Approaches and considerations in the endoscopic treatment of T1 colorectal cancer

White light endoscopic findings

White light endoscopy (WLE) is a fundamental technique for the detection and differentiation of neoplastic polyps. A meta-analysis showed the sensitivity of WLE for predicting T1 CRC was relatively low (0.21–0.46); this was inferior to the sensitivities of narrow-band imaging (NBI) and magnifying chromoendoscopy (CE). However, its specificity was relatively high (0.81–1.0) [5]. Thus, malignant polyps should be suspected when using WLE. The keys to prediction or observation of malignant polyps include their morphology, size, and location [6]. Therefore, although WLE may be less sensitive than other T1 CRC detection methods, its high specificity makes it valuable for the initial identification and suspicion of malignant polyps.

Endoscopic characteristics of T1 CRC

Lesion size is closely associated with the risk of CRC [7,8]. In a retrospective study of 755 polyps measuring ≥ 6 mm, larger polyp size was associated with higher rates of malignancy: 0%, 0.9%, 6.1%, and 38.1% for polyps measuring 6–9, 10–19, 20–29, and ≥ 30 mm, respectively [7]. Furthermore, a meta-analysis of studies concerning laterally spreading tumors (LSTs) revealed that the proportion of malignancy increased according to lesion size: 4.6%, 9.2%, and 16.5% for lesions measuring 10–19, 20–29, and ≥ 30 mm, respectively [9]. Both the US Multi-Society Task Force (USMSTF) on CRC [10] and the Clinical Guidelines of the European Society of Gastrointestinal Endoscopy [11] recommend using advanced imaging for polyps measuring ≥ 10 mm to assess the malignancy risk and depth of submucosal invasion (DSI).

Morphological features play key roles in the prediction of T1 CRC. Several studies have identified specific morphological features as indicators of submucosal invasive cancer (SMIC); such features include a demarcated depressed area, ulceration fold convergence, induration, loss of lobulation, excavation, the chicken skin sign, stalk swelling, the non-lifting sign, and spontaneous or contact bleeding [12-15]. A multicenter prospective study of 2,123 cases of T1 CRC showed that the non-lifting sign, the chicken skin sign, depressed areas, induration, and ulceration were significantly associated with deep SMIC, defined as DSI ≥ 1 mm (1,000 µm) [15]. Additionally, a retrospective study of 64 cases of T1 CRC showed that demarcated depressed areas, stalk swelling, and fullness are more common in deep SMIC than in superficial SMIC [12].

Endoscopic characteristics of LSTs

As originally proposed by Kudo et al. [16,17], LSTs are non-pedunculated adenomatous lesions measuring ≥ 10 mm with Paris 0-II and 0-Is classifications [10]. They are classified into granular (LST-G) and non-granular (LST-NG) types based on endoscopic morphology. LST-G is subdivided into homogeneous granular (HG) and nodular mixed (NM) types, whereas LST-NG is divided into the flat elevated (FE) and pseudo-depressed (PD) types (Fig. 1). The risk of malignancy in LSTs increases according to tumor size and subtype [9,18,19]. Tumor size is associated with a higher SMIC rate in LST-NG than in LST-G [18]. A meta-analysis showed that LST-G-HG has a low probability (0.5%) of SMIC, whereas the LST-G-NM, LST-NG-FE, and LST-NG-PD types have increased risks of SMIC: 10.5%, 4.9%, and 31.6%, respectively [9]. The risk of SMIC within LSTs increases when large nodules, depressions, or submucosal tumor-like elevations are present [20,21]. It is also important to be cautious about multifocal submucosal invasion. A comprehensive analysis of 2,822 LSTs revealed that LST-NG-PD has a significantly higher multifocal invasion rate (46.9%) compared with the LST-G-NM (7.9%) and LST-NG-FE (11.8%) types [18].

Figure 1.

Endoscopic images of the four endoscopic laterally spreading tumor subtypes: (A) homogenous granular; (B) granular nodular mixed; (C) non-granular flat elevated; and (D) non-granular pseudo-depressed.

The relationship between the location and risk of SMIC is unclear, but a meta-analysis showed that most LST-G-HG and LST-NG-FE types are located in the proximal colon (73% and 71%, respectively), whereas the LST-G-NM and LSTNG-PD types are more evenly distributed throughout the colon. LSTs containing SMIC are more frequently located in the distal colon, rather than the proximal colon [9].

Imaging-enhanced endoscopy

Imaging-enhanced endoscopy is an important advancement that offers various contrast enhancement methods via dye, optical, or electronic techniques. Imaging-enhanced endoscopy is broadly categorized into dye- and electronic-based CE. Notable examples of electronic-based CE include NBI, i-scan, and flexible spectral imaging color enhancement (FICE). Imaging-enhanced endoscopy plays a crucial role in detecting and distinguishing neoplastic lesions, as well as predicting the DSI of T1 CRC [22,23]. The USMSTF recommends the proficient use of electronic-based CE, such as NBI, i-scan, FICE, or blue light imaging, as well as dye-based CE. It also emphasizes the importance of proficiency in the endoscopic recognition of DSI [1].

NBI is one of the most widely used endoscopic methods for characterization of colorectal polyps. A simple classification system is essential for international standardization of the NBI observation criteria. The Colon Tumor NBI Interest Group, which comprises endoscopists from Japan, the United States, and Europe, developed the NBI International Colorectal Endoscopic (NICE) classification [24], which classifies colorectal tumors into three types via close observation using high-resolution colonoscopy, regardless of magnification. The primary advantage of this system is that it simplifies the NBI classification, facilitating learning and clinical application. In particular, NICE type 3 is characterized by distorted or missing vessels or the distortion or absence of a surface pattern. The predictive accuracy of deep SMIC for this type exceeds 95% [25,26]. Thus, these findings can reliably guide clinicians who are considering surgery.

However, NICE type 2 is excessively broad and includes histological patterns ranging from adenoma to deep SMIC. Thus, the Japanese NBI expert team (JNET classification) divided NICE type 2 into more detailed subtypes: JNET types 2A and 2B [26]. Type 2B was subdivided into types 2B-low and 2B-high by magnifying endoscopy [27], allowing more accurate histopathological prediction. These modifications are important because accurate prediction of DSI can determine the optimal treatment modality, such as ER or surgery, and reduce underestimates or overtreatments. JNET type 2A histological findings mostly comprise adenoma, whereas JNET 2B-low histological findings [26] with uniformly distributed irregular vessels are consistent with ~98% of adenomas or superficial SMIC and ~2% of deep SMIC [27]. Thus, these findings suggest that ER is feasible (Fig. 2). However, JNET type 2B-high histological findings with irregular heterogeneously distributed vessels are consistent with ~40% of high-grade adenomas or superficial SMIC and ~60% of deep SMIC [27]. These findings suggest that ER is not sufficient. Therefore, suspected cases of JNET type 2B-high should be carefully evaluated to determine the suitability of ER or surgery (Fig. 3). Dye-based CE is an established technique for predicting histological diagnoses and DSI in patients with T1 CRC. This technique involves the use of dyes, such as indigo carmine with or without crystal violet, applied via magnifying endoscopy to highlight the surface pattern of the colonic mucosa. This application is followed by the observation and interpretation of pit patterns, which are categorized according to the Kudo classification [28].

Figure 2.

Endoscopic curative resection. (A) A 20-mm non-granular pseudo-depressed laterally spreading tumor located in the transverse colon. (B) Irregular and uniform vascular and surface patterns were observed (JNET type 2B-low) on narrow-band imaging with near-focus. (C) Circumferential incision and submucosal dissection of the lesion using an endoscopic knife after submucosal injection. (D) Mucosal defect after completion of ESD. (E) Histopathological examination confirmed complete resection (R0) (22 × 17 mm, tubulovillous adenoma with low-grade dysplasia).

Figure 3.

Endoscopic non-curative resection. (A) A 20-mm non-granular pseudo-depressed laterally spreading tumor located in the transverse colon. (B) Irregular and heterogeneous vascular and surface patterns were observed (JNET type 2B-high) on narrow-band imaging with near-focus. (C) Circumferential incision and submucosal dissection of the lesion using an endoscopic knife after submucosal injection. (D) Mucosal defect after completion of endoscopic submucosal dissection. (E) Histopathological examination confirmed incomplete resection (20 × 17 mm adenocarcinoma well-differentiated, depth of submucosal invasion ≥ 2,000 μm, no lymphatic invasion, with carcinoma involvement in the vertical resection margin).

The Kudo classification defines type V_I as an irregular pit pattern in terms of shape, size, and arrangement; type V_N is considered nonstructural, characterized by the absence of a pit pattern [29,30]. A retrospective analysis of 272 colorectal neoplasms showed that dysplasia, superficial SMIC, and deep SMIC were associated with 57.9%, 11.4%, and 30.7% of type V_I pit patterns, respectively. Conversely, dysplasia, superficial SMIC, and deep SMIC were associated with 0%, 4.3%, and 95.7% of type V_N pit patterns, respectively [31]. Therefore, surgery should be considered for neoplasms categorized as type V_N under the Kudo classification; a careful decision should be made regarding the suitability of ER or surgery for Kudo classification type V_I neoplasms. Dyebased CE has several limitations, including a cumbersome time-consuming application process, the cost of the dye solution, and the toxicity-related prohibition of crystal violet use in some countries. Additionally, magnifying endoscopes are not consistently used in clinical practice worldwide.

In contrast, NBI offers a more convenient option because it is easily activated by a button on the endoscope. Accordingly, experts often recommend the initial use of NBI for predicting DSI in cases of suspected or diagnosed CRC. However, in challenging cases (e.g., JNET type 2B-high lesions) where the decision between ER and surgery is ambiguous, experts suggest the use of magnifying dye-based CE. This approach allows more precise evaluation of DSI, aiding the selection of the most appropriate treatment strategy [23,27]. Recently, research has been actively conducted on enhancing the prediction of LNM in T1 CRC by applying artificial intelligence to various endoscopic imaging methods, making it a promising field for future developments [32].

Endoscopic mucosal resection (EMR)

EMR is widely used to remove polyps, typically ranging in size from small (6–9 mm) to intermediate (10–19 mm). EMR ensures safe effective resection through injection into the submucosal layer, which lifts the lesion and separates it from the muscular layer. This approach reduces the risk of thermal injury and perforation while enhancing the feasibility of en bloc resection [36]. However, EMR usually is not recommended for en bloc resection of non-pedunculated polyps > 20 mm because of snare size limitations and the challenges associated with effective resection at the center of larger lesions [11,37].

The rate of incomplete resection increases according to lesion size. A prospective study of 346 neoplastic polyps removed by 11 endoscopists showed that the incomplete resection rate increased with increasing lesion size: 5.8%, 9.4%, 13.4%, and 23.3% for 5–7, 8–9, 10–14, and 15–20 mm, respectively [38]. Another prospective study of 102 intermediate (10–20 mm) sessile colorectal polyps removed by EMR demonstrated an en bloc resection rate (EBR) of 75% and a complete resection rate (CRR) of 50% [39]. Therefore, EMR does not consistently ensure en bloc resection or complete resection as the lesion size approaches 20 mm for lesions < 20 mm. Accordingly, for CRCs slightly smaller than 20 mm or with suspected comorbid submucosal fibrosis, or any other case where EMR may not readily achieve en bloc resection, modified EMR or endoscopic submucosal dissection (ESD) can be considered for more reliable en bloc and complete resection [40,41].

Endoscopic piecemeal mucosal resection (EPMR)

EPMR is a method for the removal of large lesions that cannot be captured by a snare, which involves cutting them into several pieces. At the lesion boundary, 2–3 mm of normal mucosa is removed and en bloc resection is attempted to the maximum possible extent for an area with suspected malignancy. The remaining lesion is then sequentially removed using a snare [42,43]. Snares measuring 10–15 mm are usually recommended. Experts also recommend beginning resection from the most inaccessible and difficult area [42].

In a meta-analysis of lesions measuring > 20 mm, the local recurrence rate was approximately sevenfold greater when the lesion was removed by piecemeal resection than when it was removed by en bloc resection [44]. Furthermore, colorectal tumor resection into > 5 pieces was associated with a high risk of recurrence [45]. In that study, the time to recurrence among cases with resection into > 5 pieces was significantly shorter than the time for cases with resection into < 4 pieces (3.8 ± 1.9 mo vs. 7.9 ± 5.0 mo, p < 0.05). EPMR is not recommended for the resection of diagnosed or suspected T1 CRC because of the associated difficulty in evaluating resection margins and the high risk of recurrence. However, if a lesion with SMIC can be resected by EPMR, the suspected carcinoma area should be resected en bloc to the maximum possible extent and follow-up should be carefully scheduled considering the potential for recurrence [42-44,46,47].

Modified EMR

Modified EMR is an advanced ER technique intended to overcome the limitations of conventional EMR. It involves using an endoscopic snare and modifications to enhance the likelihood of en bloc resection, even for large lesions, or to achieve deeper submucosal resection.

Underwater endoscopic mucosal resection (UEMR)

UEMR is a resection technique that involves submerging the lesion in water. Air is aspirated from the lumen, which is then filled with water. Next, the lesion is removed by snaring without injection of the submucosal layer. This approach is based on the notion that after water immersion, the muscularis propria of the colon remains circular; the mucosal surface tends to involute inwards and assume a collapsed state. Simultaneously, the lesion is submerged in water, causing the mucosa and submucosa to float away from the muscularis propria because of the underwater buoyancy created by the fat density of the submucosal tissue. This combined effect allows safer, more effective lesion resection [48,49].

In a multicenter randomized control trial (RCT), both UEMR and EMR showed high efficacy in removing small non-pedunculated colorectal polyps (4–9 mm), with similar EBR (94.4% for UEMR vs. 91.5% for EMR) and CRR (83.1% for UEMR vs. 87.3% for EMR), and no significant differences in complication rates [50]. Another RCT involving small polyps (6–9 mm) showed that the rates of incomplete resection in the UEMR and EMR groups were low and did not significantly differ (2% vs. 1.9%, p = 0.91) [51].

In a prospective RCT of intermediate (10–20 mm), sessile, colorectal lesions involving 210 polyps, the EBR and CRR were significantly higher in the UEMR group (89% and 69%) than in the EMR group (75% and 50%), but there were no significant differences in adverse events between the groups [39]. In a retrospective study of large lesions (20–30 mm) that compared a UEMR group (125 lesions) with an ESD group (306 lesions), the EBR and CRR were significantly lower in the UEMR group (61% and 36%, respectively) than in the ESD group (99% and 86%, respectively) [52]. In another single-center RCT that compared UEMR with EMR for 20–40 mm lesions, UEMR demonstrated superior EBR and CRR (33% and 32%, respectively) compared with EMR (18% and 16%, respectively) [53]. However, both groups had very low EBR and CRR.

UEMR can be considered for small or intermediate T1 CRC. However, it is not a reliable method for achieving en bloc or complete resection of T1 CRCs measuring ≥ 20 mm.

Anchored snare-tip EMR (ASEMR)

ASEMR, or tip-in EMR, involves making a small incision proximal to the lesion using the tip of a snare after sufficient submucosal injection. The snare tip is anchored within the submucosal layer of the incision site. Subsequently, the snare is opened to capture and resect the entire lesion. This technique has a favorable EBR for large flat lesions because anchoring of the snare tip prevents slippage from the proximal part, ensuring stable capture of the lesion [54-57].

A prospective RCT compared the efficacies of ASEMR and EMR in 82 lesions measuring 15–25 mm [58]. The EBRs for ASEMR and EMR were 90% and 73.1%, respectively. However, that study was conducted at a single center with a relatively small sample size; it did not include detailed comparisons of EBR and CRR for ASEMR and EMR in each size range (i.e., 15–20 and 20–25 mm). A large-scale retrospective study of 709 lesions measuring 20–30 mm showed that both EBR (87.4% vs. 97.8%, p < 0.001) and CRR (69.9% vs. 87.3%, p < 0.01) were significantly lower in the ASEMR group than the ESD group; this result remained statistically significant after propensity matching [59]. A multicenter retrospective study analyzing the ASEMR results for a series of 141 consecutive lesions revealed a mean lesion size, overall EBR, and CRR of 19.8 mm, 81.6%, and 70.2%, respectively; the CRR significantly decreased with increasing lesion size (82.8% for lesions < 20 mm, 55.3% for lesions 21–30 mm, and 50.0% for lesions > 30 mm; p = 0.002) [57].

Based on these results, caution is needed in the ASEMR-mediated removal of T1 CRC lesions measuring > 20 mm because the rate of incomplete resection may increase.

EMR with precutting (EMR-P)

EMR-P, also known as EMR with circumferential mucosal incision, was developed to enhance the en bloc resection of large, flat, colorectal lesions. In this technique, the tumor is either fully or partially incised along its circumference using a snare tip or endoscopic knife after injection of the submucosal layer. Subsequently, the lesion is captured and resected using the snare (Fig. 4).

Figure 4.

Endoscopic mucosal resection with precutting. (A) A 16-mm non-granular flat elevated laterally spreading tumor located in the ascending colon. (B) Irregular and uniform vascular and surface patterns were observed on narrow-band imaging with near-focus (JNET type 2B-low). (C) Complete circumferential incision of the lesion using a snare tip after submucosal injection. (D) Visual inspection of the iatrogenic polypectomy ulcer after snare-mediated mucosal resection of the lesion.

A retrospective single-center study evaluated the efficacy of EMR-P for colorectal lesions measuring > 20 mm (mean 22.3 ± 3.9 mm); it showed that EMR-P achieved high EBR (94.1%) and CRR (76.5%) [60]. Another retrospective study reviewed 523 non-pedunculated colorectal tumors measuring ≥ 20 mm that underwent ER; the respective EBR and CRR values were 42.9% and 32.9% for EMR (mean tumor size 21.7 ± 3.5 mm), 65.2% and 59.4% for EMR-P (23.5 ± 5.6 mm), and 92.7% and 87.6% for ESD (28.9 ± 12.7 mm) [61]. In a retrospective multicenter study of lesions measuring < 20 mm, the EMR-P group had significantly higher rates of EBR (98.0% vs. 85.7%, p = 0.004) and CRR (87.8% vs. 67.3%, p < 0.001) than the EMR group after propensity score matching; however, the mean procedure time was significantly longer (11.8 ± 7.5 vs. 2.8 ± 1.7 min, p < 0.001). For lesions measuring ≥ 20 mm, EMR-P had significantly higher EBR (88.6% vs. 48.5%, p < 0.001) and CRR (71.4% vs. 42.9%, p = 0.02), compared with EMR [62].

EMR-P tends to have a relatively higher probability of en bloc resection for lesions measuring ≥ 20 mm, compared with other modified EMR techniques. However, the EBR and CRR are lower for EMR-P than for ESD. The variation in EBR and CRR across studies suggests that endoscopist confidence and proficiency affect the outcome. Therefore, EMR-P could be considered for some T1 CRC lesions measuring ≥ 20 mm, depending on these factors.

ESD

ESD is an advanced ER technique used to remove large lesions with endoscopic knives, enabling en bloc resection regardless of tumor size. Colorectal ESD is typically indicated for lesions that require en bloc resection but may be challenging to manage with snare EMR [41]. EBR and CRR are significantly higher with ESD than with EMR [19], UEMR [52], ASEMR [59], or EMR-P for large colorectal lesions [60,61]. The EBR for ESD was not affected by lesion size. It remained consistently high (> 90%) in all subgroups; it was 92.8% for lesions measuring > 20 mm and 91.9% for lesions measuring > 30 mm [19] (Fig. 5). However, both EBR and CRR tend to be lower for ESD in non-Asian countries (81.2% and 71.3%, respectively) compared with Asian countries (93.0% and 85.6%, respectively) [63]. Recently, the use of pocket creation or traction-assisted ESD, which enhance submucosal layer exposure during submucosal dissection, has shown promising results for challenging cases, such as lesions with submucosal fibrosis, lesions requiring deep vertical margins, or instances of locally recurring/residual lesions [64-67].

Figure 5.

Endoscopic submucosal dissection (ESD). (A) A 70-mm granular nodular mixed laterally spreading tumor located in the rectosigmoid junction. (B) Most of the lesion had a regular vascular and surface pattern (JNET type 2A) on narrow-band imaging with near-focus, but the large nodule had an irregular and uniform vascular pattern (JNET type 2B-low). (C) Circumferential incision and submucosal dissection of the lesion using an endoscopic knife after submucosal injection. (D) Mucosal defect after completion of ESD. (E) Histopathological examination confirmed complete resection (R0) (70 × 55 mm villous adenoma with high-grade dysplasia).

Nonetheless, ESD has not been broadly adopted worldwide because of technical difficulties, long procedure time, and a high risk of complications [68-71]. In one meta-analysis, the overall perforation rate and delayed bleeding rate of ESD were 5.2% and 2.7%, respectively [63]. Another meta-analysis showed that ESD had a significantly higher perforation risk than EMR (pooled incidence 5.9% vs. 1.2%) [19].

Endoscopic full-thickness resection (EFTR)

EFTR is advantageous for efforts to secure a sufficient vertical-free margin for T1 CRC. Although it cannot be used to resect lymph nodes, its indications are identical to ESD. The most popular EFTR device is the full-thickness resection device (FTRD; Ovesco Endoscopy, Tübingen, Germany). In an analysis of data from the Multicenter Dutch EFTR registry that included consecutive EFTR procedures involving an FTRD for T1 CRC, the primary resection group (n = 132) had a median lesion size of 15 mm (12–16 mm); technical success was achieved in 89.4% of EFTR-amenable cases, whereas R0 resection was achieved in 82% of such cases. In the secondary treatment group, which included cases of previously incomplete ER (n = 198) with a median lesion size of 10 mm (7–15 mm), technical success was achieved in 85.4% of EFTR-amenable cases; R0 resection was achieved in 88.0% of such cases [72]. A meta-analysis of EFTR for colorectal lesions incorporated data from 14 studies involving 1,936 patients. The mean procedure duration was 45.4 ± 11.4 min. The pooled technical success rate was 87.6%, and the R0 resection rate was 78.8%. Procedure-associated adverse events occurred in 12.2% of cases, and the recurrence rate was 12.6% over a mean weighted follow-up of 20.1 ± 3.8 weeks. The R0 resection rate was significantly lower, and the overall procedural-associated adverse event rate was significantly higher, for lesions measuring > 20 mm than for lesions measuring ≤ 20 mm [73].

EFTR with an FTRD has a high success rate for primary treatment of T1 CRC tumors measuring < 20 mm, as well as cases with a history of incomplete ER or concomitant severe fibrosis.

Considerations based on current recommendations for curative resection

In cases of T1 CRC, DSI ≥ 1,000 µm (1 mm) is a controversial independent high-risk factor for LNM. In a study that involved 724 non-pedunculated T1 CRC lesions, the rate of LNM was 0% for DSI < 1,000 µm, whereas it was 12.5% for DSI ≥ 1000 µm; it subsequently increased (1,000 ≤ X < 1,500 µm: 11.5% LNM and 1,500 ≤ X < 2,000 µm: 12.2% LNM) [81]. Several studies have demonstrated that DSI ≥ 1,000 µm (odds ratio 2.1 to 5.4) is a risk factor for LNM in T1 CRC [80,84,85]. However, a recent meta-analysis of eight studies involving 1,146 patients revealed that DSI ≥ 1,000 µm was the sole risk factor for LNM in the absence of other histological high-risk factors, such as poor histological grade, lymphovascular invasion, or tumor budding; the results showed that the absolute risk of LNM for DSI ≥ 1,000 µm was 2.6% [86]. These findings suggest that DSI ≥ 1,000 µm in the absence of all other high-risk features is associated with a relatively low risk of LNM. Indeed, challenges are associated with the measurement of DSI [87]. These challenges include the deformed status of the muscularis mucosa and interobserver agreement regarding its status, with a kappa value of 0.67, indicating substantial but not perfect agreement [88].

Assessments of the resection margin are controversial. R0 resection is typically defined as the absence of tumor invasion within 1 mm of the transection line, whereas R1 resection is defined as the absence of tumor invasion within ≤ 1 mm. This criterion is based on findings that the risk of local residual or recurrent cancer is 0–2% in tumors with a free resection margin > 1 mm [82,89,90]; this risk increases to ≤ 16% in cases with a resection margin ≤ 1 mm [82,89]. However, recent evidence challenges this notion, demonstrating similar risks of residual disease in patients with free resection margins between 0.1 and 1 mm and patients with margins > 1 mm in the absence of other histological risk factors [91].

When piecemeal resection of T1 CRC results in a negative vertical margin but unclear lateral margin, in the absence of other histological high-risk factors for LNM, a difficult decision arises. The selection of secondary ER/EFTR, short-term surveillance, or additional surgery requires careful consideration because there is a lack of definitive information regarding residual disease. The JSCCR guideline recommends surgical resection when the vertical margin is positive. However, when piecemeal resection results in a positive horizontal margin, the guideline suggests endoscopic surveillance for approximately 6 months considering the increased risk of local recurrence [37].

When piecemeal resection is performed, especially in cases where only a single fragment exhibited malignancy, the resection margin could be accurately evaluated. However, most piecemeal resections hinder accurate histological assessment of submucosal or lymphovascular invasion. This limitation is particularly concerning in lesions classified as LST-NG, where piecemeal resection may not allow adequate analysis in cases of multifocal invasion [92,93]. Previous studies have demonstrated a significant association between EPMR and an increased risk of local recurrence [94-96]. Therefore, the Chinese national guidelines and general consensus recommend colectomy with regional lymph node dissection when the specimen is fragmented, which would limit pathological evaluation [97,98].

After piecemeal resection of T1 CRC, additional surgery should be prioritized. However, this decision can be individualized based on factors such as the estimated oncologic benefit of surgery, the operative risk, the endoscopist’s confidence in achieving complete resection, and the patient’s preferences.