Li Shuyuan, Ji Liqiang, Huang Jie, Wang Ye, Liu Peng, Zhang Wei, Lou Zheng
Department of Colorectal Surgery, the first affiliated Hospital of Naval Medical University, 168 Changhai Road, Yangpu District, Shanghai, China.
The first affiliated Hospital of Naval Medical University, Shanghai, China.
Int J Colorectal Dis. 2023 Aug 15;38(1):214. doi: 10.1007/s00384-023-04500-y.
Whether patients with asymptomatic primary tumors and unresectable metastases of colorectal cancer (CRC) should undergo primary tumor resection (PTR) remains controversial. This study aims to determine the appropriateness of PTR for these individuals by evaluating a number of outcome measures.
A systematic literature search was performed. Outcome measures included overall survival, emergency surgery rates, incidence of postoperative complications, time to initiate chemotherapy, conversion rates, and chemotherapy-related toxicities.
Patients who received PTR in addition to chemotherapy had a better overall survival rate than those who only received chemotherapy (HR = 0.62, 95%CI, 0.50-0.78, I = 84%, p < 0.00001). In the RCT subgroup, there were no significant differences with a HR of 0.72 (95%CI, 0.45-1.13, I = 17%, p = 0.15). More patients in the chemotherapy alone group could be converted to resectable status (OR = 0.47, 95%CI, 0.27-0.82, I = 0%, p = 0.008), but the incidence of emergency surgery was 23% (95%CI, 17-29%, I = 14%). The risk of chemotherapy-related toxicity was not significantly higher in the PTR group (OR = 1.5, 95%CI, 0.94-2.43, p = 0.09, I = 0%), with a 7% incidence of postoperative complications (95%CI, 0-14%, p = 0.05, I = 0%). The time to initiate chemotherapy after PTR was approximately 33.06 days (95%CI, 25.55-40.58, I = 0%).
PTR plus chemotherapy may be associated with improved survival in asymptomatic CRC patients with unresectable metastases. However, PTR did not provide a significant survival benefit in the subgroup of RCTs. Additionally, PTR did not result in a significantly increased risk of chemotherapy-related toxicity, with a postoperative complication rate of approximately 7%, and chemotherapy could be initiated at approximately 33.06 days after PTR. Compared with the PTR plus chemotherapy, chemotherapy alone could result in a significantly higher conversion rate. However, about 23% of patients receiving chemotherapy alone required emergency surgery for primary tumor-related symptoms. The above results needed to be validated in future larger prospective randomized trials.
无症状原发性肿瘤且伴有不可切除转移灶的结直肠癌(CRC)患者是否应接受原发性肿瘤切除术(PTR)仍存在争议。本研究旨在通过评估多项结局指标来确定这些患者接受PTR的合理性。
进行了系统的文献检索。结局指标包括总生存期、急诊手术率、术后并发症发生率、开始化疗的时间、转化率以及化疗相关毒性。
接受PTR联合化疗的患者总生存率高于仅接受化疗的患者(HR = 0.62,95%CI为0.50 - 0.78,I = 84%,p < 0.00001)。在随机对照试验(RCT)亚组中,HR为0.72(95%CI为0.45 - 1.13,I = 17%,p = 0.15),无显著差异。单纯化疗组更多患者可转化为可切除状态(OR = 0.47,95%CI为0.27 - 0.82,I = 0%,p = 0.008),但急诊手术发生率为23%(95%CI为17 - 29%,I = 14%)。PTR组化疗相关毒性风险无显著升高(OR = 1.5,95%CI为0.94 - 2.43,p = 0.09,I = 0%),术后并发症发生率为7%(95%CI为0 - 14%,p = 0.05,I = 0%)。PTR后开始化疗的时间约为33.06天(95%CI为25.55 - 40.58,I = 0%)。
PTR联合化疗可能与无症状CRC伴不可切除转移灶患者生存率提高相关。然而,在RCT亚组中,PTR未提供显著的生存获益。此外,PTR未导致化疗相关毒性风险显著增加,术后并发症发生率约为7%,化疗可在PTR后约33.06天开始。与PTR联合化疗相比,单纯化疗可导致显著更高的转化率。然而,约23%接受单纯化疗的患者因原发性肿瘤相关症状需要急诊手术。上述结果需要在未来更大规模的前瞻性随机试验中得到验证。