| Literature DB >> 32606963 |
Chao Lu1,2,3, Weiwei Jin1,2, Yiping Mou1,2, Hongliang Shao4, Xiaosan Wu4, Shaodong Li5, Biwu Xu4, Yuanyu Wang1,2, Qicong Zhu1,2, Tao Xia1,2, Yucheng Zhou1,2,3.
Abstract
BACKGROUND: Gastrointestinal stromal tumors (GIST) of the duodenum are rarely reported and optimal minimally invasive management has not been well proposed. Pancreaticoduodenectomy and different types of pancreas-sparing duodenectomy can be chosen; however, which to choose and its corresponding clinical outcomes and oncological concerns remain controversial. PATIENTS AND METHODS: Patients diagnosed with GIST of duodenum underwent laparoscopic pancreaticoduodenectomy (L-PD) or pancreas-sparing duodenectomy (L-PSD) in Zhejiang Provincial People's Hospital were enrolled. All prospectively maintained data were analyzed retrospectively. Patients were grouped into the L-PD group or the L-PSD group, and the clinical outcomes and oncological outcomes were analyzed.Entities:
Keywords: GIST; duodenum; pancreas-sparing duodenectomy; pancreaticoduodenectomy
Year: 2020 PMID: 32606963 PMCID: PMC7310982 DOI: 10.2147/CMAR.S254972
Source DB: PubMed Journal: Cancer Manag Res ISSN: 1179-1322 Impact factor: 3.989
Figure 1Flow diagram and indication for laparoscopic pancreaticoduodenectomy (L-PD) or laparoscopic pancreas-sparing duodenectomy (L-PSD) for duodenal GISTs.
Figure 2For lesions adjacent to papilla, laparoscopic pancreaticoduodenectomy was indicated and performed (A). The blue spot represented the duodenal GISTs. (B) Shows the resected specimen with ulcerative lesions in the same side of papilla.
Figure 3Laparoscopic pancreas-sparing duodenectomy (L-PSD) for supra-ampulla lesions. Diagnostic endoscopy was used to exclude possibility of endoscopic resections (A) and marking the tumor location to papilla (B). Supra-ampulla duodenum was gradually separated from the pancreas (C), and the distal margin was transected without stapler for preserving the ampulla intact (D). With the guidance of catheter along the common bile duct (E), intraoperative cholangiogram (IOC, 3F) was also performed to locate the papilla. With the help of catheter, the opening was closed without injury the papilla (G). (H) Shows the trocar distribution and the specimen.
Figure 4Laparoscopic pancreas-sparing duodenectomy (L-PSD) for infra-ampulla lesions. Lesions located in the 3rd part of duodenum (A). After clamping the pre-set margin (B), before transection by stapler, IOC was performed to confirm the papilla intact. (C and D) Show the trocar distribution and the resected specimen, respectively.
Demographic and Clinico-Pathological Characteristics for 22 Duodenal GISTs
| All Patients (n=22) | n (%) |
|---|---|
| Sex | 22 |
| Male | 11 (50%) |
| Female | 11 (50%) |
| Age (Median) | 58.2±9.5 (60.5) |
| Symptoms | |
| Gastrointestinal bleeding | 12 (54.5%) |
| Abdominal pain | 6 (27.2%) |
| Asymptomatic | 4 (18.2%) |
| Tumor Site | |
| D1 (1st portion of duodenum) | 2 (9.1%) |
| D2 (2nd portion of duodenum) | 13 (59.1%) |
| D3 (3rd portion of duodenum) | 6 (27.3%) |
| D4 (4th portion of duodenum) | 1 (4.5%) |
| Tumor Size | |
| | 4 (18.2%) |
| 2< | 12 (54.5%) |
| 5cm< | 4 (18.2%) |
| | 2 (9.1%) |
| Surgical management | |
| Laparoscopic pancreaticoduodenectomy (L-PD) | 13 (59.1%) |
| Laparoscopic pancreas-sparing duodenectomy (L-PSD) | 9 (40.9%) |
| Supra-ampulla L-PSD | 4 (18.2%) |
| Infra-ampulla L-PSD | 5 (22.7%) |
| Risk stratification of NIH criteria | |
| Very low risk | 4 (18.2%) |
| Low risk | 10 (45.4%) |
| Intermediate risk | 0 (0%) |
| High risk | 8 (36.4%) |
| Mitotic count | |
| ≤5/50HPF | 20 (91%) |
| >5/50HPF | 2 (9%) |
| Adjuvant Imatinib | 7 (31.8%) |
Clinico-Pathological Detail and Follow-Up of All L-PDs
| Case | Sex/Age | Symptom | Size (cm) | Location | Mitotic Count | Risk | Adjuvant Imatinib | OS | |
|---|---|---|---|---|---|---|---|---|---|
| Opposite | Sup./Inf. | ||||||||
| 1 | M/64 | Asymptomatic | 2.5 | No | Adjacent | 2/50HPF | Low | No | 81.9 months |
| 2 | M/58 | GI Bleeding | 3 | No | Inferior | 1/50HPF | Low | No | 76.2 months |
| 3 | M/42 | GI Bleeding | 3 | No | Adjacent | 5/50HPF | Low | No | 69.7 months |
| 4 | M/70 | GI Bleeding | 3 | No | Superior | 1/50HPF | Low | No | 54.5 months |
| 5 | F/59 | Pain | 8 | Yes | / | 2/50HPF | High | Yes | 54.5 months |
| 6 | M/56 | GI Bleeding | 5.5 | No | / | 2/50HPF | High | Yes | 53.9 months |
| 7 | F/63 | GI Bleeding | 4.2 | No | Adjacent | 7/50HPF | High | Yes | 45.7 months |
| 8 | F/36 | GI Bleeding | 12 | No | / | 4/50HPF | High | Yes | 41.8 months* |
| 9 | M/68 | Asymptomatic | 16 | No | / | 2/50HPF | High | No | Mortality |
| 10 | F/60 | GI Bleeding | 6 | No | Adjacent | 4/50HPF | High | Yes | 22.6 months |
| 11 | F/67 | Asymptomatic | 1.5 | No | Adjacent | 1/50HPF | Very Low | No | 12.0 months |
| 12 | F/61 | GI Bleeding | 2 | No | Adjacent | 1/50HPF | Very Low | No | 17.5 months |
| 13 | M/52 | Pain | 7 | No | Adjacent | 2/50HPF | High | Yes | 16.5 months |
Note: *Hepatic metastasis ocurred 36months after surgery, followed by sunitinib.
Clinico-Pathological Detail and Follow-Up of All L-PSDs
| Case | Sex/Age | Symptom | Size (cm) | Location to Ampulla | Mitotic Count | Risk | Adjuvant Imatinib | OS | |
|---|---|---|---|---|---|---|---|---|---|
| Opposite | Sup./Inf. | ||||||||
| 1 | F/63 | GI Bleeding | 1.6 | Yes | Superior | 5/50HPF | Very low | No | 53.1 months |
| 2 | M/59 | GI Bleeding | 3.0 | Yes | Inferior | 8/50HPF | High | Yes | 50.8 months |
| 3 | F/71 | Pain | 2.0 | Yes | Superior | 2/50HPF | Very Low | No | 44.6 months |
| 4 | M/46 | Pain | 3.3 | Yes | Superior | 1/50HPF | Low | No | 30.3 months |
| 5 | F/50 | Pain | 4.0 | Yes | Inferior | 1/50HPF | Low | No | 24.2 months |
| 6 | M/66 | Asymptomatic | 4.0 | Yes | Inferior | 1/50HPF | Low | No | 25.3 months |
| 7 | F/65 | GI Bleeding | 2.5 | Yes | Superior | 2/50HPF | Low | No | 14.9 months |
| 8 | F/44 | Pain | 4.6 | Yes | Inferior | 4/50HPF | Low | No | 14.5 months |
| 9 | M/61 | GI Bleeding | 3 | Yes | Inferior | 4/50HPF | Low | No | 14.0 months |
Peri-Operative Outcomes and Postoperative Complications
| Operative Outcomes and Complications | n (%) | ||
|---|---|---|---|
| L-PD Group | L-PSD Group | ||
| Operative time (min) | 364.2±58.7 | 230.0±12.3 | <0.001 |
| Blood loss (mL) | 176.9±85.7 | 61.1±18.2 | <0.001 |
| Blood transfusion (n) | 3(23.1%) | 0(0%) | 0.36 |
| Intensive care unit stay (n) | 2(15.4%) | 0(0%) | 0.63 |
| Retrieved lymph nodes | 11.6±7.2 | 1.3±2.0 | <0.001 |
| Metastatic lymph nodes | 0 | 0 | 1.00 |
| Postoperative complications | 8 (61.6%) | 1 (11.1%) | 0.02 |
| Minor complications (Grade I/II*) | 4 (30.8%) | 1 (11.1%) | |
| Biochemical POPF (Grade I) | 2 (15.4%) | 0 | |
| Grade A Bile leakage with draining (Grade II) | 1 (7.7%) | 0 | |
| Grade A Hemorrhage (Grade II) | 1 (7.7%) | ||
| Delayed gastric emptying (Grade II) | 0 (0%) | 1 (11.1%) | |
| Major complications (Grade III/IV/V*) | 4 (30.8%) | 0 (0%) | |
| Grade B POPF with drainage (Grade IIIa) | 1 (7.7%) | 0 | |
| Grade B Bile leakage with drainage (Grade IIIa) | 1 (7.7%) | 0 | |
| Grade C POPF with reoperation (Grade IIIb) | 2 (15.4%) | 0 | |
| Grade C POPF leading to death (Grade V) | 1 (7.7%) | 0 | |
| Late hepaticojejunostomy stricture | 1 (7.7%) | 0 (0%) | 0.84 |
| Reoperation | 3 (23.1%) | 0 (0%) | 0.36 |
| Mortality | 1 (7.7%) | 0 (0%) | 0.85 |
| Length of hospital stay (day, Median) | 20.6±11.1 (16) | 10.9±3.8 (10) | 0.021 |
Note: *Refer to Clavien-Dindo Classification of surgical complications.
Figure 5Overall survival (A) and disease-free survival (B) of patients underwent L-PD and L-PSD.