Bridge Institute of Experimental Tumor Therapy, West German Cancer Center, University Medicine EssenEssen, Germany
Division of Solid Tumor Translational Oncology, German Cancer Research Center (DKFZ) and German Cancer Consortium (DKTK), partner site EssenHeidelberg, Germany
This work is licensed under the Creative Commons Attribution 4.0 International License.
Rowcroft A, Loveday BPT, Thomson BNJ, Banting S, Knowles B. Systematic review of liver directed therapy for uveal melanoma hepatic metastases. HPB (Oxford) 2020; 22: 497–505. doi: 10.1016/j.hpb.2019.11.002RowcroftALovedayBPTThomsonBNJBantingSKnowlesBSystematic review of liver directed therapy for uveal melanoma hepatic metastasesHPB (Oxford)20202249750510.1016/j.hpb.2019.11.002Open DOISearch in Google Scholar
Singh AD, Turell ME, Topham AK. Uveal melanoma: trends in incidence, treatment, and survival. Ophthalmology 2011; 118: 1881–5. doi: 10.1016/j.ophtha.2011.01.040SinghADTurellMETophamAKUveal melanoma: trends in incidence, treatment, and survivalOphthalmology20111181881510.1016/j.ophtha.2011.01.040Open DOISearch in Google Scholar
Rietschel P, Panageas KS, Hanlon C, Patel A, Abramson DH, Chapman PB. Variates of survival in metastatic uveal melanoma. J Clin Oncol 2005; 23: 8076–80. doi: 10.1200/JCO.2005.02.6534RietschelPPanageasKSHanlonCPatelAAbramsonDHChapmanPBVariates of survival in metastatic uveal melanomaJ Clin Oncol20052380768010.1200/JCO.2005.02.6534Open DOISearch in Google Scholar
Damato BE, Coupland SE. Differences in uveal melanomas between men and women from the British Isles. Eye 2012; 26: 292–9. doi: 10.1038/eye.2011.272DamatoBECouplandSEDifferences in uveal melanomas between men and women from the British IslesEye201226292910.1038/eye.2011.272Open DOISearch in Google Scholar
Diener-West M, Reynolds SM, Agugliaro DJ, Caldwell R, Cumming K, Earle JD, et al. Development of metastatic disease after enrolment in the COMS trials for treatment of choroidal melanoma: Collaborative Ocular Melanoma Study Group Report No. 26. Arch Ophthalmol 2005; 123: 1639–43. doi: 10.1001/archopht.123.12.1639Diener-WestMReynoldsSMAgugliaroDJCaldwellRCummingKEarleJDDevelopment of metastatic disease after enrolment in the COMS trials for treatment of choroidal melanoma: Collaborative Ocular Melanoma Study Group Report No. 26Arch Ophthalmol200512316394310.1001/archopht.123.12.1639Open DOISearch in Google Scholar
Gragoudas ES, Egan KM, Seddon JM, Glynn RJ, Walsh SM, Finn SM, et al. Survival of patents with metastases from uveal melanoma. Ophthalmology 1991; 98: 383–90. doi: 10.1016/s0161-6420(91)32285-1GragoudasESEganKMSeddonJMGlynnRJWalshSMFinnSMSurvival of patents with metastases from uveal melanomaOphthalmology1991983839010.1016/s0161-6420(91)32285-1Open DOISearch in Google Scholar
Chew AL, Spilsbury K, Isaacs TW. Survival from uveal melanoma in Western Australia 1981–2005. Clin Exp Ophthalmol 2015; 43: 422–8. doi: 10.1111/ceo.12490ChewALSpilsburyKIsaacsTWSurvival from uveal melanoma in Western Australia 1981–2005Clin Exp Ophthalmol201543422810.1111/ceo.12490Open DOISearch in Google Scholar
Bedikian AY, Legha SS, Mavligit G, Carrasco CH, Khorana S, Plager C, et al. Treatment of uveal melanoma metastatic to the liver. A review of the M. D. Anderson cancer center experience and prognostic factors. Cancer 1995; 76: 1665–70. doi: 10.1002/1097-0142(19951101)76:9<1665::aidcncr2820760925>3.0.co;2-jBedikianAYLeghaSSMavligitGCarrascoCHKhoranaSPlagerCTreatment of uveal melanoma metastatic to the liver. A review of the M. D. Anderson cancer center experience and prognostic factorsCancer19957616657010.1002/1097-0142(19951101)76:9<1665::aidcncr2820760925>3.0.co;2-jOpen DOISearch in Google Scholar
Schelhorn J, Richly H, Ruhlmann M, Lauenstein TC, Theysohn JM. A single-center experience in radioembolization as salvage therapy of hepatic metastases of uveal melanoma. Acta Radiol Open 2015; 4: 2047981615570417. doi: 10.1177/2047981615570417SchelhornJRichlyHRuhlmannMLauensteinTCTheysohnJMA single-center experience in radioembolization as salvage therapy of hepatic metastases of uveal melanomaActa Radiol Open20154204798161557041710.1177/2047981615570417Open DOISearch in Google Scholar
Heusner TA, Antoch G, Wittkowski-Sterczewski A, Ladd SC, Forsting M, Verhagen R, et al. Transarterial hepatic chemoperfusion of uveal melanoma metastases: survival and response to treatment. RoFo 2011; 183: 1151–60. doi: 10.1055/s-0031-1281743HeusnerTAAntochGWittkowski-SterczewskiALaddSCForstingMVerhagenRTransarterial hepatic chemoperfusion of uveal melanoma metastases: survival and response to treatmentRoFo201118311516010.1055/s-0031-1281743Open DOISearch in Google Scholar
Leyvraz S, Piperno-Neumann S, Suciu S, Baurain JF, Zdzienicki M, Testori A, et al. Hepatic intra-arterial versus intravenous fotemustine in patients with liver metastases from uveal melanoma (EORTC 18021): a multicentric randomized trial. Ann Oncol 2014; 25: 742–6. doi: 10.1093/annonc/mdt585LeyvrazSPiperno-NeumannSSuciuSBaurainJFZdzienickiMTestoriAHepatic intra-arterial versus intravenous fotemustine in patients with liver metastases from uveal melanoma (EORTC 18021): a multicentric randomized trialAnn Oncol201425742610.1093/annonc/mdt585Open DOISearch in Google Scholar
Duran R, Chapiro J, Frangakis C, Lin M, Schlachter TR, Schernthaner RE, et al. Uveal melanoma metastatic to the liver: the role of quantitative volumetric contrast-enhanced MR imaging in the assessment of early tumor response after transarterial chemoembolization. Transl Oncol 2014; 7: 447–55. doi: 10.1016/j.tranon.2014.05.004DuranRChapiroJFrangakisCLinMSchlachterTRSchernthanerREUveal melanoma metastatic to the liver: the role of quantitative volumetric contrast-enhanced MR imaging in the assessment of early tumor response after transarterial chemoembolizationTransl Oncol201474475510.1016/j.tranon.2014.05.004Open DOISearch in Google Scholar
Erasmus JJ, Gladish GW, Broemeling L, Sabloff BS, Truong MT, Herbst RS, et al. Interobserver and intraobserver variability in measurement of non-small-cell carcinoma lung lesions: implications for assessment of tumor response. J Clin Oncol 2003; 21: 2574–82. doi: 10.1200/JCO.2003.01.144ErasmusJJGladishGWBroemelingLSabloffBSTruongMTHerbstRSInterobserver and intraobserver variability in measurement of non-small-cell carcinoma lung lesions: implications for assessment of tumor responseJ Clin Oncol20032125748210.1200/JCO.2003.01.144Open DOISearch in Google Scholar
Thiesse P, Ollivier L, Di Stefano-Louineau D, Négrier S, Savary J, Pignard K, et al. Response rate accuracy in oncology trials: reasons for interobserver variability. Groupe Français d’Immunothérapie of the Fédération Nationale des Centres de Lutte Contre le Cancer. J Clin Oncol 1997; 15: 3507–14. doi: 10.1200/JCO.1997.15.12.3507ThiessePOllivierLDi Stefano-LouineauDNégrierSSavaryJPignardKResponse rate accuracy in oncology trials: reasons for interobserver variability. Groupe Français d’Immunothérapie of the Fédération Nationale des Centres de Lutte Contre le CancerJ Clin Oncol19971535071410.1200/JCO.1997.15.12.3507Open DOISearch in Google Scholar
Koitka S, Gudlin P, Theysohn JM, Oezcelik A, Hoyer DP, Dayangac M, et al. Fully automated preoperative liver volumetry incorporating the anatomical location of the central hepatic vein. Sci Rep 2022; 12: 16479. doi: 10.1038/s41598-022-20778-4KoitkaSGudlinPTheysohnJMOezcelikAHoyerDPDayangacMFully automated preoperative liver volumetry incorporating the anatomical location of the central hepatic veinSci Rep2022121647910.1038/s41598-022-20778-4Open DOISearch in Google Scholar
Zensen S, Opitz MK, Ludwig JM, Haubold J, Richly H, Siveke JT, et al. Radiation dose aspects of hepatic artery infusion chemotherapy in uveal melanoma patients with liver metastases. Cardiovasc Intervent Radiol 2022; 45: 841–5. doi: 10.1007/s00270-022-03130-1ZensenSOpitzMKLudwigJMHauboldJRichlyHSivekeJTRadiation dose aspects of hepatic artery infusion chemotherapy in uveal melanoma patients with liver metastasesCardiovasc Intervent Radiol202245841510.1007/s00270-022-03130-1Open DOISearch in Google Scholar
Pinguet F, Culine S, Bressolle F, Astre C, Serre MP, Chevillard C, et al. A phase I and pharmacokinetic study of melphalan using a 24-hour continuous infusion in patients with advanced malignancies. Clin Cancer Res 2000; 6: 57–63. PMID: 10656432PinguetFCulineSBressolleFAstreCSerreMPChevillardCA phase I and pharmacokinetic study of melphalan using a 24-hour continuous infusion in patients with advanced malignanciesClin Cancer Res20006576310656432Search in Google Scholar
Boone BA, Perkins S, Bandi R, Santos E, McCluskey K, Bartlett DL, et al. Hepatic artery infusion of melphalan in patients with liver metastases from ocular melanoma. J Surg Oncol 2018; 117: 940–6. doi: 10.1002/jso.24984BooneBAPerkinsSBandiRSantosEMcCluskeyKBartlettDLHepatic artery infusion of melphalan in patients with liver metastases from ocular melanomaJ Surg Oncol2018117940610.1002/jso.24984Open DOISearch in Google Scholar
Eisenhauer EA, Therasse P, Bogaerts J, Schwartz LH, Sargent D, Ford R, et al. New response evaluation criteria in solid tumours: revised RECIST guideline (version 1.1). Eur J Cancer 2009; 45: 228–47. doi: 10.1016/j.ejca.2008.10.026EisenhauerEATherassePBogaertsJSchwartzLHSargentDFordRNew response evaluation criteria in solid tumours: revised RECIST guideline (version 1.1)Eur J Cancer2009452284710.1016/j.ejca.2008.10.026Open DOISearch in Google Scholar
Landis JR, Koch GG. The measurement of observer agreement for categorical data. Biometrics 1977; 33: 159–74. PMID: 843571LandisJRKochGGThe measurement of observer agreement for categorical dataBiometrics19773315974843571Search in Google Scholar
Karydis I, Gangi A, Wheater MJ, Choi J, Wilson I, Thomas K, et al. Percutaneous hepatic perfusion with melphalan in uveal melanoma: a safe and effective treatment modality in an orphan disease. J Surg Oncol 2018; 117: 1170–8. doi: 10.1002/jso.24956KarydisIGangiAWheaterMJChoiJWilsonIThomasKPercutaneous hepatic perfusion with melphalan in uveal melanoma: a safe and effective treatment modality in an orphan diseaseJ Surg Oncol20181171170810.1002/jso.24956Open DOISearch in Google Scholar
Kalkmann J, Forsting M, Stattaus J. Liver volume variations as a parameter to assess therapy response in advanced metastatic liver disease. Onkologie 2011; 34: 30–4. doi: 10.1159/000323373KalkmannJForstingMStattausJLiver volume variations as a parameter to assess therapy response in advanced metastatic liver diseaseOnkologie20113430410.1159/000323373Open DOISearch in Google Scholar
Purkiss SF, Williams NS. Growth rate and percentage hepatic replacement of colorectal liver metastases. Br J Surg 1993; 80: 1036–8. doi: 10.1002/bjs.1800800838PurkissSFWilliamsNSGrowth rate and percentage hepatic replacement of colorectal liver metastasesBr J Surg1993801036810.1002/bjs.1800800838Open DOISearch in Google Scholar
Opitz M, Zensen S, Ludwig JM, Weber M, Alatzides G, Seifert R, et al. Radiation dose aspects and establishment of diagnostic reference levels for90Y radioembolisation during angiographic procedure. J Radiol Prot 2022; 42(3). doi: 10.1088/1361-6498/ac8f9eOpitzMZensenSLudwigJMWeberMAlatzidesGSeifertRRadiation dose aspects and establishment of diagnostic reference levels for90Y radioembolisation during angiographic procedureJ Radiol Prot202242310.1088/1361-6498/ac8f9eOpen DOISearch in Google Scholar
Schaarschmidt BM, Wildgruber M, Kloeckner R, Nie J, Steinle V, Braat AJAT, et al. 90Y Radioembolization in the treatment of neuroendocrine neoplasms: results of an international multicenter retrospective study. J Nucl Med 2022; 63: 679–85. doi: 10.2967/jnumed.121.262561SchaarschmidtBMWildgruberMKloecknerRNieJSteinleVBraatAJAT90Y Radioembolization in the treatment of neuroendocrine neoplasms: results of an international multicenter retrospective studyJ Nucl Med2022636798510.2967/jnumed.121.262561Open DOISearch in Google Scholar
Schaarschmidt BM, Kloeckner R, Dertnig T, Demircioglu A, Müller L, Auer TA, et al. Real-life experience in the treatment of intrahepatic cholangiocarcinoma by 90Y radioembolization: a multicenter retrospective study. J Nucl Med 2023; 64: 529–35. doi: 10.2967/jnumed.122.264598SchaarschmidtBMKloecknerRDertnigTDemirciogluAMüllerLAuerTAReal-life experience in the treatment of intrahepatic cholangiocarcinoma by 90Y radioembolization: a multicenter retrospective studyJ Nucl Med2023645293510.2967/jnumed.122.264598Open DOISearch in Google Scholar
Krasovitsky M, Lee YC, Sim H-W, Chawla T, Moore H, Moses D, et al. Interobserver and intraobserver variability of RECIST assessment in ovarian cancer. Int J Gynecol Cancer 2022; 32: 656–61. doi: 10.1136/ijgc-2021-003319KrasovitskyMLeeYCSimH-WChawlaTMooreHMosesDInterobserver and intraobserver variability of RECIST assessment in ovarian cancerInt J Gynecol Cancer2022326566110.1136/ijgc-2021-003319Open DOISearch in Google Scholar
Suzuki C, Torkzad MR, Jacobsson H, Aström G, Sundin A, Hatschek T, et al. Interobserver and intraobserver variability in the response evaluation of cancer therapy according to RECIST and WHO-criteria. Acta Oncol 2010; 49: 509–14. doi: 10.3109/02841861003705794SuzukiCTorkzadMRJacobssonHAströmGSundinAHatschekTInterobserver and intraobserver variability in the response evaluation of cancer therapy according to RECIST and WHO-criteriaActa Oncol2010495091410.3109/02841861003705794Open DOISearch in Google Scholar
Kuhl CK, Alparslan Y, Schmoee J, Sequeira B, Keulers A, Brümmendorf TH, et al. Validity of RECIST Version 1.1 for response assessment in metastatic cancer: a prospective, multireader study. Radiology 2019; 290: 349–56. doi: 10.1148/radiol.2018180648KuhlCKAlparslanYSchmoeeJSequeiraBKeulersABrümmendorfTHValidity of RECIST Version 1.1 for response assessment in metastatic cancer: a prospective, multireader studyRadiology20192903495610.1148/radiol.2018180648Open DOISearch in Google Scholar
Gafita A, Rauscher I, Fendler WP, Murthy V, Hui W, Armstrong WR, et al. Measuring response in metastatic castration-resistant prostate cancer using PSMA PET/CT: comparison of RECIST 1.1, aPCWG3, aPERCIST, PPP, and RECIP 1.0 criteria. Eur J Nucl Med Mol Imaging 2022; 49: 4271–81. doi: 10.1007/s00259-022-05882-xGafitaARauscherIFendlerWPMurthyVHuiWArmstrongWRMeasuring response in metastatic castration-resistant prostate cancer using PSMA PET/CT: comparison of RECIST 1.1, aPCWG3, aPERCIST, PPP, and RECIP 1.0 criteriaEur J Nucl Med Mol Imaging20224942718110.1007/s00259-022-05882-xOpen DOISearch in Google Scholar
Hagen F, Mair A, Bitzer M, Bösmüller H, Horger M. Fully automated whole-liver volume quantification on CT-image data: comparison with manual volumetry using enhanced and unenhanced images as well as two different radiation dose levels and two reconstruction kernels. PloS one 2021; 16: e0255374. doi: 10.1371/journal.pone.0255374HagenFMairABitzerMBösmüllerHHorgerMFully automated whole-liver volume quantification on CT-image data: comparison with manual volumetry using enhanced and unenhanced images as well as two different radiation dose levels and two reconstruction kernelsPloS one202116e025537410.1371/journal.pone.0255374Open DOISearch in Google Scholar
Cai W, He B, Fan Y, Fang C, Jia F. Comparison of liver volumetry on contrast-enhanced CT images: one semiautomatic and two automatic approaches. J Appl Clin Med Phys 2016; 17: 118–27. doi: 10.1120/jacmp.v17i6.6485CaiWHeBFanYFangCJiaFComparison of liver volumetry on contrast-enhanced CT images: one semiautomatic and two automatic approachesJ Appl Clin Med Phys2016171182710.1120/jacmp.v17i6.6485Open DOISearch in Google Scholar
Suzuki K, Epstein ML, Kohlbrenner R, Garg S, Hori M, Oto A, et al. Quantitative radiology: automated CT liver volumetry compared with interactive volumetry and manual volumetry. AJR Am J Roentgenol 2011; 197: W706–12. doi: 10.2214/AJR.10.5958SuzukiKEpsteinMLKohlbrennerRGargSHoriMOtoAQuantitative radiology: automated CT liver volumetry compared with interactive volumetry and manual volumetryAJR Am J Roentgenol2011197W7061210.2214/AJR.10.5958Open DOISearch in Google Scholar