A Randomized Phase II Trial of Gemcitabine, Nab-Paclitaxel, Cisplatin with or without a Medically Supervised Ketogenic Diet for Patients with Metastatic Pancreatic Cancer
Jameson, G. S.; Roe, D. J.; Borazanci, E.; Hanna, D. L.; Roberts, C. G. P.; Pelster, M. S.; Frank, R. C.; Alistar, A. T.; Miller, A. M.; Wiedmeier-Nutor, J. E.; Algaze, S. D.; Zoller, A. R.; Hallberg, S. J.; Wertheim, B. C.; Cridebring, D.; Rabinowitz, J. D.; Gately, S.; Keppler, J.; Sharma, S.; Von Hoff, D. D.; Rasco, D. W.
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BackgroundIn this Phase II randomized clinical trial, we evaluated a medically supervised ketogenic diet (MSKD) compared to a usual diet (non-MSKD) when combined with the triplet chemotherapy regimen of gemcitabine, nab-paclitaxel with cisplatin in patients with treatment-naive advanced pancreatic ductal adenocarcinoma (PDAC). MethodsPatients with treatment-naive metastatic PDAC were randomized 1:1 to MSKD or non-MSKD while receiving gemcitabine, nab-paclitaxel, cisplatin on Days 1, 8 of a 21-day cycle. The MSKD was guided by tracking of daily ketone (beta-hydroxybutyrate, BHB) and glucose levels, a web-based application, education, and communication with a remote care team to maintain nutritional ketosis, targeting BHB 0.5-3.0mM. Patients with BMI < 18 kg/m2, type 1 diabetes or history of diabetic ketoacidosis were excluded. The primary endpoint was progression-free survival (PFS), tested using a one-sided alpha level of 0.20. Secondary endpoints included overall survival (OS), disease control rate (DCR; partial response + complete response + stable disease at 9 weeks), incidence and severity of adverse events (AEs) and changes in CA 19-9, fasting insulin, HbA1c, BHB, body weight, and quality of life (QLQ-C30). FindingsFifty-six patients with untreated metastatic PDAC were consented, of which 41 were eligible and 36 were enrolled and randomized. Among 32 evaluable patients (median age 65.9 years; 53% male), 16 were randomized to each arm. In the MSKD arm, 15 of 16 patients achieved nutritional ketosis at any point during the study, with mean BHB of 0.49 mM (95% CI 0.36-0.63) and median proportion of days in ketosis of 39.4% (range 0-95.8%). The study met its primary endpoint. Patients on the MSKD had a PFS by RECIST or clinical progression of 8.5 months, compared to non-MSKD of 5.5 months, HR (95% CI) = 0.53 (0.20 - 1.36) p = 0.092 (one-sided). Patients in the MSKD arm had a median OS of 13.7 months versus 10.2 months in the non-MSKD arm, HR (95% CI) = 0.58 p = 0.107 (one-sided). All MSKD-related AEs were Grade 1-2 and included fatigue, constipation, weight loss, decreased appetite, dehydration, dizziness and nausea. None of the patients stopped the MSKD due to related AEs. There were no significant differences in grade [≥]3 chemotherapy-related AEs between the arms. ConclusionsA medically supervised ketogenic diet is feasible in patients with treatment-naive metastatic pancreatic adenocarcinoma, and when combined with gemcitabine, nab-paclitaxel, and cisplatin, demonstrates significant improvements in progression-free and overall survival, without added toxicity or detriment to quality of life. Larger studies are required to definitively establish the value of ketogenic diet in pancreatic cancer treatment.
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