Immune Checkpoint Inhibitors in Small Cell Lung Cancer: A Partially Realized Potential

被引:0
作者
Samantha A. Armstrong
Stephen V. Liu
机构
[1] Georgetown University,Department of Medicine
来源
Advances in Therapy | 2019年 / 36卷
关键词
Atezolizumab; Checkpoint inhibitors; Immunotherapy; Nivolumab; SCLC;
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学科分类号
摘要
Small cell lung cancer (SCLC) is a highly lethal subtype of lung cancer that has seen few therapeutic advances, despite ongoing concerted efforts. Immunotherapy has been an effective option in other carcinogen-related cancers and has shown modest activity in SCLC. Monotherapy with the anti-PD-1 antibody nivolumab in patients with at least two prior lines of therapy was associated with a response rate of 11.9% and a median duration of response of 17.9 months, leading to accelerated approval by the Food and Drug Administration (FDA) as third-line therapy for SCLC. Second-line checkpoint inhibitors have not performed well enough to change the standard of care, and maintenance immunotherapy has not shown significant benefit. However, the incorporation of concurrent immunotherapy in the first-line treatment of SCLC has improved outcomes. The addition of the anti-PD-L1 antibody atezolizumab to standard carboplatin plus etoposide led to an improvement in progression free survival (PFS) and overall survival, the first such improvement in over 30 years leading to the approval of atezolizumab as part of first-line therapy for advanced SCLC. While these landmark approvals offer promising novel treatment options for this recalcitrant disease, more work is needed to optimize their delivery and to build upon these important advances.
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页码:1826 / 1832
页数:6
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[1]  
Shepherd FA(1997)The role of chemotherapy in the treatment of small cell lung cancer Chest Surg Clin N Am 7 113-133
[2]  
Rossi A(2012)Carboplatin- or cisplatin-based chemotherapy in first-line treatment of small-cell lung cancer: the COCIS meta-analysis of individual patient data J Clin Oncol 30 1692-1698
[3]  
Di Maio M(1992)Randomized study of cyclophosphamide, doxorubicin, and vincristine versus etoposide and cisplatin versus alternation of these two regimens in extensive small-cell lung cancer: a phase III trial of the Southeastern Cancer Study Group J Clin Oncol 10 282-291
[4]  
Chiodini P(2015)Cancer immunology. Mutational landscape determines sensitivity to PD-1 blockade in non-small cell lung cancer Science 348 124-128
[5]  
Roth BJ(2013)Signatures of mutational processes in human cancer Nature 500 415-421
[6]  
Johnson DH(2012)Integrative genome analyses identify key somatic driver mutations of small-cell lung cancer Nat Genet 44 1104-1110
[7]  
Einhorn LH(2014)Paraneoplastic syndromes associated with lung cancer World J Clin Oncol 5 197-223
[8]  
Rizvi NA(1999)Favourable prognosis in Lambert–Eaton myasthenic syndrome and small-cell lung carcinoma Lancet 353 117-118
[9]  
Hellmann MD(2000)Long-term clinical outcome of paraneoplastic cerebellar degeneration and anti-Yo antibodies Neurology 55 713-715
[10]  
Snyder A(1992)Anti-Hu-associated paraneoplastic encephalomyelitis/sensory neuronopathy. A clinical study of 71 patients Medicine (Baltimore) 71 59-72