Evidence map›Paper›PMID 41862176›Full record

ArticleCancer medicine2026

Real-World Efficacy of Nab-Paclitaxel Plus Capecitabine and a PD-1 Inhibitor in Metastatic or Locally Advanced Esophageal Cancer.

Yun Wang, Wei-Jing Zhang, Yun-Xin Lu, Shi-Liang Liu, Zhuo-Yu Zhang, Si-Min Zhang, Tian-Wan Wang, Yu Zhong, Dong-Sheng Zhang

Abstract read
In one paragraph

Article in Cancer medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

9 authors.

Yun WangDepartment of Medical Oncology, Sun Yat-sen University Cancer Center, Guangzhou, China.
Wei-Jing ZhangState Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine, Sun Yat-sen University Cancer Center, Guangzhou, China.
Yun-Xin LuDepartment of Medical Oncology, Sun Yat-sen University Cancer Center, Guangzhou, China.
Shi-Liang LiuState Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine, Sun Yat-sen University Cancer Center, Guangzhou, China.
Zhuo-Yu ZhangGuangdong Provincial Key Laboratory of Food, Nutrition and Health, and Department of Nutrition, School of Public Health, Sun Yat-sen University, Guangzhou, China.
Si-Min ZhangDepartment of Medical Oncology, Sun Yat-sen University Cancer Center, Guangzhou, China.
Tian-Wan WangDepartment of Medical Oncology, Sun Yat-sen University Cancer Center, Guangzhou, China.
Yu ZhongDepartment of Medical Oncology, Sun Yat-sen University Cancer Center, Guangzhou, China.
Dong-Sheng ZhangDepartment of Medical Oncology, Sun Yat-sen University Cancer Center, Guangzhou, China.

Funding

Tencent
6 · The paper itself

Abstract

backgroundOver half of esophageal cancer (EC) cases occur in China, where paclitaxel and platinum agents have become the preferred chemotherapeutic regimen for EC patients. However, there is a clinical need for a non-platinum-based therapeutic option.

methodsCases were collected from Sun Yat-sen University Cancer Center between January 2019 and November 2023. Patients with metastatic or locally advanced EC received 4-6 cycles of chemo-immunotherapy, including nab-paclitaxel, capecitabine, and a programmed death receptor 1 (PD-1) inhibitor, with or without subsequent surgery, radiotherapy, or maintenance therapy. The objective response rate (ORR), disease control rate (DCR), progression-free survival (PFS), pathological complete response (pCR), complete (R0) resection rate, and major pathologic response (MPR) were assessed.

resultsAmong the 72 patients retrospectively analyzed, the median PFS was 24.7 months (95% confidence interval: 7.0-42.3 months). 75% of patients were regarded as responders, with an ORR of 66.7% in 42 patients with measurable lesions. The 6-month, 1-year, and 2-year PFS rates (DCRs) were 100%, 96.2%, and 67.9%, respectively. In total, 9 patients underwent surgery, and 29 patients received radiotherapy following the regimen. The R0 resection rate was 77.8%, while both pCR and MPR were 66.7%. The most common adverse events were myelosuppression (27.8%) and liver dysfunction (25.0%).

conclusionOur study demonstrated that the combination of nab-paclitaxel, capecitabine, and a PD-1 inhibitor was an effective and tolerable strategy for EC patients and a promising first-line or neoadjuvant treatment option.

Indexed as

AlbuminsAntineoplastic Combined Chemotherapy ProtocolsCapecitabineEsophageal NeoplasmsImmune Checkpoint InhibitorsPaclitaxelAdultAgedFemaleHumansMaleMiddle AgedPathologic Complete ResponseRetrospective StudiesTreatment Outcome130-nm albumin-bound paclitaxelAlbuminsCapecitabineImmune Checkpoint InhibitorsPaclitaxelanti‐PD‐1 inhibitorcapecitabineesophageal cancernab‐paclitaxel

Identifiers

PMID41862176
PMCPMC13093792

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