Local and systemic recurrence following total neoadjuvant therapy (TNT) and resection for borderline resectable and locally advanced pancreatic adenocarcinoma: Long-term follow up from two phase II studies.

Authors

null

Grace E. Ryan

Massachusetts General Hospital, Boston, MA

Grace E. Ryan , Janet E. Murphy , Christine A. Ulysse , Beow Y. Yeap , Jennifer Yon-Li Wo , Colin D. Weekes , Jeffrey William Clark , Jill N. Allen , Lawrence Scott Blaszkowsky , Ryan David Nipp , Lorraine C. Drapek , Aparna Raj Parikh , Christine Bolton , Jacob Maruna , Cristina R. Ferrone , Motaz Qadan , Keith D. Lillemoe , David P. Ryan , Carlos Fernandez Del-Castillo , Theodore S. Hong

Organizations

Massachusetts General Hospital, Boston, MA, Hematology/Oncology, Massachusetts General Hospital, Boston, MA, University of Colorado Comprehensive Cancer Center, Aurora, CO, Department of Medicine, Division of Hematology & Oncology, Massachusetts General Hospital & Harvard Medical School, Boston, MA, Department of Radiation Oncology, Massachusetts General Hospital, Boston, MA, University of California San Francisco, San Francisco, CA, Memorial Sloan Kettering Cancer Center, New York, NY, Department of Surgery, Massachusetts General Hospital, Harvard Medical School, Boston, MA

Research Funding

No funding received
None

Background: With the advent of FOLFIRINOX, the management of pancreatic cancer has undergone a profound change. There has been a shift to TNT with FOLFIRINOX followed by radiation and an attempt at surgical resection. Recent trials of TNT have demonstrated an ability to resect locally advanced (LA) and borderline resectable disease. There is a lack of prospective data demonstrating local and systemic recurrence rates after TNT. Methods: Two previously reported prospective clinical trials (Murphy JE, et al, JAMA Oncol 2018, 2019) of total neoadjuvant therapy were conducted between 2012 and 2018 for borderline and LA disease (NCT01591733, NCT01821729). Patients received FOLFIRINOX for 8 cycles. Upon restaging, patients with resolution of vascular involvement received short-course chemoradiotherapy (5 Gy x 5 with protons or 3 Gy x 10 w photons) with capecitabine (N=34). Patients with persistent vascular involvement received long-course chemoradiotherapy with capecitabine (N=56). All patients were considered for resection after TNT except for those patients with metastatic or unresectable disease. Results: 97 eligible patients were enrolled and started treatment on the borderline resectable (n = 48) and locally advanced (n= 49) study. 90 patients completed therapy. 80 patients were taken to the operating room. 61 patients had R0 resection and 5 patients had R1 resection. The table shows the distribution of local recurrences, local recurrences and metastatic disease, and metastatic disease alone. With a median follow-up of 5.2 years (range: 2.4-6.0), of the 61 R0 patients, 22 patients remained alive and free of disease, 7 patients had a local recurrence, 4 patients had locoregional and metastatic recurrence, and 24 patients had a metastatic recurrence. 3 patients who underwent R0 resection died of unrelated causes. Median survival for patients undergoing R0 resection is 43.8 months. Conclusions: Total neoadjuvant therapy for locally advanced and borderline resectable pancreatic cancer is potentially curable and may change the pattern of spread.

N
mOS (mos)
LR only
LR+M
M alone
DwD nos
DwoD
NED
All
97
32.3
16
7
40
2
6
26
Unresected*
31
14.5
8
3
14
1
2
3
R0+R1
66
43.8
8
4
26
1
4
23
R0
61
43.8
7
4
24
1
3
22
R1
5
46.0
1
0
2
0
1
1

*Unresected: unresectable and off-study early due to progression, toxicity or withdrawal. mOS: median survival; DwD nos: died of disease, recurrence sites unknown; DwoD: died of unrelated cause; NED: alive free of disease.

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Abstract Details

Meeting

2021 ASCO Annual Meeting

Session Type

Poster Session

Session Title

Gastrointestinal Cancer—Gastroesophageal, Pancreatic, and Hepatobiliary

Track

Gastrointestinal Cancer—Gastroesophageal, Pancreatic, and Hepatobiliary

Sub Track

Pancreatic Cancer

Citation

J Clin Oncol 39, 2021 (suppl 15; abstr 4133)

DOI

10.1200/JCO.2021.39.15_suppl.4133

Abstract #

4133

Poster Bd #

Online Only

Abstract Disclosures