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Optimising the use of cetuximab in the continuum of care for patients with metastatic colorectal cancer

机译:优化西妥昔单抗在转移性结直肠癌患者护理中的应用

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摘要

The anti-epidermal growth factor receptor (EGFR) monoclonal antibody cetuximab in combination with chemotherapy is a standard of care in the first-line treatment of RAS wild-type (wt) metastatic colorectal cancer (mCRC) and has demonstrated efficacy in later lines. Progressive disease (PD) occurs when tumours develop resistance to a therapy, although controversy remains about whether PD on a combination of chemotherapy and targeted agents implies resistance to both components. Here, we propose that some patients may gain additional clinical benefit from the reuse of cetuximab after having PD on regimens including cetuximab in an earlier treatment line. We conducted a non-systematic literature search in PubMed and reviewed published and ongoing clinical trials, focusing on later-line cetuximab reuse in patients with mCRC. Evidence from multiple studies suggests that cetuximab can be an efficacious and tolerable treatment when continued or when fit patients with mCRC are retreated with it after a break from anti-EGFR therapy. Furthermore, on the basis of available preclinical and clinical evidence, we propose that longitudinal monitoring of RAS status may identify patients suitable for such a strategy. Patients who experience progression on cetuximab plus chemotherapy but have maintained RAS wt tumour status may benefit from continuation of cetuximab with a chemotherapy backbone switch because they have probably developed resistance to the chemotherapeutic agents rather than the biologic component of the regimen. Conversely, patients whose disease progresses on cetuximab-based therapy due to drug-selected clonal expansion of RAS-mutant tumour cells may regain sensitivity to cetuximab following a defined break from anti-EGFR therapy. Looking to the future, we propose that RAS status determination at disease progression by liquid, needle or excisional biopsy may identify patients eligible for cetuximab continuation and rechallenge. With this approach, treatment benefit can be extended, adding to established continuum-of-care strategies in patients with mCRC.
机译:抗表皮生长因子受体(EGFR)单克隆抗体西妥昔单抗联合化疗是RAS野生型(wt)转移性结直肠癌(mCRC)一线治疗的标准治疗方法,并已在以后的治疗中证明其疗效。当肿瘤对治疗产生耐药性时会发生进行性疾病(PD),尽管关于化学疗法和靶向药物联合使用的PD是否暗示对这两种成分都有耐药性仍存在争议。在此,我们建议一些患者在较早的治疗方案中对包括西妥昔单抗在内的治疗方案进行PD治疗后,可以通过重复使用西妥昔单抗获得更多的临床益处。我们在PubMed中进行了非系统性文献检索,并回顾了已发表和正在进行的临床试验,重点关注mCRC患者中西妥昔单抗的再利用。来自多项研究的证据表明,西妥昔单抗在继续治疗或适合的mCRC患者在停止抗EGFR治疗后用其治疗时,可能是一种有效且可耐受的治疗方法。此外,根据现有的临床前和临床证据,我们建议纵向监测RAS状况可以确定适合这种策略的患者。继续接受西妥昔单抗加化学疗法治疗但仍具有RAS wt肿瘤状态的患者,可通过继续进行化学疗法主治而受益于西妥昔单抗的继续治疗,因为他们可能已对化疗药物产生了耐药性,而不是该方案的生物学成分。相反,由于药物选择的RAS突变肿瘤细胞的克隆扩增,其疾病在以西妥昔单抗为基础的治疗中进展的患者可能会在抗EGFR治疗明确中断后恢复对西妥昔单抗的敏感性。展望未来,我们建议通过液体,针头或切除活检在疾病发展过程中确定RAS状态,可以确定符合西妥昔单抗持续治疗和再挑战性条件的患者。通过这种方法,可以扩大治疗获益,为mCRC患者增加既定的连续治疗策略。

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