30-Second Takeaway
- Use post-FOLFIRINOX restaging factors and CA19-9/e19-9 dynamics to individualize pancreatic surgery and adjuvant intensity.
- Treat major pathologic response in PDAC as strongly prognostic and consider adjuvant de-escalation in these patients.
- Avoid extensive debulking for multiorgan mCRC; it adds morbidity without survival benefit over chemotherapy alone.
Week ending March 21, 2026
Surgical oncology decisions: refining selection, response assessment, and de-escalation
Eight-variable post-FOLFIRINOX calculator stratifies survival in localized PDAC
This international cohort included 2338 patients with localized PDAC treated first-line with (m)FOLFIRINOX and then restaged. Eight factors independently predicted overall survival: baseline resectability, tumor site, WHO status, restaging metastases, post-induction CA19-9, CA19-9 change, post-induction tumor size, and tumor size change. These variables were combined into a web-based calculator that stratified patients into four risk groups with 3-year survival from 6.0% to 65.8%. The tool can aid prognosis counseling, selection for resection, and tailoring adjuvant therapy intensity after neoadjuvant FOLFIRINOX.
Major pathologic response after preop therapy in PDAC predicts excellent survival and limited adjuvant benefit
This multi-institution retrospective series analyzed 739 PDAC patients undergoing pancreatectomy after preoperative treatment using Evans grading. Major pathologic response (Evans III/IV) occurred in 11.5% and was associated with markedly longer overall survival (71.5 vs 40.9 months) and recurrence-free survival (55.5 vs 15.2 months). MPR remained an independent prognostic factor for overall survival on multivariable analysis. Among MPR patients, adjuvant chemotherapy did not significantly affect overall or recurrence-free survival and was not an independent prognostic factor. Chemoradiotherapy, preoperative duration ≥6 months, post-treatment normal CA19-9, and radiologic response predicted achieving MPR, informing neoadjuvant and postoperative discussions.
ORCHESTRA: extensive tumor debulking fails to improve survival in multiorgan mCRC
In this randomized trial, 382 patients with multiorgan mCRC responding or stable after oxaliplatin-based chemotherapy were assigned to chemotherapy alone or additional debulking. More than 80% debulking via surgery, radiotherapy, and/or ablation had to be technically feasible before randomization. Median overall survival was similar: 27.5 months with chemotherapy alone versus 30.0 months with debulking plus chemotherapy (adjusted HR 0.88; P = .26). Progression-free survival was also similar, but serious adverse events were more frequent with debulking (53% vs 39%; P = .006). These data argue against routine aggressive multivisceral debulking for multiorgan mCRC outside carefully selected oligometastatic settings.
Omitting axillary surgery in node-negative early breast cancer preserves survival with modestly higher axillary recurrence
This meta-analysis pooled seven randomized trials including 8806 patients with early breast cancer and clinically node-negative axillae. Omitting axillary surgery versus sentinel lymph node biopsy or axillary dissection did not worsen overall survival (OR 1.02; 95% CI 0.86-1.20) or disease-free survival. Axillary surgery significantly reduced axillary recurrence risk (OR 0.18; 95% CI 0.10-0.31), although absolute recurrence rates were low. Findings support omitting axillary surgery in carefully staged, node-negative patients when prioritizing functional outcomes and morbidity reduction.
References
Numbered in order of appearance. Click any reference to view details.
Additional Reads
Optional additional studies from this edition.