| Literature DB >> 24822196 |
Dedrick Kok-Hong Chan1, Choon-Seng Chong1, Bettina Lieske1, Ker-Kan Tan1.
Abstract
Laparoscopic colectomy for colon cancer is a well-established procedure supported by several well-conducted large-scale randomised controlled trials. Patients could now be conferred the benefits of the minimally invasive approach while retaining comparable oncologic outcomes to the open approach. However, the benefits of laparoscopic proctectomy for rectal cancer remained controversial. While the laparoscopic approach is more technically demanding, results from randomised controlled trials regarding long term oncologic outcomes are only beginning to be reported. The impacts of bladder and sexual functions following proctectomy are considerable and are important contributing factors to the patients' quality of life in the long-term. These issues present a delicate dilemma to the surgeon in his choice of operative approach in tackling rectal cancer. This is compounded further by the rapid proliferation of various laparoscopic techniques including the hand assisted, robotic assisted, and single port laparoscopy. This review article aims to draw on the significant studies which have been conducted to highlight the short- and long-term outcomes and evidence for laparoscopic resection for rectal cancer.Entities:
Mesh:
Year: 2014 PMID: 24822196 PMCID: PMC4009228 DOI: 10.1155/2014/347810
Source DB: PubMed Journal: Biomed Res Int Impact factor: 3.411
Short-term outcomes.
| Trial | Type | Surgical method in comparison | Numbers | Mean/median lymph nodes harvested | CRM positivity | TME complete | Conversion to open (%) | Duration of intervention (min) | Blood loss (mL) | Length of hospital stay (days) | Morbidity within 28 days (%) | Mortality within 28 days (%) |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| CLASICC | Multicentre RCT-UK | Open versus laparoscopic assisted | 254 (O) versus 127 (L) | NA | 14 versus 16 (NA) | NA | 34% | 135 versus 180 (no significance calculated) | NA | 13 versus 11 (no significance calculated) | 40 versus 37 | NA |
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| COREAN | Multicentre RCT—South Korea | Open versus laparoscopic assisted | 170 versus 170 | 18 versus 17 | 4.1 versus 2.9 (1 mm from margin) | 74.7 versus 72.4 | 1.20% | 197 versus 245* | 217.5 versus 200* | 9 versus 8 | 23.5 versus 21.2 | 0 versus 0 |
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| COLOR II | Multicentre RCT—30 centres in 8 countries | Open versus laparoscopic assisted | 364 versus 739 | 14 versus 13 | 10 versus 10 (2 mm from margin) | 92 versus 88 | 17% | 188 versus 240* | 400 versus 200* | 9 versus 8 | 37 versus 40 | 2 versus 1 |
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| Lujan et al. | Multicentre non randomised-72 centres in Spain | Open versus laparoscopic assisted | 3018 versus 1387 | 14.75 versus 14.53 | 16.3 versus 9.5 (1 mm from margin)* | 75.6 versus 82.4 | 17.37% | 186.38 versus 217.83* | NA | 11 versus 8* | 45.6 versus 38.3* | 3.6 versus 1.2* |
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| Lujan et al. | Single centre RCT-Spain | Open versus laparoscopic assisted | 103 versus 101 | 11.6 versus 13.6 | 2.9 versus 4.0 (1 mm from margin) | NA | 7.90% | 172.9 versus 193.7 | 234.2 versus 127.8 | 9 versus 8 | 33.0 versus 33.7 | 2.9 versus 1.9 |
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| Ng et al. | Single centre RCT-HK | Open versus laparoscopic APR | 48 versus 51 | 13 versus 12.4 | 4.2 versus 5.9 (NA) | NA | 9.80% | 163.7 versus 213.5 | 555.6 versus 321.7 | 11.5 versus 10.8 | 52.1 versus 42.1 | 2.8 versus 2.5 |
*P < 0.05.
Long-term outcomes-oncological.
| Trial | Type | Surgical method in comparison | Numbers | Median follow-up period (months) | Local recurrence | Neoadjuvant therapy administered | Disease-free survival (months) | Median overall survival (months) |
|---|---|---|---|---|---|---|---|---|
| CLASICC | Multicentre RCT—UK | Open versus laparoscopic assisted | 254 (O) versus 127 (L) | 62.9 in both arms | NA | Not controlled | 67.1 versus 70.8 | 65.8 versus 82.7 |
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| Lujan et al. | Single centre RCT—Spain | Open versus laparoscopic assisted | 103 versus 101 | 34.1, 32.8 | 5.3 versus 4.8 | 77 versus 73, no statistical significance | 81.0 versus 84.8 | 75.3 versus 72.1 |
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| Ng et al. | Single centre RCT—UK | Open versus laparoscopic assisted | 142 versus 136 | 136.6, 124.5 | 9.3 versus 5.5 | Neoadjuvant not included in trial | ∗ | + |
*Trial calculated probability of being disease-free at 15 years, 71.4% versus 79%.
+Trial calculated probability of overall survival at 15 years, 51.4% versus 47.4%.
Open versus HAL [28].
| Open | HALS | |
|---|---|---|
| Incision length (cm) | 17 ± 2* | 6 ± 1* |
| Procedure time (min) | 140 ± 20* | 161 ± 35* |
| Surgical blood loss (mL) | 380 ± 85* | 310 ± 96* |
| Hospital stay (days) | 15 ± 3* | 12 ± 2* |
| Complications | 9 | 5 |
| Pathological | ||
| Median lymph nodes resected | 15 | 16 |
| Median length of distal margin | 2 | 2 |
| Number of specimens with involved | 0 | 0 |
*P < 0.05.
Comparison of HALS versus standard laparoscopic approach.
| Surgical method | Trial | Numbers | Estimated blood loss (mL) | Operating time (min) | Hospitalisation stay | Complications (%) | Number of LN harvested | Distal tumour margin (cm) | CRM | Involved CRM |
|---|---|---|---|---|---|---|---|---|---|---|
| Standard laparoscopic |
Tjandra et al. | 31 | 152.9 | 188.2 | 5.8 | 25.8 | 17.4 | 2.6 | 8.3 | 1 |
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| HALS |
Tjandra et al. | 32 | 158.1 | 169.8 | 5.9 | 21.9 | 17.4 | 2.6 | 8.5 | 1 |
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| HALS |
Pendlimari et al. | 129 | 250 | 204 | 5 | 3 | ∗ | ∗ | ∗ | ∗ |
*Pendlimari et al.'s [31] analysed results for both rectal and colon cancers. No subdivision was made between the two types and hence cannot be accurately reflected here.
Open versus standard laparoscopic versus RAS [43].
| Open | Laparoscopic | RAS | |
|---|---|---|---|
| Procedure time (min) | 252.6* | 277.8* | 309.7* |
| Surgical blood loss (mL) | 275.4* | 140.1* | 133* |
| Hospital stay (days) | 16* | 13.5* | 10.8* |
| Complications (%) | 24.8 | 27.9 | 20.6 |
| Pathological | |||
| Median lymph nodes resected | 17.4 | 15.6 | 15 |
| Median length of distal | 2.2 | 2 | 1.9 |
| Number of specimens with | 17 | 11 | 7 |
*P < 0.05.