12885-023-11133-5
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BackgroundPatients with recurrent or metastatic head and neck squamous cell carcinoma (R/M-HNSCC) have a poor prognosis and limited therapeutic options. Immune checkpoint inhibitors (ICIs) are effective in patients with tumor progression < 6 months following first-line, platinum-based chemotherapy (PBC), but data are missing for patients with progression & GE; 6 months after the last platinum dose.MethodsRetrospective analysis (six French centers, 2008-2019) of all consecutive R/M-HNSCC patients. treated first-line with PBC and tumor progression & GE; 6 months after the last platinum dose. Primary endpoint: progression-free survival after second-line therapy (PFS2). Additional endpoints: overall survival from Day 1 of first-line (OS1) and second-line (OS2) therapy.ResultsR/M-HNSCC patients (n = 144) received cisplatinum (n = 67, 47%) or carboplatinum (n = 77, 53%) first-line. Response after first-line: complete response (CR; n = 16, 11%); partial response (PR; n = 77, 53%); stable disease (n = 22, 15%). Second-line therapy: PBC (n = 95, 66%); platinum-free regimen (PFR) (n = 25, 17%); ICI (n = 24, 17%). Median [95% confidence interval] PFS (months): PBC 5.0 [3.8-6.2]; PFR 4.0 [1-7.0]; ICI 2.0 [0.4-3.6] (p = 0.16). For PBC, PFR, and ICI, respectively: OS1 30, 23, and 29 months (p = 1.02); OS2 14, 10, and 16 months (p = 0.25); PR, 26%, 16%, and 21% patients; CR, 0%, 8%, and 4% patients. For subsequent lines, ICIs were administered for PBC (n = 11, 12%) and PFR (n = 2, 8%). No predictive factor for efficacy (PFS, OS) was identified.ConclusionsOur retrospective study suggests similar efficacy regarding OS2 for second-line chemotherapy or ICI in R/M-HNSCC patients with progression & GE; 6 months after the last first-line platinum dose.
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