Parikh P, Prabhash K, Naik R, Vaid A K, Goswami C, Rajappa S, Noronha V, Joshi A, Chacko R T, Aggarwal S, Doval D C
Department of Medical Oncology, Lung/Head and Neck Cancer, Tata Memorial Hospital, Mumbai, Maharashtra, India.
Indian J Cancer. 2016 Jan-Mar;53(1):87-91. doi: 10.4103/0019-509X.180863.
Tyrosine kinase inhibitors (TKIs) are a pharmaceutical class of small molecules, orally available with manageable safety profile, approved worldwide for the treatment of several neoplasms, including lung, breast, kidney and pancreatic cancer as well as gastro-intestinal stromal tumours and chronic myeloid leukaemia. In recent years, management of lung cancer has been moving towards molecular-guided treatment, and the best example of this new approach is the use of the tyrosine kinase inhibitors (TKIs) in patients with mutations in the epidermal growth factor receptor (EGFR). The identification of molecular predictors of response can allow the selection of patients who will be the most likely to respond to these tyrosine kinase inhibitors (TKIs). Gastrointestinal (GI) adverse events (AEs) are frequently observed in patients receiving EGFR tyrosine kinase inhibitor therapy and are most impactful on the patient's quality of life. Dermatologic side effects are also relatively common among patients treated with EGFR inhibitors. Evidence has emerged in recent years to suggest that the incidence and severity of rash, positively correlated with response to treatment.These skin disorders are generally mild or moderate in severity and can be managed by appropriate interventions or by reducing or interrupting the dose. Appropriate and timely management make it possible to continue a patient's quality of life and maintain compliance; however if these adverse events (AEs) are not managed appropriately, and become more severe, treatment cessation may be warranted compromising clinical outcome. Strategies to improve the assessment and management of TKI related skin AEs are therefore essential to ensure compliance with TKI therapy, thereby enabling patients to achieve optimal benefits. This article provides a consensus on practical recommendation for the prevention and management of diarrhoea and rash in Non-Small Cell Lung Cancer (NSCLC) patients receiving TKIs.
酪氨酸激酶抑制剂(TKIs)是一类小分子药物,口服给药,安全性可控,在全球范围内被批准用于治疗多种肿瘤,包括肺癌、乳腺癌、肾癌和胰腺癌以及胃肠道间质瘤和慢性髓性白血病。近年来,肺癌的治疗已朝着分子导向治疗发展,这种新方法的最佳例子是在表皮生长因子受体(EGFR)发生突变的患者中使用酪氨酸激酶抑制剂(TKIs)。确定反应的分子预测指标可以帮助选择最有可能对这些酪氨酸激酶抑制剂(TKIs)产生反应的患者。接受EGFR酪氨酸激酶抑制剂治疗的患者经常出现胃肠道(GI)不良事件(AEs),对患者的生活质量影响最大。在接受EGFR抑制剂治疗的患者中,皮肤副作用也相对常见。近年来有证据表明,皮疹的发生率和严重程度与治疗反应呈正相关。这些皮肤疾病的严重程度一般为轻度或中度,可以通过适当的干预措施或减少或中断剂量来处理。适当及时的处理可以使患者维持生活质量并保持依从性;然而,如果这些不良事件(AEs)处理不当且变得更加严重,则可能需要停药,从而影响临床结果。因此,改善对TKI相关皮肤不良事件的评估和管理策略对于确保TKI治疗的依从性至关重要,从而使患者能够获得最佳疗效。本文就接受TKIs治疗的非小细胞肺癌(NSCLC)患者腹泻和皮疹的预防及管理提供了实用建议的共识。