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The IPLA-OVCA Trial, Intra-Peritoneal Local Anaesthetics in Ovarian Cancer (IPLA-OVCA)

Primary Purpose

Advanced Ovarian Cancer

Status
Recruiting
Phase
Phase 3
Locations
Sweden
Study Type
Interventional
Intervention
Ropivacaine
Saline Solution
Sponsored by
Karolinska Institutet
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Advanced Ovarian Cancer focused on measuring Local Anesthesia, Time-interval from surgery to adjuvant chemotherapy, advanced ovarian cancer

Eligibility Criteria

18 Years - 80 Years (Adult, Older Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  • ASA I-III
  • Scheduled for upfront cytoreductive surgery for presumed stage III or IV epithelial ovarian cancer
  • Signed written informed consent

Exclusion Criteria:

  • Contraindication to epidural anesthesia
  • Allergy to any component drugs used during epidural or intraperitoneal anesthesia (Ropivacaine, Sufentanil)
  • Uncontrolled renal, liver, heart failure or ischemic heart disease
  • Speech, language or cognitive difficulties
  • Women in whom cytoreductive surgery is not attempted at time of upfront laparotomy due to extent of disease

Sites / Locations

  • Karolinska Hospital, SolnaRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Placebo Comparator

Experimental

Arm Label

Placebo

Experimental

Arm Description

Normal saline administered intraperitoneally at defined times during upfront surgery and intermittently postoperatively for 72 hours

Local anesthetic (ropivacaine) administered intraperitoneally at defined times during upfront surgery and intermittently postoperatively for 72 hours

Outcomes

Primary Outcome Measures

Time-interval from upfront surgery to adjuvant chemotherapy
Days from surgery to first infusion of adjuvant chemotherapy

Secondary Outcome Measures

Postoperative complications
Assessed according to the Clavien-Dindo Nomenclature
Overall survival
Death of any reason
Postoperative quality of recovery
As measured by validated instruments
Postoperative morbidity
As measured by validated instruments

Full Information

First Posted
August 19, 2019
Last Updated
June 23, 2022
Sponsor
Karolinska Institutet
Collaborators
Skane University Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT04065009
Brief Title
The IPLA-OVCA Trial, Intra-Peritoneal Local Anaesthetics in Ovarian Cancer
Acronym
IPLA-OVCA
Official Title
A Randomized Double Blind, Multicenter Trial to Assess Time-interval Between Cytoreductive Surgery and Adjuvant Chemotherapy After Administration of Local Anesthetic Intraperitoneally/Perioperatively in Advanced Epithelial Ovarian Cancer
Study Type
Interventional

2. Study Status

Record Verification Date
June 2022
Overall Recruitment Status
Recruiting
Study Start Date
August 26, 2020 (Actual)
Primary Completion Date
December 26, 2023 (Anticipated)
Study Completion Date
August 26, 2028 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Karolinska Institutet
Collaborators
Skane University Hospital

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Surgery and chemotherapy combined constitute first line treatment in women with advanced ovarian cancer. The aim of surgery apart from staging is cytoreduction, i.e. surgical resection of tumour. Radical resection of all tumour visible by the naked eye followed by adjuvant chemotherapy is associated with best chance of prolonged survival. However, because of tumour dissemination in the peritoneal cavity, radical surgery is often very extensive with surgery in all quadrants of the abdomen and multi-organ resection with substantial risk of postoperative severe complications and subsequent delay in administration of adjuvant chemotherapy. Longer time-interval between surgery to start of adjuvant chemotherapy has been associated with decrease in survival. Surgery presents opportunities not only for eradicating tumours but, paradoxically, also for proliferation and invasion of residual cancer cells. It increases the shedding of malignant cells into the blood and lymphatic circulations, inhibits their apoptosis and potentiates their invasion capacity. Additionally, the immune system, the inflammatory system and the neuroendocrine system react to surgery with important changes, which have been proven to promote progression of cancer. Several anaesthesia-related factors play an important role in perioperative tumorigenesis such as inhalational anaesthetics, opiate analgesics, local anaesthetics and regional anaesthesia, all of which may impact short-term morbidity and long-term mortality. A previous randomized placebo-controlled pilot study suggests that women who receive local anesthetics intraperitoneally preoperatively have a significantly decreased time-interval to initiation of adjuvant chemotherapy. In a prospective, randomised, multi-centre study, we plan to further assess if intraperitoneal local anaesthetics administered perioperatively during 72 h leads to early start of chemotherapy compared to placebo in patients undergoing cytoreductive surgery for FIGO stage III-IV ovarian cancer.
Detailed Description
Epithelial ovarian cancer (EOC) is the common term for cancer that originate from the surface of the ovary, lining of the fallopian tube and the peritoneum. There are different histopathological subtypes with high grade serous adenocarcinomas being the most prevalent (70%) followed by endometrioid (10%), clear cell (10%), low-grade serous (5%) and mucinous adenocarcinomas (3%).The pattern of dissemination is foremost through early exfoliation or seeding of tumour-cells in the peritoneum (carcinomatosis) and the majority of women have advanced stage disease at presentation, why ovarian cancer is the gynecologic malignancy with highest mortality. Ovarian cancer affects 295 000 women every year globally and causes 185 000 cancer-related deaths annually . The highest incidence is seen in Northern Europe and North America and the lowest in South East Asia and parts of Africa. In the Nordic countries 2300 women are diagnosed annually and the corresponding number in Sweden is 700. Ovarian cancer constitutes 3% of all female cancers in Sweden and the risk of developing disease before the age of 75 is 1.1%. A decline in incidence is evident since the 1970s most probably due to increase in use of contraceptive pills but also change in criteria for diagnosis (an adnexal biopsy is mandatory for diagnosis today). The median age at diagnosis is 63 years. Risk-factors include genetic mutations, family history, hormone replacement therapy and endometriosis. Pregnancy, lactation, contraceptive pills, sterilization, salpingectomy, hysterectomy and salpingoophorectomy are all factors associated with decreased risk of developing EOC. Staging of ovarian cancer is surgical and according to the International Federation of Gynecology and Obstetrics (FIGO), latest revised in 2014 (7). In stage III and IV, advanced ovarian cancer, extra-pelvic dissemination is evident. Stage of disease is a strong prognostic factor for survival. The total 5-year relative survival in Sweden is 50% but ranges from 90% for stage I to 20% for stage IV. However, treatment is also an important prognostic factor and may increase survival even in advanced stage. Surgical treatment of advanced EOC is often accompanied by a severe inflammatory and immuno-compromised perioperative course associated with early morbidity, delayed rehabilitation and, sometimes, delayed start of chemotherapy. Early start of chemotherapy has been repeatedly associated with improved survival. For this reason, perioperative factors such as choice of anaesthesia and analgesia and fluid replacement may be important. Tumorigenesis and the perioperative environment Surgery, perioperative stress and anaesthesia may all modulate the immuno-surveillance mechanisms and compromise host defences that normally maintain a balance between immunity & tumorigenesis. There is increasing evidence that surgery itself may promote the recurrence and metastases of cancer, which depends largely on the tumour's ability to metastasise, combined with the host immunity and inflammatory response. Natural killer (NK) cells act as a primary defence against perioperative cancer metastases. Negative effects of anaesthetics and analgesics on NK-cell activity may promote pro-inflammatory effects and may also activate cancer cell survival pathways. Additionally, concentrations of tumour-related anti-angiogenic factors are decreased while angiogenic factors such as vascular endothelial growth factor (VEGF) are increased. Hypoxia inducing factor (HIF-1) is a transcriptional factor that has also been shown to play an important role for tumour survival. Hypoxia in solid tumours leads to activation of HIF-1, which in turn increases cancer cell survival . Similarly, hyperoxia may, paradoxically, lead to activation of HIF-1 and potentially worsen long-term survival. Inhalational anaesthetics but not propofol have been shown to affect VEGF as well as transforming growth factor-beta (TGF-β) in patients undergoing breast surgery that may affect long-term survival. VEGF and TGF-β play a significant role in establishing tumour blood supply and cell proliferation. Other factors such as surgical stress, blood transfusions, hypothermia, hyperglycaemia, and postoperative pain may also affect immunity and the tumour microenvironment. Role of anaesthetics and analgesics in cancer metastases Preventing a major systemic inflammatory response and preserving immuno-surveillance in the perioperative period are fundamental in promoting improved postoperative outcome in cancer surgery. The severity of injury correlates with the magnitude of inflammation. In vitro studies have shown that amide local anaesthetics have cytotoxic activity, which could prove to be beneficial in preventing cancer recurrence. These potential cytotoxic effects of LA may effectively reduce postoperative morbidity and promote early start of chemotherapy. Anaesthetic drugs, specifically inhalation anaesthetics, impair numerous immune functions, including those of neutrophils, macrophages, dendritic cells, T-cell, and natural killer (NK) cells. Upregulation of hypoxia-inducible-factors (HIF) in tumour cells by volatile anaesthetics may contribute to a tumour's recurrence by stimulating cytoprotective or pro-tumorigenic behaviour in residual cells. However, propofol may not depress the immune function and does not upregulate synthesis of HIF. Opioid analgesics inhibit both cellular and humoral immune function, increase angiogenesis, and promote breast tumour growth in rodents. Opioids interfere with immune function by depressing NK cell activity . The use of epidural anaesthesia and analgesia thus prevents the stress response to surgery, reduces the need for opiates and may prolong survival. Fluid dynamics and early recovery Fluid optimization remains a challenge because of several factors: preoperative fluid shifts and accumulation of ascitic fluid, low preoperative albumin from malnutrition, as well as perioperative fluid and blood loss. Both hypo- and hypervolemia have been shown to have adverse effects and may delay recovery and start of chemotherapy and a large prospective, randomised study concluded that hypovolemia may even lead to renal insufficiency. The primary objective of this Phase 3 double blind placebo controlled trial is to investigate if local anesthetics administered intraperitoneally perioperatively at time of upfront surgery for advanced ovarian cancer reduces the time-interval between surgery and adjuvant chemotherapy. Secondary objectives are to investigate, postoperative morbidity, complications and long term survival. The trial entails a translational part with the following specific aims: I. To examine if surgical peritoneal stress evolves during the course of surgery, as measured by pro-inflammatory cytokines and biomarkers in the mesothelium, tumour tissues and blood, coupled to analysis of the circulating tumour DNA II. To test if intraperitoneally administered anti-inflammatory analgesics may reduce the (mesothelial) inflammation. III. To use functional ex vivo assays for exploring how the above identified surgical tissue responses and induced or inhibited pathways affect the aggressive EOC cell functions and properties including tumour invasion and chemo-resistance.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Advanced Ovarian Cancer
Keywords
Local Anesthesia, Time-interval from surgery to adjuvant chemotherapy, advanced ovarian cancer

7. Study Design

Primary Purpose
Other
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Model Description
Randomised, double blind, prospective, multicenter
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Masking Description
Study drugs are blinded and administered perioperatively. Fully blinded for all (participants, assessors etc)
Allocation
Randomized
Enrollment
220 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Normal saline administered intraperitoneally at defined times during upfront surgery and intermittently postoperatively for 72 hours
Arm Title
Experimental
Arm Type
Experimental
Arm Description
Local anesthetic (ropivacaine) administered intraperitoneally at defined times during upfront surgery and intermittently postoperatively for 72 hours
Intervention Type
Drug
Intervention Name(s)
Ropivacaine
Other Intervention Name(s)
Narop
Intervention Description
Experimental drug will be administered intraperitoneally
Intervention Type
Drug
Intervention Name(s)
Saline Solution
Other Intervention Name(s)
Normal saline
Intervention Description
Placebo will be administered intraperitoneally
Primary Outcome Measure Information:
Title
Time-interval from upfront surgery to adjuvant chemotherapy
Description
Days from surgery to first infusion of adjuvant chemotherapy
Time Frame
Number of days to start of adjuvant chemotherapy (0 - 60 days)
Secondary Outcome Measure Information:
Title
Postoperative complications
Description
Assessed according to the Clavien-Dindo Nomenclature
Time Frame
30 days postoperatively
Title
Overall survival
Description
Death of any reason
Time Frame
3 and 5 years after surgery
Title
Postoperative quality of recovery
Description
As measured by validated instruments
Time Frame
Perioperatively
Title
Postoperative morbidity
Description
As measured by validated instruments
Time Frame
Perioperatively

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: ASA I-III Scheduled for upfront cytoreductive surgery for presumed stage III or IV epithelial ovarian cancer Signed written informed consent Exclusion Criteria: Contraindication to epidural anesthesia Allergy to any component drugs used during epidural or intraperitoneal anesthesia (Ropivacaine, Sufentanil) Uncontrolled renal, liver, heart failure or ischemic heart disease Speech, language or cognitive difficulties Women in whom cytoreductive surgery is not attempted at time of upfront laparotomy due to extent of disease
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Sahar Salehi, MD, PhD
Phone
08-51770000
Email
sahar.salehi@sll.se
First Name & Middle Initial & Last Name or Official Title & Degree
Emma Hasselgren, MD
Phone
08-51770000
Email
emma.hasselgren@sll.se
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Sahar Salehi, MD, PhD
Organizational Affiliation
Karolinska Institute and Karolinska University Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Karolinska Hospital, Solna
City
Stockholm
ZIP/Postal Code
17176
Country
Sweden
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Katja Tobin Klinisk prövningsledare/Clinical Research Manager
Phone
+46 8 517 745 15
Email
katja.tobin@sll.se
First Name & Middle Initial & Last Name & Degree
Katja Wiklund Clinical Research Manager/Quality coordinator
Phone
+46 8 517 725 84
Email
katja.wiklund@sll.se

12. IPD Sharing Statement

Plan to Share IPD
No
IPD Sharing Plan Description
All study data will be retained at site of patient recruitment. Primary investigator and statistician will only have access to coded patient identity
Citations:
PubMed Identifier
32172954
Citation
Hayden JM, Oras J, Block L, Thorn SE, Palmqvist C, Salehi S, Nordstrom JL, Gupta A. Intraperitoneal ropivacaine reduces time interval to initiation of chemotherapy after surgery for advanced ovarian cancer: randomised controlled double-blind pilot study. Br J Anaesth. 2020 May;124(5):562-570. doi: 10.1016/j.bja.2020.01.026. Epub 2020 Mar 13.
Results Reference
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The IPLA-OVCA Trial, Intra-Peritoneal Local Anaesthetics in Ovarian Cancer

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