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Poster Display session

169P - THASSOS-INTL Türkiye subset: Unveiling treatment patterns and clinical outcomes in resectable early-stage NSCLC

Date

28 Mar 2025

Session

Poster Display session

Presenters

Ahmet Sezer

Citation

Journal of Thoracic Oncology (2025) 20 (3): S98-S120. 10.1016/S1556-0864(25)00632-X

Authors

A. Sezer1, A. Isikdogan2, S. Sezgin Goksu3, T. Goksel4, D. Erdem5, O. Yazici6, M. Kiyik7, Y. Kilic8

Author affiliations

  • 1 Baskent University, Adana/TR
  • 2 Dicle University Medical Faculty, 21280 - Diyarbakir/TR
  • 3 Akdeniz University Faculty of Medicine, Antalya/TR
  • 4 Ege University Faculty of Medicine, Izmir/TR
  • 5 Samsun Medical Park Hospital, Samsun/TR
  • 6 Gazi University Faculty of Medicine, 06560 - Ankara/TR
  • 7 Istanbul Provincial Directorate of Health, Yedikule Chest Diseases and Thoracic Surgery Training and Research Hospital, Istanbul/TR
  • 8 AstraZeneca, Istanbul/TR

Resources

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Abstract 169P

Background

Evolving treatment (Tx) options for early-stage NSCLC warrants understanding the real-world Tx patterns and associated survival outcomes to help refine current practice and inform future strategies.

Methods

The THASSOS-INTL (NCT04808050) Türkiye cohort, an observational, retrospective study, abstracted data of adult patients (pts) with clinical stage (CS) IA-IIIB resectable NSCLC (Jan 2013-Dec 2017) until their disease progression, death (last medical record) or Dec 2020. Primary objectives included Tx patterns and 3-year survival rates.

Results

Of 119 pts (median [range] age 60 [22–80] yrs; 77.3% [92/119] males; 83.2% [89/107] current/former smokers) enrolled, 25.2% had CS I, 37.0% CS II and 37.8% CS III. Most pts had adenocarcinoma (70.0%, 70/100) in right lung (68.9%, 82/119) with pN0 in 54.6% (65/119). Of 22 (18.5%) pts tested 1 had EGFR mutation; 3/5 pts had PD-L1 expression >1%. Overall, 71.4% (85/119) pts underwent curative surgery, majorly lobectomy (70.6%, 60/85) with R0 resection (81.2%, 69/85); 15.1% (18/119) pts underwent only surgery. Neo-adjuvant therapy (NT) was recorded in 10.1% (12/119) pts (systemic therapy [ST]: 75%, 09; ST + radiotherapy [RT]: 25%, 03). Adjuvant therapy (AT) was recorded in 77.3% (92/119) pts (ST: 73.9%, 68; RT: 2.2%, 02; ST + RT: 23.9%, 22). Both NT and AT were recorded in only 4 pts. At 3 years, 83.2% were alive with mOS of 8.7 yrs (95% CI: 8.0-NE). Disease progression was reported in 32.8% (39/119) pts ─ intra-thoracic and regional lymph node (51.3%), distant (41.0%), CNS (2.6%), unknown (5.1%). Post-progression, 66.7% (26/39) pts received ST and 46.2% (18/39) received RT.

Table 169P
Tx Patterns and Survival
Tx pattern, n (%)Overall N=119CS 1A (11, 9.2%)CS IB (19, 16.0%)CS IIA (30,25.2%)CS 11B (14,11.8%)CS 111A(30,25.2%)CS 111B (15, 12.6%)
Sx only18 (15.1)7 (63.6)7 (36.8)3 (10.0)001 (6.7)
NT + Sx12 (10.1)002 (6.7)2 (14.3)5 (16.7)3 (20.0)
Sx + AT92 (77.3)4 (36.4)12 (63.2)26 (86.7)13 (92.9)26 (86.7)11 (73.3)
NT + Sx + AT4 (3.4)001 (3.3)1 (7.1)2 (6.7)0
Survival (95% CI)
3-yr survival rate (%)83.2 (76.6–90.4)100 (100.0–100.0)88.5 (74.8–100.0)88.9 (77.8–100.0)85 7 (69 2–100 0)78.1 (64.0–95.3)60.0 (39.7–90.7)
mOS (yrs)8.7 (8.0-NE)NE8.0 (7.8-NE)NE8.7 (7.1-NE)9.0 (5.1-NE)NE

Conclusions

About 3/4th of pts receiving AT in the Türkiye cohort and a mOS of 8.7 yrs demonstrates adherence to the Tx recommendations. However, the 3-yr survival rates varied from 100% for CS IA to 60% for CS IIIB, emphasizing the need for optimized Tx sequencing and novel approaches. The poor biomarker testing rates underscore upfront testing at NSCLC diagnosis.

Clinical trial identification

NCT04808050.

Editorial acknowledgement

Medical writing support was provided by Dr. Purva Thatai and Prajakta Nachane of Fortrea Scientific Pvt Ltd.

Legal entity responsible for the study

AstraZeneca International.

Funding

AstraZeneca International.

Disclosure

S. Sezgin Goksu: Other, Institutional, Invited Speaker: Novartis, Pfizer, MSD, AstraZeneca; Other, Institutional, Advisory Role: Novartis, MSD. Y. Kilic: Financial Interests, Institutional, Full or part-time Employment: AstraZeneca. All other authors have declared no conflicts of interest.

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