Back to Search Start Over

Fasting mimicking diet as an adjunct to neoadjuvant chemotherapy for breast cancer in the multicentre randomized phase 2 DIRECT trial

Authors :
Groot, S. de
Lugtenberg, R.T.
Cohen, D.
Welters, M.J.
Ehsan, I.
Vreeswijk, M.P.G.
Smit, V.
Graaf, H. de
Heijns, J.B.
Portielje, J.E.
Wouw, A.J. van de
Imholz, Alexander L. T.
Kessels, L.W.
Vrijaldenhoven, S.
Baars, A.
Kranenbarg, E.M.
Carpentier, M.D.
Putter, H.
Hoeven, J.J.M. van der
Nortier, J.W.
Longo, V.D.
Pijl, H.
Kroep, J.R.
Groot, S. de
Lugtenberg, R.T.
Cohen, D.
Welters, M.J.
Ehsan, I.
Vreeswijk, M.P.G.
Smit, V.
Graaf, H. de
Heijns, J.B.
Portielje, J.E.
Wouw, A.J. van de
Imholz, Alexander L. T.
Kessels, L.W.
Vrijaldenhoven, S.
Baars, A.
Kranenbarg, E.M.
Carpentier, M.D.
Putter, H.
Hoeven, J.J.M. van der
Nortier, J.W.
Longo, V.D.
Pijl, H.
Kroep, J.R.
Source :
Nature Communications; 2041-1723; 1; 11; 3083; ~Nature Communications~~~~~2041-1723~1~11~~3083
Publication Year :
2020

Abstract

Contains fulltext : 225860.pdf (publisher's version ) (Open Access)<br />Short-term fasting protects tumor-bearing mice against the toxic effects of chemotherapy while enhancing therapeutic efficacy. We randomized 131 patients with HER2-negative stage II/III breast cancer, without diabetes and a BMI over 18 kg m(-2), to receive either a fasting mimicking diet (FMD) or their regular diet for 3 days prior to and during neoadjuvant chemotherapy. Here we show that there was no difference in toxicity between both groups, despite the fact that dexamethasone was omitted in the FMD group. A radiologically complete or partial response occurs more often in patients using the FMD (OR 3.168, P = 0.039). Moreover, per-protocol analysis reveals that the Miller&Payne 4/5 pathological response, indicating 90-100% tumor-cell loss, is more likely to occur in patients using the FMD (OR 4.109, P = 0.016). Also, the FMD significantly curtails chemotherapy-induced DNA damage in T-lymphocytes. These positive findings encourage further exploration of the benefits of fasting/FMD in cancer therapy. Trial number: NCT02126449.

Details

Database :
OAIster
Journal :
Nature Communications; 2041-1723; 1; 11; 3083; ~Nature Communications~~~~~2041-1723~1~11~~3083
Publication Type :
Electronic Resource
Accession number :
edsoai.on1366923379
Document Type :
Electronic Resource