Evidence map›Paper›PMID 40921945›Full record

ArticleInvestigational new drugs2025

Association of different approvals with Chinese Society of Clinical Oncology recommendation levels for solid tumor drugs: a cross-sectional analysis.

Lirong Zhang, Hongbin Yi, Liping Kuai, Sheng Han, Hong Sun, Jiaqin Cai, Xiaoxia Wei

Abstract read
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Article in Investigational new drugs, 2025. 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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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

7 authors.

Lirong Zhang *Department of Pharmacy, Shengli Clinical Medical College of Fujian Medical University, Fuzhou, China.
Hongbin Yi *International Research Centre for Medicinal Administration, Peking University, Beijing, China.
Liping KuaiScience and Technology Development Center, Chinese Pharmaceutical Association, Beijing, China.
Sheng HanInternational Research Centre for Medicinal Administration, Peking University, Beijing, China.
Hong SunDepartment of Pharmacy, Shengli Clinical Medical College of Fujian Medical University, Fuzhou, China.
Jiaqin CaiDepartment of Pharmacy, Shengli Clinical Medical College of Fujian Medical University, Fuzhou, China.
Xiaoxia WeiDepartment of Pharmacy, Shengli Clinical Medical College of Fujian Medical University, Fuzhou, China. xxwei0321@outlook.com.

Funding

Fujian provincial health technology project 2022GGA010Fujian provincial Joint Funding Project of Scientific and Technological Innovation 2023Y9347Natural Science Foundation of Fujian, China 2021J01397
6 · The paper itself

Abstract

In China, many solid tumor drugs have been approved via the accelerated approval (AA) pathway. We extracted data regarding indications for solid tumor-treating drugs approved by the National Medical Products Administration (NMPA) between 2015 and 2023, along with their corresponding Chinese Society of Clinical Oncology (CSCO) guideline recommendation levels and inclusion data. Descriptive statistics, Fisher's exact tests, and t-tests were used to examine associations between NMPA approval pathways and CSCO guideline recommendation levels. The study included 92 solid tumor drugs comprising 191 indications. Sixty-three indications were approved via the regular approval (RA), and 128 were approved via the AA. One hundred fifty-seven indications obtained CSCO guideline recommendation level I, 28 obtained level II, and 6 obtained level III. No significant difference in the recommendation level was observed between the approval pathways. The average time for the indications approved via the RA to obtain the recommendation level was 2.03 months before NMPA approval. The average time for the indications approved via the AA to obtain the level was 6.66 months after NMPA approval. Compared with initial levels, 57 indications had their recommendation levels upgraded. Most indications obtain the CSCO guideline recommendation level I, with similar likelihoods across obtaining different approval pathways. Indications approved via the RA tended to obtain the CSCO guideline recommendation earlier than those via the AA. Given the limitations in data completeness and CSCO guideline coverage, these findings should be interpreted with caution. Clearer criteria for evaluating recommendation levels and standardizing rating procedures will enable CSCO guidelines to better support clinicians and patients.

Indexed as

Antineoplastic AgentsDrug ApprovalNeoplasmsChinaCross-Sectional StudiesHumansMedical OncologyPractice Guidelines as TopicSocieties, MedicalAntineoplastic AgentsAccelerate approvalChinese Society of Clinical OncologyNational Medical Products AdministrationSolid tumor

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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.