# The Safety and Effectiveness of Bevacizumab in Metastatic Colorectal Cancer With Unresectable Metastases: A Real-Life Study From the South of Morocco

**Authors:** Ghizlane Rais, Farah Boutaagount, Rania Mokfi, Meryem Maskrout, Soundous Bennour, Chaymae Senoussi, Fadoua Rais, Laila Lahlou

PMC · DOI: 10.7759/cureus.56733 · Cureus · 2024-03-22

## TL;DR

This study examines the real-world effectiveness and safety of bevacizumab combined with chemotherapy for treating metastatic colorectal cancer in Morocco.

## Contribution

The study provides real-life data on bevacizumab's use in metastatic colorectal cancer treatment in a specific Moroccan region.

## Key findings

- Median overall survival was 14 months with bevacizumab plus chemotherapy.
- Patients with right-sided tumors and maintenance treatment had longer survival.
- Only 6% of patients were eligible for metastasis resection.

## Abstract

Background

Colorectal cancer constitutes a significant public health challenge, despite remarkable strides made in the last two decades, particularly in the medical management of metastatic stages. Notable progress has been achieved through targeted therapies such as anti-epidermal growth factor receptors or anti-angiogenic antibodies, as well as advancements in surgical approaches for hepatic metastases. This study seeks to assess the efficacy and safety of bevacizumab plus chemotherapy in individuals with metastatic colorectal cancer.

Methodology

This is an observational, cross-sectional, retrospective study of all patients who were followed up for metastatic colorectal cancer with unresectable metastases and were treated with bevacizumab in combination with standard chemotherapy from January 2010 until December 2019 in the medical oncology department of the Centre Hospitalier Universitaire (CHU) Souss-Massa of Agadir.

Results

Of the total 162 cases, 117 (72%) had metastatic disease, and 45 (28%) progressed to metastatic disease after initial treatment. The median age of the patients was 55 years (range = 23-79 years) with a sex ratio of 1.1 (M/F). The tumor was located in the left colon in 135 (83.3%) patients. The results represented adenocarcinoma in 137 (84.6) cases and mucinous subtype in 23 (14.19) cases. The three most common sites of metastasis were the liver (99, 61.1), peritoneum (67, 41.3), and lung (33, 20.3). In the first line, all patients received bi-chemotherapy plus bevacizumab, i.e., fluorouracil, oxaliplatin, and leucovorin in 34 (20.9%) patients; capecitabine plus oxaliplatin in 88 (54.3%) patients; leucovorin, fluorouracil, and irinotecan in 17 (10.4%) patients; and capecitabine plus irinotecan in 23 (14.1%) patients. Response after first-line treatment was progression in 74 (45.7) cases, stability in 42 (25.9) cases, partial response in 35 (21.6) cases, and complete response in 11 (6.8) cases. Nine (6%) patients were able to benefit from surgical resection of metastatic lesions. Overall, 77 (47%) patients received second-line chemotherapy, i.e., 5-FU with irinotecan in 40 (51.8%) cases or with oxaliplatin in 30 (38.8%) cases. Two patients developed undesirable side effects under bevacizumab (hypertension). The median progression-free survival and median overall survival of the study cohort were 9 months and 14 months, respectively. Nevertheless, patients who underwent primary tumor resection (p = 0.048), those with right‑sided tumors (p = 0.022), those who received a higher number of treatment cycles (p = 0.020), and those who received maintenance treatment (p = 0.001) had a longer median overall survival.

Conclusions

Chemotherapy combination with bevacizumab is considered as the cornerstone of metastatic colorectal cancer treatment in our region. With the new healthcare and social security systems, easier access to expensive treatments and molecular pathology tests is currently available. It is important to highlight that real-world data can offer valuable insights into the daily clinical practice of medical oncology.

## Linked entities

- **Chemicals:** fluorouracil (PubChem CID 3385), oxaliplatin (PubChem CID 9887053), leucovorin (PubChem CID 135403648), capecitabine (PubChem CID 60953), irinotecan (PubChem CID 60838), 5-FU (PubChem CID 3385)
- **Diseases:** colorectal cancer (MONDO:0005575)

## Full-text entities

- **Diseases:** metastatic disease (MESH:D000092182), hypertension (MESH:D006973), tumor (MESH:D009369), Metastases (MESH:D009362), adenocarcinoma (MESH:D000230), mucinous (MESH:D002288), Colorectal Cancer (MESH:D015179)
- **Chemicals:** irinotecan (MESH:D000077146), 5-FU (MESH:D005472), oxaliplatin (MESH:D000077150), fluorouracil, oxaliplatin, (-), Bevacizumab (MESH:D000068258), leucovorin (MESH:D002955), capecitabine (MESH:D000069287)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

27 references — full list in the complete paper: https://tomesphere.com/paper/PMC11033042/full.md

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Source: https://tomesphere.com/paper/PMC11033042