Virtual Poster Session in NETs From Munich - prIME Oncology
Virtual Poster
Virtual Poster

Virtual Poster Session in NETs From Munich

Practical Application of Key Data Presented During the 2018 European Oncology Congress

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View CME-certified poster presentations and downloadable slides covering the most up-to-date clinical trial data on neuroendocrine tumors (NETs) from the 2018 European Oncology Congress in Munich.

Interactive Presentation

Interactive Presentation

Downloadable Slides

Downloadable Slides



1 AMA PRA Category 1 Credit™

Release Date

Release Date

Nov 1, 2018

Expiration Date

Nov 2, 2019

Jaume Capdevila, MD, PhD

Abstract #1307O: Efficacy of lenvatinib in patients with advanced pancreatic (panNETs) and gastrointestinal (giNETs) grade 1/2 (G1/G2) neuroendocrine tumors: Results of the international phase II TALENT trial (GETNE 1509)

Featured Expert: Jaume Capdevila, MD, PhD

Dieter Hörsch, MD, PhD

Abstract #1314P: Efficacy and safety of telotristat ethyl (TE) in combination with lanreotide (LAN) in patients with a neuroendocrine tumour and carcinoid syndrome (CS) diarrhoea (CSD): Meta-analysis of phase 3 double-blind placebo (PBO)-controlled TELESTAR and TELECAST studies

Featured Expert: Dieter Hörsch, MD, PhD

Jonathan Strosberg, MD

Abstract #1316P: Impact of liver tumor burden on therapeutic effect of 177Lu-DOTATATE treatment in NETTER-1 study

Featured Expert: Jonathan Strosberg, MD

Filippo de Braud, MD

Abstract #1319P: Post-hoc analysis of CLARINET phase III study to investigate the influence of diabetic status on progression-free survival (PFS) of patients with neuroendocrine tumours (NETs) treated with lanreotide (LAN) or placebo (PBO)

Featured Expert: Filippo de Braud, MD

Vikas Prasad, MD, PhD

Abstract #1331P: Tumour growth rate (TGR) when using lanreotide Autogel® (LAN) before, during and after peptide receptor radionuclide therapy (PRRT) in advanced neuroendocrine tumours (NETs)

Featured Expert: Vikas Prasad, MD, PhD

  • Filippo de Braud, MDFondazione IRCCS - Istituto Nazionale dei Tumori
    Milan, Italy
  • Jaume Capdevila, MD, PhDVall d’Hebron University Hospital
    Barcelona, Spain
  • Dieter Hörsch, MD, PhDCenter for Neuroendocrine Tumors Bad Berka
    Bad Berka, Germany
  • Vikas Prasad, MD, PhDUniversity of Ulm
    Ulm, Germany
  • Jonathan Strosberg, MDMoffitt Cancer Center
    Tampa, Florida, United States

This activity is specifically designed for physicians, nurses, and other clinicians who are cancer specialists.

After successful completion of this educational activity, participants should be able to:

  • Discuss key NET data from the conference
  • Apply key NET data from the conference to clinical practice, as appropriate


Colorectal Cancer

Abstract #LBA18_PR: Durable clinical benefit with nivolumab (NIVO) plus low-dose ipilimumab (IPI) as first-line therapy in microsatellite instability-high/mismatch repair deficient (MSI-H/dMMR) metastatic colorectal cancer (mCRC)
Featured Expert: Heinz-Josef J. Lenz, MD

Abstract #LBA20: TRIBE2: A phase III, randomized strategy study by GONO in the 1st- and 2nd-line treatment of unresectable metastatic colorectal cancer (mCRC) patients (pts)
Featured Expert: Chiara Cremolini, MD

Abstract #463P: Real-world dosing of regorafenib (REG) in metastatic colorectal cancer (mCRC): Final results from the prospective, observational CORRELATE study
Featured Expert: Juan Manuel O’Connor, MD

Abstract #464P: Safety and efficacy of trifluridine/tipiracil (FTD/TPI) in metastatic colorectal cancer (mCRC) patients according to previous treatment with regorafenib in the international phase 3b PRECONNECT study
Featured Expert: Julien Taїeb, MD, PhD

Abstract #466P: Phase II trial to evaluate efficacy and tolerance of regorafenib monotherapy in patients (pts) over 70 with previously treated metastatic colorectal adenocarcinoma (mCRC) FFCD 1404 – REGOLD
Featured Expert: Thomas Aparicio, MD

Hepatocellular Carcinoma

Abstract #LBA26: Updated safety and clinical activity results from a phase Ib study of atezolizumab + bevacizumab in hepatocellular carcinoma (HCC)
Featured Expert: Michael J. Pishvaian, MD, PhD

Abstract #710P: Practice patterns and deterioration of liver function after transarterial chemoembolization (TACE) in hepatocellular carcinoma (HCC): Final analysis of OPTIMIS in Europe and Canada
Featured Expert: Jean-Luc Raoul, MD, PhD

Head & Neck

Abstract #LBA8_PR: KEYNOTE-048: Phase 3 study of first-line pembrolizumab (P) for recurrent/metastatic head and neck squamous cell carcinoma (R/M HNSCC)
Featured Expert: Barbara Burtness, MD

Abstract #1045O: A phase II window of opportunity study of preoperative olaparib (O) with cisplatin (C) or durvalumab (D) or olaparib alone in in patients with operable squamous cell head and neck carcinoma (HNSCC) (OPHELIA)
Featured Expert: Amanda Psyrri, MD, PhD


Abstract #LBA42: OpACIN-neo – A multicenter phase 2 study to identify the optimal neo-adjuvant combination scheme of ipilimumab (IPI) and nivolumab (NIVO)
Featured Expert: Christian U. Blank, MD, PhD

Abstract #LBA45: Phase 1b/2, open label, multicenter, study of the combination of SD-101 and pembrolizumab in patients with advanced melanoma who are naïve to anti-PD-1 therapy
Featured Expert: Antoni Ribas, MD, PhD

 Abstract #1265P – Phase 1b/2 study of the combination of SD-101 and pembrolizumab in patients with advanced melanoma who had progressive disease on or after prior anti-PD-1 therapy
Featured Expert:  Antoni Ribas, MD, PhD 

Abstract #LBA47: Initial results from a phase 3b/4 study evaluating two dosing regimens of nivolumab (NIVO) in combination with ipilimumab (IPI) in patients with advanced melanoma (CheckMate 511)
Featured Expert: Celeste Lebbé, MD

 Abstract #1244O: KEYNOTE-022 Part 3: Phase 2 randomized study of 1L dabrafenib (D) and trametinib (T) plus pembrolizumab (Pembro) or placebo (PBO) for BRAF-mutant advanced melanoma
Featured Expert: Paolo A. Ascierto, MD

Abstract #1248PD: Efficacy of pembrolizumab (Pembro) in patients (Pts) with advanced melanoma with stable brain metastases (BM) at baseline: A pooled retrospective analysis
Featured Expert: Omid Hamid, MD


Abstract #LBA53: IMpower130: Progression-free survival (PFS) and safety analysis from a randomised phase 3 study of carboplatin + nab-paclitaxel (CnP) with or without atezolizumab (atezo) as first-line (1L) therapy in advanced non-squamous NSCLC
Featured Expert: Federico Cappuzzo, MD, PhD

Abstract #LBA54: IMpower132: efficacy of atezolizumab (atezo) + carboplatin (carbo)/cisplatin (cis) + pemetrexed (pem) as 1L treatment in key subgroups with stage IV non-squamous non-small cell lung cancer (NSCLC)
Featured Expert: Fabrice Barlesi, MD, PhD

Abstract #LBA62: Health-related quality of life (HRQoL) for pembrolizumab or placebo plus carboplatin and paclitaxel or nab-paclitaxel in patients with metastatic squamous NSCLC: data from KEYNOTE-407
Featured Expert: Julien Mazières, MD, PhD

Abstract #LBA63: Long-term survival in patients (pts) with advanced NSCLC in the KEYNOTE-010 study overall and in pts who completed 2 years of pembrolizumab (pembro)
Featured Expert: Roy Herbst, MD, PhD

Abstract #1469P: EVIDENS: An observational study of nivolumab-treated patients in advanced non-small cell lung cancer (NSCLC) in a real-world setting: Initial results on 1394 patients
Featured Expert: Fabrice Barlesi, MD, PhD


Abstract #LBA6_PR: JAVELIN Renal 101: a randomized, phase 3 study of avelumab + axitinib vs sunitinib as first-line treatment of advanced renal cell carcinoma (aRCC)
Featured Expert: Manuela Schmidinger, MD

Abstract #LBA31: Molecular correlates differentiate response to atezolizumab (atezo) + bevacizumab (bev) vs sunitinib (sun): results from a Phase III study (IMmotion151) in untreated metastatic renal cell carcinoma (mRCC)
Featured Expert: Brian I Rini, MD

Abstract #874P: Treatment-free interval (TFI) following discontinuation of first-line nivolumab plus ipilimumab (N+I) or sunitinib (S) in patients (Pts) with advanced renal cell carcinoma (aRCC): CheckMate 214 analysis
Featured Expert: David McDermott, MD

Abstract #875P: Characterization of response to nivolumab plus ipilimumab (N+I) or sunitinib (S) in patients (Pts) with previously untreated advanced renal cell carcinoma (aRCC): CheckMate 214
Featured Expert: Brian I Rini, MD

This educational activity is supported by grants from Bayer HealthCare Pharmaceuticals, Inc.; Bristol-Myers Squibb; Ipsen; and Merck and Co, Inc.

Continuing Education

prIME Oncology is accredited by the Accreditation Council for Continuing Medical Education (ACCME) to provide continuing medical education for physicians.

prIME Oncology designates this enduring material for a maximum of 1 AMA PRA Category 1 Credit™. Physicians should claim only the credit commensurate with the extent of their participation in the activity.


This activity is provided by prIME Oncology.

Disclosure Information

Method of Participation

There are no fees for participating in and receiving CME credit for this activity. In order to receive credit, participants must successfully complete the online activity evaluation. Your participation in this CME activity will be recorded in prIME Oncology’s database. However, upon request, your CME credit certificate will be emailed to you. Technical requirements may be found under the Terms of Use.

Disclosure of Relevant Financial Relationships

prIME Oncology assesses relevant financial relationships with its instructors, planners, managers, and other individuals who are in a position to control the content of CME activities. Any potential conflicts of interest that are identified are thoroughly vetted by prIME Oncology for fairness, balance, and scientific objectivity of data, as well as patient care recommendations. prIME Oncology is committed to providing its learners with high-quality CME activities and related materials that promote improvements or quality in healthcare and not a specific proprietary business interest of a commercial entity.

The faculty reported the following financial relationships or relationships to products or devices they or their spouses/life partners have with commercial interest related to the content of this activity:

Dr de Braud has disclosed has disclosed participation in advisory boards for Amgen, Daiichi Sankyo, Ignyta, Incyte, Novartis, Octimet Oncology NV,  Pfizer, Pharm Research Associated (U.K) Ltd, and Teofarma S.r.l. He also disclosed speaking at congresses or courses for ACCMED, Aiom, Bristol-Myers Squibb, Events Srl, Dephaforum S.r.l., Fondazione Quarta, Fondazione Menarini, G. C. Congress, Motore Sanità, Merck Sharp & Dohme, Nadirex, Novartis, Roche, SOS S.r.l., and UNIMI. He also disclosed his role as principal investigator for Bayer, Boehringer Ingelheim, Bristol-Myers Squibb, Celgene, Eli-Lilly, Genentech, GlaxoSmithKline, Ignyta, Lilly, MedImmune, Merck Sharp & Dohme, Nektar, Novartis, Pfizer Italia, Philogen, Roche, and Servier. He has agreed to disclose any unlabeled/unapproved uses of drugs or products referenced in his presentation.

Dr Capdevila has disclosed has disclosed that he has been on an advisory board and served as a speaker for Adacap, Amgen, Bayer, Eisai, Exelixis, Ipsen, Merck Serono, Novartis, Pfizer, and Sanofi. Furthermore, he also received grants for research from Adacap, AstraZeneca, Bayer, Eisai, Novartis, and Pfizer. He also disclosed his role as principal investigator of clinical trials funded by AstraZeneca and Eisai. He disclosed his role as a steering committee participant of clinical trials funded by Eisai and Exelixis. He has agreed to disclose any unlabeled/unapproved uses of drugs or products referenced in his presentation.

Dr Hörsch has disclosed has disclosed board membership and membership on advisory committees or review panels for Ipsen and Novartis. He has agreed to disclose any unlabeled/unapproved uses of drugs or products referenced in his presentation.

Dr Prasad has disclosed has disclosed that he has received consulting fees from Bayer, Ipsen, and ITM. He also disclosed independent contracting for Bayer, Ipsen, and ITM. He has agreed to disclose any unlabeled/unapproved uses of drugs or products referenced in his presentation.

Dr Strosberg has disclosed has disclosed that he has received consulting fees from Ipsen and Novartis. He disclosed honoraria for promotional speaker’s bureaus from Ipsen and Lexicon. He has agreed to disclose any unlabeled/unapproved uses of drugs or products referenced in his presentation.

The employees of prIME Oncology have disclosed:

  • Sanneke Koekkoek, RN (scientific content reviewer/planner) – no relevant financial relationships
  • Jessica Mastrodomenico, MPH (editorial content reviewer) – no relevant financial relationships


Participants have an implied responsibility to use the newly acquired information to enhance patient outcomes and their own professional development. The information presented in this activity is not meant to serve as a guideline for patient management. Any procedures, medications, or other courses of diagnosis or treatment discussed or suggested in this activity should not be used by clinicians without evaluation of their patients’ conditions and possible contraindications or dangers in use, review of any applicable manufacturer’s product information, and comparison with recommendations of other authorities.

Disclosure Regarding Unlabeled Use

This activity may contain discussion of published and/or investigational uses of agents that are not indicated by the US Food and Drug Administration or European Medicines Agency. Please refer to the official prescribing information for each product discussed for discussions of approved indications, contraindications, and warnings.