SYSTEMATIC REVIEW article

Front. Surg., 11 October 2022

Sec. Surgical Oncology

Volume 9 - 2022 | https://doi.org/10.3389/fsurg.2022.989065

Meta-analysis of robotic versus open pancreaticoduodenectomy in all patients and pancreatic cancer patients

  • 1. Department of General Surgery, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China

  • 2. Clinical Immunology Center, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China

Abstract

Purposes:

To compare perioperative outcomes of robotic pancreaticoduodenectomy (RPD) to open pancreaticoduodenectomy (OPD) using evidence from cohort studies.

Methods:

Outcomes of interest include operative time, blood loss, R0 resection rate, lymph nodes harvested, overall complication rate, pancreatic fistula rate, delayed gastric emptying rate and 90-day mortality.

Results:

6 prospective studies and 15 retrospective studies were included. Five of these studies were limited to patients with pancreatic cancer. Operative time was significantly longer in RPD (WMD: 64.60 min; 95% CI: 26.89 to 102.21; p = 0.001). Estimated blood loss was lower in RPD (WMD: −185.44 ml; 95% CI: −239.66 to −131.21; p < 0.001). Overall complication rates (OR: 0.66; 95% CI: 0.44 to 0.97; p < 0.001) and pancreatic fistula rate (OR: 0.67; 95% CI: 0.55 to 0.82; p < 0.001) were both lower in RPD. Length of hospital stay was longer in OPD (WMD: −1.90; 95% CI: −2.47 to −1.33). 90-day mortality was lower in RPD [odds ratio (OR): 0.77; 95% CI: 0.45 to 0.95; p = 0.025].

Conclusion:

At current level of evidence, RPD is a safer alternative than OPD with regard to post-operative outcomes and blood loss. However, in terms of oncological outcomes RPD show no advantage over OPD, and the cost of RPD was higher. In general, RPD is now considered a reliable technology, but high-quality randomized controlled trial (RCT) studies are still needed to support this conclusion.

1. Introduction

Pancreaticoduodenectomy (PD) has been universally accepted to be indicated in benign or malignant lesions of the pancreatic head, duodenum, and distal common bile duct. In 1994, Gagner reported the first laparoscopic pancreaticoduodenectomy, since when minimally invasive pancreaticoduodenectomy (MIPD) are increasingly being performed over the world (1). The development of the Da Vinci robotic platform takes MIPD a step further. Laparoscopic surgery has some shortcomings compared to robotic surgery, including limited vision and flexibility. And this contributed to the popularity of robotic surgery over the world (2). The first case of robotic-assistant pancreaticoduodenectomy (RAPD) was reported in 2007, and since then many studies have compared the safety and efficacy between open pancreaticoduodenectomy (OPD) and robotic pancreaticoduodenectomy (RPD). There have been several meta-analyses evaluating the effect between OPD and RPD. However, robotic surgery technology developed rapidly in these years, and the studies used in the existing meta-analyses are not new enough. Therefore, we focused on those studies published in the last 5 years (in or after 2016) to provide high-quality evidence for further clinical practice.

2. Methods

2.1. Literature-search strategy

A systematic review of the literature was performed in PubMed and Web of Science from January 2016 to October 2021. These key words were used: robot, robotic, robotic-assisted, open, and pancreaticoduodenectomy. Studies included should fulfill the following PICOS criteria in our meta-analyses. P (patients): Male or female patients with a benign or malignant disease that requires elective PD; I (intervention): RPD; C (control): OPD; O (outcome): At least 1 of the interested outcomes; S (study design): randomized controlled trials (RCTs) and observative studies.

References of the acquired articles were manually searched to broaden the search. When multiple researches describing the same population were published, the most complete or recent research was used.

2.2. Inclusion and exclusion criteria

The inclusion criteria were as followed: (1) comparative study of RPD and OPD; (2) papers written in English; (3) papers published in or after 2016. Abstracts, case reports, reviews, letters to the editor, non-comparative studies, and articles without available data were excluded.

2.3. Data extraction and outcome of interest

All references were reviewed and evaluated by two researchers independently. Only full-length articles were eligible for extraction. The following data of included articles were extracted: first author, year of publication, study design, number of operated subjects, operative time, blood loss, R0 resection rate, lymph nodes harvested, overall complication rate, pancreatic fistula rate, delayed gastric emptying and 90-day mortality.

2.4. Quality assessment

The Newcastle–Ottawa Scale (NOS) was used to evaluate the methodological quality of non-randomized studies. Scores of each observational study range from 0 to 9, and studies having six or more stars were considered to be high-quality studies.

2.5. Statistical analysis

This meta-analysis was performed using Stata MP 16.0 software. The odds ratios (OR) and the weighted mean difference (WMD) with a 95% confidence interval (95% CI) were used to estimate dichotomous and continuous variables, respectively. p < 0.05 was considered statistically significant. For studies that reported continuous data as median and range values (or quartile and median), the standard deviations were calculated using the method described by Luo et al. (3). Heterogeneity was evaluated by the Chi-square test, and p < 0.100 was considered significant. I2 values were used for the evaluation of statistical heterogeneity. An I2 value of 50% or more indicated the presence of heterogeneity. The fixed effect model (FEM) and random effect model (REM) were used based on the value of I2. FEM was used in the case of I2 < 50% while REM was adopted in the case of I2 > 50%.

3. Result

3.1. Literature-search results

The first search strategy generated 518 studies. 21 articles including 5,756 patients (2,561 cases for RPD and 3,285 cases for OPD) fulfilled the predefined inclusion criteria and were included in this meta-analysis (4–24). All studies were non-RCTs, of which 6 studies were prospective while 15 studies were retrospective. The selection process is shown in Figure 1.

Figure 1

3.2. Study characteristics and quality assessment

The study characteristics and study quality are shown in Table 1. We screened articles published in 2016 and beyond. This is a worldwide meta-analysis, in which eight articles are from America, six articles are from China, four articles are from Italy, two articles are from Korea, and one article is from Spain. In most studies the robotic surgery group carried out RPD, while in four studies RAPD were used, where robots were only involved in some parts of the surgery. In five studies patients were limited to pancreatic cancer, while in other studies the indication for surgery were wide, including benign and malignant disease. All the studies were of high quality according to the Newcastle–Ottawa Scale (NOS) (Supplementary Table S1).

Table 1

ArticleCountryDesignNumber of patients (robotic)Number of patients (open)Quality scoreRobotic techniqueIndication for surgery (benign or malignant disease)
Emanuele 2018ItalyRetrospective24266RPDM
Hassan 2021AmericaRetrospective3103108RPDM
Shyr 2021ChinaProspective65656RPDM
Maria 2020AmericaRetrospective38387RPDM
Weng 2020ChinaRetrospective1052108RAPDM
Amer 2016AmericaRetrospective2118176RPDB/M
Matthew 2016AmericaRetrospective1521527RPDB/M
Mejia 2020AmericaRetrospective102546RPDB/M
Wang 2018ChinaProspective87878RPDB/M
Kim 2018KoreaRetrospective511867RPDB/M
Varley 2018AmericaRetrospective1331497RPDB/M
Cai 2019AmericaProspective4604058RPDB/M
Paolini 2021ItalyRetrospective65536RPDB/M
Benedetto 2018SpainProspective17177RPDB/M
Marino 2019ItalyProspective35358RAPDB/M
Shi 2021ChinaRetrospective1871878RAPDB/M
Bencini 2020ItalyRetrospective35358RPDB/M
Hyeyeon 2020KoreaRetrospective55557RAPDB/M
Oosten 2020AmericaRetrospective961928RPDB/M
Shyr 2020ChinaRetrospective2841696RPDB/M
Wang 2021ChinaProspective49437RPDB/M

Characteristics of the included studies and quality assessment.

Patients’ baseline characteristics are summarized in Table 2.

Table 2

ArticleAge (years)
Gender (male) (%)
BMI
Tumor diameter (cm)
Preoperative CA 199
RPDOPDRPDOPDRPDOPDRPDOPDRPDOPD
Emanuele 201865 (58.5–74.75)72.5 (59.75–78.75)50.054.123.1 ± 3.224.1 ± 3.12.7 ± 0.62.7 ± 0.9353.3 ± 528.61362.7 ± 4497
Hassan 202166 ± 21.368.1 ± 19.350.151.1NMNMNMNMNMNM
Shyr 202166 ± 1366 ± 1152.340.024 ± 422 ± 33.1 ± 0.83.1 ± 0.7NMNM
Maria 202066 (38–84)a68 (42–81)a42.142.124.7 (19.6–39.1)a25.7 (15.8–44.8)a3 (0.5–6)a2.9 (0.9–7)aNMNM
Weng 202063 (57–68)64 (58–70)61.765.922.8 ± 2.822.6 ± 3.13 (2.2–3.5)3.0 (2.3–3.8)144.4 (40.1–375.4)153.4 (46.0–505.2)
Amer 201667 (15–86)a65 (15–93)a52.955.527.5 (18.1–47.6)a26.1 (14.7–85.5)a2.5 (0.1–26.0)a2.9 (0–5.0)aNMNM
Matthew 2016NMNMNMNMNMNMNMNMNMNM
Mejia 202066 ± 10.661.7 ± 14.15255.6NMNM3.4 ± 1.63.7 ± 2.1NMNM
Wang 2018NMNM5056.7NMNMNMNMNMNM
Kim 201860.7 ± 11.965.4 ± 10.147.158.122.7 ± 2.524.0 ± 3.1NMNMNMNM
Varley 201866.3 ± 10.667.0 ± 10.5485327.5 ± 6.126.7 ± 5.6NMNMNMNM
Cai 201966.5 ± 11.067.5 ± 10.75552.127.8 ± 5.827.2 ± 5.9NMNMNMNM
Paolini 202170 (42–85)a73 (45–91)a50.953.826 (17–33)a23 (14–33)a2.3 (0.7–6)a2.5 (0.6–8.2)a85.0 (1.6–1,617.0)a132.3 (1.6–91,000.0)a
Benedetto 201866.8 ± 9.561.4 ± 11.947.158.823.8 ± 4.124.6 ± 3.3624.1 ± 5.424.8 ± 6.1NMNM
Marino 201960.4 (43–72)a62.3 (45–73)a54.342.923.8 (19.4–30.9)a23.5 (18.8–28.1)a2.35 (1.6–3.4)a2.22 (1.2–3.5)aNMNM
Shi 202160.9 ± 11.460.1 ± 10.858.357.2NMNM2.7 ± 1.12.7 ± 1.3NMNM
Bencini 202070.5 (42–85)a69 (50–88)a56.345.726 (18–32)a24 (18–38)a30 (18–40)a37 (2–51)a143 (2–1,617)a70 (2–2,617)a
Hyeyeon 202058.6 ± 8.359.9 ± 13.447.354.523.7 ± 2.823.9 ± 3.62.6 ± 1.22.6 ± 1.8NMNM
Oosten 202067 (60–73)67 (58–73)NMNM26 (23–30)27 (23–29)NMNMNMNM
Shyr 202065 ± 1264 ± 1153.353.524 ± 423 ± 33.2 ± 1.53.7 ± 2.5NMNM
Wang 202164.7 ± 11.864.8 ± 11.651.953.427.7 ± 5.627.4 ± 5.8NMNMNMNM

Comparison of patients’ baseline characteristics in robotic vs. open pancreaticoduodenectomy.

BMI, body mass index; expressed in mean ± SD and median (IQR).

a

Expressed in median (range).

3.3. Meta-analysis results

All 21 studies were included in this meta-analysis. The summarized result of meta-analysis is shown in Table 3.

Table 3

OutcomesStudies, nRPDOPDWMD/OR (95% CI)p valueHeterogeneity
I2Tau2
Intraoperative outcomes
 Operative time171,9242,69064.60 (26.89 to 102.21)0.0010.978
 Estimated blood loss141,6041,583−185.44 (−239.66 to −131.21)<0.0010.927
Oncological outcomes
 Lymph nodes harvested131,3371,6991.13 (−0.27 to 2.54)0.1150.8284.69
 R0 resection109551,0261.02 (0.79 to 1.30)0.8890n
Post-operative outcomes
 Overall complication rates131,1921,8560.66 (0.44 to 0.97)<0.0010.7620.3524
 Pancreatic fistula131,9382,1040.67 (0.55 to 0.82)<0.0010.269n
 Length of stay202,4963,220−1.90 (−2.47 to −1.33)<0.0010.6850.6432
 90-day mortality121,8412,5910.77 (0.45 to 0.95)0.0250.038n

Outcomes of the included studies.

3.3.1. Intraoperative outcomes

3.3.1.1. Operative time

Operative time was reported in 17 studies (1,924 RPD vs. 2,690 OPD). According to the results of this meta-analysis, operative time was significantly longer in RPD group (WMD: 64.60 min; 95% CI: 26.89 to 102.21; p = 0.001), with high heterogeneity (I2 = 97.8%; Tau2 = 2133.45) in the REM (Figure 2A).

Figure 2

3.3.1.2. Estimated blood loss

Estimated blood loss was reported in 14 studies (1,604 RPD vs. 1,583 OPD) and was significantly lower in RPD (WMD: −185.44 ml; 95% CI: −239.66 to −131.21; p < 0.001) with high among-study statistical heterogeneity (I2 = 92.7%; Tau2 = 3152.37) (Figure 2B).

3.3.2. Oncological outcomes

3.3.2.1. Lymph nodes harvested

13 studies reported the results of lymph nodes harvested (1,337 RPD vs. 1,699 OPD). No statistically significant differences were found between the two groups (WMD: 1.13; 95% CI: −0.27 to 2.54; p = 0.115), with a high heterogeneity (I2 = 82.8%, Tau2 = 4.69) in the REM (Figure 3A).

Figure 3

3.3.2.2. Lymph nodes harvested (in pancreatic cancer)

Four studies reporting the results of lymph nodes harvested are limited in pancreatic cancer patients (518 RPD vs. 623 OPD). No statistically significant differences were found between the two groups (WMD: 0.4; 95% CI: −0.59 to 1.40; p = 0.425), with a low heterogeneity (I2 = 0%) in the FEM (Figure 3B).

3.3.2.3. R0 resection

Ten studies reported the results of lymph nodes harvested (955 RPD vs. 1,026 OPD). No statistically significant differences were found between the two groups (OR: 1.02; 95% CI: 0.79 to 1.30; p = 0.889), with a low heterogeneity (I2 = 0%) in the FEM (Figure 3C).

3.3.3. Post-operative outcomes

3.3.3.1. Overall complication rates

Overall complication rate was reported in 13 studies (1,192 RPD vs. 1,856 OPD) and was significantly lower in RPD (OR: 0.66; 95% CI: 0.44 to 0.97; p < 0.001) with high among-study statistical heterogeneity (I2 = 76.2%; Tau2 = 0.3524) in the REM (Figure 4A).

Figure 4

3.3.3.2. Pancreatic fistula

Pancreatic fistula was reported in 13 studies (1,938 RPD vs. 2,104 OPD) and was significantly lower in RPD (OR: 0.67; 95% CI: 0.55 to 0.82; p < 0.001) with low among-study statistical heterogeneity (I2 = 26.9%) in the FEM (Figure 4B).

3.3.3.3. Delayed gastric emptying

Thirteen studies reported the results of delayed gastric emptying (1,055 RPD vs. 1,257 OPD). No statistically significant differences were found between the two groups (OR: 0.67; 95% CI: 0.38 to 1.18; p = 0.165), with a high heterogeneity (I2 = 51.3%, Tau2 = 0.4918) in the REM (Figure 4C).

3.3.3.4. Length of stay

20 studies reported the data of length of stay (2,496 RPD vs. 3,220 OPD). The meta-analysis showed OPD has significant longer length of stay than RPD (WMD: −1.90; 95% CI: −2.47 to −1.33; p < 0.001), with a high heterogeneity (I2 = 68.5%, Tau2 = 0.6432) in the REM (Figure 4D).

3.3.3.5. 90-day Mortality

12 studies reported the data of 90-day mortality (1,841 RPD vs. 2,591 OPD). The meta-analysis showed RPD has significant lower 90-day mortality than OPD (OR: 0.65; 95% CI: 0.45 to 0.95; p = 0.025), with a low heterogeneity (I2 = 3.8%) in the FEM (Figure 4E).

4. Discussion

Since first RAPD was reported in 2007, RPD technology has developed rapidly. With the improvement of equipment and doctors gradually through the learning curve, the safety and efficiency of RPD comparing to OPD is gradually improved. Hence, the relevant research results have timeliness. Therefore, although there have been previous meta-analyses comparing clinical outcomes between OPD and RPD, these meta-analyses contained some former studies and can't sufficiently represent current situation. So, we screened articles published after 2016 in our meta-analyses and contained several new studies in this year in order to show the latest RPD development as far as possible.

4.1. Findings in our meta-analyses

According to the result of our meta-analysis, RPD has a longer operative time and lower blood loss comparing to OPD, which is also supported by previous researches. As a significant advantage of robotic surgery, RPD showed a lower blood loss. And it may be explained by high-quality three-dimensional (3-D), optical 10–15 magnification vision, and greater precision (25). Multiple factors may lead to the longer operative time in RPD. On one hand, the long time for preparation of machine before operation resulted in a longer operative time. On the other hand, surgeons in these studies not passing through the learning curve may also contribute to longer operative time. What deserve attention is that the result of operative time and estimated blood loss showed high heterogeneity. According to the forest plot of operative time (Figure 2A), most studies raised up that operative time was higher in RPD group, but four studies reached the opposite conclusion (7, 14, 15, 19). Many factors can affect the operation time, of which the most important factor is the proficiency of the surgeon. In addition, the equipment of the center and the surgery team also influence the operative time. The heterogeneity of estimated blood loss was also high (I2 = 0.927). One study showed obvious different conclusion comparing with other studies (7). It's obvious that the exclusion of this study will not influence the conclusion of our article. Blood loss can be affected by the proficiency of the surgeon and the condition of the patients (e.g., the location and kind of cancer).

Lymph nodes harvested and margin status are considered to be consistent with prognosis of pancreatic cancer. Although various methods of margin quantification in different studies increase the complexity to assessment, margin status is still recognized to have prognostic significance for overall survival of pancreatic ductal adenocarcinoma (PDAC) in PD (26). Similarly, the number of lymph nodes harvested also plays a role in the reveal of prognostic performance (27). Historically, a mass of researches on OPD and RPD compared their differences in margin status, and previous meta-analysis also counted the oncological outcomes of the two groups. Except the meta-analysis of Dong et al. demonstrated that the RPD group has a larger number of lymph nodes harvested and a lower resection margin involvement rate, another two meta-analyses early and this meta-analysis all reveal that there is no difference of those oncological outcomes in the two groups (28–30). The heterogeneity of lymph nodes harvested and overall complication rate is high. The composition of patients’ tumor varies in different studies, which may lead to the heterogeneity of lymph nodes harvested. Besides, different operation centers may have different diagnostic criteria and definition for post-operative complications, causing the heterogeneity of overall complication rate.

Furthermore, we analyzed the oncological outcomes in studies limited to pancreatic cancer. Five studies analyzed patients with only pancreatic cancer, and other studies contained patients with kinds of disease which accepted RPD or OPD. In most studies, patients accepted PD because of different diseases, including pancreatic cancer, ampullary adenocarcinoma, and neuroendocrine tumor. Obviously, the malignancy of these tumors is different, reducing the credibility of the comparison of the prognosis indicator between OPD and RPD.

Of the five studies limited to pancreatic cancer, four involved lymph nodes harvested, and analysis of these four articles also showed no difference in RPD and OPD groups. Only two articles limited in pancreatic cancer mentioned R0 resection which is too few to analyze. Comparing the results of the two meta-analyses, no different conclusions were reached.

The safety of RPD has been proved in previous studies. As expected, our meta-analysis revealed that clinical outcomes favor RPD, including overall complication rates, pancreatic fistula rate, and length of hospital stay. Besides, different from the previous meta-analysis, this meta-analysis demonstrated that 90-day mortality also favors RPD.

4.2. Strengths

The safety and efficiency of RPD comparing to OPD is gradually improved, owing to the improvement of equipment and doctors gradually through the learning curve. This is the latest meta-analyses that included all eligible studies published in these 5 years. The number of studies is one strength of our article. Furthermore, to our knowledge, this is the first meta-analyses and systematic review that included all studies limited to patients with pancreatic cancer.

4.3. Limitations

Although we found 5 studies researching RPD and OPD in pancreatic cancer patients, most studies mix patients with various diseases together for analysis, making it impossible to conduct subgroup analysis. Besides, lack of RCTs in our meta-analysis is another limitation.

4.4. Implications for clinical practice

This meta-analysis found that RPD showed lower blood loss, overall complication rates, pancreatic fistula, and 90-day mortality compared with OPD. Besides, length of hospital stay was shorter in RPD. Although the operative time is longer in RPD group, and there were no differences in R0 resection and lymph nodes harvested, RPD has shown benefits over OPD and seemed to be proposed as an equivalent alternative to OPD. However, all the current studies about OPD and RPD are not RCTs, and high-quality studies are still needed. In addition, centers with the ability to perform a sufficient number of surgeries and professional surgeons who have overcome the learning curve are essential for successful implementation of RPD. What's more, RPD costs much higher than OPD, which is also an important factor in the choice of surgical methods.

Statements

Data availability statement

The original contributions presented in the study are included in the article/Supplementary Material, further inquiries can be directed to the corresponding author/s.

Author contributions

Conception and design of the work: YF and JQ. Data acquisition and analysis: YF and YY. Interpretation of the data: YF and YY. Drafting the manuscript: YF and JQ. Critical revision of the manuscript: YY and DW. Agreement to be accountable for all aspects of the work: YF, JQ, YY, DW, and TZ. All authors contributed to the article and approved the submitted version.

Funding

This study was supported by grants from the National Key R/D Program of China (2018YFE0118600); National Natural Science Foundation of China (No. 81972258); National Multidisciplinary Cooperative Diagnosis and Treatment Capacity Building Project for Major Diseases.

Conflict of interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Publisher’s note

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.

Supplementary material

The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fsurg.2022.989065/full#supplementary-material.

References

  • 1.

    GagnerMPompA. Laparoscopic pylorus-preserving pancreatoduodenectomy. Surg Endosc. (1994) 8(5):408–10. 10.1007/BF00642443

  • 2.

    KornaropoulosMMorisDBealEWMakrisMCMitrousiasAPetrouAet alTotal robotic pancreaticoduodenectomy: a systematic review of the literature. Surg Endosc. (2017) 31(11):4382–92. 10.1007/s00464-017-5523-z

  • 3.

    LuoDWanXLiuJTongT. Optimally estimating the sample mean from the sample size, median, mid-range, and/or mid-quartile range. Stat Methods Med Res. (2018) 27(6):1785–805. 10.1177/0962280216669183

  • 4.

    KauffmannEFNapoliNMenonnaFIacopiSLombardoCBernardiniJet alA propensity score-matched analysis of robotic versus open pancreatoduodenectomy for pancreatic cancer based on margin status. Surg Endosc. (2019) 33(1):234–42. 10.1007/s00464-018-6301-2

  • 5.

    AzizHKhanMKhanSSerraGPGoodmanMDGenykYet alAssessing the perioperative complications and outcomes of robotic pancreaticoduodenectomy using the national cancer database: is it ready for prime time?J Robot Surg. (2022)16(3):687–94. 10.1007/s11701-021-01296-3

  • 6.

    ShyrBUShyrBSChenSCShyrYMWangSE. Propensity score-matched comparison of the oncological feasibility and survival outcomes for pancreatic adenocarcinoma with robotic and open pancreatoduodenectomy. Surg Endosc. (2022) 36(2):1507–14. 10.1007/s00464-021-08437-7

  • 7.

    Baimas-GeorgeMWatsonMMurphyKJIannittiDBakerEOcuinLet alRobotic pancreaticoduodenectomy may offer improved oncologic outcomes over open surgery: a propensity-matched single-institution study. Surg Endosc. (2020) 34(8):3644–9. 10.1007/s00464-020-07564-x

  • 8.

    WengYJiangYFuNJinJShiYHuoZet alOncological outcomes of robotic-assisted versus open pancreatoduodenectomy for pancreatic ductal adenocarcinoma: a propensity score-matched analysis. Surg Endosc. (2021) 35(7):3437–48. 10.1007/s00464-020-07791-2

  • 9.

    ZureikatAHPostlewaitLMLiuYGillespieTWWeberSMAbbottDEet alA multi-institutional comparison of perioperative outcomes of robotic and open pancreaticoduodenectomy. Ann Surg. (2016) 264(4):640–9. 10.1097/SLA.0000000000001869

  • 10.

    McMillanMTZureikatAHHoggMEKowalskySJZehHJSprysMHet alA propensity score-matched analysis of robotic vs open pancreatoduodenectomy on incidence of pancreatic fistula. JAMA Surg. (2017) 152(4):327–35. 10.1001/jamasurg.2016.4755

  • 11.

    MejiaAShahJVivianEAcharyaP. Analysis of 102 fully robotic pancreaticoduodenectomies: clinical and financial outcomes. Pancreas. (2020) 49(5):668–74. 10.1097/MPA.0000000000001545

  • 12.

    WangSEShyrBUChenSCShyrYM. Comparison between robotic and open pancreaticoduodenectomy with modified blumgart pancreaticojejunostomy: a propensity score-matched study. Surgery. (2018) 164(6):1162–7. 10.1016/j.surg.2018.06.031

  • 13.

    KimHSHanYKangJSKimHKimJRKwonWet alComparison of surgical outcomes between open and robot-assisted minimally invasive pancreaticoduodenectomy. J Hepatobiliary Pancreat Sci. (2018) 25(2):142–9. 10.1002/jhbp.522

  • 14.

    VarleyPRZenatiMSKlobukaAToblerJHamadAHoggMEet alDoes robotic pancreaticoduodenectomy improve outcomes in patients with high risk morphometric features compared to the open approach. HPB. (2019) 21(6):695–701. 10.1016/j.hpb.2018.10.016

  • 15.

    CaiJRamanathanRZenatiMSAl AbbasAHoggMEZehHJet alRobotic pancreaticoduodenectomy is associated with decreased clinically relevant pancreatic fistulas: a propensity-matched analysis. J Gastrointest Surg. (2020) 24(5):1111–8. 10.1007/s11605-019-04274-1

  • 16.

    PaoliniCBenciniLGabelliniLUrciuoliIPaccianiSTribuziAet alRobotic versus open pancreaticoduodenectomy: is there any difference for frail patients?Surg Oncol. (2021) 37:101515. 10.1016/j.suronc.2020.12.009

  • 17.

    IelpoBCarusoRDuranHDiazEFabraIMalavéLet alRobotic versus standard open pancreatectomy: a propensity score-matched analysis comparison. Updates Surg. (2019) 71(1):137–44. 10.1007/s13304-018-0529-1

  • 18.

    MarinoMVPoddaMGomez RuizMFernandezCCGuarrasiDGomez FleitasM. Robotic-assisted versus open pancreaticoduodenectomy: the results of a case-matched comparison. J Robot Surg. (2020) 14(3):493–502. 10.1007/s11701-019-01018-w

  • 19.

    ShiYJinJQiuWWengYWangJZhaoSet alShort-term outcomes after robot-assisted vs open pancreaticoduodenectomy after the learning curve. JAMA Surg. (2020) 155(5):389–94. 10.1001/jamasurg.2020.0021

  • 20.

    BenciniLTofaniFPaoliniCVaccaroCCheccacciPAnnecchiaricoMet alSingle-centre comparison of robotic and open pancreatoduodenectomy: a propensity score-matched study. Surg Endosc. (2020) 34(12):5402–12. 10.1007/s00464-019-07335-3

  • 21.

    KimHParkSYParkYKwonJLeeWSongKBet alAssessment of learning curve and oncologic feasibility of robotic pancreaticoduodenectomy: a propensity score-based comparison with open approach. J Hepatobiliary Pancreat Sci. (2022) 29(6):649–58. 10.1002/jhbp.837

  • 22.

    van OostenAFDingDHabibJRIrfanASchmockerRKSereniEet alPerioperative outcomes of robotic pancreaticoduodenectomy: a propensity-matched analysis to open and laparoscopic pancreaticoduodenectomy. J Gastrointest Surg. (2021) 25(7):1795–804. 10.1007/s11605-020-04869-z

  • 23.

    ShyrBUShyrBSChenSCShyrYMWangSE. Robotic and open pancreaticoduodenectomy: results from Taipei veterans general hospital in Taiwan. Updates Surg. (2021) 73(3):939–46. 10.1007/s13304-020-00899-z

  • 24.

    WangWLiuQZhaoZMTanXLWangZZZhangKDet alComparison of robotic and open pancreaticoduodenectomy for primary nonampullary duodenal adenocarcinoma: a retrospective cohort study. Langenbecks Arch Surg. (2022) 407(1):167–73. 10.1007/s00423-021-02303-9

  • 25.

    ShyrYMWangSEChenSCShyrBUShyrBS. Robotic pancreaticoduodenectomy for pancreatic head cancer and periampullary lesions. Ann Gastroenterol Surg. (2021) 5(5):589–96. 10.1002/ags3.12457

  • 26.

    PineJKHaugkBRobinsonSMDarneAWilsonCSenGet alProspective assessment of resection margin status following pancreaticoduodenectomy for pancreatic ductal adenocarcinoma after standardisation of margin definitions. Pancreatology. (2020) 20(3):537–44. 10.1016/j.pan.2020.01.004

  • 27.

    YouMSLeeSHChoiYHShinBSPaikWHRyuJKet alLymph node ratio as valuable predictor in pancreatic cancer treated with R0 resection and adjuvant treatment. BMC Cancer. (2019) 19(1):952. 10.1186/s12885-019-6193-0

  • 28.

    Da DongXFelsenreichDMGognaSRojasAZhangEDongMet alRobotic pancreaticoduodenectomy provides better histopathological outcomes as compared to its open counterpart: a meta-analysis. Sci Rep. (2021) 11(1):3774. 10.1038/s41598-021-83391-x

  • 29.

    YanQXuLBRenZFLiuC. Robotic versus open pancreaticoduodenectomy: a meta-analysis of short-term outcomes. Surg Endosc. (2020) 34(2):501–9. 10.1007/s00464-019-07084-3

  • 30.

    PengLLinSLiYXiaoW. Systematic review and meta-analysis of robotic versus open pancreaticoduodenectomy. Surg Endosc. (2017) 31(8):3085–97. 10.1007/s00464-016-5371-2

Summary

Keywords

robotic pancreaticoduodenectomy, open pancreaticoduodenectomy, pancreatic cancer, outcome, meta-analysis

Citation

Fu Y, Qiu J, Yu Y, Wu D and Zhang T (2022) Meta-analysis of robotic versus open pancreaticoduodenectomy in all patients and pancreatic cancer patients. Front. Surg. 9:989065. doi: 10.3389/fsurg.2022.989065

Received

08 July 2022

Accepted

20 September 2022

Published

11 October 2022

Volume

9 - 2022

Edited by

Andrew Gumbs, Centre Hospitalier Intercommunal de Poissy, France

Reviewed by

Xiaohang Li, The First Affiliated Hospital of China Medical University, China Xu Che, Cancer Hospital Shenzhen Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, China

Updates

Copyright

*Correspondence: Taiping Zhang

†

These authors have contributed equally to this work

Specialty Section: This article was submitted to Surgical Oncology, a section of the journal Frontiers in Surgery

Disclaimer

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.

Outline

Figures

Cite article

Copy to clipboard


Export citation file


Share article

Article metrics