Tagrisso plus chemotherapy reduced the risk of disease progression in the brain by 42% in patients with EGFR-mutated advanced lung cancer and brain metastases at baseline

On October 21, 2023 Astrazeneca reported results from a prespecified exploratory analysis of the FLAURA2 Phase III trial showed Tagrisso (osimertinib) with the addition of chemotherapy demonstrated a 42% improvement in central nervous system (CNS) progression-free survival (PFS), compared to Tagrisso alone for patients with locally advanced or metastatic epidermal growth factor receptor-mutated (EGFRm) non-small cell lung cancer (NSCLC) and brain metastases at baseline, reprsenting 40% of patients in the trial, as assessed by blinded independent central review (BICR) (Press release, AstraZeneca, OCT 21, 2023, View Source [SID1234636187]).

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These results were presented today in an oral presentation at the European Society for Medical Oncology (ESMO) (Free ESMO Whitepaper) Congress in Madrid, Spain (abstract #LBA68).

In this group of patients, Tagrisso with the addition of chemotherapy reduced the risk of CNS disease progression or death by 42% compared to Tagrisso alone (based on a hazard ratio [HR] of 0.58; 95% confidence interval [CI] 0.33-1.01) as assessed by BICR. With two years of follow-up, 74% of patients treated with Tagrisso plus chemotherapy had not experienced CNS disease progression or death versus 54% of patients treated with Tagrisso monotherapy. Results also showed a higher proportion of patients demonstrated CNS complete response (CR) with Tagrisso plus chemotherapy (59%) versus Tagrisso alone (43%).

David Planchard, MD, PhD, thoracic oncologist at Gustave Roussy Institute of Oncology and principal investigator for the trial, said: "Osimertinib has a proven ability to cross the blood-brain barrier and improve outcomes for patients with lung cancer and central nervous system metastases, who often face a poorer prognosis than patients whose disease has not spread to the brain. In FLAURA2, the addition of chemotherapy to osimertinib led to a complete response and the disappearance of these tumours in the brain, in more than half of these patients."

Susan Galbraith, Executive Vice President, Oncology R&D, AstraZeneca, said: "In this trial, patients with brain metastases at baseline saw a meaningful benefit with the FLAURA2 regimen, offering hope for patients whose cancer has spread to the brain. These data build on the recent positive progression-free survival results from FLAURA2, further reinforcing Tagrisso as the backbone therapy in EGFR-mutated non-small cell lung cancer."

The safety profile of Tagrisso with the addition of chemotherapy was generally manageable and consistent with the established profiles of the individual medicines. Adverse event (AEs) rates were higher in the Tagrisso plus chemotherapy arm, driven by well-characterised chemotherapy-related AEs. Tagrisso discontinuation rates were low in both arms of the trial (11% for the Tagrisso plus chemotherapy arm and 6% for the monotherapy arm).

In the Tagrisso plus chemotherapy arm, patients remained on Tagrisso for a median duration of 22.3 months, while patients had a median exposure to platinum-based chemotherapy of 2.8 months and a median exposure to pemetrexed of 8.3 months.

Summary of results: FLAURA2 CNS efficacyi

Tagrisso plus chemotherapy

(n=118)

Tagrisso monotherapy

(n=104)

PFS HR (95% CI)

0.58 (0.33-1.01)

Median PFS (months; 95% CI)

30.2 (28.4-NCii)

27.6 (22.1-NC)

CNS objective response rate, n (%)

86 (73)

72 (69)

CR, n (%)

70 (59)

45 (43)

Median CNS duration of response (in months; 95% CI)

NRiii (23.8-NC)

26.2 (19.4-NC)

i The data cut-off date was 3 April, 2023.
ii NC, non-calculable
iii NR, not reached

Earlier this month, Tagrisso with the addition of chemotherapy was granted Priority Review by the Food and Drug Administration (FDA) for the 1st-line treatment of adult patients with locally advanced or metastatic EGFRm NSCLC based on positive PFS data from the FLAURA2 Phase III trial recently presented at the International Association for the Study of Lung Cancer 2023 World Conference on Lung Cancer. In August 2023, Tagrisso with the addition of chemotherapy also received Breakthrough Therapy Designation from the FDA in this setting.

Notes

Lung cancer
Lung cancer is the leading cause of cancer death among both men and women, accounting for about one-fifth of all cancer deaths.1 Lung cancer is broadly split into NSCLC and small cell lung cancer.2 The majority of all NSCLC patients are diagnosed with advanced disease.3

Patients with EGFRm NSCLC are particularly sensitive to treatment with an EGFR-tyrosine kinase inhibitor (EGFR-TKI) which blocks the cell-signalling pathways that drive the growth of tumour cells.4

FLAURA2
FLAURA2 is a randomised, open-label, multi-centre, global Phase III trial in the 1st-line treatment of patients with locally advanced (Stage IIIB-IIIC) or metastatic (Stage IV) EGFRm NSCLC. Patients were treated with Tagrisso 80mg once daily oral tablets in combination with chemotherapy (pemetrexed (500mg/m2) plus cisplatin (75mg/m2) or carboplatin (AUC5) every three weeks for four cycles, followed by Tagrisso with pemetrexed maintenance every three weeks.

The trial enrolled 557 patients in more than 150 centres across more than 20 countries, including in the US, Europe, South America and Asia. The primary endpoint is PFS. The trial is ongoing and will continue to assess the secondary endpoint of overall survival (OS).

Tagrisso
Tagrisso (osimertinib) is a third-generation, irreversible EGFR-TKI with proven clinical activity in NSCLC, including against CNS metastases. Tagrisso (40mg and 80mg once-daily oral tablets) has been used to treat nearly 700,000 patients across its indications worldwide and AstraZeneca continues to explore Tagrisso as a treatment for patients across multiple stages of EGFRm NSCLC.

Tagrisso is approved as monotherapy in more than 100 countries including in the US, EU, China and Japan. These include for 1st-line treatment of patients with locally advanced or metastatic EGFRm NSCLC, locally advanced or metastatic EGFR T790M mutation-positive NSCLC, and adjuvant treatment of early-stage (IB, II and IIIA) EGFRm NSCLC, where Tagrisso recently demonstrated a statistically significant and clinically meaningful OS benefit.

There is an extensive body of evidence supporting the use of Tagrisso in EGFRm NSCLC. Tagrisso is the only targeted therapy to improve survival in both early-stage disease in the ADAURA Phase III trial and late-stage disease in the FLAURA Phase III trial.

AstraZeneca also has several ongoing Phase III trials focused on earlier stages of lung cancer, including a trial in the Stage IA2-IA3 adjuvant resectable setting (ADAURA2), in the neoadjuvant setting (NeoADAURA), and in the Stage III locally advanced unresectable setting (LAURA).

The Company is also researching ways to address tumour mechanisms of resistance through the SAVANNAH and ORCHARD Phase II trials, and the SAFFRON Phase III trial, which test Tagrisso plus savolitinib, an oral, potent and highly selective MET TKI, as well as other potential new medicines.

Sumgen Biotech’s First-In-Class ADC SG2918 Has Received IND Clearance From The National Medical Products Administration

On October 20, 2023 Hangzhou Sumgen Biotech Co., Ltd. (hereinafter referred to as "Sumgen Biotech") reported that it has received regulatory approval from the National Medical Products Administration (NMPA) to commence clinical trials for its proprietary novel ADC drug candidate SG2918 for injection, for the treatment of advanced malignant tumors (Press release, Sumgen Biotech, OCT 20, 2023, View Source;a=nav&id=355 [SID1234656271]). SG2918 is the first ADC candidate from Sumgen Biotech’s pipeline to be approved for clinical use, and it is first-in-class ADC approved for clinical trials.

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BreakBio Corp receives IND approval from the FDA for BreakVax

On October 20, 2023 BreakBio Corp., a biotech company dedicated to advancing innovative solutions in vaccine development for the treatment of cancer, reported that it has received Investigational New Drug (IND) approval from the U.S. Food and Drug Administration (FDA) for its investigational new personalized immunotherapy drug, BreakVax, on October 20, 2023 (Press release, Break Bio, OCT 20, 2023, View Source [SID1234644908]).

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This represents a significant milestone in the company’s commitment to addressing unmet medical needs and improving global health outcomes. This IND approval marks the culmination of extensive research and development by BreakBio Corp.’s dedicated team of oncologists, bioinformaticians, immunologists, and personalized cancer vaccine specialists.

BreakVax is a cutting-edge personalized peptide immunotherapy designed by mass spec, ML and manufactured per patient. Leveraging breakthrough technology and scientific expertise, BreakVax aims to provide a safe and effective treatment for solid cancers.

"We are thrilled to receive IND approval for BreakVax, as it underscores our unwavering dedication to advancing immunotherapies that have the potential to transform solid cancer treatments," said Roy de Souza, CEO of BreakBio Corp. "This milestone brings us one step closer to fulfilling our mission of improving survival rates, and aiming for cures for all solid cancers."

BreakBio Corp. remains committed to advancing BreakVax through the next stages of development, including our First In Human clinical trial in first indication (colorectal cancer) in 2024, with the ultimate goal of achieving the FDA’s Breakthrough Designation and making this personalized immunotherapy available to cancer patients who need it.

BRUKINSA® Receives Positive Recommendation from NICE in U.K. for Adult Patients with Chronic Lymphocytic Leukemia

On October 20, 2023 BeiGene, Ltd. (Nasdaq: BGNE; HKEX: 06160; SSE: 688235), a global biotechnology company, reported the National Institute for Health and Care Excellence (NICE) of the United Kingdom (U.K.) has issued a final draft guidance (FDG) recommending BRUKINSA (zanubrutinib) for the treatment of eligible adult patients with (Press release, BeiGene, OCT 20, 2023, View Source [SID1234636171]):

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Untreated chronic lymphocytic leukemia (CLL) if there is a 17p deletion or TP53 mutation (high risk) or
Untreated CLL without a 17p deletion or TP53 mutation, and fludarabine-cyclophosphamide-rituximab (FCR) or bendamustine plus rituximab (BR) is unsuitable and
Relapsed or refractory CLL
"We are delighted that NICE has recognized the clinical and economic benefit of BRUKINSA for patients with CLL," said Dr. Robert Mulrooney, General Manager, U.K. & Ireland at BeiGene. "This follows the previous approval of BRUKINSA by NICE in July 2022 as the only cost-effective treatment for patients with Waldenstrom’s macroglobulinemia. Although we are a relatively new player in the U.K. market, we are rapidly establishing ourselves as a company that can make innovative cancer medicines accessible and affordable for U.K. patients."

As stated in the FDG, for the untreated CLL population that is high-risk or for whom FCR or BR is unsuitable and for the relapsed/refractory CLL population, zanubrutinib had lower incremental costs and more incremental quality adjusted life years compared with other BTK inhibitors. The committee considered that zanubrutinib is a cost-effective use of NHS resources in CLL.

"This decision represents a significant milestone for patients in England and Wales with CLL, the most common form of leukemia in adults," said Nick York, Patient Advocacy Healthcare Liaison Officer, U.K. Leukemia Care. "Despite continued treatment advances, many patients with CLL will relapse and need additional treatment options. Furthermore, a proportion of patients have a disease which is refractory to initial treatment."

BRUKINSA is the third BTKi for CLL to be recommended by NICE for routine commissioning.

"Zanubrutinib has demonstrated superior efficacy and a favorable safety profile in two global Phase 3 trials, SEQUOIA and ALPINE, in adult patients with CLL," said Dr. Talha Munir, consultant hematologist at Leeds Teaching Hospitals NHS Trust, Leeds, U.K.i,ii "The positive recommendation from NICE will allow patients with CLL in England and Wales to access this important new treatment option."

In addition, on October 9, 2023, BRUKINSA received approval by the Scottish Medicines Consortium for the treatment of adult patients with CLL in whom chemo-immunotherapy is unsuitable.

BRUKINSA is approved in more than 65 countries, including the U.S., China, EU, Great Britain, Canada, Australia, South Korea, and Switzerland, in selected indications and under development for additional indications globally. The global BRUKINSA development program includes more than 5,000 subjects enrolled to date in 29 countries and regions.

About Chronic Lymphocytic Leukemia (CLL)
A life-threatening cancer of adults, CLL is a type of mature B-cell malignancy in which abnormal leukemic B lymphocytes (a type of white blood cells) arise from the bone marrow and flood peripheral blood, bone marrow, and lymphoid tissues.iii,iv CLL is the most common type of leukemia in adults, accounting for about one-quarter of new cases of leukemia.iv,v Approximately 3,800 people in the U.K. are diagnosed with CLL every year.vi,vii

About BRUKINSA (zanubrutinib)
BRUKINSA is a small molecule inhibitor of Bruton’s tyrosine kinase (BTK) discovered by BeiGene scientists that is currently being evaluated globally in a broad clinical program as a monotherapy and in combination with other therapies to treat various B-cell malignancies. Because new BTK is continuously synthesized, BRUKINSA was specifically designed to deliver complete and sustained inhibition of the BTK protein by optimizing bioavailability, half-life, and selectivity. With differentiated pharmacokinetics compared to other approved BTK inhibitors, BRUKINSA has been demonstrated to inhibit the proliferation of malignant B cells within a number of disease relevant tissues.

Novartis Financial Results – Q3 2023

On October 24, 2023 Novartis reported a very strong quarter, with double-digit sales and core operating income growth leading to a further upgrade to 2023 guidance (Press release, Novartis, OCT 20, 2023, View Source [SID1234636263]). We have successfully executed the spin-off of Sandoz, allowing us to fully focus on high-value innovative medicines. Our growth drivers, including Kesimpta, Entresto, Kisqali and Pluvicto, continue to perform well in the market. Our robust pipeline also continues to deliver, and we have achieved important innovation milestones for Pluvicto, iptacopan, remibrutinib and Lutathera. We are confident in our mid-term growth outlook and remain committed to creating value for our shareholders."

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