Highlights
- •Platinum doublets and chemoimmunotherapy showed similar efficacy with ORR 20–25%.
- •TP53 mutations and brain metastases conferred shorter survival after platinum and TKI.
- •More tumour CD8+ and less Th1 cells were associated with longer overall survival.
- •No difference in outcome by exon20 insertion site or use of pemetrexed or bevacizumab.
- •Occasionally long responses under EGFR TKI for both ‘near-’ and ‘far-loop’ variants.
Abstract
Background
EGFR exon20 insertions (ex20ins) are targeted by novel compounds in non-small-cell lung
cancer (NSCLC). However, data about outcome under conventional therapies and the influence
of molecular features are scarce.
Patients and methods
We retrospectively analysed 118 patients with evaluation of radiologic response based
on RECIST v1.1. TP53 status was available for 88 cases.
Results
Platinum doublets and chemoimmunotherapy showed similar response rates (20–25%), disease
control rates (80%) and median progression-free survival (mPFS, ≈7 months), which
were longer compared to monochemotherapy (9%, 59%, 4.1 months), EGFR inhibitors (0%,
46%, 3.0) and PD-(L)1 inhibitors (0%, 30%, 2.1; p < 0.05). Overall survival (OS) was
not dependent on the choice of first-line treatment, but related to more lines of
systemic therapy (p < 0.05). TP53 mutations and brain metastases were associated with shorter PFS under platinum doublets
and EGFR inhibitors (HR 3.3–6.1, p < 0.01), and shorter OS for patients receiving
both treatments (p < 0.05). More tumour CD8+ and less Th1 cells were associated with longer OS independent of brain and TP53 status (p < 0.01). No difference in outcome was noted according to the ex20ins site
and use of pemetrexed (vs. other cytotoxics) or bevacizumab. Long-lasting responses (>1 year) occasionally occurred
under EGFR inhibitors for both ‘near-’ and ‘far-loop’ variants.
Conclusions
Platinum doublets and chemoimmunotherapy have the highest activity with ORR of 20–25%
and mPFS of approximately 7 months, regardless of the cytotoxic partner, while PD-(L)1
inhibitors show limited efficacy. TP53 mutations, brain metastases and a lower tumour CD8/Th1-cell ratio are independently
associated with shorter survival.
Keywords
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Article info
Publication history
Published online: May 20, 2022
Accepted:
April 13,
2022
Received in revised form:
March 22,
2022
Received:
January 19,
2022
Identification
Copyright
© 2022 Elsevier Ltd. All rights reserved.