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ORIC-101, a Glucocorticoid Receptor Antagonist, in Combination with Nab-Paclitaxel in Patients with Advanced Solid Tumors.
Chen, Christopher T; Khanna, Vishesh; Kummar, Shivaani; Abdul-Karim, Raghad M; Sommerhalder, David; Tolcher, Anthony W; Ueno, Naoto T; Davis, Sarah Lindsey; Orr, Douglas W; Hamilton, Erika; Patel, Manish R; Spira, Alexander I; Jauhari, Shekeab; Florou, Vaia; Duff, Maureen; Xu, Rongda; Wang, Jian; Barkund, Shravani R; Zhou, Haiying; Pankov, Aleksandr; Kong, Wayne; Jahchan, Nadine S; Jackson, Erica L; Sun, Jessica D; Junttila, Melissa R; Multani, Pratik S; Daemen, Anneleen; Chow Maneval, Edna; Munster, Pamela N.
Afiliación
  • Chen CT; Division of Oncology, Department of Medicine, Stanford University School of Medicine, Palo Alto, California.
  • Khanna V; Division of Oncology, Department of Medicine, Stanford University School of Medicine, Palo Alto, California.
  • Kummar S; Division of Oncology, Department of Medicine, Stanford University School of Medicine, Palo Alto, California.
  • Abdul-Karim RM; Knight Cancer Institute, Oregon Health and Science University, Portland, Oregon.
  • Sommerhalder D; NEXT Oncology, San Antonio, Texas.
  • Tolcher AW; NEXT Oncology, San Antonio, Texas.
  • Ueno NT; NEXT Oncology, San Antonio, Texas.
  • Davis SL; University of Texas MD Anderson Cancer Center, Houston, Texas.
  • Orr DW; University of Colorado Cancer Center, Aurora, Colorado.
  • Hamilton E; Mary Crowley Cancer Research, Dallas, Texas.
  • Patel MR; Sarah Cannon Research Institute, Nashville, Tennessee.
  • Spira AI; Florida Cancer Specialists/Sarah Cannon Research Institute, Sarasota, Florida.
  • Jauhari S; Virginia Cancer Specialists, Fairfax, Virginia.
  • Florou V; Florida Cancer Specialists/Sarah Cannon Research Institute, Lake Mary, Florida.
  • Duff M; 1Huntsman Cancer Institute, University of Utah, Salt Lake City, Utah.
  • Xu R; ORIC Pharmaceuticals, South San Francisco, California.
  • Wang J; ORIC Pharmaceuticals, South San Francisco, California.
  • Barkund SR; ORIC Pharmaceuticals, South San Francisco, California.
  • Zhou H; ORIC Pharmaceuticals, South San Francisco, California.
  • Pankov A; ORIC Pharmaceuticals, South San Francisco, California.
  • Kong W; ORIC Pharmaceuticals, South San Francisco, California.
  • Jahchan NS; ORIC Pharmaceuticals, South San Francisco, California.
  • Jackson EL; ORIC Pharmaceuticals, South San Francisco, California.
  • Sun JD; ORIC Pharmaceuticals, South San Francisco, California.
  • Junttila MR; ORIC Pharmaceuticals, South San Francisco, California.
  • Multani PS; ORIC Pharmaceuticals, South San Francisco, California.
  • Daemen A; ORIC Pharmaceuticals, South San Francisco, California.
  • Chow Maneval E; ORIC Pharmaceuticals, South San Francisco, California.
  • Munster PN; ORIC Pharmaceuticals, South San Francisco, California.
Cancer Res Commun ; 4(9): 2415-2426, 2024 Sep 01.
Article en En | MEDLINE | ID: mdl-39177285
ABSTRACT

PURPOSE:

In preclinical models, glucocorticoid receptor (GR) signaling drives resistance to taxane chemotherapy in multiple solid tumors via upregulation of antiapoptotic pathways. ORIC-101 is a potent and selective GR antagonist that was investigated in combination with taxane chemotherapy as an anticancer regimen preclinically and in a phase 1 clinical trial. PATIENTS AND

METHODS:

The ability of ORIC-101 to reverse taxane resistance was assessed in cell lines and xenograft models, and a phase 1 study (NCT03928314) was conducted in patients with advanced solid tumors to determine the dose, safety, and antitumor activity of ORIC-101 with nab-paclitaxel.

RESULTS:

ORIC-101 reversed chemoprotection induced by glucocorticoids in vitro and achieved tumor regressions when combined with paclitaxel in both taxane-naïve and -resistant xenograft models. In the phase 1 study, 21 patients were treated in dose escalation and 62 patients were treated in dose expansion. All patients in dose expansion had previously progressed on a taxane-based regimen. In dose escalation, five objective responses were observed. A preplanned futility analysis in dose expansion showed a 3.2% (95% confidence interval, 0.4-11.2) objective response rate with a median progression-free survival of 2 months (95% confidence interval, 1.8-2.8) across all four cohorts, leading to study termination. Pharmacodynamic analysis of tissue and plasma showed GR pathway downregulation in most patients in cycle 1.

CONCLUSIONS:

ORIC-101 with nab-paclitaxel showed limited clinical activity in taxane-resistant solid tumors. Despite clear inhibition of GR pathway signaling, the insufficient clinical signal underscores the challenges of targeting a single resistance pathway when multiple mechanisms of resistance may be in play.

SIGNIFICANCE:

Glucocorticoid receptor (GR) upregulation is a mechanism of resistance to taxane chemotherapy in preclinical cancer models. ORIC-101 is a small molecule GR inhibitor. In this phase 1 study, ORIC-101 plus nab-paclitaxel did not show meaningful clinical benefit in patients who previously progressed on taxanes despite successful GR pathway downregulation.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Protocolos de Quimioterapia Combinada Antineoplásica / Receptores de Glucocorticoides / Paclitaxel / Albúminas / Neoplasias Límite: Adult / Aged / Animals / Female / Humans / Male / Middle aged Idioma: En Revista: Cancer Res Commun Año: 2024 Tipo del documento: Article Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Protocolos de Quimioterapia Combinada Antineoplásica / Receptores de Glucocorticoides / Paclitaxel / Albúminas / Neoplasias Límite: Adult / Aged / Animals / Female / Humans / Male / Middle aged Idioma: En Revista: Cancer Res Commun Año: 2024 Tipo del documento: Article Pais de publicación: Estados Unidos