TY - JOUR
T1 - Interdisciplinary multimodality management of stage III nonsmall cell lung cancer
AU - Huber, Rudolf M.
AU - De Ruysscher, Dirk
AU - Hoffmann, Hans
AU - Reu, Simone
AU - Tufman, Amanda
N1 - Funding Information:
Conflict of interest: R.M. Huber reports personal fees from AstraZeneca (Germany), Boehringer Ingelheim (Germany), BMS (Germany), Lilly, Pfizer (Germany), Roche (Germany), Takeda and MSD (Germany), outside the submitted work. D. De Ruysscher reports grants and other funding from BMS and AstraZeneca, and other funding from Roche/ Genentech, Merck/Pfizer and Celgene, during the conduct of the study. H. Hoffmann has nothing to disclose. S. Reu has nothing to disclose. A. Tufman reports personal fees from Boehringer Ingelheim, Lilly, Roche and Chugai, outside the submitted work.
Publisher Copyright:
© ERS 2019.
PY - 2019/6/30
Y1 - 2019/6/30
N2 - Stage III nonsmall cell lung cancer (NSCLC) comprises about one-third of NSCLC patients and is very heterogeneous with varying and mostly poor prognosis. It is also called "locoregionally or locally advanced disease". Due to its heterogeneity a general schematic management approach is not appropriate. Usually a combination of local therapy (surgery or radiotherapy, depending on functional, technical and oncological operability) with systemic platinum-based doublet chemotherapy and, recently, followed by immune therapy is used. A more aggressive approach of triple agent chemotherapy or two local therapies (surgery and radiotherapy, except for specific indications) has no benefit for overall survival. Until now tumour stage and the general condition of the patient are the most relevant prognostic factors. Characterising the tumour molecularly and immunologically may lead to a more personalised and effective approach. At the moment, after an exact staging and functional evaluation, an interdisciplinary discussion amongst the tumour board is warranted and offers the best management strategy.
AB - Stage III nonsmall cell lung cancer (NSCLC) comprises about one-third of NSCLC patients and is very heterogeneous with varying and mostly poor prognosis. It is also called "locoregionally or locally advanced disease". Due to its heterogeneity a general schematic management approach is not appropriate. Usually a combination of local therapy (surgery or radiotherapy, depending on functional, technical and oncological operability) with systemic platinum-based doublet chemotherapy and, recently, followed by immune therapy is used. A more aggressive approach of triple agent chemotherapy or two local therapies (surgery and radiotherapy, except for specific indications) has no benefit for overall survival. Until now tumour stage and the general condition of the patient are the most relevant prognostic factors. Characterising the tumour molecularly and immunologically may lead to a more personalised and effective approach. At the moment, after an exact staging and functional evaluation, an interdisciplinary discussion amongst the tumour board is warranted and offers the best management strategy.
KW - GROWTH-FACTOR-RECEPTOR
KW - RANDOMIZED PHASE-III
KW - LEUKEMIA-GROUP-B
KW - HYPERFRACTIONATED RADIATION-THERAPY
KW - INDIVIDUAL PATIENT DATA
KW - INDUCTION CHEMOTHERAPY
KW - CONCURRENT CHEMORADIOTHERAPY
KW - PREOPERATIVE CHEMOTHERAPY
KW - ACCELERATED RADIOTHERAPY
KW - THORACIC RADIOTHERAPY
U2 - 10.1183/16000617.0024-2019
DO - 10.1183/16000617.0024-2019
M3 - (Systematic) Review article
C2 - 31285288
SN - 0905-9180
VL - 28
JO - European Respiratory Review
JF - European Respiratory Review
IS - 152
M1 - 190024
ER -