Abstract 1820
Background
mCRC is a non-immunogenic tumour type with poor response to checkpoint inhibitors, hypothetically due to low tumour T-cell levels and incomplete blockade of MAPK-mediated growth factor signalling. Combining the anti-tumour immunity effects of the anti–PD-L1 Ab (atezo), MEK inhibitor (cobi) and anti-VEGF Ab (bev) in pts with mCRC may improve response. Atezo enhances T-cell priming/activation, cobi decreases tumour growth and increases tumour antigen presentation via MHC I and bev increases T-cell infiltration. Therefore, bev + atezo + cobi may enhance immune recognition of mCRC. This report is the primary analysis of a Phase Ib study of this combination.
Methods
This study assessed the safety and activity of atezo (840 mg q2w IV) + bev (5 mg/kg q2w IV) + cobi (60 mg qd 21 on/7 off oral) in pts with mCRC who progressed on ≥ 1 prior line of treatment (tx) containing 5-FU and oxaliplatin/irinotecan. After safety run-in, dose-expansion and biopsy cohorts were enrolled. The primary objective was to assess safety.
Results
In the primary analysis (Sep 21, 2018, cutoff), 49 pts were evaluated. Median safety follow-up was 7.8 mo (range, 1.4-25.4 mo). Median prior lines of tx was 2 (range, 1-7). 33 pts (67%) had RAS-mutant tumours. 45 pts (92%) had microsatellite stable disease; 4 pts (8%) had unknown microsatellite status. 48 pts (98%) had tx-related AEs (TRAEs), 30 pts (61%) had G3-5 TRAEs and 1 pt (2%) had bev-related G5 GI necrosis. AEs led to tx withdrawal in 9 pts (18%). Most common AEs were diarrhoea (78%), acneiform dermatitis (51%), fatigue (49%), rash (41%) and CPK increase (35%). Confirmed ORR was 8% in the overall population. See Table for activity by tx line and RAS status.Table:
603P
2L therapy (n = 25) | 3L+ therapy (n = 24) | Overall (N = 49) | |
---|---|---|---|
Confirmed response per RECIST 1.1, n (%)a | 2 (8%) | 2 (8%) | 4 (8%) |
mPFS (range), moa | 5.5 (3.6-9.4) | 5.8(2.4-9.0) | 5.5 (3.6-7.5) |
mOS (range), mo | NE(11.7-NE) | 11.8 (8.7-21.8) | 11.8 (9.0-21.8) |
RAS mutant (n = 33) | RAS wild-type/ unknown (n = 16) | Pb HR (95% CI) | |
DCR, n (%)c (95% CI) | 12 (36) (20, 55) | 5 (31) (11, 59) | – |
mPFS, mo (95% CI) | 5.8 (3.6, 11.6) | 3.6 (2.6, 7.3) | 0.05 2.2 (1.1, 4.5) |
mOS, mo (95% CI) | 21.8 (9.0, NE) | 9.1 (3.6, 14.5) | 0.34 1.8 (0.6, 5.5) |
Ab, antibody; DCR, disease control rate; HR, hazard ratio; mPFS, median progression-free survival; mOS, median overall survival; NE, not estimable; RECIST, Response Evaluation Criteria in Solid Tumours.
aInvestigator assessed.
bP values not controlled for type I error and are descriptive only.
cAt 4 mo.
Conclusions
Atezo + bev + cobi had an acceptable safety profile with manageable AEs with improved activity over that reported with SOC in 2L+ mCRC. A greater benefit trend was seen in pts with a RAS mutation vs wild-type tumours.
Clinical trial identification
NCT02876224.
Editorial acknowledgement
Chris Lum, PhD, of Health Interactions, funded by F. Hoffmann-La Roche, Ltd.
Legal entity responsible for the study
F. Hoffmann-La Roche, Ltd.
Funding
F. Hoffmann-La Roche, Ltd.
Disclosure
J. Bendell: Advisory / Consultancy, Research grant / Funding (institution), Travel / Accommodation / Expenses: Gilead; Advisory / Consultancy, Research grant / Funding (institution), Travel / Accommodation / Expenses: Roche/Genentech; Advisory / Consultancy, Research grant / Funding (institution), Travel / Accommodation / Expenses: Bristol-Myers Squibb; Advisory / Consultancy, Research grant / Funding (institution): Five Prime; Advisory / Consultancy, Research grant / Funding (institution), Travel / Accommodation / Expenses: Lilly; Advisory / Consultancy, Research grant / Funding (institution), Travel / Accommodation / Expenses: Merck; Advisory / Consultancy, Research grant / Funding (institution), Travel / Accommodation / Expenses: MedImmune; Advisory / Consultancy, Research grant / Funding (institution), Travel / Accommodation / Expenses: Celgene; Research grant / Funding (institution): EMD Serono; Advisory / Consultancy, Research grant / Funding (institution), Travel / Accommodation / Expenses: Taiho; Advisory / Consultancy, Research grant / Funding (institution): Macrogenics; Advisory / Consultancy, Research grant / Funding (institution): GSK; Advisory / Consultancy, Research grant / Funding (institution), Travel / Accommodation / Expenses: Novartis; Advisory / Consultancy, Research grant / Funding (institution), Travel / Accommodation / Expenses: OncoMed; Advisory / Consultancy, Research grant / Funding (institution): LEAP; Advisory / Consultancy, Research grant / Funding (institution): TG Therapeutics; Advisory / Consultancy, Research grant / Funding (institution): AstraZeneca; Advisory / Consultancy, Research grant / Funding (institution), Travel / Accommodation / Expenses: BI; Advisory / Consultancy, Research grant / Funding (institution): Daiichi Sankyo; Advisory / Consultancy, Research grant / Funding (institution): Bayer; Advisory / Consultancy, Research grant / Funding (institution): Incyte; Advisory / Consultancy, Research grant / Funding (institution): Apexigen; Research grant / Funding (institution): Koltan; Research grant / Funding (institution): SynDevRex; Research grant / Funding (institution): Forty Seven; Research grant / Funding (institution): AbbVie; Advisory / Consultancy, Research grant / Funding (institution): Array; Research grant / Funding (institution): Onyx; Advisory / Consultancy, Research grant / Funding (institution): Sanofi; Research grant / Funding (institution): Takeda; Research grant / Funding (institution): Eisai; Research grant / Funding (institution): Celldex; Research grant / Funding (institution): Agios; Research grant / Funding (institution): Cytomx; Research grant / Funding (institution): Nektar; Advisory / Consultancy, Research grant / Funding (institution), Travel / Accommodation / Expenses: ARMO; Research grant / Funding (institution): Boston Biomedical; Advisory / Consultancy, Research grant / Funding (institution), Travel / Accommodation / Expenses: Ipsen; Advisory / Consultancy, Research grant / Funding (institution): Merrimack; Research grant / Funding (institution): Tarveda; Research grant / Funding (institution): Tyrogenex; Advisory / Consultancy, Research grant / Funding (institution), Travel / Accommodation / Expenses: Oncogenex; Research grant / Funding (institution): Marshall Edwards; Research grant / Funding (institution): Pieris; Research grant / Funding (institution): Mersana; Research grant / Funding (institution): Calithera; Research grant / Funding (institution): Blueprint; Research grant / Funding (institution): Evelo; Advisory / Consultancy, Research grant / Funding (institution), Travel / Accommodation / Expenses: FORMA; Research grant / Funding (institution): Jacobio; Research grant / Funding (institution): Effector; Research grant / Funding (institution): Novocare; Research grant / Funding (institution): Arrys; Research grant / Funding (institution): Tracon; Research grant / Funding (institution): Sierra; Advisory / Consultancy, Research grant / Funding (institution): Arch Oncology; Advisory / Consultancy, Research grant / Funding (institution): Prelude Oncology; Research grant / Funding (institution): Unum Therapeutics; Research grant / Funding (institution): Vyriad; Research grant / Funding (institution): Harpoon; Research grant / Funding (institution): ADC; Advisory / Consultancy, Research grant / Funding (institution): Amgen; Research grant / Funding (institution): Pfizer; Research grant / Funding (institution): Millennium; Research grant / Funding (institution): Imclone; Research grant / Funding (institution): Acerta Pharma; Research grant / Funding (institution): Rgenix; Research grant / Funding (institution): Bellicum; Advisory / Consultancy: Phoenix Bio; Advisory / Consultancy: Cyteir; Advisory / Consultancy: Molecular Partners; Advisory / Consultancy: Innate; Advisory / Consultancy: Torque; Advisory / Consultancy: Tizona; Advisory / Consultancy: Janssen; Advisory / Consultancy: Tolero; Advisory / Consultancy: TD2 (Translational Drug Development); Advisory / Consultancy: Seattle Genetics; Advisory / Consultancy: Moderna Therapeutics; Advisory / Consultancy: Tanabe Research Laboratories; Advisory / Consultancy: Beigene; Advisory / Consultancy: Continuum Clinical; Advisory / Consultancy: Agios. C. Lieu: Honoraria (self): Foundation Medicine. K.P.S. Raghav: Honoraria (self): Genentech, Inc.; Honoraria (self): Bayer, Inc.; Travel / Accommodation / Expenses: Tracon, Inc. G. Argilés: Full / Part-time employment: VHIO; Research grant / Funding (institution): Bayer; Research grant / Funding (self): Spains Society Against Cancer; Honoraria (self), Travel / Accommodation / Expenses: Roche; Honoraria (self), Travel / Accommodation / Expenses: Amgen; Honoraria (self), Travel / Accommodation / Expenses: Merck Serono; Honoraria (self): BMS; Honoraria (self), Travel / Accommodation / Expenses: Servier; Honoraria (self), Travel / Accommodation / Expenses: Bayer. A. Cubillo: Advisory / Consultancy, Research grant / Funding (institution): Servier; Research grant / Funding (institution): Adacap; Research grant / Funding (institution): Merck; Advisory / Consultancy: Amgen. X. Qu: Shareholder / Stockholder / Stock options, Full / Part-time employment: Genentech Inc. Y. Yan: Shareholder / Stockholder / Stock options, Full / Part-time employment: Genentech/Roche. M. Merchant: Full / Part-time employment: Genentech/Roche. H. Zeuner: Full / Part-time employment: Roche. J.D. Gallo: Shareholder / Stockholder / Stock options, Full / Part-time employment: Genentech Inc. N.H. Segal: Advisory / Consultancy, Research grant / Funding (institution): Roche/Genentech; Advisory / Consultancy, Research grant / Funding (institution): Pfizer; Advisory / Consultancy, Research grant / Funding (institution): Merck; Advisory / Consultancy, Research grant / Funding (institution): BMS; Advisory / Consultancy, Research grant / Funding (institution): MedImmune/AstraZeneca; Research grant / Funding (institution): Incyte; Advisory / Consultancy: Boehringer Ingelheim; Advisory / Consultancy: Pieris; Advisory / Consultancy: PsiOxus; Advisory / Consultancy: Synlogic; Advisory / Consultancy: Aduro; Advisory / Consultancy: Kyn Therapautics; Advisory / Consultancy: Pure Tech Ventrures; Advisory / Consultancy: Horizon Pharma; Advisory / Consultancy: EMD Serono; Advisory / Consultancy: Gritstone Oncology; Advisory / Consultancy: Chugai; Advisory / Consultancy: TRM Oncology; Advisory / Consultancy: IFM Therapeutics; Advisory / Consultancy: Cstone Pharmaceuticals.
Resources from the same session
5295 - Predictive factors and survival outcomes with stereotactic body radiation therapy in treatment of oligometastases in colorectal cancer
Presenter: Vibhay Pareek
Session: Poster Display session 2
Resources:
Abstract
5887 - Factors of importance in procuring tumoroids from colorectal liver metastasis biopsies for precision medicine.
Presenter: Lars Henrik Jensen
Session: Poster Display session 2
Resources:
Abstract
2196 - FUSAFE individual patient data meta-analysis (MA) to assess the performance of dihydropyrimidine dehydrogenase (DPD) gene polymorphisms for predicting grade 4-5 fluoropyrimidine (FP) toxicity
Presenter: Marie-Christine Etienne-Grimaldi
Session: Poster Display session 2
Resources:
Abstract
2859 - Treatments (tx) after progression to first-line FOLFOXIRI + bevacizumab (bev) in metastatic colorectal cancer (mCRC) patients (pts): A pooled analysis of TRIBE and TRIBE-2 studies by GONO.
Presenter: Daniele Rossini
Session: Poster Display session 2
Resources:
Abstract
3888 - Randomized phase III study of sequential treatment with capecitabine or 5-fluorouracil (FP) plus bevacizumab (BEV) followed by the addition with oxaliplatin (OX) versus initial combination with OX+FP+ BEV in the first-line chemotherapy for metastatic colorectal cancer: The C-cubed study
Presenter: Takeshi Nagasaka
Session: Poster Display session 2
Resources:
Abstract
1065 - Early tumour shrinkage (ETS), depth of response (DpR) and associated survival outcomes in patients (pts) with RAS wild type (WT) metastatic colorectal cancer (mCRC) classified according to Köhne prognostic category: retrospective analysis of the panitumumab (Pmab) PRIME study
Presenter: Andrea Sartore-Bianchi
Session: Poster Display session 2
Resources:
Abstract
1702 - Randomized phase II trial of CAPOX with planned oxaliplatin stop-and-go strategy as adjuvant chemotherapy after curative resection of colon cancer (CCOG-1302 study)
Presenter: Hiroyuki Yokoyama
Session: Poster Display session 2
Resources:
Abstract
5104 - A metabolomic recurrence score for risk-stratification of elderly patients (pts) with early colorectal cancer (eCRC)
Presenter: Samantha Di Donato
Session: Poster Display session 2
Resources:
Abstract
5285 - RAS mutant allele fraction in plasma predicts benefit to anti-angiogenic based first line treatment in metastatic colorectal cancer
Presenter: Giulia Martini
Session: Poster Display session 2
Resources:
Abstract
1790 - Impact of prophylactic systemic antibiotics (SA) on outcome of patients (pts) with RAS-wildtype (RAS-wt) metastatic colorectal carcinoma (mCRC) treated with cetuximab-based first-line therapy. Subgroup analysis of the german non-interventional study ERBITAG
Presenter: Stephan Sahm
Session: Poster Display session 2
Resources:
Abstract