Journal: Annals of surgery
Study question
Does using broad-spectrum perioperative prophylaxis with piperacillin-tazobactam (PTZ), compared with cefoxitin, during pancreatoduodenectomy influence long-term oncologic outcomes, including adjuvant chemotherapy use and survival?
Design and data source
- Registry-linked analysis of a prior randomized clinical trial comparing PTZ vs cefoxitin for surgical site infection (SSI) prevention in pancreatoduodenectomy.
- Data linkage: Trial participants from the ACS NSQIP database were linked to the National Cancer Database to assess oncologic outcomes.
- Statistical methods (chemotherapy): Multivariable logistic regression evaluated factors associated with delivery of indicated adjuvant chemotherapy.
- Statistical methods (survival): Survival was assessed using Kaplan–Meier and Cox proportional hazards models.
Cohort
- Original trial size: 778 patients.
- Eligible for linkage: 471 patients treated at Commission on Cancer–accredited centers.
- Successfully matched: 426 patients total
- PTZ group: 203 patients.
- Cefoxitin group: 223 patients.
Key findings
- Adjuvant chemotherapy omission among those with an indication:
- PTZ: 9.4%
- Cefoxitin: 15.4% (P = 0.097)
- Factors not significantly associated with receipt of indicated adjuvant chemotherapy:
- PTZ vs cefoxitin: OR 1.49; 95% CI 0.56–3.95
- Presence of SSI: OR 0.58; 95% CI 0.21–1.65
- Survival impact: Postoperative SSI was associated with significantly worse 3‑year overall survival (HR 1.69; 95% CI 1.20–2.38).
Interpretation for practice
- Antibiotic choice: Broad-spectrum prophylaxis with PTZ, while previously shown to reduce SSI, did not significantly alter the delivery of indicated adjuvant chemotherapy or other measured oncologic care processes.
- Impact of complications: Occurrence of SSI itself is associated with worse long-term survival after pancreatoduodenectomy, reinforcing the importance of preventing perioperative complications in oncologic surgery.
- Methodologic value: The study also demonstrates the value of linking clinical trial data with cancer registries to evaluate long-term oncologic outcomes.