4.7 Article

Phase I Study of Everolimus, Letrozole, and Trastuzumab in Patients with Hormone Receptor-positive Metastatic Breast Cancer or Other Solid Tumors

Journal

CLINICAL CANCER RESEARCH
Volume 27, Issue 5, Pages 1247-1255

Publisher

AMER ASSOC CANCER RESEARCH
DOI: 10.1158/1078-0432.CCR-20-2878

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Funding

  1. Novartis
  2. Sabin Family Foundation
  3. MD Anderson Cancer Center [NIH/NCI P30 CA016672]
  4. Clinical Translational Science Award [NIH/HHS 1UL1 TR003167]
  5. Cancer Prevention Research Institute of Texas (CPRIT) [RP150535]
  6. Sheikh Khalifa Bin Zayed Al Nahyan Institute for Personalized Cancer Therapy

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The combination therapy of everolimus, letrozole, and trastuzumab showed favorable safety profile and encouraging signs of anticancer activity in patients with heavily pretreated hormone receptor- and HER2-positive advanced cancers. Some patients, particularly those with HER2 amplification, had partial responses to the treatment.
Purpose: Doublets of everolimus with letrozole or trastuzumab have demonstrated activity against HER2-positive breast cancer, suggesting that the triple combination can have synergistic anticancer activity. Patients and Methods: This first-in-human dose-escalation study (NCT02152943) enrolled patients with hormone receptor-positive, HER2-positive (defined by amplification, overexpression, or mutation) treatment-refractory advanced cancers to receive escalating doses (3+3 design) of daily oral letrozole (days 1-21), daily oral everolimus (days 1-21), and intravenous trastuzumab (day 1) every 21 days to determine dose-limiting toxicities (DLT) and MTD or recommended phase II dose (RP2D). Results: A total of 32 patients with hormone receptor-positive, HER2-positive (amplification, n = 27; overexpression, n = 1; and mutation, n = 4) advanced breast cancer (n = 26) or other cancers (n = 6) were enrolled. The most frequent grade >= 3 adverse events included hyperglycemia (n = 4), anemia (n = 3), thrombocytopenia (n = 2), and mucositis (n = 2). DLTs included grade 3 mucositis and grade 4 neutropenia, and trastuzumab given as an 8 mg/kg loading dose on day 1 of cycle 1 followed by a 6 mg/kg maintenance dose on day 1 of subsequent cycles plus 10 mg everolimus daily and 2.5 mg letrozole daily every 21 days was declared as RP2D. Five patients with breast cancer (four with HER2 amplification and one with HER2 mutation) had partial responses. HER2 amplification in circulating cell-free DNA at baseline was associated with shorter progression-free and overall survival durations (P < 0.05). Conclusions: Everolimus, letrozole, and trastuzumab have a favorable safety profile and elicit encouraging signals of anticancer activity in patients with heavily pretreated hormone receptor- and HER2-positive advanced cancers.

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