Phase III APACT trial of adjuvant nab-paclitaxel plus gemcitabine (nab-P + Gem) versus gemcitabine (Gem) alone for patients with resected pancreatic cancer (PC): Outcomes by geographic region.

Authors

null

Michele Reni

IRCCS Ospedale, San Raffaele Scientific Institute, Milan, Italy

Michele Reni , Hanno Riess , Eileen Mary O'Reilly , Joon Oh Park , Hassan Hatoum , Berta Laquente Saez , Tapio Salminen , Helmut Oettle , Rafael Lopez , Scot D. Dowden , Meinolf Karthaus , Josep Tabernero , Eric Van Cutsem , Philip Agop Philip , David Goldstein , Jordan Berlin , Margaret A. Tempero

Organizations

IRCCS Ospedale, San Raffaele Scientific Institute, Milan, Italy, Charité Universitätsmedizin, Berlin, Germany, Memorial Sloan Kettering Cancer Center, New York, NY, Division of Hematology-Oncology, Department of Medicine, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, South Korea, University of Oklahoma Health Sciences Center, Oklahoma City, OK, Institut d'Investigació Biomédica de Bellvitge (IDIBELL), Barcelona, Spain, University of Tampere, Tampere, Finland, Onkologische und Hamatologische Schwerpunktpraxis, Friedrichshafen, Germany, Head of Medical Oncology Department, Complexo Hospitalario Universitario, Santiago de Compostela, Spain, University of Calgary Tom Baker Cancer Centre, Calgary, AB, Canada, Hematology, Oncology, and Palliative Medicine, Klinikum Neuperlach and Harlaching, Munich, Germany, Vall d'Hebron University Hospital, Vall d'Hebron Institute of Oncology (VHIO), Barcelona, Spain, University Hospitals Gasthuisberg Leuven, KU Leuven, Leuven, Belgium, Karmanos Cancer Institute, Detroit, MI, Nelune Cancer Centre, Prince of Wales Hospital and University of New South Wales, Randwick, NSW, Australia, Vanderbilt University, Nashville, TN, School of Medicine, University of California, San Francisco, CA

Research Funding

Other
Bristol-Myers Squibb

Background: The APACT trial was one of the largest and most geographically diverse trials of adjuvant chemotherapy for resected PC, allowing for comparison of outcomes by geographic region. In this analysis, we report updated overall survival (OS) results for the intent-to-treat (ITT) population and examine outcomes by geographic region. Methods: Treatment-naive patients with histologically confirmed PC, macroscopic complete resection, Eastern Cooperative Oncology Group performance status 0 or 1, and carbohydrate antigen 19-9 < 100 U/mL were eligible. Stratification factors were resection status (R0/R1) and lymph node status (positive/negative). Treatment was initiated ≤ 12 weeks postsurgery. Patients received nab-P 125 mg/m2 + Gem 1000 mg/m2 or Gem 1000 mg/m2 on days 1, 8, and 15 of six 28-day cycles. The primary endpoint was disease-free survival by independent review. Secondary endpoints were OS and safety. Results: The updated OS analysis (data cutoff date, January 2020) revealed a median OS of 41.8 months with nab-P + Gem compared with 37.7 months with Gem alone (hazard ratio [HR] 0.81; 95% CI, 0.68 - 0.97; nominal P = 0.047; Table). In each geographic region, the median OS with nab-P + Gem was numerically longer than with Gem alone. Conclusions: The updated OS analysis of the ITT population supports the previously reported trend favoring nab-P + Gem. The geographic regional analyses reveal numerically longer OS with nab-P + Gem vs Gem alone and variable outcomes by region; however, the differences do not support the trend observed in the ITT population, potentially due to limited sample sizes. Registration: EudraCT (2013-003398-91). Clinical trial information: NCT01964430.

Survival Outcomes by Geographic Region.

Groupnab-P + Gem
Gem
HR
(95% CI)
P value
nMedian (95% CI) OS, monMedian (95% CI) OS, mo
ITT population43241.8
(35.55 - 46.75)
43437.7
(31.11 - 40.51)
0.81
(0.68 - 0.97)
0.047
North America14438.5
(32.56 - 53.13)
15635.0
(28.25 - 41.33)
0.73
(0.54 - 0.99)
0.11
Europe20341.8
(32.82 - 48.03)
20538.1
(30.72 - 43.40)
0.88
(0.68 - 1.13)
0.40
Australia3031.5
(19.06 - NA)
2028.1
(17.05 - 43.01)
0.65
(0.30 - 1.38)
0.39
Asia Pacific5545.5
(27.01 - NA)
5340.6
(24.21 - NA)
0.83
(0.50 - 1.39)
0.43

NA, not applicable

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Abstract Details

Meeting

2020 ASCO Virtual Scientific Program

Session Type

Poster Discussion Session

Session Title

Gastrointestinal Cancer—Gastroesophageal, Pancreatic, and Hepatobiliary

Track

Gastrointestinal Cancer—Gastroesophageal, Pancreatic, and Hepatobiliary

Sub Track

Pancreatic Cancer

Clinical Trial Registration Number

NCT01964430

Citation

J Clin Oncol 38: 2020 (suppl; abstr 4515)

DOI

10.1200/JCO.2020.38.15_suppl.4515

Abstract #

4515

Poster Bd #

123

Abstract Disclosures