Neoadjuvant Radiotherapy After (m)FOLFIRINOX for Borderline Resectable Pancreatic Adenocarcinoma: A TAPS Consortium Study

Author:

Janssen Quisette P.12,van Dam Jacob L.2,Prakash Laura R.3,Doppenberg Deesje4,Crane Christopher H.5,van Eijck Casper H.J.2,Ellsworth Susannah G.6,Jarnagin William R.1,O’Reilly Eileen M.7,Paniccia Alessandro8,Reyngold Marsha5,Besselink Marc G.4,Katz Matthew H.G.3,Tzeng Ching-Wei D.3,Zureikat Amer H.8,Groot Koerkamp Bas2,Wei Alice C.1,_ _

Affiliation:

1. 1Department of Surgery, Memorial Sloan Kettering Cancer Center, New York, New York;

2. 2Department of Surgery, Erasmus MC Cancer Institute, University Medical Center Rotterdam, Rotterdam, the Netherlands;

3. 3Department of Surgical Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas;

4. 4Department of Surgery, Amsterdam UMC, University of Amsterdam, Cancer Center Amsterdam, Amsterdam, the Netherlands;

5. 5Department of Radiation Oncology, Memorial Sloan Kettering Cancer Center, New York, New York;

6. 6Department of Radiation Oncology, University of Pittsburgh Medical Center, Pittsburgh, Pennsylvania;

7. 7Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York; and

8. 8Department of Surgery, Division of Surgical Oncology, University of Pittsburgh Medical Center, Pittsburgh, Pennsylvania.

Abstract

Background: The value of neoadjuvant radiotherapy (RT) after 5-fluorouracil with leucovorin, oxaliplatin, and irinotecan, with or without dose modifications [(m)FOLFIRINOX], for patients with borderline resectable (BR) pancreatic ductal adenocarcinoma (PDAC) is uncertain. Methods: We conducted an international retrospective cohort study including consecutive patients with BR PDAC who received (m)FOLFIRINOX as initial treatment (2012–2019) from the Trans-Atlantic Pancreatic Surgery Consortium. Because the decision to administer RT is made after chemotherapy, patients with metastases or deterioration after (m)FOLFIRINOX or a performance score ≥2 were excluded. Patients who received RT after (m)FOLFIRINOX were matched 1:1 by nearest neighbor propensity scores with patients who did not receive RT. Propensity scores were calculated using sex, age (≤70 vs >70 years), WHO performance score (0 vs 1), tumor size (0–20 vs 21–40 vs >40 mm), tumor location (head/uncinate vs body/tail), number of cycles (1–4 vs 5–8 vs >8), and baseline CA 19-9 level (≤500 vs >500 U/mL). Primary outcome was overall survival (OS) from diagnosis. Results: Of 531 patients who received neoadjuvant (m)FOLFIRINOX for BR PDAC, 424 met inclusion criteria and 300 (70.8%) were propensity score–matched. After matching, median OS was 26.2 months (95% CI, 24.0–38.4) with RT versus 32.8 months (95% CI, 25.3–42.0) without RT (P=.71). RT was associated with a lower resection rate (55.3% vs 72.7%; P=.002). In patients who underwent a resection, RT was associated with a comparable margin-negative resection rate (>1 mm) (70.6% vs 64.8%; P=.51), more node-negative disease (57.3% vs 37.6%; P=.01), and more major pathologic response with <5% tumor viability (24.7% vs 8.3%; P=.006). The OS associated with conventional and stereotactic body RT approaches was similar (median OS, 25.7 vs 26.0 months; P=.92). Conclusions: In patients with BR PDAC, neoadjuvant RT following (m)FOLFIRINOX was associated with more node-negative disease and better pathologic response in patients who underwent resection, yet no difference in OS was found. Routine use of RT cannot be recommended based on these data.

Publisher

Harborside Press, LLC

Subject

Oncology

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