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Summary

The Prophylactic Antibiotic Regimens in Tumor Surgery (PARITY) trial is the first ever international multi-center randomized controlled trial in bone cancer surgery. In order to avoid amputation for bone cancer in the leg, complex limb-saving operations are performed. However, infections with devastating complications following surgery are common. Surgeons from across the world will randomize patients to receive either short- or long-duration antibiotic regimens after surgery with the goal of identifying the best regimen to reduce these infections.

Conditions

Infection, Bone Neoplasms

Recruitment Status

Completed

Detailed Description

Long-bone sarcomas were historically managed with amputation. In the current era of osteosarcoma management, amputations are generally avoided by complex surgeries in which the malignancy is removed and the limb is reconstructed with advanced surgical techniques. This process of limb salvage is possible with improvements in chemotherapeutic regimens, advanced imaging techniques and surgical innovations such as modular metallic implants. However, the risk for surgical complications is high due to the complexity of the surgeries themselves. The most common and devastating complication is a surgical site infection. Background work and data from our pilot study indicates that infection rates approach 15%. Multiple surgical attempts at eradication of the infection fail in 50% of these cases, resulting in amputation. Published guidelines for post-operative antibiotic prophylaxis following many standard and less complex elective surgical procedures dictate that prophylactic antibiotics be discontinued after 24 hours. However, the most effective duration of treatment in sarcoma surgery has not previously been examined. Given the limitations of the evidence, it has not been possible for orthopaedic oncologists to draw firm conclusions and, therefore, clinical practice is highly varied, particularly with respect to antibiotic duration. Our international, multi-center randomized controlled trial will determine whether a 5-day regimen of post-operative prophylactic antibiotics in comparison to a standard 24-hour regimen decreases the rate of surgical site infections after limb salvage surgery within 1-year follow-up.

Eligibility Criteria

Inclusion Criteria:

primary bone malignancies or aggressive benign bone tumors of the femur or tibia, soft-tissue sarcomas which have invaded the femur or tibia, or oligometastatic bone disease of the femur or tibia in a patient expected to live at least one year post-operatively; and
treatment by surgical excision and endoprosthetic replacement of the femur or tibia.

Exclusion Criteria:

current known Methicillin-resistant Staphylococcus Aureus (MRSA) colonization;
current known Vancomycin Resistant Enterococcus (VRE) colonization;
documented anaphylaxis or angioedema to penicillin or cefazolin (Ancef);
current surgical procedure is a revision surgery for implant failure or infection;
prior local infection within the surgical field of the affected limb;
current known immunologically-deficient disease conditions (not including recent chemotherapy);
known renal insufficiency with estimated creatinine clearance (eGRF) of less than 54 mL/min;
reconstruction to include structural allograft;
enrolled in a competing study; and
weight of less than or equal to 45 kg (for sites using cefuroxime only).

Intervention

Intervention Type

Intervention Name

Drug

24-Hour Prophylactic Cefazolin* Antibiotic Regimen

Drug

5-Days Prophylactic Cefazolin* Antibiotic Regimen

Phase

Phase 3

Gender

All

Minimum Age

12 Years

Maximum Age

N/A

Download Date

March 11, 2021

Principal Investigator

Michelle Ghert, MD, FRCSC

Primary Contact Information

For more information on this trial, visit clinicaltrials.gov.

Contact

For more information and to contact the study team: