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Poster session 05

2005P - Anlotinib combined with chemotherapy in the treatment of first-line extensive-stage small cell lung cancer (ES-SCLC): A real-world study

Date

21 Oct 2023

Session

Poster session 05

Topics

Tumour Site

Small Cell Lung Cancer

Presenters

Fangfang Gao

Citation

Annals of Oncology (2023) 34 (suppl_2): S1062-S1079. 10.1016/S0923-7534(23)01926-9

Authors

Y. Zhao1, X. Li2, Y. Li3, T. Ma4, Q. Li5, X. Tang6, X. Han7, S. Yi8, F. Gao1

Author affiliations

  • 1 Respiratory Department Of Internal Medicine, Henan Cancer Hospital/Affiliated Cancer Hospital of Zhengzhou University, 450008 - Zhengzhou/CN
  • 2 Department Of Oncology, The First Affiliated Hospital of Zhengzhou University, 450052 - Zhengzhou/CN
  • 3 Respiratory Department Of Internal Medicine, Shangqiu First People 's Hospital, Shangqiu/CN
  • 4 Department Of Oncology, Luohe Central Hospital, 462005 - Luohe/CN
  • 5 Department Of Oncology, Xinxiang Central Hospital, 453059 - Xinxiang/CN
  • 6 Department Of Oncology, The First Affiliated Hospital of Xinxiang Medical University, 453100 - Xinxiang/CN
  • 7 Department Of Oncology, Xinyang Central Hospital, Xinyang/CN
  • 8 Department Of Oncology, Zhengzhou central hospital, Zhenzhou/CN

Resources

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Abstract 2005P

Background

Small cell lung cancer (SCLC) makes up about 15% of all newly diagnosed cases of lung cancer, approximately 70% diagnosed with extensive-stage SCLC (ES-SCLC). For ES-SCLC, the safety and efficacy data of anti-angiogenesis combined with chemotherapy are still seriously lacking. The median PFS of first-line standard regimen (PD-L1 combined with chemotherapy) in the treatment of ES-SCLC is about 5 months, which is comparable to that of chemotherapy alone. Therefore, we conducted a real-world study to observe and evaluate the efficacy and safety of anlotinib combined with chemotherapy in the treatment of first-line ES-SCLC.

Methods

Eligible ES-SCLC pts (histologically or cytologically proven inoperable ES-SCLC; not received systematic treatment before; age≥18years; ECOG PS 0-2) were received anlotinib + etoposide + platinum for 4∼6 cycles, then anlotinib maintenance until the disease progresses or intolerable adverse reactions occur. During the treatment, dose reduction of anlotinib was permitted, which could be reduced to 10mg or 8mg if it was intolerable. The primary endpoint was progression-free survival (PFS), and secondary endpoints were objective response rate (ORR), disease control rate (DCR), overall survival (OS) and safety.

Results

Between March 2022 and April 2023, 60 patients were enrolled in this study and 34 patients were included in the evaluation of the treatment, with an average age of 65.5 (53.0-79.0) years old, 28 males (82.3%) and 6 females (17.7%). The ORR was 70.6%, and the DCR was 100.0%. The median PFS was 6.2 months (95% CI: 5.19 to 6.37). The median OS has not yet reached. The common grade 1-2 treatment-related adverse events (TRAEs) were hypertriglyceridemia (11.8%), hypercholesterolemia (11.8%), lymphocyte count decreased (8.8%), GGT increased (5.9%), cough (5.9%), platelet decreased (2.9%), grade 3 and above TRAEs included lymphocyte count decreased (5.9%), leukocyte decreased (5.9%), GGT increased (2.9%), hypodynamia (2.9%), neutrophil declined (2.9%). No higher-grade adverse reactions.

Conclusions

Anlotinib combined with chemotherapy in the treatment of ES-SCLC shows good efficacy and controllable safety; no unexpected toxicity has been observed.

Clinical trial identification

Editorial acknowledgement

Legal entity responsible for the study

Henan Cancer Hospital.

Funding

Has not received any funding.

Disclosure

All authors have declared no conflicts of interest.

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