TUMORES NEUROENDOCRINOS. Miguel Navarro. Salamanca

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Transcription:

TUMORES NEUROENDOCRINOS Miguel Navarro. Salamanca

Introduction to Neuroendocrine Tumours (NETs) NETs are relatively RARE At least 40 different entities are described arising in different organs. Different terminologies have also caused confusion.

Most NETs 70% are non functional

Diagnostic challenges in NET Wide variety of clinical presentations Late presentation Over 60% of NETs are advanced at the time of diagnosis The median survival for patients with advanced NET is 33 months

Incidence Trends of NETs Dasari A et al. JAMA Oncol. April 2017

NETs Are Second Most Prevalent Gastrointestinal Tumor Median survival Localized 203 months Regional 114 months Distant 39 months

Confusion Caused by the Term Carcinoid Oberndorfer coined the term karzinoide in 1907. This term implies that these tumours are benign; this is an unfortunate misnomer for the majority of NET. NET have malignant potential and metastasize, generally to the liver.

Histologic classification

Treatment challenges in NET One Treatment Does Not Fit All

Treatment challenges in NET

Somatostatin Analogues AAS

Telotristat. A Tryptophan Hydroxylase (TPH) Inhibitor to treat carcinoid syndrome diarrhea Indicated for carcinoid syndrome diarrhea in combination with somatostatin analog (SSA) therapy in adults inadequately controlled by SSA therapy

Telotristat Patients who received telotristat etiprate also experienced a lower frequency of flushing episodes and less intense abdominal pain compared to placebo, though these differences did not reach statistical significance.

Where does telotristat fit in? Active in controlling diarrhea from carcinoid syndrome. Does it have QOL benefits beyond diarrhea control? Flushing? Abdominal pain? Is there a role in prevention of carcinoid heart disease?

New options in NETs

Treatment challenges in NET cancers in slow motion WATCHFUL WAITING

Somatostatin Analogues AAS

PROMID Trial

CLARINET Trial

Somatostatin Analogues AAS Previous restrictions on the use of AAS in non functioning tumors are no longer justified. Favorable side effects profile. Appropriate 1st line agents in most well-differenciated NETs. Early antitumor therapy

Indications for cytotoxic chemotherapy

QT en NETS

Newer chemotherapy regimens have demonstrated acceptable toxicity in advanced NET

Cap/Tem Example of response Baseline Maximal response

Targeting NETs

Targeting NETs

Targeting NETs

AAS

Targeting NETS

Targeting NETS There are several biological agents being evaluated. Pazopanib (Votrient) Cabozantinib (Cabometyx) Axitinib (Inlyta) Lenvatinib (Lenvima)

Radionuclide Therapy Theranostics-Diagnosis and Therapy

n engl j med 376;2 nejm.org January 12, 2017

Number of deaths: LU-Dotate: 14 Control: 26 Estimated risk of death 60% lower n engl j med 376;2 nejm.org January 12, 2017

Case Report 58 yo m. Large cell Neuroendocrine carcinoma. Surgery. Stage Ib Cisplatin-Vp16 (Ady) 2009-2015 Liver- Bone Mtx Carboplatin-Vp16, Lanreotide, Everolimus,Pazopanib,TMZ-Cap Topotecan ECOG -2. Oxycontin 60 mg/12 h plus oxinorm 2016-2017 ECOG-0, weight gain 20 KG, no opioids PRRT

Case Report 2 2018 Progression If patient had responded to the first few rounds of Lutathera and then the tumors start to grow again, it can be given safely for a second time? 5 round of Lutathera May/18

Where does PRRT fit in? Phase 3 randomized data only in midgut NETs. Early phase data suggesting higher response rates in non-midgut NETs COMPETE trial. Somatostatin-receptor (SSTR) expression is strong predictive marker. Consider as 2nd line therapy in patients with strong SSTR expression. Advantages: Limited treatment course (4x), exceptionally long-pfs, low toxicity Are there long-term risks to consider?

Inmunotherapy NETs do not have many mutations. Merkel cell carcinoma (MCC). Rare and aggressive neuroendocrine tumor of the skin. MCC incidence is higher in immunocompromised populations. Tumour oncogenesis is linked to Merkel cell polyomavirus integration and ultravioletradiation-induced mutations, providing rationale for treatment with immunotherapy antibodies that target the PD-L1/PD-1 pathway. CarboVp16 Rt - Avelumab

Ongoing clinical trials

Take Home Messages Nets are not rare. Consider patient and tumor characteristic. Increasing number of treatment options Octeotride / Lanreotide Telotristat Sunitinib / Everolimus Temozolomide. PPRT Exciting Decade in Neuroendocrine Tumor Treatment

Muchas gracias lmnavarro@saludcastillayleon.es