Chiang C L, Choi H C, Lam K O, Chan B Y, Lee S F, Yeung S Y, Lau K S, Chan S Y, Choy T S, Yuen K K
Department of Clinical Oncology, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong, China.
Clinical Oncology Center, The University of Hong Kong-Shenzhen Hospital, Shenzhen, China.
Asia Pac J Clin Oncol. 2019 Mar;15 Suppl 2:5-13. doi: 10.1111/ajco.13114. Epub 2019 Mar 19.
To investigate treatment patterns and outcomes of metastatic colorectal cancer (mCRC) patients beyond second progression (PD2) since regorafenib and TAS-102 became available in Hong Kong.
The clinical records of consecutive mCRC patients who were treated beyond PD2 at Department of Clinical Oncology, Queen Mary Hospital between June 2013 and February 2018, were retrospectively reviewed.
Of 176 PD2 patients (76.7% Eastern Cooperative Oncology Group performance status 0/1 and a median follow-up time of 6.6 [range, 0.4-37.2] months), 104 (59%) underwent palliative care only and 72 (41%) received active third-line (3L) treatment: regorafenib (n = 22), TAS-102 (n = 6), chemotherapy + antiepidermal growth factor receptor (n = 12), chemotherapy + antivascular endothelial growth factor (n = 28) or clinical trials (n = 4). Patients on active 3L treatment had significantly longer OS than those on palliative care only: 11.7 versus 5.5 months (adjusted hazard ratio = 0.41, 95% confidence interval: 0.28-0.61, P < 0.001). For those on active treatment, OS was significantly associated with the time from diagnosis of metastasis to PD2 (P < 0.001) and post-3L treatments (P = 0.009). When analyzing treatment eligibility according to trial criteria, half of the eligible patients (54/109) did not receive active treatment, but both eligible and ineligible patients achieved better OS when receiving active 3L treatment versus palliative care only (P < 0.001 and P = 0.002). No unexpected toxicity was reported.
Active 3L and beyond treatment significantly prolonged OS versus palliative care, even in selected "trial ineligible" patients. Given a high rate of palliation only care in eligible patients, improved patient access to medicine and counseling may be needed to maximize outcomes.
自瑞戈非尼和TAS-102在香港上市以来,调查转移性结直肠癌(mCRC)患者二线进展(PD2)后的治疗模式及疗效。
回顾性分析2013年6月至2018年2月在玛丽医院临床肿瘤科接受PD2后治疗的连续性mCRC患者的临床记录。
176例PD2患者中(76.7%东部肿瘤协作组体能状态为0/1,中位随访时间为6.6[范围0.4 - 37.2]个月),104例(59%)仅接受姑息治疗,72例(41%)接受积极的三线(3L)治疗:瑞戈非尼(n = 22)、TAS-102(n = 6)、化疗 + 抗表皮生长因子受体(n = 12)、化疗 + 抗血管内皮生长因子(n = 28)或临床试验(n = 4)。接受积极3L治疗的患者总生存期显著长于仅接受姑息治疗的患者:11.7个月对5.5个月(校正风险比 = 0.41,95%置信区间:0.28 - 0.61,P < 0.001)。对于接受积极治疗的患者,总生存期与从转移诊断到PD2的时间(P < 0.001)及3L治疗后(P = 0.009)显著相关。根据试验标准分析治疗资格时,一半符合条件的患者(54/109)未接受积极治疗,但与仅接受姑息治疗相比,符合条件和不符合条件的患者在接受积极3L治疗时均获得了更好的总生存期(P < 0.001和P = 0.002)。未报告意外毒性。
即使在部分“不符合试验条件”的患者中,积极的3L及后续治疗与姑息治疗相比也显著延长了总生存期。鉴于符合条件的患者中仅接受姑息治疗的比例较高,可能需要改善患者获得药物和咨询的机会以实现最佳疗效。