Phase II study of olaratumab with paclitaxel/carboplatin (P/C) or P/C alone in previously untreated advanced NSCLC
Jazyk angličtina Země Irsko Médium print-electronic
Typ dokumentu klinické zkoušky, fáze II, časopisecké články, multicentrická studie, randomizované kontrolované studie, Research Support, N.I.H., Extramural, práce podpořená grantem
Grantová podpora
K24 CA201543
NCI NIH HHS - United States
PubMed
28838379
PubMed Central
PMC5672830
DOI
10.1016/j.lungcan.2017.07.009
PII: S0169-5002(17)30388-4
Knihovny.cz E-zdroje
- Klíčová slova
- NSCLC, Olaratumab, PDGFR, Paclitaxel/carboplatin,
- MeSH
- analýza přežití MeSH
- indukce remise MeSH
- kombinovaná terapie MeSH
- lidé středního věku MeSH
- lidé MeSH
- monoklonální protilátky aplikace a dávkování MeSH
- nádory plic farmakoterapie mortalita patologie MeSH
- nemalobuněčný karcinom plic farmakoterapie mortalita patologie MeSH
- paclitaxel aplikace a dávkování MeSH
- protokoly protinádorové kombinované chemoterapie škodlivé účinky terapeutické užití MeSH
- rozvrh dávkování léků MeSH
- senioři MeSH
- staging nádorů MeSH
- výsledek terapie MeSH
- Check Tag
- lidé středního věku MeSH
- lidé MeSH
- mužské pohlaví MeSH
- senioři MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- klinické zkoušky, fáze II MeSH
- multicentrická studie MeSH
- práce podpořená grantem MeSH
- randomizované kontrolované studie MeSH
- Research Support, N.I.H., Extramural MeSH
- Názvy látek
- monoklonální protilátky MeSH
- olaratumab MeSH Prohlížeč
- paclitaxel MeSH
BACKGROUND: In non-small cell lung cancer (NSCLC), platelet-derived growth factor receptor (PDGFR) mediates angiogenesis, tissue invasion, and tumor interstitial pressure. Olaratumab (IMC-3G3) is a fully human anti-PDGFRα monoclonal antibody. This Phase II study assessed safety and efficacy of olaratumab+paclitaxel/carboplatin (P/C) versus P/C alone for previously untreated advanced NSCLC. MATERIALS AND METHODS: Patients received up to six 21-day cycles of P 200mg/m2 and C AUC 6 (day 1)±olaratumab 15mg/kg (days 1 and 8). Primary endpoint was PFS. Olaratumab was continued in the olaratumab+P/C arm until disease progression. RESULTS: 131 patients were: 67 with olaratumab+P/C and 64 with P/C; 74% had nonsquamous NSCLC. Median PFS was similar between olaratumab+P/C and P/C (4.4 months each) (HR 1.29; 95% CI [0.86-1.93]; p=0.21). Median OS was similar between olaratumab+P/C (11.8 months) and P/C (11.5 months) (HR 1.04; 95% CI [0.68-1.57]; p=0.87). Both arms had similar toxicity profiles. All evaluable cases were PDGFR-negative by immunohistochemistry. Tumor stroma PDGFR expression was evaluable in 23/131 patients, of which 78% were positive. CONCLUSIONS: The addition of olaratumab to P/C did not result in significant prolongation of PFS or OS in advanced NSCLC. Olaratumab studies in other patient populations, including soft tissue sarcoma (NCT02783599), pancreatic cancer (NCT03086369), and pediatric malignancies (NCT02677116) are underway.
Case Western Reserve University Cleveland OH 44106 USA
Cleveland Clinic Cleveland OH 44195 USA
Eli Lilly and Company Bridgewater NJ 08807 USA
Eli Lilly and Company Indianapolis IN 46285 USA
Eli Lilly and Company United Kingdom of Great Britain and Northern Ireland UK
Eli Lilly and Company Windlesham GU20 6PH UK
Hematology Oncology Associates of the Treasure Coast Port Saint Lucie FL 34952 USA
Oregon Health and Science University Portland OR 97239 USA
Scott and White Clinic Hematology Oncology Temple TX 76508 USA
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