Abstract 1914MO
Background
Anaplastic thyroid cancer (ATC) is a rare/aggressive cancer with no standard radiation-based local treatment. Achieving locoregional disease control in the neck is critical due to major concerns of airway and esophageal compromise. Based on data suggesting synergy between pazopanib (P) and paclitaxel (T) in ATC, NRG Oncology conducted a randomized phase II study comparing concurrent T and intensity modulated radiation therapy (IMRT) with either P or placebo (C).
Methods
The study arm evaluated 2-3 weeks of weekly T (80 mg/m2) and daily P suspension (PS) 400 mg followed by concurrent weekly T (50 mg/m2), daily PS (300 mg), and IMRT 66 Gy. The standard arm substituted C for PS. Inclusion criteria included pathologic diagnosis of M0/M1 ATC (central path review), Zubrod 0-2, no recent hemoptysis/bleeding, no brain metastases. Target accrual was 88 patients (pts) (79 eligible) to show a >37.5% reduction in the hazard rate for overall survival (OS) with addition of PS (1-sided alpha 0.15, beta 0.2). Final analysis, after accounting for 1 interim analysis, was 1-sided log-rank test at 0.1379 level in eligible pts.
Results
89 pts (71 eligible) were accrued from 6/23/14-12/30/16, completing accrual 14 months earlier than projected. Pts excluded per protocol in each arm - PS 6; C 12. Median age 65 years. Female 52.1%. Zubrod 0-1 91.5%. Total thyroidectomy 36.6%; partial thyroidectomy 21.1%. M0 disease 56.3%. OS was not significantly higher with PS compared to C (p=0.28); hazard ratio (PS/C) was 0.86 (95% CI 0.52 - 1.43). OS and adverse events (AE) rates are in the table. Table: 1914MO
Pazopanib (n=36) | Placebo (n=35) | |
OS rate (95% CI) | ||
1-year | 37.1% (21.1-53.2%) | 29.0% (13.2-44.8%) |
2-year | 20.0% (6.7-33.3%) | 12.9% (1.1-24.6%) |
3-year | 17.1% (4.7-29.6%) | 9.7% (0-20.0%) |
Highest treatment-related AE | (n=36) | (n=34) |
Grade 3 | 52.8% | 55.9% |
Grade 4 | 33.3% | 26.5% |
Grade 5 | 2.8% (1 pt) | 2.9% (1 pt) |
Conclusions
NRG-RTOG 0912 is the largest randomized ATC study that completed accrual demonstrating feasibility in the cooperative group setting. Although a statistically significant improvement in OS was not seen with PS added to T and IMRT, the OS rates and feasibility data from this prospective clinical trial will be useful to help design future studies in this rare and aggressive disease.
Clinical trial identification
RTOG 0912.
Editorial acknowledgement
Legal entity responsible for the study
NRG/RTOG Oncology.
Funding
This project was supported by grants UG1CA189867 (NRG Oncology NCORP), U10CA180868 (NRG Oncology Operations), U10CA180822 (NRG Oncology SDMC), & U24CA180803 (IROC) from the National Cancer Institute (NCI) and Novartis.
Disclosure
E.J. Sherman: Honoraria (self), Advisory/Consultancy: Novartis; Honoraria (self), Advisory/Consultancy: Eisai; Honoraria (self), Advisory/Consultancy, Research grant/Funding (institution): Regeneron; Honoraria (self), Advisory/Consultancy, Research grant/Funding (institution): Eli Lilly/Loxo; Research grant/Funding (institution): Roche; Research grant/Funding (institution): Plexxicon. P. Xia: Honoraria (self), Advisory/Consultancy, Research grant/Funding (institution), Travel/Accommodation/Expenses: Philips Healthcare; Research grant/Funding (institution): Advanced Oncotherapy. C.H. Chung: Advisory/Consultancy, Research grant/Funding (institution): Bristol-Myers Squibb; Advisory/Consultancy: CUE Biopharma; Advisory/Consultancy, Research grant/Funding (institution): Ignyta; Speaker Bureau/Expert testimony, Travel/Accommodation/Expenses: Mirati Therapeutics; Research grant/Funding (institution), Travel/Accommodation/Expenses: AstraZeneca; Research grant/Funding (institution): IRX Therapeutics; Research grant/Funding (institution): Eli Lilly; Research grant/Funding (institution): Lion Biotechnologies; Research grant/Funding (institution): Merck; Research grant/Funding (institution): Pfizer; Research grant/Funding (institution): Regeneron. R.L. Foote: Licensing/Royalties: Bionix; Travel/Accommodation/Expenses: Hitachi Chemical. S. Yom: Research grant/Funding (institution): BioMimetix; Research grant/Funding (institution): Bristol-Myers Squibb; Research grant/Funding (institution): Genentech; Research grant/Funding (institution): Merck. S.J. Wong: Research grant/Funding (institution): Merck; Research grant/Funding (institution): Novartis. S. Koyfman: Research grant/Funding (institution): Merck Sharp & Dohme. S. Khan: Honoraria (institution), Advisory/Consultancy: Ariad; Honoraria (self), Advisory/Consultancy: EMD Serono; Honoraria (self), Advisory/Consultancy, Research grant/Funding (institution), Travel/Accommodation/Expenses: Genentech/Roche; Honoraria (self), Speaker Bureau/Expert testimony: Genzyme; Advisory/Consultancy, Research grant/Funding (institution): Bayer/Onyx; Advisory/Consultancy: Foundation Medicine; Advisory/Consultancy, Research grant/Funding (institution): Guardant Health; Advisory/Consultancy, Speaker Bureau/Expert testimony: Takeda; Research grant/Funding (institution): AbbVie; Research grant/Funding (institution): Bristol-Myers Squibb; Research grant/Funding (institution): Celldex; Research grant/Funding (institution): Formation Biologics; Research grant/Funding (institution): Gilead Sciences; Research grant/Funding (institution): Loxo; Research grant/Funding (institution): Merck; Research grant/Funding (institution), Travel/Accommodation/Expenses: Novartis; Research grant/Funding (institution): Pfizer; Research grant/Funding (institution): Threshold Pharmaceuticals. Q-T. Le: Advisory/Consultancy: Merck; Shareholder/Stockholder/Stock options: Aldea; Travel/Accommodation/Expenses: Genentech; Advisory/Consultancy: Grail. N. Lee: Advisory/Consultancy: Eli Lilly; Advisory/Consultancy: Merck; Advisory/Consultancy, Research grant/Funding (institution): Pfizer; Advisory/Consultancy: Vertex. All other authors have declared no conflicts of interest.
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