# Comparative efficacy of antibody-drug conjugates and chemotherapy for malignant tumors: a systematic review and meta-analysis

**Authors:** Xin Gao, Linghui Tao, Wen Hao, Xiaqiu Wu, Feiye Zhu, Shengxia Lv, Yongsheng Zhang

PMC · DOI: 10.3389/fonc.2025.1697340 · Frontiers in Oncology · 2026-01-09

## TL;DR

This study compares antibody-drug conjugates and chemotherapy for cancer, finding that ADCs improve survival without increasing serious side effects.

## Contribution

A meta-analysis showing ADCs improve overall and progression-free survival compared to chemotherapy in cancer patients.

## Key findings

- ADCs improved overall survival (HR = 0.67) compared to chemotherapy.
- ADCs improved progression-free survival (HR = 0.76) compared to chemotherapy.
- Adverse events were similar between ADCs and chemotherapy.

## Abstract

Despite advancements in cancer treatment, malignant tumors remain a significant global health challenge. Drawbacks of chemotherapy, such as drug resistance and strong side effects, have prompted the exploration of antibody-drug conjugates (ADCs), which combine targeting capabilities with potent cytotoxins to enhance therapeutic efficacy.

We searched PubMed, Cochrane, and EMBASE library databases up to June 8, 2025, for eligible randomized controlled trials (RCTs) and extracted relevant data. The primary outcome measures were overall survival (OS) and progression-free survival (PFS), with subgroup analysis and sensitivity analysis conducted to assess the heterogeneity of statistical results.

A total of thirteen RCTs involving 5,927 patients were included. The results indicated that ADCs offered superior OS (HR = 0.67, 95%CI: 0.55-0.81) and PFS (HR = 0.76; 95% CI: 0.66-0.86) compared to chemotherapy drugs. The any adverse event (96.8% vs. 93.6%), grade 3–5 adverse event (51.7% vs. 51.8%) and serious adverse event (25.3% vs. 22.4%) caused to patients were generally similar between ADCs and chemotherapy.

Our meta-analysis demonstrates that compared to chemotherapy drugs, ADC drugs can prolong both OS and PFS in cancer patients, with no significant difference in adverse reactions.

http://www.crd.york.ac.uk/PROSPERO, identifier CRD42024592020.

## Full-text entities

- **Diseases:** cancer (MESH:D009369)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12827071/full.md

## References

54 references — full list in the complete paper: https://tomesphere.com/paper/PMC12827071/full.md

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Source: https://tomesphere.com/paper/PMC12827071