Randomized Phase II trial of nintedanib, afatinib and sequential combination in castration-resistant prostate cancer.
Τίτλος | Randomized Phase II trial of nintedanib, afatinib and sequential combination in castration-resistant prostate cancer. |
Publication Type | Journal Article |
Year of Publication | 2014 |
Authors | L Molife, R., Omlin A., Jones R. J., Karavasilis V., Bloomfield D., Lumsden G., Fong P. C., Olmos D., O'Sullivan J. M., Pedley I., Hickish T., Jenkins P., Thompson E., Oommen N., Wheatley D., Heath C., Temple G., Pelling K., & de Bono J. S. |
Journal | Future Oncol |
Volume | 10 |
Issue | 2 |
Pagination | 219-31 |
Date Published | 2014 Feb |
ISSN | 1744-8301 |
Λέξεις κλειδιά | Aged, Aged, 80 and over, Antineoplastic Combined Chemotherapy Protocols, Humans, Indoles, Male, Middle Aged, Neoplasm Grading, Neoplasm Metastasis, Neoplasm Staging, Prostatic Neoplasms, Castration-Resistant, Quinazolines, Treatment Outcome |
Abstract | AIMS: The aim of this article was to evaluate afatinib (BIBW 2992), an ErbB family blocker, and nintedanib (BIBF 1120), a triple angiokinase inhibitor, in castration-resistant prostate cancer patients.PATIENTS & METHODS: Patients were randomized to receive nintedanib (250 mg twice daily), afatinib (40 mg once daily [q.d.]), or alternating sequential 7-day nintedanib (250 mg twice daily) and afatinib (70 mg q.d. [Combi70]), which was reduced to 40 mg q.d. (Combi40) due to adverse events. The primary end point was progression-free rate at 12 weeks.RESULTS: Of the 85 patients treated 46, 20, 16 and three received nintedanib, afatinib, Combi40 and Combi70, respectively. At 12 weeks, the progression-free rate was 26% (seven out of 27 patients) for nintedanib, and 0% for afatinib and Combi40 groups. Two patients had a ≥50% decline in PSA (nintedanib and the Combi40 groups). The most common drug-related adverse events were diarrhea, nausea, vomiting and lethargy.CONCLUSION: Nintedanib and/or afatinib demonstrated limited anti-tumor activity in unselected advanced castration-resistant prostate cancer patients. |
DOI | 10.2217/fon.13.250 |
Alternate Journal | Future Oncol |
PubMed ID | 24490608 |