Plain language summary of SUNLIGHT: trifluridine/tipiracil and bevacizumab for refractory metastatic colorectal cancer.

IF 3 4区 医学 Q2 ONCOLOGY Future oncology Pub Date : 2024-07-02 DOI:10.1080/14796694.2024.2366100
Gerald W Prager, Julien Taieb, Marwan Fakih, Fortunato Ciardiello, Eric Van Cutsem, Elena Élez, Lucjan Wyrwicz, Daniil Stroyakovskiy, Gabor Liposits, Igor Bondarenko, Dominik P Modest, Nadia Amellal, Josep Tabernero
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Abstract

What is this summary about?: This is a summary describing the results from a phase 3 clinical trial called SUNLIGHT. The study looked at treatment with orally administered trifluridine/tipiracil plus intravenously administered bevacizumab in people with metastatic colorectal cancer (mCRC) that is refractory to treatment.This study included people whose cancer had grown or spread beyond its original location after no more than two previous treatments. People in the study received either the combination of trifluridine/tipiracil plus bevacizumab or they received trifluridine/tipiracil alone. The aims of the study were to see how long people lived after treatment with trifluridine/tipiracil plus bevacizumab compared with trifluridine/tipiracil alone and to find out how well the combination of trifluridine/tipiracil plus bevacizumab worked at slowing down the spread of the cancer. Researchers also looked at side effects from taking the medicines and at how treatment affected people's physical functioning.

What are the key takeaways?: People in the combination group lived longer (a median of 10.8 months) than people who received trifluridine/tipiracil alone (7.5 months). In addition, the time it took for the cancer to worsen was longer for those who received the combination treatment (a median of 5.6 months) compared with those who received trifluridine/tipiracil alone (2.4 months). People's physical functioning took longer to worsen with combination therapy (a median of 9.3 months) than it did with trifluridine/tipiracil alone (6.3 months), as measured by the impact of treatment on people's ability to carry out daily living activities. The most common side effects in both treatment groups were low levels of white blood cells, known as neutrophils (neutropenia), nausea, and low levels of healthy red blood cells (anemia).

What were the main conclusions reported by the researchers?: The results from the study suggest that treatment with oral trifluridine/tipiracil plus intravenous (IV) bevacizumab could help people with refractory mCRC live longer and maintain good physical functioning, and it could slow the worsening of their cancer.Clinical Trial Registration: NCT04737187 (SUNLIGHT) (ClinicalTrials.gov).

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SUNLIGHT: 曲氟尿苷/替比西嘧啶和贝伐珠单抗治疗难治性转移性结直肠癌的通俗语言摘要。
本摘要是关于什么的? 本摘要描述了一项名为 "SUNLIGHT "的三期临床试验的结果。该研究观察了口服曲氟尿苷/替比拉嘧啶加静脉注射贝伐珠单抗治疗难治性转移性结直肠癌(mCRC)患者的情况。参加研究的人要么接受曲氟尿苷/替比拉西联合贝伐珠单抗治疗,要么只接受曲氟尿苷/替比拉西治疗。这项研究的目的是了解接受曲氟尿苷/替吡拉西嗪加贝伐单抗治疗的患者与单独接受曲氟尿苷/替吡拉西嗪治疗的患者相比能活多久,并了解曲氟尿苷/替吡拉西嗪加贝伐单抗联合疗法在延缓癌症扩散方面的效果如何。研究人员还考察了服用药物的副作用以及治疗对患者身体机能的影响:联合用药组患者的生存期(中位数为10.8个月)比单独服用三氟尿苷/替吡西林组患者的生存期(7.5个月)要长。此外,与单独接受曲氟尿苷/替吡嘧啶治疗的患者(2.4 个月)相比,接受联合治疗的患者癌症恶化的时间更长(中位数为 5.6 个月)。根据治疗对患者日常生活能力的影响来衡量,接受联合疗法的患者身体功能恶化的时间(中位数为9.3个月)长于单独接受曲氟啶/替吡嘧啶疗法的患者(6.3个月)。两个治疗组中最常见的副作用是白细胞(即中性粒细胞)水平低(中性粒细胞减少症)、恶心和健康红细胞水平低(贫血):研究结果表明,口服曲氟尿苷/替比拉嘧啶加静脉注射贝伐珠单抗可以帮助难治性mCRC患者延长寿命并保持良好的身体机能,而且可以延缓癌症的恶化:NCT04737187(SUNLIGHT)(ClinicalTrials.gov)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Future oncology
Future oncology ONCOLOGY-
CiteScore
5.40
自引率
3.00%
发文量
335
审稿时长
4-8 weeks
期刊介绍: Future Oncology (ISSN 1479-6694) provides a forum for a new era of cancer care. The journal focuses on the most important advances and highlights their relevance in the clinical setting. Furthermore, Future Oncology delivers essential information in concise, at-a-glance article formats - vital in delivering information to an increasingly time-constrained community. The journal takes a forward-looking stance toward the scientific and clinical issues, together with the economic and policy issues that confront us in this new era of cancer care. The journal includes literature awareness such as the latest developments in radiotherapy and immunotherapy, concise commentary and analysis, and full review articles all of which provide key findings, translational to the clinical setting.
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