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BriaCell Reports 12.0 Months Overall Survival Benefit in Advanced Breast Cancer; 100% Resolution of ‘Eye-Bulging’ Tumor

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BriaCell Therapeutics Corp. (Nasdaq: BCTX, BCTXW) reports significant overall survival data for advanced breast cancer patients treated with its candidate, Bria-IMT™. Patients demonstrated a 12.0 months average overall survival, with 13.4 months for those with 2+ HLA matches and 12.5 months for Grade I/II tumors. A top responder achieved 21.4 months survival and complete resolution of an orbital tumor. These results significantly outperform historical treatments, which average 7.2-9.8 months survival. The findings position BriaCell as a promising option for patients resistant to existing therapies.

Positive
  • Average overall survival of 12.0 months in treated patients.
  • Patients with 2+ HLA matches experienced survival of 13.4 months.
  • Top responder achieved 21.4 months survival with complete tumor resolution.
  • Results significantly exceed historical survival rates of 7.2-9.8 months.
Negative
  • None.
  • 12.0 months average overall survival benefit, including 13.4 months in patients with 2+ HLA matches and 12.5 months in patients with Grade I/II tumors(1)
  • Top Responder: 21.4 months survival plus 100% resolution of ‘eye-bulging’ orbital tumor
  • Compares to 7.2-9.8 months survival in historical comparison treatment trials(2)

BERKELEY, Calif. and VANCOUVER, British Columbia, June 02, 2021 (GLOBE NEWSWIRE) -- BriaCell Therapeutics Corp. (Nasdaq: BCTX, BCTXW) (TSX-V:BCT) (“BriaCell” or the “Company”), a clinical-stage biotechnology company specializing in targeted immunotherapies for advanced breast cancer, today provides an update on the overall survival (OS) data on its previously disclosed advanced breast cancer patients. These women were treated with BriaCell’s lead candidate Bria-IMT™ as monotherapy and also in combination with checkpoint inhibitors, including pembrolizumab (KEYTRUDA®; manufactured by Merck & Co., Inc.) and Incyte’s retifanlimab (manufactured and provided under a corporate collaboration with Incyte Corporation).

HLA-Typing: Cells with HLA (human leukocyte antigen) molecules on their surface determine and trigger the body’s immune response. BriaCell’s immunotherapy treatment appears most effective when the patient’s HLA-type matches with Bria-IMT™, allowing BriaCell to potentially identify patients most likely to respond. HLA-typing is a simple and widely available test.

Tumor Grade: BriaCell has noted clinical benefit in its patients with grade I and grade II tumors, suggesting another subgroup of patients for whom BriaCell’s treatment would be most effective.

BriaCell Treatment 1 Leading Treatment Comparison 2
N =FilterPrior RegimensOverall Survivalvs.Prior RegimensOverall Survival
7Combination Therapy912.0 months 27.2 - 9.8 months
91+ HLA812.1 months   
52+ HLA513.4 months   
6Tumor Grade I/II1212.5 months   
Patient 06-005 32 HLA; Grade II1321.4 months   

1) BriaCell treats severely sick patients, as indicated by the “Prior Regimens” column. To more accurately present survival data, BriaCell has included only those women able to mount an immune response. Patients from both the monotherapy and combination therapy are included unless otherwise indicated.
2) Overall survival of 7.2-9.8 months in similar patients with metastatic breast cancer who have failed 2 prior therapy attempts (third line setting); Kazmi S, et al. Breast Cancer Res Treat. 2020 Aug 17.
3) Remarkable Responder highlighted; included within subsets “Tumor Grade I/II” and “2+ HLA”.

Highlighting BriaCell’s Top Responder:
Initially announced on Sep. 19, 2019 and subsequently on Jan. 13, 2020, BriaCell has continued to emphasize this patient’s positive response to BriaCell’s treatment. Prior to BriaCell’s treatment, the patient had received 12 regimens with 16 agents (incl. 13 chemotherapies), yet her condition worsened and included a gruesome orbital tumor that metastasized behind her left eye and caused the eye to bulge from its socket (proptosis).   After just six months of BriaCell’s treatment, the orbital tumor had been completely eliminated, and she survived for over 21 months, a significant clinical benefit.

Media Snippet - June 1, 2021

Figure 1: The figure shows MRI scans of the top responder patient. The arrows on the images (baseline scans) show the location of the orbital tumors. As shown on the images on the right hand side, the tumors were eliminated following 6 months of treatment with the Bria-IMT combination regimen.

In the figure above, and with tumors indicated by white arrows, complete resolution of the orbital tumor was observed after six months on BriaCell’s treatment. Of note, she had two HLA matches with Bria-IMT™ and a grade II tumor, supporting BriaCell’s hypotheses outlined above.

"Women with advanced breast cancer often are fighting a deadly disease that does not respond to currently-available treatments," said Dr. Bill Williams, BriaCell’s President and CEO. "We are pleased to report that our immunotherapy regimen appears to offer clinical benefit for these patients in desperate need of new therapy options."

About BriaCell Therapeutics Corp.

BriaCell is an immuno-oncology focused biotechnology company developing targeted and effective approaches for the management of cancer.

For additional information on BriaCell, please visit: https://briacell.com/.

Forward Looking Statements

This press release contains “forward-looking statements” that are subject to substantial risks and uncertainties. All statements, other than statements of historical fact, contained in this press release are forward-looking statements. Forward-looking statements contained in this press release may be identified by the use of words such as “anticipate,” “believe,” “contemplate,” “could,” “estimate,” “expect,” “intend,” “seek,” “may,” “might,” “plan,” “potential,” “predict,” “project,” “target,” “aim,” “should,” "will” “would,” or the negative of these words or other similar expressions, although not all forward-looking statements contain these words. Forward-looking statements are based on BriaCell’s current expectations and are subject to inherent uncertainties, risks and assumptions that are difficult to predict. Further, certain forward-looking statements are based on assumptions as to future events that may not prove to be accurate. These and other risks and uncertainties are described more fully under the heading "Risks and Uncertainties" in the Company's most recent Management’s Discussion and Analysis, under “Risks and Uncertainties” and in the Company's other filings with the Canadian securities regulatory authorities and the U.S. Securities and Exchange Commission, all of which are available under our profiles on SEDAR at www.sedar.com and on EDGAR at www.sec.gov. . Forward-looking statements contained in this announcement are made as of this date, and BriaCell Therapeutics Corp. undertakes no duty to update such information except as required under applicable law.

Neither TSX Venture Exchange nor its Regulation Services Provider (as that term is defined in the policies of the TSX Venture Exchange) accepts responsibility for the adequacy or accuracy of this release.

Contact Information

Company Contact:
William V. Williams, MD

President & CEO
1-888-485-6340
info@briacell.com

Media Relations:
Jules Abraham
Director of Public Relations
CORE IR
917-885-7378
julesa@coreir.com 

Investor Relations Contact:
CORE IR
investors@briacell.com


FAQ

What is BriaCell's recent survival data for BCTX and BCTXW?

BriaCell reported a 12.0 months average overall survival for advanced breast cancer patients, with 13.4 months for those with 2+ HLA matches.

How does BriaCell's treatment compare to historical treatments?

BriaCell's treatment shows a significant improvement, with historical treatments averaging 7.2-9.8 months of survival.

What results did the top responder achieve with BriaCell's therapy?

The top responder experienced 21.4 months of survival and complete resolution of an orbital tumor.

What type of tumors showed clinical benefit in BriaCell's study?

Clinical benefit was noted in patients with Grade I and II tumors, indicating targeted effectiveness.

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