Looking for DNA changes in 303 CUP tissue samples collected in 2018, Prof. Jeffrey Ross (Upstate Medical University, Syracuse, USA) and colleagues used cutting edge technology to reveal that 32% of the tumours investigated could have been targeted by the latest medicines [1]. The same technology is now being used in the ongoing prospective CUPISCO trial. This current study is being followed up by one in which patients with CUP are being randomised to individualised targeted treatment or immunotherapy based on genetic alternations in their tumour, or to standard platinum-based chemotherapy. Initial results are expected within the next few years.
The need for a greater understanding of CUP tumour biology and a wider range of targeted therapies is reinforced by results of the also reported GEFCAPI 04 trial [2]. Started in 2012, this study used gene expression technology to identify the most likely primary tumour source in patients with CUP. However, best available targeted and other treatment tailored to primary tumours failed to improve disease progression or survival compared with standard platinum–based chemotherapy.
“The GEFCAPI 04 results are disappointing but many of the patients had pancreatic, biliary, and other kinds of cancer which are extremely difficult to treat and for which there are no targeted treatments. In a small number of patients who had suspected primary cancers unlikely to respond to empiric chemotherapy, molecular testing allowed use of a targeted agent or better tailored chemotherapy or immunotherapy. But there were probably not enough to make a difference to the overall results of the study,” said presenting author Prof. Karim Fizazi (University of Paris Sud, France).
- Ross J et al. ESMO Congress 2019. Abstract 1983PD_ PR.
- Fizazi K et al. ESMO Congress 2019. Abstract LBA15_PR.
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Table of Contents: ESMO 2019
Featured articles
Interview with ESMO President Prof. Josep Tabernero
Breast Cancer
Triple negative breast cancer gets positive news: KEYNOTE-522 interim results
CDK4/6 inhibitors change landscape of breast cancer treatment: 2 studies
Veliparib-chemo combo prolongs survival without disease progression in some advanced breast cancer patients
Lung Cancer
Improved response rates without survival benefit with pembrolizumab in pretreated mesothelioma
Frontline ipilimumab/nivolumab improves OS in advanced NCLSC
First-line osimertinib significantly lengthens OS in NSCLC
Liquid biopsy to decide the best treatment for NSCLC
Melanoma
Long-term data from CheckMate 067
Adjuvant nivolumab provides benefit
Nivolumab+ipilimumab superior to monotherapy for melanoma brain metastases
GI Cancers
Preoperative chemotherapy for colon cancer
Nivolumab improves OS in advanced oesophageal cancer
Liquid biopsy identifies relapse in patients with colorectal cancer after surgery
In hepatocellular carcinoma, CheckMate 459 misses OS endpoint, but some interesting trends emerge
Heavily pre-treated GIST: ripretinib improves PFS
FGFR2+ cholangiocarcinoma: pemigatinib active as second-line treatment
IDH1+ cholangiocarcinoma: phase 3 results show improved PFS
Advanced colorectal cancer and BRAF mutations: triplet combination improves survival
Genitourinary Cancers
25% reduction in the risk of death in patients with nmCRPC treated with apalutamide
Enfortumab vedotin and pembrolizumab in advanced bladder cancer: initial results
PARP inhibition in selected patients slows progression on advanced prostate cancer
PFS extension with immunotherapy + chemotherapy in urothelial cancer
Third-line in mCRPC: CARD trial
Prostate cancer: spare radiotherapy after surgery
Novel mode of action for kidney cancer treatment
Gynaecological Cancers
Ovarian cancer patients benefit from combined maintenance therapy
Combination of PARP inhibition plus chemotherapy in ovarian cancer
PFS benefit with niraparib as first-line maintenance in ovarian cancer
CNS Tumours
Ceritinib in ALK+ NSCLC brain metastases
Solid Tumours/Pan-Tumour Data
Mixed data: AMG 510 in tumours with KRASG12C
DNA profiling of carcinoma of unknown primary should inform treatment
Larotrectinib: safe and effective in TRK fusion-positive tumours
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