TY - JOUR
T1 - Small cell lung cancer
T2 - Novel treatments beyond immunotherapy
AU - Meijer, Job-Joris
AU - Leonetti, Alessandro
AU - Airò, Giulia
AU - Tiseo, Marcello
AU - Rolfo, Christian
AU - Giovannetti, Elisa
AU - Vahabi, Mahrou
N1 - Funding Information:
This work was supported by the Cancer Center Amsterdam (grant 2018 ), KWF Dutch Cancer Society (KWF grant# 11957 ), and Associazione Italiana per la Ricerca sul Cancro (AIRC/IG-grant 24444 ).
Publisher Copyright:
© 2022 The Authors
PY - 2022/11
Y1 - 2022/11
N2 - Small cell lung cancer (SCLC) arises in peribronchial locations and infiltrates the bronchial submucosa, including about 15% of lung cancer cases. Despite decades of research, the prognosis for SCLC patients remains poor because this tumor is characterized by an exceptionally high proliferative rate, strong tendency for early widespread metastasis and acquired chemoresistance. Omics profiling revealed that SCLC harbor extensive chromosomal rearrangements and a very high mutation burden. This led to the development of immune-checkpoint inhibitors as single agents or in combination with chemotherapy, which however resulted in a prolonged benefit only for a small subset of patients. Thus, the present review discusses the rationale and limitations of immunotherapeutic approaches, presenting the current biological understanding of aberrant signaling pathways that might be exploited with new potential treatments. In particular, new agents targeting DNA damage repair, cell cycle checkpoint, and apoptosis pathways showed several promising results in different preclinical models. Epigenetic alterations, gene amplifications and mutations can act as biomarkers in this context. Future research and improved clinical outcome for SCLC patients will depend on the integration between these omics and pharmacological studies with clinical translational research, in order to identify specific predictive biomarkers that will be hopefully validated using clinical trials with biomarker-selected targeted treatments.
AB - Small cell lung cancer (SCLC) arises in peribronchial locations and infiltrates the bronchial submucosa, including about 15% of lung cancer cases. Despite decades of research, the prognosis for SCLC patients remains poor because this tumor is characterized by an exceptionally high proliferative rate, strong tendency for early widespread metastasis and acquired chemoresistance. Omics profiling revealed that SCLC harbor extensive chromosomal rearrangements and a very high mutation burden. This led to the development of immune-checkpoint inhibitors as single agents or in combination with chemotherapy, which however resulted in a prolonged benefit only for a small subset of patients. Thus, the present review discusses the rationale and limitations of immunotherapeutic approaches, presenting the current biological understanding of aberrant signaling pathways that might be exploited with new potential treatments. In particular, new agents targeting DNA damage repair, cell cycle checkpoint, and apoptosis pathways showed several promising results in different preclinical models. Epigenetic alterations, gene amplifications and mutations can act as biomarkers in this context. Future research and improved clinical outcome for SCLC patients will depend on the integration between these omics and pharmacological studies with clinical translational research, in order to identify specific predictive biomarkers that will be hopefully validated using clinical trials with biomarker-selected targeted treatments.
KW - Apoptosis
KW - Cell cycle checkpoints
KW - DNA damage repair
KW - Immunotherapy
KW - Small cell lung cancer (SCLC)
KW - Targeted therapy
UR - http://www.scopus.com/inward/record.url?scp=85130951386&partnerID=8YFLogxK
U2 - 10.1016/j.semcancer.2022.05.004
DO - 10.1016/j.semcancer.2022.05.004
M3 - Review article
C2 - 35568295
SN - 1044-579X
VL - 86
SP - 376
EP - 385
JO - Seminars in Cancer Biology
JF - Seminars in Cancer Biology
ER -