Real-world efficacy and safety of anlotinib combined with chemotherapy for advanced pancreatic cancer: a retrospective study

Background Pancreatic cancer (PC) is often diagnosed at advanced stages, limiting surgical options. There is no standardized treatment for second-line or beyond therapies, necessitating alternative treatments. This study evaluates the efficacy and safety of anlotinib combined with chemotherapy in ad...

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Main Authors: Zhiyong Li, Zhiming Wang, Hexia Gan, Feng Shen, Lisha Cheng, Xiuping Zhang
Format: Article
Language:English
Published: Taylor & Francis Group 2025-12-01
Series:Future Science OA
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Online Access:https://www.tandfonline.com/doi/10.1080/20565623.2025.2532327
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author Zhiyong Li
Zhiming Wang
Hexia Gan
Feng Shen
Lisha Cheng
Xiuping Zhang
author_facet Zhiyong Li
Zhiming Wang
Hexia Gan
Feng Shen
Lisha Cheng
Xiuping Zhang
author_sort Zhiyong Li
collection DOAJ
description Background Pancreatic cancer (PC) is often diagnosed at advanced stages, limiting surgical options. There is no standardized treatment for second-line or beyond therapies, necessitating alternative treatments. This study evaluates the efficacy and safety of anlotinib combined with chemotherapy in advanced PC patients receiving second-line or subsequent treatments.Methods A retrospective analysis of 68 advanced PC patients was conducted. Twenty-six patients treated with anlotinib and chemotherapy were compared to 42 controls who received chemotherapy only. Demographic data, efficacy, survival, and adverse reactions were analyzed.Results In the anlotinib group, the therapeutic responses were as follows: Complete Response: 0, Partial Response: 2 (7.7%), Stable Disease: 13 (50.0%), and Progressive Disease: 11 (42.3%), the Objective Remission Rate was 7.7%, and the Disease Control Rate was 57.7%. The median Progression-Free Survival was 4.5 months. The Overall Survival was significantly longer in the anlotinib group compared to controls. Common adverse reactions included fatigue, bone marrow suppression, and hypertension, mostly grade 1–3. The potential toxicity and cumulative toxicity of long-term use is hand-foot syndrome, hypothyroidism and hypertension.Conclusion The data generated suggest that anlotinib combined with chemotherapy may be an effective and tolerable option for second-line and subsequent treatment of advanced PC.
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spelling doaj-art-7d209d702b08408b9d77d4ddaf80a6262025-08-20T03:50:32ZengTaylor & Francis GroupFuture Science OA2056-56232025-12-0111110.1080/20565623.2025.2532327Real-world efficacy and safety of anlotinib combined with chemotherapy for advanced pancreatic cancer: a retrospective studyZhiyong Li0Zhiming Wang1Hexia Gan2Feng Shen3Lisha Cheng4Xiuping Zhang5Department of Medical Oncology, Zhongshan Hospital (Xiamen), Fudan University, Xiamen, Fujian, ChinaDepartment of Medical Oncology, Zhongshan Hospital (Xiamen), Fudan University, Xiamen, Fujian, ChinaDepartment of Medical Oncology, Zhongshan Hospital (Xiamen), Fudan University, Xiamen, Fujian, ChinaDepartment of Medical Oncology, Zhongshan Hospital (Xiamen), Fudan University, Xiamen, Fujian, ChinaDepartment of Medical Oncology, Zhongshan Hospital (Xiamen), Fudan University, Xiamen, Fujian, ChinaDepartment of Medical Oncology, Zhongshan Hospital (Xiamen), Fudan University, Xiamen, Fujian, ChinaBackground Pancreatic cancer (PC) is often diagnosed at advanced stages, limiting surgical options. There is no standardized treatment for second-line or beyond therapies, necessitating alternative treatments. This study evaluates the efficacy and safety of anlotinib combined with chemotherapy in advanced PC patients receiving second-line or subsequent treatments.Methods A retrospective analysis of 68 advanced PC patients was conducted. Twenty-six patients treated with anlotinib and chemotherapy were compared to 42 controls who received chemotherapy only. Demographic data, efficacy, survival, and adverse reactions were analyzed.Results In the anlotinib group, the therapeutic responses were as follows: Complete Response: 0, Partial Response: 2 (7.7%), Stable Disease: 13 (50.0%), and Progressive Disease: 11 (42.3%), the Objective Remission Rate was 7.7%, and the Disease Control Rate was 57.7%. The median Progression-Free Survival was 4.5 months. The Overall Survival was significantly longer in the anlotinib group compared to controls. Common adverse reactions included fatigue, bone marrow suppression, and hypertension, mostly grade 1–3. The potential toxicity and cumulative toxicity of long-term use is hand-foot syndrome, hypothyroidism and hypertension.Conclusion The data generated suggest that anlotinib combined with chemotherapy may be an effective and tolerable option for second-line and subsequent treatment of advanced PC.https://www.tandfonline.com/doi/10.1080/20565623.2025.2532327Advanced pancreatic canceranlotinibchemotherapysecond-line treatmentprogression-free survivaladverse reactions
spellingShingle Zhiyong Li
Zhiming Wang
Hexia Gan
Feng Shen
Lisha Cheng
Xiuping Zhang
Real-world efficacy and safety of anlotinib combined with chemotherapy for advanced pancreatic cancer: a retrospective study
Future Science OA
Advanced pancreatic cancer
anlotinib
chemotherapy
second-line treatment
progression-free survival
adverse reactions
title Real-world efficacy and safety of anlotinib combined with chemotherapy for advanced pancreatic cancer: a retrospective study
title_full Real-world efficacy and safety of anlotinib combined with chemotherapy for advanced pancreatic cancer: a retrospective study
title_fullStr Real-world efficacy and safety of anlotinib combined with chemotherapy for advanced pancreatic cancer: a retrospective study
title_full_unstemmed Real-world efficacy and safety of anlotinib combined with chemotherapy for advanced pancreatic cancer: a retrospective study
title_short Real-world efficacy and safety of anlotinib combined with chemotherapy for advanced pancreatic cancer: a retrospective study
title_sort real world efficacy and safety of anlotinib combined with chemotherapy for advanced pancreatic cancer a retrospective study
topic Advanced pancreatic cancer
anlotinib
chemotherapy
second-line treatment
progression-free survival
adverse reactions
url https://www.tandfonline.com/doi/10.1080/20565623.2025.2532327
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