Phase I study of trametinib in combination with whole brain radiation therapy for brain metastases. (May 2022)
- Record Type:
- Journal Article
- Title:
- Phase I study of trametinib in combination with whole brain radiation therapy for brain metastases. (May 2022)
- Main Title:
- Phase I study of trametinib in combination with whole brain radiation therapy for brain metastases
- Authors:
- Palmer, Joshua D.
Prasad, Rahul N.
Fabian, Denise
Wei, Lai
Yildiz, Vedat O.
Tan, Yubo
Grecula, John
Welliver, Meng
Williams, Terence
Elder, James B.
Raval, Raju
Blakaj, Dukagjin
Haglund, Karl
Bazan, Jose
Kendra, Kari
Arnett, Andrea
Beyer, Sasha
Liebner, David
Giglio, Pierre
Puduvalli, Vinay
Chakravarti, Arnab
Wuthrick, Evan - Abstract:
- Highlights: Trametinib is a MEK inhibitor with intracranial activity used for BRAF+ disease. Even subtherapeutic trametinib doses are toxic with whole brain radiation therapy. The overall response rate was 33% with a median survival of 2.2 months. Abstract: Introduction: Trametinib is a MEK inhibitor with intracranial activity indicated for BRAF-mutant metastatic malignancies. Yet, the safety of trametinib concurrent with whole brain radiation therapy (WBRT) is unknown. We performed a single-institution, prospective, 3 + 3, phase I clinical trial to determine the maximum tolerated dose (MTD) of trametinib with WBRT. Methods and Materials: Patients with brain metastases (BM) received daily trametinib for 28 days, starting 7 days prior to and continuing through WBRT (37.5 Gy/15 fractions). Dose levels (DL)1–3 were 1.0, 1.5, and 2.0 mg. The MTD of trametinib plus WBRT, the max dose where ≤1 of 6 patients experienced a dose limiting toxicity (DLT), was the primary endpoint. Results: 10 patients were enrolled (median age-59 [47–64], BM-5 [1–10], 50% melanoma). Three and 7 patients were assigned to DL1 and 2. One DL2 patient withdrew. 89% of remaining patients completed therapy per protocol, but 1 DL2 patient with systemic progression discontinued therapy at 30 Gy. Thirteen grade (G)3–4 toxicities were observed, of which 12 occurred at DL2 (4/6 of patients). DLT was reached at DL2 (G4 thrombocytopenia and G3 diarrhea, 1 each). There were no G5 toxicities. Median overall survivalHighlights: Trametinib is a MEK inhibitor with intracranial activity used for BRAF+ disease. Even subtherapeutic trametinib doses are toxic with whole brain radiation therapy. The overall response rate was 33% with a median survival of 2.2 months. Abstract: Introduction: Trametinib is a MEK inhibitor with intracranial activity indicated for BRAF-mutant metastatic malignancies. Yet, the safety of trametinib concurrent with whole brain radiation therapy (WBRT) is unknown. We performed a single-institution, prospective, 3 + 3, phase I clinical trial to determine the maximum tolerated dose (MTD) of trametinib with WBRT. Methods and Materials: Patients with brain metastases (BM) received daily trametinib for 28 days, starting 7 days prior to and continuing through WBRT (37.5 Gy/15 fractions). Dose levels (DL)1–3 were 1.0, 1.5, and 2.0 mg. The MTD of trametinib plus WBRT, the max dose where ≤1 of 6 patients experienced a dose limiting toxicity (DLT), was the primary endpoint. Results: 10 patients were enrolled (median age-59 [47–64], BM-5 [1–10], 50% melanoma). Three and 7 patients were assigned to DL1 and 2. One DL2 patient withdrew. 89% of remaining patients completed therapy per protocol, but 1 DL2 patient with systemic progression discontinued therapy at 30 Gy. Thirteen grade (G)3–4 toxicities were observed, of which 12 occurred at DL2 (4/6 of patients). DLT was reached at DL2 (G4 thrombocytopenia and G3 diarrhea, 1 each). There were no G5 toxicities. Median overall survival was 2.2 months. During the study period, changing practice patterns favored utilization of stereotactic radiosurgery (SRS). Thus, the trial closed early prior to completion. Conclusions: In a patient population representative of modern candidates for WBRT, trametinib plus WBRT is highly toxic with a MTD <1.5 mg. The safety of trametinib with SRS remains an important question for future study. … (more)
- Is Part Of:
- Radiotherapy and oncology. Volume 170(2022)
- Journal:
- Radiotherapy and oncology
- Issue:
- Volume 170(2022)
- Issue Display:
- Volume 170, Issue 2022 (2022)
- Year:
- 2022
- Volume:
- 170
- Issue:
- 2022
- Issue Sort Value:
- 2022-0170-2022-0000
- Page Start:
- 21
- Page End:
- 26
- Publication Date:
- 2022-05
- Subjects:
- BM brain metastases -- WBRT whole brain radiation therapy -- SRS stereotactic radiosurgery -- SRT stereotactic radiotherapy -- RT radiation therapy -- MEK mitogen-activated extracellular signal regulated kinase -- ECOG Eastern Cooperative Oncology Group -- MRI magnetic resonance imaging -- CTCAE Common Terminology Criteria for Adverse Events -- G grade -- CT computed tomography -- MTD maximum tolerated dose -- DLT dose limiting toxicity -- AE adverse events -- ORR objective response rate -- LC local control -- nPFS neurologic progression free survival -- OS overall survival -- RECIST Response Evaluation Criteria in Solid Tumors -- CR complete response -- PR partial response -- SD stable disease -- PD progressive disease
Brain metastases -- Clinical trial -- Dose limiting toxicity -- MEK inhibitor -- Trametinib -- Whole brain radiation therapy
Oncology -- Periodicals
Radiotherapy -- Periodicals
Tumors -- Periodicals
Medical Oncology -- Periodicals
Neoplasms -- radiotherapy -- Periodicals
Radiotherapy -- Periodicals
Radiothérapie -- Périodiques
Cancérologie -- Périodiques
Tumeurs -- Périodiques
Electronic journals
616.9940642 - Journal URLs:
- http://www.sciencedirect.com/science/journal/01678140 ↗
http://www.clinicalkey.com/dura/browse/journalIssue/01678140 ↗
http://www.clinicalkey.com.au/dura/browse/journalIssue/01678140 ↗
http://www.estro.org/ ↗
http://www.elsevier.com/journals ↗
http://www.journals.elsevier.com/radiotherapy-and-oncology/ ↗ - DOI:
- 10.1016/j.radonc.2022.03.016 ↗
- Languages:
- English
- ISSNs:
- 0167-8140
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- Legaldeposit
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