Evidence map›Paper›PMID 34105207›Full record

Trial reportThe oncologist2021

Anlotinib Monotherapy for Refractory Metastatic Colorectal Cancer: A Double-Blinded, Placebo-Controlled, Randomized Phase III Trial (ALTER0703).

Yihebali Chi, Yongqian Shu, Yi Ba, Yuxian Bai, Baoli Qin, Xiuwen Wang, Jianping Xiong, Nong Xu, Helong Zhang, Jianfeng Zhou and 25 more

Open access · bronzeAbstract readClinical Trial, Phase IIIMulticenter StudyRandomized Controlled Trial
In one paragraph

Trial report in The oncologist, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers, 5 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed, 5 pooled it
7.6field-weighted citation impact, top 2% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

41 citing papers in PubMed, 5 syntheses or guidelines pooled it, 63 citations in OpenAlex.

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  15. Efficacy of Anlotinib in Treating Progressive Glioblastoma: Insights From a Single-Center Study.Medical science monitor : international medical journal of experimental and clinical research · 2025
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

35 authors at 20 institutions in 1 country.

Yihebali ChiDepartment of Medical Oncology, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, People's Republic of China.
Yongqian ShuDepartment of Medical Oncology, Jiangsu Province Hospital, Nanjing, People's Republic of China.
Yi BaDepartment of Digestive Oncology, Tianjin Medical University Cancer Institute & Hospital, Tianjin, People's Republic of China.
Yuxian BaiDepartment of Medical Oncology, Harbin Medical University Cancer Hospital, Harbin, People's Republic of China.
Baoli QinDepartment of Gastrointestinal Oncology, Liaoning Cancer Hospital & Institute, Shenyang, People's Republic of China.
Xiuwen WangDepartment of Chemotherapy, Qilu Hospital of Shandong University, Jinan, People's Republic of China.
Jianping XiongDepartment of Medical Oncology, The First Affiliated Hospital of Nanchang University, Nanchang, People's Republic of China.
Nong XuDepartment of Medical Oncology, The First Affiliated Hospital, Zhejiang University, Hangzhou, People's Republic of China.
Helong ZhangDepartment of Medical Oncology, Tangdu Hospital, Air Force Medical University, Xi'an, People's Republic of China.
Jianfeng ZhouDepartment of Medical Oncology, Peking Union Medical College Hospital, Beijing, People's Republic of China.
Jianming XuDepartment of Gastrointestinal Oncology, 307 Hospital of PLA, Academy of Military Medical Sciences, Beijing, People's Republic of China.
Ying ChengDepartment of Medical Oncology, Jilin Cancer Hospital, Changchun, People's Republic of China.
Jifeng FengDepartment of Medical Oncology, Jiangsu Cancer Hospital, Nanjing, People's Republic of China.
Chunhong HuDepartment of Oncology, the Second Xiangya Hospital, Central South University, Changsha, People's Republic of China.
Yigui ChenDepartment of Abdominal Oncology, Fujian Cancer Hospital, Fuzhou, People's Republic of China.
Zhendong ChenDepartment of Oncology, The Second Hospital of Anhui Medical University, Hefei, People's Republic of China.
Jufeng WangDepartment of Oncology, Henan Cancer Hospital, Zhengzhou, People's Republic of China.
Chengxue DangDepartment of Surgical Oncology, The First Affiliated Hospital of Xi'an Jiaotong University, Xi'an, People's Republic of China.
Jianhong WangDepartment of Medical Oncology, Nantong Tumor Hospital, Nantong, People's Republic of China.
Yiye WanDepartment of Medical Oncology, Jiangxi Cancer Hospital, Nanchang, People's Republic of China.
Yong TangDepartment of Digestive Internal Medicine, The Affiliated Tumor Hospital of Xinjiang Medical University, Urumqi, People's Republic of China.
Donglin WangDepartment of Medical oncology, Chongqing Cancer Hospital, Chongqing, People's Republic of China.
Jiang LiuDepartment of Medical Oncology, People's Hospital of Xinjiang Uygur Autonomous Region, Urumqi, People's Republic of China.
Minhui WuDepartment of integrated Chinese and Western Medicine, Shaanxi Provincial Cancer Hospital, Xi'an, People's Republic of China.
Yanhong DengDepartment of Medical Oncology, The Sixth Affiliated Hospital of Sun Yat-sen University, Guangzhou, People's Republic of China.
Xingwen LiDepartment of Gastrointestinal Surgery, Gansu Provincial Cancer Hospital, Lanzhou, People's Republic of China.
Yongqiang LiDepartment of Medical Oncology, Affiliated Tumor Hospital of Guangxi Medical University, Nanning, People's Republic of China.
Jian DongFirst Department of Medical Oncology, Yunnan Cancer Hospital, Kunming, People's Republic of China.
Da JiangDepartment of Medical Oncology, Forth Hospital of Hebei Medical University, Hebei, People's Republic of China.
Guisheng LiDepartment of Medical Oncology, Liuzhou Worker's Hospital, Liuzhou, People's Republic of China.
Qiong WuDepartment of Medical Oncology, The First Affiliated Hospital of Bengbu Medical College, Bengbu, People's Republic of China.
Jin LiDepartment of Medical Oncology, Shanghai East Hospital, Tongji University School of Medicine, Shanghai, People's Republic of China.
Yujuan QiDepartment of Medical Oncology, Qinghai Provincial People's Hospital, Xining, People's Republic of China.
Yongkun SunDepartment of Medical Oncology, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, People's Republic of China.
Jianqiang CaiDepartment of Hepatobiliary Surgery, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, People's Republic of China.
Chinese Academy of Medical Sciences & Peking Union Medical College · CN307th Hospital of Chinese People’s Liberation Army · CNAir Force Medical University · CNAnhui Medical University · CNChongqing Cancer Hospital · CNFirst Affiliated Hospital of Bengbu Medical College · CNFirst Affiliated Hospital of Xi'an Jiaotong University · CNFirst Affiliated Hospital Zhejiang University · CNFirst People's Hospital of Yunnan Province · CNFourth Affiliated Hospital of Guangxi Medical University · CNFujian Provincial Cancer Hospital · CNGansu Provincial Hospital · CNHebei Medical University · CNHenan Cancer Hospital · CNJiangsu Cancer Hospital · CNJiangsu Province Hospital · CNJiangxi Provincial Cancer Hospital · CNJilin Province Tumor Hospital · CNLiaoning Cancer Hospital & Institute · CNNanchang University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundTreatment options for refractory metastatic colorectal cancer (mCRC) were limited. Anlotinib is a novel multitarget tyrosine kinase inhibitor. ALTER0703 study was conducted to assess efficacy and safety of anlotinib for patients with refractory mCRC. MATERIALS AND

methodsThis was a multicenter, double-blinded, placebo-controlled, randomized phase III trial involving 33 hospitals in China. Patients had taken at least two lines of therapies were 2:1 randomized to receive oral anlotinib (12 mg/day; days 1-14; 21 days per cycle) or placebo, plus best supportive care. Randomization was stratified by previous VEGF-targeting treatments and time from diagnosis to metastases. The primary endpoint was overall survival (OS). The secondary endpoints were progression-free survival (PFS), objective response rate (ORR), disease control rate (DCR), quality of life (QoL), and safety.

resultsA total of 419 patients (anlotinib: 282; placebo: 137) were treated from December 2014 to August 2016. The median PFS was improved in anlotinib group (4.1 months; 95% confidence interval [CI], 3.4-4.5) over placebo group (1.5 months; 95% CI, 1.4-1.5), with a hazard ratio (HR) of 0.34 (95% CI, 0.27-0.43; p < .0001). However, median OS was similar between two groups (8.6 months; 95% CI, 7.8-9.7 vs. 7.2 months; 95% CI, 6.2-8.8; HR, 1.02; p = .870). Improvements of ORR and DCR were observed in anlotinib over placebo. The most common grade ≥ 3 anlotinib related adverse events were hypertension (20.92%), increased γ-GT (7.09%), and hand-foot skin reaction (6.38%).

conclusionAnlotinib was tolerated in Chinese patients with refractory mCRC. Although OS did not reach significant difference, anlotinib still provided clinical benefits by substantially prolonged PFS in these patients. IMPLICATIONS FOR PRACTICE: In this randomized clinical trial that included 419 patients with refractory metastatic colorectal cancer, substantial prolonged in progression-free survival was noted in patients who received anlotinib compared with those given placebo. Improvements on objective response rate and disease control rate was also observed in anlotinib group. However, overall survival was similar between the two groups. In a word, in third-line or above treatment of Chinese patients with refractory metastatic colorectal cancer, anlotinib provided clinical benefit by significantly prolonged progression-free survival.

Indexed as

Colorectal NeoplasmsQuinolinesDouble-Blind MethodHumansIndolesQuality of LifeanlotinibIndolesQuinolinesAdverse eventsAnlotinibColorectal cancerMetastaticProgression-free survivalSurvival

Identifiers

PMID34105207
PMCPMC8488800
OpenAlexW3169953522

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.