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Clinical outcomes in stage III non-small cell lung cancer patients treated with durvalumab after sequential or concurrent platinum-based chemoradiotherapy – single institute experience Cover

Clinical outcomes in stage III non-small cell lung cancer patients treated with durvalumab after sequential or concurrent platinum-based chemoradiotherapy – single institute experience

Open Access
|Nov 2021

Figures & Tables

Figure 1

Progression free survival of patients treated with durvalumab after sequential or concurrent platinum-based chemoradiotherapy.

Figure 2

Progression free survival regarding response after durvalumab completion.

Figure 3

Overall survival of patients treated with durvalumab after sequential or concurrent platinum-based chemoradiotherapy.

Univariate and multivariate analysis of predictors for progression free survival

VariableUnivariate analysisMultivariate analysis

HR (95% CI)pHR (95 % CI)p
Age< 63 years0.67 (0.35–1.29)0.231
≥ 63 years
GenderMale0.62 (0.32–1.20)0.156
Female
ECOG PS00.66 (0.34–1.28)0.226
1–2
StageIIIA0.89 (0.54–1.48)0.663
IIIB
IIIC
HistologyAdenocarcinoma0.84 (0.41–1.70)0.635
Squamous Cell
Smoking statusNever0.59 (0.33–1.07)0.0841.72 (0.26–11.00)0.567
Ex-smokers
Smoking at diagnosis
Mutational statusNo0.99 (0.87–1.12)0.881
KRAS
PD-L1< 1%1.03 (0.67–1.59)0.882
1%–49%
> 50%
Time to durvalumab< 57 days0.63 (0.32–1.24)0.186
≥ 57 days
RT dose< 60 Gy1.10 (0.43–2.84)0.838
≥ 60 Gy
No of ChTUp to 32.06 (0.94–4.51)0.0690.83 (0.23–2.99)0.783
4–5
ChTSequential1.51 (0.79–2.85)0.209
Concurrent
Response after ITCR0.066 (0.008–0.518)0.0100.067 (0.008–0.535)0.011
PR/SD
Durvalumab treatment time< 10.8 months3.16 (1.62–6.17)0.0011.18 (0.227–6.170.841
≥ 10.8 months

Chemoradiotherapy treatment characteristics

N = 85 (%)
N of ChT13 (3.5%)
213 (15.3%)
341 (48.2%)
427 (31.8%)
51 (1.2%)
ChTGem/cis79 (92.9%)
Etop/cis52 (61.2%)
Pem/cis3 (3.5%)
ChTInduction82 (96.5%)
Sequential only31 (36.5%)
Concurrent54 (63.5%)
Concurrent only3 (3.5%)
RT dose (Gy)Median (range)60 (5 –66)
V20 (Gy)Median (range)27.2 (7.0–35.6)
MLD (Gy)Median (range)15.7 (4.0–20.2)
PTV (cm3)Median (range)416.6 (172.3–1282.6)
Evaluation after ChT-RTCR10 (11.8%)
PR70 (82.3%)
SD5 (5.9 %)
Time between RT-IT (days)Median (range)57 (12–99)

Durvalumab treatment characteristics and influence on overall survival

Treatment characteristicsN (%)P
Time between RT-ITMedian (days)57 (12–99)0.689
< 57
≥ 57
Treatment time of IT*Median (months)10.8 (0.5–12.0)< 0.001
< 10.8
≥ 10.8
Treatment with ITCompleted41 (48.2%)0.095
Early stopped due to AE25 (29.4%)
Progression16 (18.8%)
Other3 (3.6%)
Response after IT**CR29 (34.1%)0.213
PR11 (12.9%)
SD15 (17.6%)
PD10 (11.8%)
Progression***Loco-regional21 (24.7%)0.217
Metastatic10 (11.7%)
Metastatic and local5 (5.9%)
Metastatic spreadCNS5 (5.9%)0.101
Other10 (11.7 %)

Pattern of progression

Progression (N of patients)Loco-regional onlyMetastaticp
GenderMale12100.563
Female95
StageIIIA730.663
IIIB119
IIIC33
HistologyAdenocarcinoma290.002
Squamous cell195
Other01
MutationKRAS07< 0.001
No mutation218
PD-L1< 1%34
1%–49 %860.435
50 %104

Baseline characteristics of patients treated with durvalumab

N = 85
GenderFemale25 (29.4 %)
Male60 (70.6 %)
AgeMedian (range)
< 6363 (36 – 73)
≥ 63
ECOG PS037 (43.5 %)
146 (54.1 %)
22 (2.4 %)
Smoking historyNever2 (2.4 %)
Ex-smokers35 (41.6 %)
Smoking at diagnosis47 (56.0 %)
HistologyAdenocarcinoma31 (36.5 %)
Squamous Cell50 (58.8 %)
Other4 (4.7 %)
AJCC 8th Edition StageIIIA26 (30.6%)
IIIB48 (56.5 %)
IIIC11 (12.9 %)
PD-L1 Expression< 1%13 (15.3 %)
1%-49%33 (38.8 %)
> 50%32 (37.7 %)
Unavailable7 (8.2 %)
Mutational statusNo mutations65 (76.5 %)
KRAS16 (18.8 %)
Unavailable4 (4.7 %)
DOI: https://doi.org/10.2478/raon-2021-0044 | Journal eISSN: 1581-3207 | Journal ISSN: 1318-2099
Language: English
Page range: 482 - 490
Submitted on: Aug 19, 2021
|
Accepted on: Oct 7, 2021
|
Published on: Nov 19, 2021
In partnership with: Paradigm Publishing Services
Publication frequency: 4 issues per year

© 2021 Martina Vrankar, Karmen Stanic, Stasa Jelercic, Eva Ciric, Ana Lina Vodusek, Jasna But-Hadzic, published by Association of Radiology and Oncology
This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 License.