# Long-Term Outcomes of Patients Undergoing Conversion Surgery After Induction Chemotherapy: Turkish Oncology Group Study

**Authors:** Furkan Ceylan, Selin Aktürk Esen, Olçun Ümit Ünal, Ferit Aslan, İlknur Deliktaş Onur, Öztürk Ateş, Erkut Demirciler, İlkay Tuğba Ünek, Ahmet Gülmez, Esra Özen Engin, Semra Taş, Gamze Gököz Doğu, Melih Şimşek, Hacı Mehmet Türk, Ali İnal, Gökhan Şahin, Haydar Çağatay Yüksel, Ateş Kutay Tenekeci, Mutlu Hızal, Mehmet Ali Nahit Şendur, Doğan Uncu

PMC · DOI: 10.3390/medicina61050776 · 2025-04-22

## TL;DR

This study evaluates the long-term outcomes of patients with liver metastatic colorectal cancer who underwent surgery after chemotherapy, finding that surgical resection improves survival.

## Contribution

The study provides insights into the efficacy of combining biological therapies with chemotherapy for liver metastatic colorectal cancer patients undergoing conversion surgery.

## Key findings

- Median progression-free survival was 21.1 months and overall survival was 53.7 months.
- No significant survival benefit was observed from adding Anti-VEGF therapy in RAS/RAF mutant tumors.
- Advanced tumor stage and lack of response to chemotherapy were linked to shorter survival.

## Abstract

Background and Objectives: Conversion surgery for liver metastatic colorectal cancer (mCRC) has been associated with prolonged survival. This study aimed to evaluate the efficacy and safety of integrating biological therapies with fluorouracil-based induction chemotherapy in patients with isolated liver mCRC who subsequently underwent curative resection of both the primary tumor and liver metastases. Materials and Methods: This multicenter, retrospective study, conducted by the Turkish Oncology Group (TOG), included 116 patients from 11 tertiary centers who underwent conversion surgery following induction chemotherapy between 2009 and 2024. Results: The median age was 57 years, with 62% male patients. The median follow-up period was 55.3 months. The median progression-free survival (PFS) and overall survival (OS) were 21.1 and 53.7 months, respectively. No significant differences in PFS or OS were observed based on biological therapy use or tumor localization. Among patients with RAS/RAF wild-type tumors, PFS and OS were comparable between those receiving Anti-EGFR and Anti-VEGF therapy. In RAS/RAF mutant tumors, the addition of Anti-VEGF therapy did not confer a survival benefit. Factors associated with shorter PFS included advanced tumor stage (ypT3-T4), lymph node metastasis, and multiple metastases, while shorter OS was linked to advanced tumor stage and lack of objective response. Conclusions: Surgical resection plays a pivotal role in improving survival outcomes in patients with potentially resectable liver mCRC. Optimizing induction chemotherapy regimens may enhance conversion rates and prolong long-term survival. Further studies are needed to refine treatment selection based on tumor localization, mutation status, and molecular biomarkers.

## Linked entities

- **Genes:** ras (resistance to audiogenic seizures) [NCBI Gene 19412], ZHX2 (zinc fingers and homeoboxes 2) [NCBI Gene 22882]
- **Chemicals:** fluorouracil (PubChem CID 3385)
- **Diseases:** colorectal cancer (MONDO:0005575)

## Full-text entities

- **Genes:** ZHX2 (zinc fingers and homeoboxes 2) [NCBI Gene 22882] {aka AFR1, RAF}, EGFR (epidermal growth factor receptor) [NCBI Gene 1956] {aka ERBB, ERBB1, ERRP, HER1, NISBD2, NNCIS}, VEGFA (vascular endothelial growth factor A) [NCBI Gene 7422] {aka L-VEGF, MVCD1, VEGF, VPF}
- **Diseases:** liver metastases (MESH:D009362), lymph node metastasis (MESH:D008207), tumor (MESH:D009369), metastatic (MESH:D000092182), colorectal cancer (MESH:D015179)
- **Chemicals:** fluorouracil (MESH:D005472)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12113550/full.md

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Source: https://tomesphere.com/paper/PMC12113550