TY - JOUR
T1 - Molecular targeted positron emission tomography imaging and radionuclide therapy of pancreatic ductal adenocarcinoma
AU - Poels, Thomas T.
AU - Vuijk, Floris A.
AU - de Geus-Oei, Lioe-Fee
AU - Vahrmeijer, Alexander L.
AU - Oprea-Lager, Daniela E.
AU - Swijnenburg, Rutger-Jan
N1 - Funding Information: Author Contributions: Conceptualization, T.T.P., D.E.O.-L. and R.-J.S.; methodology, T.T.P., DA.uEt.Oho.-rLC. oanndtr iRb.u-Jt.iSo.n; sfo: rCmoanlc eapntaulyalsiizsa, tTio.Tn,.PT..,T D.P..,ED.O.E.-.LO.. -aLn.da nRd.-RJ..S-.J;. Si.n;vmeestthigoadtioolnog, yT,.TT..TP..P,. ,DD.E.E.O.O.-.-LL. . aanndd RR..--JJ..SS..;; froersmouarlcaens,alTy.sTis.P,T., .TD.P.E.,.DO..E-L.O. .a-nLd. aRnd.-JR.S..-;J .wS.;riitninvge—stiograitgioinna,lT d.Tr.aPf.,t Dp.rEe.pOa.r-aLt.ioann,d TR..T-J.P.S..,; Dre.Eso.Our.-cLes. ,aTn.dT.RP..,-DJ.S.E.;.Ow.r-iLti.nagn—d rRe.v-Ji.eSw.; w anridtinedg—itinorgi,gTin.Ta.lPd.,r aDft.Ep.Ore.p-Lar.,aRti.o-nJ.,ST.,.TF..PA.,.VD..,E L.O.-F.-.Ld..Gan.-dOR. .a-Jn.Sd.; A.L.V.; visualization, T.T.P., D.E.O.-L. and R.-J.S.; supervision, D.E.O.-L. and R.-J.S.; project admin-iTst.Tra.Pt.i,oDn,.ET.O.T..-PL.., aDn.dE.RO..--JL.S..a; nsudpRer.-vJ.iSsi.o; nfu,nDd.Ein.Og .a-Lcq. uanisditRio.n-J,.SR.;.-pJ.rSo.jeAcltl aadumthionrisst hraatvioenr,eTa.dT.aP.n,dD a.Eg.rOe.e-dL . taon tdheR p.-uJ.Sb.l;isfhuendd ivnegrsaicoqnu oisfittihoen m, Ra.n-Ju.Ss.cAripllta. uthors have read and agreed to the published version of the manuscript. Funding: This research was funded by the Dutch Cancer Society (KWF) Young Investigator Grant [FDurn. dRi.nJ.gS: wThijinsernebsueargrc]h [gwraasntfunnudmedbebry 1t1h2e8D9]u atcnhd Cbayn cCearnScoecri eCtyen(tKeWr AF)mYsoteurndgamIn v(eCsCtiAga) to[Dr rG. rRa.nJ.t S[wDrij.neRn.Jb.uSrwg]i j[ngernabnut rngu]m[gbrearn CtCnAum20b1e9r-21-12228].9 ] and by Cancer Center Amsterdam (CCA) [Dr. R.J. Swijnenburg] [grant number CCA2019-2-22]. Conflicts of Interest: The authors declare no conflicts of interest. Conflicts of Interest: The authors declare no conflict of interest. Funding Information: This research was funded by the Dutch Cancer Society (KWF) Young Investigator Grant [Dr. R.J. Swijnenburg] [grant number 11289] and by Cancer Center Amsterdam (CCA) [Dr. R.J. Swijnenburg] [grant number CCA2019-2-22]. Publisher Copyright: © 2021 by the authors. Licensee MDPI, Basel, Switzerland.
PY - 2021/12/1
Y1 - 2021/12/1
N2 - Pancreatic ductal adenocarcinoma (PDAC) has an inauspicious prognosis, mainly due to difficulty in early detection of the disease by the current imaging modalities. The upcoming development of tumour-specific tracers provides an alternative solution for more accurate diagnostic imaging techniques for staging and therapy response monitoring. The future goal to strive for, in a patient with PDAC, should definitely be first to receive a diagnostic dose of an antibody labelled with a radionuclide and to subsequently receive a therapeutic dose of the same labelled antibody with curative intent. In the first part of this paper, we summarise the available evidence on tumour-targeted diagnostic tracers for molecular positron emission tomography (PET) imaging that have been tested in humans, together with their clinical indications. Tracers such as radiolabelled prostate-specific membrane antigen (PSMA)—in particular,18 F-labelled PSMA—already validated and successfully implemented in clinical practice for prostate cancer, also seem promising for PDAC. In the second part, we discuss the theranostic applications of these tumour-specific tracers. Although targeted radionuclide therapy is still in its infancy, lessons can already be learned from early publications focusing on dose fractioning and adding a radiosensitiser, such as gemcitabine.
AB - Pancreatic ductal adenocarcinoma (PDAC) has an inauspicious prognosis, mainly due to difficulty in early detection of the disease by the current imaging modalities. The upcoming development of tumour-specific tracers provides an alternative solution for more accurate diagnostic imaging techniques for staging and therapy response monitoring. The future goal to strive for, in a patient with PDAC, should definitely be first to receive a diagnostic dose of an antibody labelled with a radionuclide and to subsequently receive a therapeutic dose of the same labelled antibody with curative intent. In the first part of this paper, we summarise the available evidence on tumour-targeted diagnostic tracers for molecular positron emission tomography (PET) imaging that have been tested in humans, together with their clinical indications. Tracers such as radiolabelled prostate-specific membrane antigen (PSMA)—in particular,18 F-labelled PSMA—already validated and successfully implemented in clinical practice for prostate cancer, also seem promising for PDAC. In the second part, we discuss the theranostic applications of these tumour-specific tracers. Although targeted radionuclide therapy is still in its infancy, lessons can already be learned from early publications focusing on dose fractioning and adding a radiosensitiser, such as gemcitabine.
KW - Pancreatic ductal adenocarcinoma
KW - Positron emission tomography
KW - Radionuclide
KW - Tu-mour tracer
UR - http://www.scopus.com/inward/record.url?scp=85120644416&partnerID=8YFLogxK
U2 - https://doi.org/10.3390/cancers13246164
DO - https://doi.org/10.3390/cancers13246164
M3 - Review article
C2 - 34944781
SN - 2072-6694
VL - 13
JO - Cancers
JF - Cancers
IS - 24
M1 - 6164
ER -