# Expert opinion on treatment patterns in metastatic colorectal cancer management in Eastern Europe

**Authors:** László Torday, Alinta Hegmane, Biljana Kukić, Edita Baltruškevičienė, Elina Sivina, Ioana Luca, Juraj Prejac, Marija Ristić, Martina Reberšek, Nikola Milašević, Rossitza Krasteva Ruseva, Saša Jungić, Velko Todorov Minchev, Tina Roblek, Viktor Uršič

PMC · DOI: 10.1186/s12919-026-00369-1 · BMC Proceedings · 2026-03-23

## TL;DR

This paper summarizes expert opinions on treating metastatic colorectal cancer in Eastern Europe, highlighting challenges and the potential role of fruquintinib.

## Contribution

The paper provides new insights into treatment practices and challenges for metastatic colorectal cancer in Eastern Europe, focusing on expert perspectives and fruquintinib's potential.

## Key findings

- Experts identified challenges like limited access to targeted therapies and the need for molecular profiling.
- Fruquintinib is seen as a potential later-line therapy with efficacy comparable to other third-line treatments.
- Experts emphasized the importance of real-world evidence and patient participation in clinical trials.

## Abstract

Colorectal cancer (CRC) is the third most prevalent malignancy globally and the second leading cause of cancer-related mortality. Approximately 15%–30% of patients are diagnosed with metastatic CRC (mCRC), and despite increasing survival rates, mCRC remains fatal. There are notable variations in the incidence and mortality rates of CRC across European countries, which may be attributed to the differences in lifestyle patterns and variations in cancer diagnosis and management practices. Standard initial treatments for mCRC include chemotherapeutic agents and targeted therapies. This report presents the findings of a virtual meeting held from 21 January to 2 February 2025. The meeting included healthcare professionals from 10 Eastern European countries (Bosnia and Herzegovina, Bulgaria, Croatia, Hungary, Latvia, Lithuania, Montenegro, Romania, Serbia, and Slovenia). The experts shared their opinions on various topics such as the current clinical practice and existing clinical challenges in the treatment of patients with mCRC, factors influencing treatment choices, and the place of fruquintinib therapy in the management of mCRC. The discussion was facilitated using open-ended questions. The primary objective of this article was to provide an overview of the experts’ opinions and experiences related to the current treatment approaches to mCRC management, with a focus on fruquintinib in Eastern Europe. The experts identified the need for molecular and genetic profiling, multidisciplinary coordination, limited availability of and access to targeted and newly approved medications, and lack of reimbursement as key challenges in managing patients with mCRC in these regions. The experts also highlighted the importance of patient education and participation in regional and international clinical trials of new therapeutics. They also noted the need for generating real-world evidence on the safety and efficacy of fruquintinib, its comparative efficacy versus other later-line therapies, its efficacy as an earlier line of therapy, and its sequencing in the current treatment practices. Furthermore, despite the lack of direct experience with fruquintinib, most experts acknowledged its potential efficacy as a later-line therapy for mCRC and considered its effectiveness to be comparable to that of other third-line treatments.

## Linked entities

- **Chemicals:** fruquintinib (PubChem CID 44480399)
- **Diseases:** colorectal cancer (MONDO:0005575)

## Full-text entities

- **Genes:** BRAF (B-Raf proto-oncogene, serine/threonine kinase) [NCBI Gene 673] {aka B-RAF1, B-raf, BRAF-1, BRAF1, NS7, RAFB1}, KRAS (KRAS proto-oncogene, GTPase) [NCBI Gene 3845] {aka 'C-K-RAS, C-K-RAS, CFC2, K-RAS2A, K-RAS2B, K-RAS4A}, RBBP4 (RB binding protein 4, chromatin remodeling factor) [NCBI Gene 5928] {aka NURF55, RBAP48, lin-53}, ERBB2 (erb-b2 receptor tyrosine kinase 2) [NCBI Gene 2064] {aka CD340, HER-2, HER-2/neu, HER2, MLN 19, MLN-19}, RET (ret proto-oncogene) [NCBI Gene 5979] {aka CDHF12, CDHR16, HSCR1, MEN2A, MEN2B, MTC1}, EGFR (epidermal growth factor receptor) [NCBI Gene 1956] {aka ERBB, ERBB1, ERRP, HER1, NISBD2, NNCIS}, TXK (TXK tyrosine kinase) [NCBI Gene 7294] {aka BTKL, PSCTK5, PTK4, RLK, TKL}, UGT1A (UDP glucuronosyltransferase family 1 member A complex locus) [NCBI Gene 7361] {aka GNT1, UGT, UGT1, UGT1A@}, KDR (kinase insert domain receptor) [NCBI Gene 3791] {aka CD309, FLK1, VEGFR, VEGFR2}, NRAS (NRAS proto-oncogene, GTPase) [NCBI Gene 4893] {aka ALPS4, CMNS, N-ras, NCMS, NRAS1, NS6}, KIT (KIT proto-oncogene, receptor tyrosine kinase) [NCBI Gene 3815] {aka C-Kit, CD117, MASTC, PBT, SCFR}, DPYD (dihydropyrimidine dehydrogenase) [NCBI Gene 1806] {aka DHP, DHPDHASE, DPD, DYPD}, VEGFA (vascular endothelial growth factor A) [NCBI Gene 7422] {aka L-VEGF, MVCD1, VEGF, VPF}, FGFR1 (fibroblast growth factor receptor 1) [NCBI Gene 2260] {aka BFGFR, CD331, CEK, ECCL, FGFBR, FGFR-1}
- **Diseases:** MSI-H (MESH:D053842), liver metastasis (MESH:D009362), renal, hepatic, and/or thyroid dysfunction (MESH:D007674), cardiovascular complications (MESH:D002318), toxicity (MESH:D064420), dermatologic toxicity (MESH:D000168), CRC (MESH:D015179), neuroblastoma rat sarcoma viral (MESH:D014777), Cancer (MESH:D009369), hypertension (MESH:D006973), metastatic (MESH:D000092182), WD (MESH:D006527)
- **Chemicals:** ipilimumab (MESH:D000074324), ESMO (-), Regorafenib (MESH:C559147), tipiracil (MESH:C000613754), FOLFOX (MESH:C410216), oxaliplatin (MESH:D000077150), fluorouracil (MESH:D005472), irinotecan (MESH:D000077146), Folinic acid (MESH:D002955), nivolumab (MESH:D000077594), cetuximab (MESH:D000068818), Fruquintinib (MESH:C000591844), bevacizumab (MESH:D000068258), trifluridine (MESH:D014271), panitumumab (MESH:D000077544), pembrolizumab (MESH:C582435)
- **Species:** Homo sapiens (human, species) [taxon 9606]
- **Mutations:** G12C

## Full text

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## Figures

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## References

4 references — full list in the complete paper: https://tomesphere.com/paper/PMC13007362/full.md

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Source: https://tomesphere.com/paper/PMC13007362