Influence of tumor location on short- and long-term outcomes after laparoscopic surgery for rectal cancer: a propensity score matched cohort study

Rectal cancer is one of the most common malignant diseases worldwide. Nowadays, surgery remains the cornerstone for the treatment of rectal cancer. However, the treatment strategy for rectal cancer has changed dramatically in the past decades, for instance, the introduction of total mesorectal excision (TME), neoadjuvant chemoradiotherapy and minimally invasive surgery. Laparoscopic surgery for rectal cancer is widely performed all over the world in recent years. A number of clinical studies including some randomized clinical trials have confirmed that laparoscopic surgery was feasible and safe for rectal cancer, with favorable short-term benefits and similar oncological outcomes compared with open surgery [1‐7]. Laparoscopic surgery for rectal cancer is considered to be a technically demanding procedure, especially for low rectal cancer. Some studies have already revealed that the tumor distance from the anal verge was related to the difficulty of laparoscopic surgery [8, 9]. Although several studies have explored the impact of rectal cancer height on clinical management and outcomes in patients undergoing curative resection, few studies have particularly compared the clinical and oncological outcomes of laparoscopic surgery at different heights of rectal cancer [10‐13].

Therefore, the aim of the present study was to evaluate the influence of tumor location on short- and long-term outcomes of rectal cancer after laparoscopic resection with curative intent by propensity score analysis.

According to the inclusion and exclusion criteria, a total of 373 patients were enrolled in our analysis, including 138 patients in the LRC group and 235 patients in the M/HRC group. After propensity score matching at a ratio of 1:1 based on the variables mentioned above, 99 LRC patients were matched with 99 M/HRC patients.

Over the past few decades, minimally invasive surgery has been introduced into the treatment of rectal cancer, and more excisions were performed laparoscopically. Our center is one of the earliest medical institutions to carry out laparoscopic resection of rectal cancer in China. In the present study, laparoscopic surgery for LRC required longer operative time and more blood loss volume than M/HRC. The main reason for this was that the difficulty of laparoscopic resection for LRC may be increased due to narrow space and complex anatomy at the bottom of the pelvic, and requiring more non-restorative surgery or protective ostomy during operation. Though a trend to higher overall morbidity was observed in the LRC group compared with the M/HRC group, which may prolong the duration of postoperative hospital stay, the reoperation rate and 30-day mortality did not increase. Akiyoshi et al. [8] demonstrated that the tumor distance from the anal verge was one of the independent predictors of pelvic operative time and postoperative morbidity. Ogiso et al. [9] also concluded that tumor location was an independent predictor of operative time, which was related to intraoperative blood loss.

In addition, our results showed that 5-year OS and DFS rates were poorer for LRC patients compared with M/HRC patients after laparoscopic surgery, which is consistent with previous literatures [10, 14], although these studies were not focused exclusively on laparoscopic surgery. Chiang et al. [10] noted that the rectal cancer level significantly affected the long-term survival and patterns of distant metastases for patients who underwent surgical resection. Compared with mid-rectal and upper-rectal cancers, LRC had the worst prognosis. Cheng et al. [14] divided T3/T4 rectal cancer patients who underwent surgery into high and mid/low rectal cancer, they found that patients with stage III high rectal cancer demonstrated better prognosis than those with mid/low rectal cancer, and tumor location was an independent prognostic factor for long-term survival. However, other studies have come to different conclusions, meaning that tumor location has no influence on long-term outcome. Bhangu et al. [11] concluded that low height of rectal cancer after curative surgery did not lead to worse survival, LRC showed equivalent oncological outcome compared with M/HRC. Similarly, Khan et al. [12] also found that although the level of rectal cancer affected the use of NAT and R0 resection rate, it did not affect recurrence rate and long-term survival.

In our matched cohort, the pathological TNM stage of LRC and M/HRC patients was nearly equal, so the long-term survival of the two groups was more comparable. Considering there were more patients of LRC received non-restorative surgery compared with M/HRC, and this may have some impact on long-term survival, multivariate analysis was carried out. On multivariate analysis, we came to the conclusion that tumor location remained as an independent predictor for PFS, but not for OS. When comparing the total recurrence between the two groups, LRC patients had higher risk of tumor relapse. This may explain why LRC patients had worse long-term survival than M/HRC patients. However, when analyzed separately, there was no significant difference in the local recurrence rate between the two groups, though the distant metastasis rate tended to be higher in LRC patients. Considering the small number of patients with recurrence in the series, this finding should be regarded with caution. Cheng et al. [14] found that the location of rectal cancer was a significant risk factor for local recurrence, lung metastasis, bone metastasis and systemic lymph node metastasis, as the tumor distance from the anal verge decreased, the risk for recurrence significantly increased. Frambach et al. [16] retrospectively analyzed 378 patients with locally advanced rectal cancer treated with NAT and curative surgery. They concluded that a distance of the tumor from the anal verge ≤5 cm was the risk factor for recurrence, and it was the only factor associated with increased risk of lung metastasis. Since LRC is more prone to distant metastasis after surgery, its perioperative treatment should be strengthened. At present, preoperative radiotherapy combined with intensive chemotherapy for advanced rectal cancer is one of the research hotspots. In addition, some studies have shown that adjuvant chemotherapy is still necessary for patients with obvious tumor downstaging after NAT, even if complete pathological response has been achieved [17, 18].

The results of this study showed that overall positive CRM rate in the matched cohort was lower (3.0%) than most previous studies have reported [3, 19, 20], and did not differ significantly between LRC and M/HRC patients. The COLOR II study [3, 4] presented that positive CRM rate was 10% after laparoscopic surgery for rectal cancer, and the rate of local recurrence was 5% at 3 years. The presence of involved CRM after laparoscopic surgery in the ALaCaRT [19] and the ACOSOG Z6051 [20] randomized clinical trials was 12 and 7%, respectively. While some other studies have reported relatively low positive CRM rates. The COREAN study [1] noted that CRM positivity was 2.9% after laparoscopic surgery for mid/low rectal cancer after NAT. Park et al. [21] demonstrated that positive CRM rate was 2.3% after laparoscopic intersphincteric resection for low rectal cancer, and 3-year local recurrence rate was 2.6%. We speculated the main reason for the low rate of positive CRM in our research was that pathologists may have underestimated the rate of CRM involvement. Besides this, all the operations in this study were performed by a same surgical team and may be related to this result, because in this case surgical standards and procedures were easily unified to ensure high quality of operations. However, considering the postoperative local recurrence rate was 9.1 and 4.0% for LRC and M/HRC patients, respectively, we deem the actual positive CRM rate would be a little higher than observed in this group.

Compared with M/HRC, LRC was more likely to harvest less than 12 lymph nodes in the total cohort. The proportion of dissected lymph nodes less than 12 in the two groups was 39.9 and 20.9%, respectively. This result can be explained by the fact that more patients in the LRC group had received NAT, which accounted for 47.8 and 11.5% for LRC and M/HRC patients, respectively. Several studies have shown that NAT was frequently associated with decreased number of harvested lymph nodes, regardless of the application of TME principle and appropriate pathologic evaluation [22‐25]. Moreover, some of the findings also noted that retrieval of less than 12 lymph nodes in the proctectomy specimen of rectal cancer treated with NAT had no adverse effect on long-term survival and may be a marker of higher tumor response [26‐29]. On the contrary, other studies indicated that lymph node yield was an independent predictor of survival in rectal cancer irrespective of NAT [30, 31]. In our matched cohort, propensity score matching basically eliminated the difference in NAT between LRC and M/HRC patients. The number of harvested lymph nodes were equivalent and the results were comparable between the two groups. The univariate analysis showed that harvested lymph nodes less than 12 was an inferior predictor of PFS, which should be taken seriously.

To our knowledge, this is the only study comparing the short- and long-term outcomes of laparoscopic surgery for LRC and M/HRC by propensity score analysis. However, the present study has a few limitations, such as retrospective design and small samples which introduce inherent selection bias and limit the generalizability of the results. Furthermore, in this study, we divided rectal cancer into LRC and M/HRC, mainly referring to the grouping approach of previous literatures [11, 12]. From a surgical point of view, laparoscopic surgery for low rectal cancer is considered to be more challenging, with higher rates of positive CRM and permanent stoma, whereas the surgical procedures and difficulties of mid and high rectal cancer are more alike. However, this grouping method has some limitations, especially the perioperative treatment is different depending on tumor location, and NAT is more often recommended for mid/low rectal cancer but less for high rectal cancer. Finally, due to the limitations of patient compliance and economic condition, the treatment options for the cases included in this study were not always reasonable. For example, some patients who required NAT accepted surgery immediately, and other patients who were recommended for adjuvant chemotherapy refused it.

In conclusion, our study showed that tumor location of the rectal cancer significantly affected the clinical and oncological outcomes after laparoscopic surgery. Lower level of the rectal cancer was related to longer operative time and more blood loss volume, and inclined to have higher postoperative morbidity. Patients of LRC presented significantly inferior OS and DFS, and tended to develop more distant metastasis compared to M/HRC. Besides, tumor location was an independent predictor of DFS for rectal cancer after laparoscopic surgery.