TY - JOUR
T1 - The Impact of the Availability of Immunotherapy on Patterns of Care in Stage III NSCLC
T2 - A Dutch Multicenter Analysis
AU - Ronden, Merle I.
AU - Bahce, Idris
AU - Claessens, Niels J. M.
AU - Barlo, Nicole
AU - Dahele, Max R.
AU - Daniels, Johannes M. A.
AU - Tissing-Tan, Caroline
AU - Hekma, Edo
AU - Hashemi, Sayed M. S.
AU - van der Wel, Antoinet
AU - Spoelstra, Femke O. B.
AU - Verbakel, Wilko F. A. R.
AU - Tiemessen, Marian A.
AU - van Laren, Marjolein
AU - Becker, Annemarie
AU - Tarasevych, Svitlana
AU - Haasbeek, Cornelis J. A.
AU - Maassen van den Brink, Karen
AU - Dickhoff, Chris
AU - Senan, Suresh
N1 - Funding Information: Disclosure: Dr. Bahce reports receiving grants from AstraZeneca during the conduct of the study and grants from AstraZeneca outside of the submitted work. Dr. Dahele reports receiving grants from Varian Medical Systems outside of the submitted work. Mr. Verbakel reports receiving grants from Varian Medical Systems and personal fees and nonfinancial support from Varian Medical Systems outside of the submitted work. Dr. Senan reports receiving research grants and personal fees (advisory boards and speaker fees) from AstraZeneca and personal fees (advisory boards) from Merck, Merck Sharp & Dohme, and Celgene outside of the submitted work. The remaining authors declare no conflict of interest. Funding Information: Disclosure: Dr. Bahce reports receiving grants from AstraZeneca during the conduct of the study and grants from AstraZeneca outside of the submitted work. Dr. Dahele reports receiving grants from Varian Medical Systems outside of the submitted work. Mr. Verbakel reports receiving grants from Varian Medical Systems and personal fees and nonfinancial support from Varian Medical Systems outside of the submitted work. Dr. Senan reports receiving research grants and personal fees (advisory boards and speaker fees) from AstraZeneca and personal fees (advisory boards) from Merck , Merck Sharp & Dohme , and Celgene outside of the submitted work. The remaining authors declare no conflict of interest. Publisher Copyright: © 2021 The Authors
PY - 2021/7/1
Y1 - 2021/7/1
N2 - Introduction: Treatment patterns in stage III NSCLC can vary considerably between countries. The PACIFIC trial reported improvements in progression-free and overall survival with adjuvant durvalumab after concurrent chemoradiotherapy (CCRT). We studied treatment decision-making by three Dutch regional thoracic multidisciplinary tumor boards between 2015 and 2019, to identify changes in practice when adjuvant durvalumab became available. Methods: Details of patients presenting with stage III NSCLC were retrospectively collected. Both CCRT and multimodality schemes incorporating planned surgery were defined as being radical-intent treatment (RIT). Results: Of 855 eligible patients, most (95%) were discussed at a thoracic multidisciplinary tumor board, which recommended a RIT in 63% (n = 510). Only 52% (n = 424) of the patients finally received a RIT. Predictors for not recommending RIT were age greater than or equal to 70 years, WHO performance score greater than or equal to 2, Charlson comorbidity index greater than or equal to 2 (excluding age), forced expiratory volume in 1 second less than 80% of predicted value, N3 disease, and period of diagnosis. Between 2015 to 2017 and 2018 to 2019, the proportion of patients undergoing CCRT increased from 34% to 42% (p = 0.02) and use of sequential chemoradiotherapy declined (21%–16%, p = 0.05). Rates of early toxicity and 1-year mortality were comparable for both periods. After 2018, 57% of the patients who underwent CCRT (90 of 159) received adjuvant durvalumab. Conclusions: After publication of the PACIFIC trial, a significant increase was observed in the use of CCRT for patients with stage III NSCLC with rates of early toxicity and mortality being unchanged. Since 2018, 57% of the patients undergoing CCRT went on to receive adjuvant durvalumab. Nevertheless, approximately half of the patients were still considered unfit for a RIT.
AB - Introduction: Treatment patterns in stage III NSCLC can vary considerably between countries. The PACIFIC trial reported improvements in progression-free and overall survival with adjuvant durvalumab after concurrent chemoradiotherapy (CCRT). We studied treatment decision-making by three Dutch regional thoracic multidisciplinary tumor boards between 2015 and 2019, to identify changes in practice when adjuvant durvalumab became available. Methods: Details of patients presenting with stage III NSCLC were retrospectively collected. Both CCRT and multimodality schemes incorporating planned surgery were defined as being radical-intent treatment (RIT). Results: Of 855 eligible patients, most (95%) were discussed at a thoracic multidisciplinary tumor board, which recommended a RIT in 63% (n = 510). Only 52% (n = 424) of the patients finally received a RIT. Predictors for not recommending RIT were age greater than or equal to 70 years, WHO performance score greater than or equal to 2, Charlson comorbidity index greater than or equal to 2 (excluding age), forced expiratory volume in 1 second less than 80% of predicted value, N3 disease, and period of diagnosis. Between 2015 to 2017 and 2018 to 2019, the proportion of patients undergoing CCRT increased from 34% to 42% (p = 0.02) and use of sequential chemoradiotherapy declined (21%–16%, p = 0.05). Rates of early toxicity and 1-year mortality were comparable for both periods. After 2018, 57% of the patients who underwent CCRT (90 of 159) received adjuvant durvalumab. Conclusions: After publication of the PACIFIC trial, a significant increase was observed in the use of CCRT for patients with stage III NSCLC with rates of early toxicity and mortality being unchanged. Since 2018, 57% of the patients undergoing CCRT went on to receive adjuvant durvalumab. Nevertheless, approximately half of the patients were still considered unfit for a RIT.
KW - Immunotherapy
KW - Multidisciplinary tumor board (MDT)
KW - Non–small cell lung cancer (NSCLC)
KW - Patterns of care
KW - Stage III
UR - https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85122767428&origin=inward
UR - https://www.ncbi.nlm.nih.gov/pubmed/34590040
U2 - https://doi.org/10.1016/j.jtocrr.2021.100195
DO - https://doi.org/10.1016/j.jtocrr.2021.100195
M3 - Article
C2 - 34590040
SN - 2666-3643
VL - 2
JO - JTO Clinical and Research Reports
JF - JTO Clinical and Research Reports
IS - 7
M1 - 100195
ER -