TY - JOUR
T1 - Immune checkpoint inhibitors for advanced non-small cell lung cancer
T2 - emerging sequencing for new treatment targets
AU - Aguiar, Pedro Nazareth
AU - De Mello, Ramon Andrade
AU - Barreto, Carmelia Maria Noia
AU - Perry, Luke Alastair
AU - Penny-Dimri, Jahan
AU - Tadokoro, Hakaru
AU - De Lima Lopes, Gilberto
PY - 2017/1/1
Y1 - 2017/1/1
N2 - Lung cancer is the leading cause of cancer-related deaths in the world. Immune checkpoint inhibitors (ICI) stimulate cytotoxic lymphocyte activity against tumour cells. These agents are available for the treatment of non-small cell lung cancer (NSCLC) after failure of platinum-based therapy. One recent study has demonstrated that ICI monotherapy was superior to platinum-based chemotherapy for first-line treatment. Nevertheless, this benefit was only for a minority of the population (30%) whose tumour programmed death receptor ligand-1 (PD-L1) expression was above 50%. Therefore, several strategies are under investigation. One option for patients with PD-L1 expression lower than 50% may be the combination of ICI with platinum-based chemotherapy or with ICIs against different targets. However, all of these combinations are at an early stage of investigation and may be very expensive or toxic, producing several harmful adverse events.
AB - Lung cancer is the leading cause of cancer-related deaths in the world. Immune checkpoint inhibitors (ICI) stimulate cytotoxic lymphocyte activity against tumour cells. These agents are available for the treatment of non-small cell lung cancer (NSCLC) after failure of platinum-based therapy. One recent study has demonstrated that ICI monotherapy was superior to platinum-based chemotherapy for first-line treatment. Nevertheless, this benefit was only for a minority of the population (30%) whose tumour programmed death receptor ligand-1 (PD-L1) expression was above 50%. Therefore, several strategies are under investigation. One option for patients with PD-L1 expression lower than 50% may be the combination of ICI with platinum-based chemotherapy or with ICIs against different targets. However, all of these combinations are at an early stage of investigation and may be very expensive or toxic, producing several harmful adverse events.
KW - atezolizumab
KW - immunotherapy
KW - nivolumab
KW - non-small cell lung cancer
KW - pembrolizumab
UR - http://www.scopus.com/inward/record.url?scp=85048045353&partnerID=8YFLogxK
U2 - 10.1136/esmoopen-2017-000200
DO - 10.1136/esmoopen-2017-000200
M3 - Review Article
C2 - 29209522
AN - SCOPUS:85048045353
SN - 2059-7029
VL - 2
JO - ESMO Open
JF - ESMO Open
IS - 3
M1 - e000200
ER -