Blood-Based Biomarker Analysis for Predicting Efficacy of Chemoradiotherapy and Durvalumab in Patients with Unresectable Stage III Non-Small Cell Lung Cancer
We recruited 50 patients with unresectable stage III NSCLC who received CCRT between March 2020 and March 2021. Durvalumab consolidation (DC) was administered to patients ( = 23) without progression after CCRT and programmed death-ligand 1 (PD-L1) ≥ 1%. Blood samples were collected before (C0) and a...
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Published in | Cancers Vol. 15; no. 4; p. 1151 |
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Main Authors | , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Switzerland
MDPI AG
10.02.2023
MDPI |
Subjects | |
Online Access | Get full text |
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Summary: | We recruited 50 patients with unresectable stage III NSCLC who received CCRT between March 2020 and March 2021. Durvalumab consolidation (DC) was administered to patients (
= 23) without progression after CCRT and programmed death-ligand 1 (PD-L1) ≥ 1%. Blood samples were collected before (C0) and after CCRT (C1) to calculate PBC counts and analyze CTCs. CTCs, isolated by the CD-PRIME
system, exhibited EpCAM/CK+/CD45- phenotype in BioViewCCBS
. At median follow-up of 27.4 months, patients with residual CTC clusters at C1 had worse median PFS than those without a detectable CTC cluster (11.0 vs. 27.8 months,
= 0.032), and this trend was noted only in the DC group (
= 0.034). Patients with high platelets at C1 (PLT
, >252 × 10
/µL) had worse median PFS than those with low platelets (PLT
) (5.9 vs. 17.1 months,
< 0.001). In multivariable analysis, PLT
and residual CTC clusters at C1 were independent risk factors for PFS, and DC group with PLT
and residual CTC clusters at C1 showed the worst median PFS (2.6 months, HR 45.16,
= 0.001), even worse than that of the CCRT alone group with PLT
(5.9 months, HR 15.39,
= 0.001). The comprehensive analysis of CTCs and PBCs before and after CCRT revealed that the clearance of CTC clusters and platelet counts at C1 might be potential biomarkers for predicting survival. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 2072-6694 2072-6694 |
DOI: | 10.3390/cancers15041151 |