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Poster Display

80P - Efficacy and Safety of Tislelizumab Combined with Anlotinib and 2-cycles Chemotherapy as First-line Treatment for Advanced NSCLC(TISAL-FE-01)

Date

07 Dec 2023

Session

Poster Display

Presenters

jun Tang

Citation

Annals of Oncology (2023) 20 (suppl_1): 100535-100535. 10.1016/iotech/iotech100535

Authors

J.W. Tang1, X. Qian2, J. Luo2, S. Lin2, J. Xu2, Y. Zhou2, Z. Li2, Y. Zeng2, B. Li2, H. Lin2

Author affiliations

  • 1 The Second Affiliated Hospital of Hainan Medical College, Haikou City/CN
  • 2 The Second Affiliated Hospital of Hainan Medical University, Haikou/CN

Resources

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Abstract 80P

Background

Although IMpower150 demonstrated atezolizumab combined with bevacizumab plus chemotherapy was a standard of care for advanced NSCLC, the efficacy and safety remained to be improved. This study was aimed to evaluate the efficacy and safety of tislelizumab (tis)plus anlotinib (anlo) combined with 2-cycles chemotherapy as first-line treatment for advanced NSCLC.

Methods

This study was a single-arm, one set and phase II study. Eligible patients were histologically confirmed locally advanced or metastatic (Stage IIIB-IV) NSCLC and untreated, excluding driver mutations. Twenty patients received 2 cycles of tis (200mg, iv, Q3W) plus anlo (12mg, QD for 2W, Q3W) and platinum-based dual agent chemotherapy, followed by tis plus anlo maintenance therapy. The primary endpoint was progression free survival. The second endpoints included over survival, object response rate, during of response, disease control rate and safety. The number of planned enrollment patients was 30.

Results

As of the data cutoff of August 31, 2023, the median follow-up time was 8 months (95%CI 4-12).There were 20 pts eligible for inclusion,18/20 pts were stage IV and 14/20 pts were non-squamous NSCLC. The median PFS was 8.5months(95%CI:4.5-NA), the 6m-PFS% and 12m-PFS% were 75.9% (95%CI 0.477-0.902) and 36.1% (95%CI 0.103-0.634) respectively. The median OS has not arrived, the 12m-OS% was 77.9% (95%CI 0.440-0.927). The ORR was 75% and DCR was 100%, the median DOR was 5.2months (95%CI 1.68-NA). The safety was manageable and none ≥3TRAE and ≥3irAE occurred. Table: 80P

AEs, n (%) N=20
Any TEAEs 20(100)
TEAEs ≥15% Grade1-2 Grade 3
WBC decreased 6 (30) 2 (10)
Neutrophil count decreased 6 (30) 2 (10)
Canker sores 5 (25) 1 (5)
Rash 5 (25) 1 (5)
Anemia 5 (25)
Hand-foot-syndrome 5 (25) 2 (10)
Decreased platelet count 5 (25) 2 (10)
Pulmonary infection 4 (20)
Hypertension 4 (20) 1 (5)
GGT increased 4 (20)
Hypertriglyceridemia 3 (15)
Hyperuricemia 3 (15)
Vomiting 3 (15)

Conclusions

The preliminary result of this study indicated that tislelizumab, anlotinib combined with 2-cycles chemotherapy as first-line treatment for advanced NSCLC showed promising efficacy and good safety.

Clinical trial identification

TISAL-FE-01.

Legal entity responsible for the study

The authors.

Funding

BeiGene and Nanjing Zhengda Tianqing Pharmaceutical Co., Ltd.

Disclosure

All authors have declared no conflicts of interest.

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