Literature DB >> 19421811

Total pelvic exenteration for primary and recurrent malignancies.

F T J Ferenschild1, M Vermaas, C Verhoef, A C Ansink, W J Kirkels, A M M Eggermont, J H W de Wilt.   

Abstract

INTRODUCTION: Complete resection is the most important prognostic factor in surgery for pelvic tumors. In locally advanced and recurrent pelvic malignancies, radical margins are sometimes difficult to obtain because of close relation to or growth in adjacent organs/structures. Total pelvic exenteration (TPE) is an exenterative operation for these advanced tumors and involves en bloc resection of the rectum, bladder, and internal genital organs (prostate/seminal vesicles or uterus, ovaries and/or vagina).
METHODS: Between 1994 and 2008, a TPE was performed in 69 patients with pelvic cancer; 48 with rectal cancer (32 primary and 16 recurrent), 14 with cervical cancer (1 primary and 13 recurrent), 5 with sarcoma (3 primary and 2 recurrent), 1 with primary vaginal, and 1 with recurrent endometrial carcinoma. Ten patients were treated with neoadjuvant chemotherapy and 66 patients with preoperative radiotherapy to induce down-staging. Eighteen patients received IORT because of an incomplete or marginal complete resection.
RESULTS: The median follow-up was 43 (range, 1-196) months. Median duration of surgery was 448 (range, 300-670) minutes, median blood loss was 6,300 (range, 750-21,000) ml, and hospitalization was 17 (range, 4-65) days. Overall major and minor complication rates were 34% and 57%, respectively. The in-hospital mortality rate was 1%. A complete resection was possible in 75% of all patients, a microscopically incomplete resection (R1) in 16%, and a macroscopically incomplete resection (R2) in 9%. Five-year local control for primary locally advanced rectal cancer, recurrent rectal cancer, and cervical cancer was 89%, 38%, and 64%, respectively. Overall survival after 5 years for primary locally advanced rectal cancer, recurrent rectal cancer, and cervical cancer was 66%, 8%, and 45%.
CONCLUSIONS: Total pelvic exenteration is accompanied with considerable morbidity, but good local control and acceptable overall survival justifies the use of this extensive surgical technique in most patients, especially patients with primary locally advanced rectal cancer and recurrent cervical cancer.

Entities:  

Mesh:

Year:  2009        PMID: 19421811      PMCID: PMC2691931          DOI: 10.1007/s00268-009-0066-7

Source DB:  PubMed          Journal:  World J Surg        ISSN: 0364-2313            Impact factor:   3.352


Introduction

Locally advanced pelvic tumors without distant metastases can cause severe local problems, such as pain, voiding, and defecation problems, and may result in a decreased quality of life [1, 2]. Extensive surgery often is the only possibility for complete resection, thereby attempting to provide local control and palliation. In case of involvement of the base or trigone of the bladder or the prostate, a total pelvic exenteration (TPE) with resection of the rectum together with bladder, lower ureters, and internal genital organs could potentially salvage the patient [3]. After resection of the bladder, an ileal conduit is usually constructed according to the technique described by Bricker [4]. TPE has been performed in primary or recurrent cancer of the cervix, rectum, vagina, uterine corpus, vulva, prostate, bladder, and for pelvic sarcoma [5, 6]. Since the introduction of the technique by Brunswick in 1948, the initially poor quality of life and high mortality and morbidity associated with the technique have substantially improved [7-9]. However, morbidity after this extensive surgical procedure is still high and reported to be between 13% and 64% [10-12]. Five-year survival rates after TPE for patients with primary disease range between 32% and 66% and in patients with recurrent disease from 0% to 23% [3, 7, 12]. Hence, a careful selection in a multidisciplinary setting of patients is of paramount importance. In the present study, all patients who underwent a pelvic exenteration were reviewed. Preoperative morbidity and mortality, local recurrence, disease-free, and overall survival rates were studied and prognostic factors for local control or survival were analyzed.

Patients and methods

In the Erasmus University Medical Center-Daniel den Hoed Cancer Center, 69 TPEs were performed during the period from 1994 to 2008 for locally advanced primary or locally recurrent pelvic malignancies. Forty-eight patients with rectal cancer (32 primary locally advanced and 16 recurrent), 14 with cervical cancer (1 primary and 13 recurrent), 5 with pelvic sarcoma (3 primary and 2 recurrent), 1 with primary vagina carcinoma, and 1 with recurrent endometrial carcinoma. Fifty patients were men, with a median age of 61 (range, 30–76) years. Patients were preoperatively analyzed and selected using CT or MRI scanning, or both, of the small pelvis (90% and 59%, respectively). On indication, a cystoscopy was performed to rule out or establish bladder involvement. Screening for distant metastases was performed using thoracic and abdominal CT scan in all patients. All 32 patients with primary rectal cancer received 50 Gy preoperative (chemo)radiation. Thirteen of 26 patients (10 cervical, 2 sarcoma, and 1 rectal cancer patient) with recurrent cancer previously received radiotherapy during treatment of the primary tumor (median dosage, 50 (range, 46–60) Gy. One patient was re-irradiated (27 Gy) after 50 Gy adjuvant radiation after primary treatment for rectal cancer. One patient with recurrent rectal cancer received chemotherapy as primary treatment. Primary treatment for patients with recurrent cancer is described in Table 1.
Table 1

Previous procedures of patients with recurrent pelvic cancer

Rectal(n = 16)Abdominal perineal resection8
Low anterior resection5
Rectosigmoid resection and end colostomy3
Cervical(n = 13)Radical hysterectomy7
Extrafascial abdominal hysterectomy3
Vaginal hysterectomy1
Chemoradiation2
Sarcoma (n = 2)Local excision1
Hysterectomy1
Endometrial(n = 1)Abdominal uterus extirpation1
Previous procedures of patients with recurrent pelvic cancer In 1997 an intraoperative radiation therapy (IORT) program was started in our hospital and the technique was described previously [13]. Briefly, IORT with HDR brachytherapy was given to patients who had a minimal circumferential-free resection margin ≤2 mm. The resection margin was judged on frozen sections taken during surgery. IORT was performed using the Flexible Intraoperative Template (FIT) developed at our department, delivering a dose of 10 Gy, usually at 1-cm depth from the applicator surface.

Pathology

All staging, except from the staging of sarcoma, was performed according to the AJCC TNM criteria, and completeness of resection was divided in R0 (complete resection of tumor), R1 (microscopic tumor remnant in circumferential margin), and R2 (macroscopically not complete resection). Recurrent rectal tumors were staged according to the Wanebo classification for recurrent tumors [14]. Since 2002, all pathology examinations for rectal cancer have been performed according to the guidelines of Quirke et al. [15].

Evaluation of morbidity and mortality

Hospital charts were studied to collect patient characteristics, operation techniques, and follow-up. Surgery-related morbidity was divided into major and minor complications. Major morbidity was defined as a complication that requires (surgical) reintervention. All other complications were classified as minor.

Statistical analysis of survival and local control

Survival time was calculated from the date of resection of the tumor until the last follow-up attendance or until death. Local control was calculated from the date of resection until the histological or evident radiological presence of a local recurrence. The cumulative survival and local control rate after surgery were calculated using the Kaplan–Meier method [16]. Univariate survival comparisons were executed using the log-rank test. Cox proportional hazards analysis was used for multivariate analysis of prognostic factors for local control and overall survival [17]. The level of significance was defined as p < 0.05.

Results

At the time of diagnosis patients presented with complaints of pain (19%), changes in defecation (25%), changes in urinary miction (7%), perineal pressure (6%), and a combination of these complaints (33%). Only seven patients (10%) did not have complaints and were diagnosed during routine follow-up. At the preoperative physical examination, 47% of the gynecological tumors were clinically fixed to the rectum and 74% percent of the rectal tumors were clinically fixed to the prostate and bladder. An exploratory staging laparotomy to create a colostomy or ileostomy was performed in 15 patients (1 sarcoma, 1 recurrent cervical, 12 primary locally advanced, and 1 recurrent rectal cancer). No distant metastases were found during previous surgery and preoperative screening.

Preoperative treatment

Ten patients (14%) received neoadjuvant chemotherapy (5 rectal cancer, 1 primary, 3 recurrent cervical, and 1 vagina carcinoma). Forty-six patients (67%) received preoperative radiotherapy (median dosage, 50 (range, 27–67) Gy).

Surgery

The median duration of surgery was 448 (range, 300–670) minutes. The median blood loss was 6,300 (range, 750–21,000) ml. Fifty-eight patients received a small bowel as urostoma and 11 patients a colon conduit. None of the patients had liver or diffuse peritoneal metastatic disease. In all but six patients, an omentoplasty, and in five patients, an unilateral gracilis muscle transposition was used for primary pelvic reconstruction. Indirect reconstruction with gracilis transposition (one bilateral and three unilateral) was performed in three patients because of persistent perineal wounds. No flap necrosis occurred and eventually after secondary reconstruction all perineal wounds closed in a median of 86 (range, 43–304) days.

Intraoperative and postoperative treatment

IORT was applied in 18 patients (6 primary rectal, 10 recurrent rectal, 2 recurrent cervical cancer): 8 with a marginal radical (R0) resection, 9 with a microscopically irradical resection (R1), and 1 with macroscopic tumor mass (R2). One primary sarcoma and two recurrent cervical tumors were postoperatively irradiated. None of the patients received adjuvant chemotherapy.

Postoperative

TNM and Wanebo stages and completeness of resection are depicted in Table 2. All sarcomas underwent a complete resection. The TNM stage for one vagina carcinoma was T4N0 and T3N0 for the recurrent endometrial carcinoma. Both tumors were resected complete. The median postoperative hospital stay was 17 (range, 4–65) days with an increase for the recurrent tumors compared to the primary-treated tumors (20 vs. 14 days).
Table 2

Pathology characteristics

RectalCervical
PrimRecPrimRec
Total no.(32)(16)(1)(13)
T stageT08%a9%
T29%
T335%25%b36%
T465%67%c100%45%
N stageN057%42%100%45%
N19%16%
N29%
Nx26%42%54%
CompletenessR082%58%100%64%
R19%25%36%
R29%17%

aWanebo classification for recurrent rectal cancer stage Tr 0 (no recurrence)

bWanebo classification for recurrent rectal cancer stage Tr 3 (growth into surrounding soft tissue)

cWanebo classification for recurrent rectal cancer stage Tr 4 (penetration anterior structures)

Pathology characteristics aWanebo classification for recurrent rectal cancer stage Tr 0 (no recurrence) bWanebo classification for recurrent rectal cancer stage Tr 3 (growth into surrounding soft tissue) cWanebo classification for recurrent rectal cancer stage Tr 4 (penetration anterior structures) Complications are depicted in Table 3. The most common minor complications were a superficial wound infection (34%) and pulmonary infections (8%). Forty-eight percent of all reinterventions were performed because of complications related to the construction of the urostomy. All of these patients had received radiotherapy (1 in primary treatment, 9 in neoadjuvant setting, and 1 in previous treatment, intraoperatively as in adjuvant treatment).
Table 3

Complications and reinterventions

Prim rectum (n = 32)Rec rectum (n = 16)Cervix (n = 14)Others (n = 7)Total (n = 69)
Complications
Minor only 12 (38%)5 (31%)2 (14%)3 (43%)22 (32%)
Major only4 (25%)4 (6%)
Major and minor9 (28%)4 (25%)6 (43%)1 (14%)20 (29%)
No complication11 (34%)3 (18%)6 (43%)3 (43%)23 (33%
Minor complications
Wound infection perineal4 (12%)1 (6%)3 (21%)2 (28%)10 (14%)
Wound infection midline6 (19%)3 (19%)3 (21%)1 (14%)13 (19%)
Pneumonia4 (12%)1 (6%)1 (7%)1 (14%)7 (10%)
Central venous catheter sepsis1 (3%)1 (6%)2 (3%)
Fever without known cause1 (3%)1 (1%)
Urinary tract infection3 (9%)2 (14%)1 (14%)6 (9%)
Neuropathy1 (3%)1 (6%)2 (3%)
TIA1 (6%)1 (1%)
Decubitus1 (3%)1 (6%)2 (3%)
Major complications / required reintervention
Urostomy-related
    Nefrodrain placement2 (6%)2 (13%)2 (14%)6 (9%)
    Small-bowel leakage-repair2 (6%)1 (6%)1 (7%)4 (6%)
    Reimplantation ureter1 (3%)1 (7%)2 (3%)
Other
    Gracilis flap wound-repair2 (6%)1 (1%)
    Sartorius flap fistula repair1 (6%)1 (1%)
    Abdominal dehiscence repair1 (3%)1 (1%)
    Ileus relaparotomy1 (6%)1 (1%)
    Bleeding relaparotomy1 (14%)1 (1%)
    Abscess drainage2 (12%)3 (21%)1 (14%)6 (9%)
    Suture leakage repair (ileostomy)1 (7%)1 (1%)
    Enterocutaneous fistula repair1 (7%)1 (1%)

Major complication: a complication that causes the need for reintervention or is the cause of prolonged hospitalization

Minor complication: a complication that does not cause the need for reintervention or is the cause of prolonged hospitalization

Complications and reinterventions Major complication: a complication that causes the need for reintervention or is the cause of prolonged hospitalization Minor complication: a complication that does not cause the need for reintervention or is the cause of prolonged hospitalization The major and minor complication rates were not significantly different for patients treated with or without radiotherapy.

Local control

The 5-year local control of primary rectal, recurrent rectal, and other cancer was 89%, 38%, and 64% (Fig. 1). All four patients with a soft-tissue sarcoma and the patients with a primary cervical tumor and primary vaginal tumor remained without local recurrence after 5 years. A recurrence at the urethra was observed 10 months after resection in the patient who was operated for a third recurrence of an endometrial tumor. The recurrence was treated with local palliative resection and the patient received systemic chemotherapy.
Fig. 1

Kaplan–Meier curve for local control

Kaplan–Meier curve for local control At univariate analysis, significant prognostic factors for an improved local control were the interval from primary resection to local recurrence more than 12 months (p = 0.012), type of tumor (primary rectal; p = 0.009), completeness of resection (p < 0.001), and absence of preoperative pain (p < 0.001). Sex, age, preoperative radiotherapy, and positive lymph nodes did not have prognostic value on local control.

Overall survival

The 5-year overall survival of patients with primary, recurrent rectal, and other cancer was 66%, 8%, and 45% (Fig. 2). All patients with soft-tissue sarcoma were alive after 5 years. At the last follow-up, 46 months after resection, the patient with primary cervical cancer was alive without evidence of disease. The patient with a primary vaginal tumor remained under local control but developed bone metastases 16 months after TPE and died 6 months later. The patient with the third recurrence of endometrial cancer was lost to follow-up 9 months after developing a local recurrence.
Fig. 2

Kaplan–Meier curve for overall survival

Kaplan–Meier curve for overall survival An interval from primary resection to local recurrence of more than 12 months, type of tumor (primary rectum), and completeness of resection were prognostic factors for improved survival (p = 0.01, p = 0.01, and p < 0.001, respectively). Sex, age, preoperative radiotherapy, and positive lymph nodes did not have prognostic value on overall survival.

Discussion

The technique of total pelvic exenteration was introduced as a palliative procedure for patients with advanced gynecological cancer. Currently it is performed with curative intent in the treatment of locally advanced and recurrent pelvic disease (rectal, cervical, endometrial, vaginal, vulvar tumors, and soft-tissue sarcoma) [8]. In locally advanced tumors (without distant metastasis), complete resection is the only possibility for cure, and in patients with rectal cancer, the overall survival rate of 66% and local control rate of 89% after 5 years shows that survival with excellent local control is possible after TPE [10, 12, 13]. These results combined with the high R0 rate and acceptable complication rate justify the performance of TPE in this subgroup [3]. The results of TPE for recurrent rectal cancer, with local control of 38% and 8% overall survival after 5 years, indicate the poor prognosis and questionable benefit of major surgery in this group. These results are comparable with rates after nonexenterative surgery for recurrent rectal cancer and the high occurrence of distant metastasis emphasizes the importance of thorough patient selection [5, 10, 12, 13]. The majority of TPE in gynecological cancer is performed in recurrent cervical cancer [18-20]. The treatment of choice for locally advanced cervical cancer is chemoradiation. One-third of patients with primary carcinoma of the cervix will have residual disease or recurrent disease, and in up to 25% of these patients there is only local disease without systemic metastases [21]. The treatment for recurrent cervical cancer can be chemoradiation, and in a selected population, without distant metastases, exenterative surgery (posterior, anterior, or total exenteration). However, this extensive, disfiguring procedure with a relatively high complication rate should only be performed in highly motivated patients. The 5-year overall survival after treatment of recurrent cervical cancer of 45% in the present study compares to rates reported in the last decade varying from 24–54% [18, 19, 22]. This also holds true for local recurrence-free rate of 64% after 5 years, which is comparable with rates varying from 40–78% in the literature [18, 22]. For more uncommon tumors, case reports or small series describe different results. Barakat et al. described that surgery for recurrent endometrial cancer is associated with only 20% long-term survival and high morbidity [23]. Preoperatively irradiated patients with locally advanced vaginal cancer are appropriate candidates for TPE with >50% survival after 5 years according to Berek et al [19]. Pelvic sarcomas are rare tumors that originate from the stroma of pelvic viscera or from the retroperitoneum. Complete resection and tumor grade are the main prognostic factors for survival [24]. The four patients with sarcomas (2 primary and 2 recurrent) in the present study were all completely resected and did not recur in the pelvis. The 100% overall survival without local relapse in this small cohort compares favorably to the 66% survival after 2 years, which recently described by Lopes et al [6]. Above all, surgery is the only option in these kinds of tumors because there is no clear benefit of any kind of chemotherapy. Overall complete resection rate in the present study was 75% for all tumors. The curative potential of resection differs between primary and recurrent tumors. A complete resection in patients with recurrent disease was possible in 65% of the patients in the present study, which was substantially lower than for patients with a primary tumor (85%). Complete resection is more difficult in recurrent cancer because of primary resection of visceral fascia. Successful complete resection of recurrent disease often is restricted to selected patients, for example with early-detected or limited tumor mass. As described in previous reports, complete resection of tumor is a significant prognostic factor for local control and survival [5, 10, 12, 25]. All four patients with a macroscopically incomplete resection (2 primary and 2 recurrent rectal cancer) died during follow-up, with a mean survival of 13 months. Morbidity rates reported after TPE for primary and locally recurrent rectal cancer vary from 13–78% [10, 11, 26]. We have previously reported overall morbidity rates of 61% in primary rectal cancer (26% major and 35% minor) and 83% in recurrent rectal cancer (50% major and 58% minor) [3]. Infectious complications, such as midline (14%) and perineal (19%) wound infection, fistula (4%), and abscesses (12%), are the most common complications after TPE. Preoperative radiotherapy did not lead to an increase in complications, which is in contrast to what has been described by Lopez et al., who identified significant higher complication rates in the irradiated group of patients [27]. Thirty-eight percent of all major complications were related to the construction of the urinary conduit. Houvenaeghel et al. [28] showed similar complications (42%) related to the construction of a noncontinent urostomy. High complication rates after construction of a Bricker urostomy in irradiated patients often have been reported because of postradiation fibrosis. The Bricker procedure remains the most performed technique for urinary diversion. Other procedures using intestinal segment outside of the radiation field, such as jejunum or colon, have been proposed; however, each have their own related complications. Use of jejunum can lead to metabolic complications and colon conduits are reserved for patients without previous colon resection to prevent absorption problems [29, 30]. The use of continent pouches is increasingly reported, with related functional advantages leading to improved quality of life but also have 46% pouch-related complications [30]. For many years, age was considered a contraindication for the performance of TPE. In the present study, patients older than aged 70 years had a similar outcome after TPE compared with younger patients, which is confirmed by other recent studies [20, 22]. Not age but physical condition and comorbidities are considered important criteria in selecting patients for TPE. As a specialized cancer center, a weekly multidisciplinary meeting is held. All patients with pelvic tumors are presented and the treatment program for each individual patient is discussed and planned.

Conclusions

Total pelvic exenteration is accompanied with considerable morbidity; however, good local control and acceptable overall survival justifies the use of this extensive surgical technique in selected patients with primary locally advanced and recurrent pelvic tumors.
  28 in total

1.  Improvements in pelvic exenteration: factors responsible for reducing morbidity and mortality.

Authors:  J M Goldberg; M S Piver; R E Hempling; C Aiduk; L Blumenson; F O Recio
Journal:  Ann Surg Oncol       Date:  1998 Jul-Aug       Impact factor: 5.344

Review 2.  Metabolic consequences of continent urinary diversion.

Authors:  R D Mills; U E Studer
Journal:  J Urol       Date:  1999-04       Impact factor: 7.450

3.  Pelvic exenteration and sphincter preservation in the treatment of soft tissue sarcomas.

Authors:  A Lopes; A H O Poletto; A L Carvalho; E A Ribeiro; N M Granja; B M Rossi
Journal:  Eur J Surg Oncol       Date:  2004-11       Impact factor: 4.424

4.  Total pelvic exenteration. A 50-year experience at the Ellis Fischel Cancer Center.

Authors:  M J Lopez; S B Standiford; J L Skibba
Journal:  Arch Surg       Date:  1994-04

5.  Major complications of urinary diversion after pelvic exenteration for gynecologic malignancies: a 23-year mono-institutional experience in 124 patients.

Authors:  G Houvenaeghel; V Moutardier; G Karsenty; F Bladou; B Lelong; M Buttarelli; J R Delpero
Journal:  Gynecol Oncol       Date:  2004-02       Impact factor: 5.482

6.  Curative surgery for local pelvic recurrence of rectal cancer.

Authors:  Norio Saito; Keiji Koda; Nobuhiro Takiguchi; Kenji Oda; Masato Ono; Masanori Sugito; Kiyotaka Kawashima; Masaaki Ito
Journal:  Dig Surg       Date:  2003       Impact factor: 2.588

7.  Management of advanced pelvic cancer by exenteration.

Authors:  D M Kecmanovic; M J Pavlov; P A Kovacevic; A V Sepetkovski; M S Ceranic; A B Stamenkovic
Journal:  Eur J Surg Oncol       Date:  2003-11       Impact factor: 4.424

Review 8.  Retroperitoneal soft-tissue sarcoma: analysis of 500 patients treated and followed at a single institution.

Authors:  J J Lewis; D Leung; J M Woodruff; M F Brennan
Journal:  Ann Surg       Date:  1998-09       Impact factor: 12.969

9.  High-dose-rate intraoperative radiotherapy for close or positive margins in patients with locally advanced or recurrent rectal cancer.

Authors:  Joost J Nuyttens; Inger-Karine K Kolkman-Deurloo; Maarten Vermaas; Floris T Ferenschild; Wilfried J Graveland; Johannes H De Wilt; Patrick E Hanssens; Peter C Levendag
Journal:  Int J Radiat Oncol Biol Phys       Date:  2004-01-01       Impact factor: 7.038

10.  Local recurrence of rectal adenocarcinoma due to inadequate surgical resection. Histopathological study of lateral tumour spread and surgical excision.

Authors:  P Quirke; P Durdey; M F Dixon; N S Williams
Journal:  Lancet       Date:  1986-11-01       Impact factor: 79.321

View more
  24 in total

1.  Systematic review of outcomes following pelvic exenteration for the treatment of primary and recurrent locally advanced rectal cancer.

Authors:  E Platt; G Dovell; S Smolarek
Journal:  Tech Coloproctol       Date:  2018-12-01       Impact factor: 3.781

2.  Pelvic exenteration for the treatment of locally advanced colorectal and bladder malignancies in the modern era.

Authors:  Paul J Speicher; Ryan S Turley; Jason L Sloane; Christopher R Mantyh; John Migaly
Journal:  J Gastrointest Surg       Date:  2013-11-08       Impact factor: 3.452

3.  Anti-miRNA-221 sensitizes human colorectal carcinoma cells to radiation by upregulating PTEN.

Authors:  Qi Xue; Kai Sun; Hai-Jun Deng; Shang-Tong Lei; Jing-Qing Dong; Guo-Xin Li
Journal:  World J Gastroenterol       Date:  2013-12-28       Impact factor: 5.742

Review 4.  Locally Advanced Disease and Pelvic Exenterations.

Authors:  Christos Kontovounisios; Paris Tekkis
Journal:  Clin Colon Rectal Surg       Date:  2017-12-01

5.  [Total pelvic exenteration].

Authors:  U Heger; M Koch; M W Büchler; J Weitz
Journal:  Chirurg       Date:  2010-10       Impact factor: 0.955

6.  Factors affecting hospital length of stay following pelvic exenteration surgery.

Authors:  Ying Guo; Eugene Chang; Mehtap Bozkurt; Minjeong Park; Diane Liu; Jack B Fu
Journal:  J Surg Oncol       Date:  2017-10-16       Impact factor: 3.454

7.  [Locally recurrent rectal cancer].

Authors:  A Troja; H R Raab
Journal:  Chirurg       Date:  2010-10       Impact factor: 0.955

8.  Locally recurrent colorectal cancer: results of surgical therapy.

Authors:  M Kruschewski; M Ciurea; S Lipka; S Daum; L Moser; B Meyer; J Gröne; J Budczies; H J Buhr
Journal:  Langenbecks Arch Surg       Date:  2012-06-28       Impact factor: 3.445

9.  Post operative stereotactic radiosurgery for positive or close margins after preoperative chemoradiation and surgery for rectal cancer.

Authors:  Nergiz Dagoglu; Elena Nedea; Vitaliy Poylin; Deborah Nagle; Anand Mahadevan
Journal:  J Gastrointest Oncol       Date:  2016-06

10.  Minimally invasive surgery techniques in pelvic exenteration: a systematic and meta-analysis review.

Authors: 
Journal:  Surg Endosc       Date:  2018-07-17       Impact factor: 4.584

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.