Trial E3311 validates a less intense treatment for HPV+ throat cancer

On May 13, 2020 The ECOG-ACRIN Cancer Research Group reported that the final results of the randomized phase two trial E3311 will be presented at the American Society of Clinical Oncology (ASCO) (Free ASCO Whitepaper) annual meeting, to occur virtually from May 29-31 (Press release, ECOG-ACRIN, MAY 13, 2020, View Source [SID1234557899]). The trial, conducted in patients undergoing transoral robotic surgery (TORS), tested reduced postoperative radiation therapy in patients with human papillomavirus-associated oropharynx squamous cell carcinoma at intermediate risk for recurrence. ASCO (Free ASCO Whitepaper) is highlighting the importance of the positive results by making it the first presentation in its Head and Neck Oral Abstract Session (Abstract 6500). The ECOG-ACRIN Cancer Research Group designed and conducted the trial with funding from the National Cancer Institute, part of the National Institutes of Health.

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"Transoral resection followed by low-dose radiation is safe in patients with intermediate-risk locally advanced oropharynx cancer, with very good oncologic outcome," said lead investigator Robert L. Ferris, MD, PhD, director, UPMC Hillman Cancer Center in Pittsburgh and a surgical oncologist specializing in head and neck cancer (pictured). "These results present a promising deintensification approach."

Most pharynx cancers caused by HPV have a very good outcome, and the cancer does not return or spread to other parts of the body after treatment. Dr. Ferris and colleagues sought to prove the benefits of using tumor pathologic features, obtained in specimens collected at surgery, to determine patients’ risk of recurrence–low, intermediate or high. In particular, they sought to more clearly define the prognostic and predictive role of traditional pathologic biomarkers such as extensive nodal or extranodal disease, to give the right amount of postoperative treatment for each risk group.

Patients at low risk were observed. Patients at intermediate risk were randomized to two arms of radiation alone, both at doses lower (50Gy or 60Gy) than usual (60-66Gy). At the time the trial opened in 2013, the optimal dose of radiation therapy was not defined. Patients at high risk were assigned to usual radiation therapy plus chemotherapy.

"Study E3311 met its primary endpoint," said Dr. Ferris. "For intermediate risk patients–those with uninvolved surgical margins, less than five involved nodes, and less than 1mm extranodal extension–reduced-dose postoperative radiation therapy without chemotherapy appears sufficient. In our study, this group had better outcomes than the group on usual high-dose radiation plus chemotherapy, showing that our patient stratification identified low and intermediate risk patients well, preserving patients’ throat function and sparing them unnecessary short- and long-term toxicities."

For patients with low-risk disease, two-year progression-free survival (PFS) was favorable without postoperative therapy (observation alone). All arms had two-year survival rates above 90% and there was no excess of local recurrences with reduction in radiation or chemotherapy (Arms B and C). Risk stratification appeared to appropriately select patients for observation (Arm A).

The overall intent of E3311 was to gather essential data for the design of a future, randomized phase three trial. The primary endpoint was to determine the feasibility and oncologic efficacy of a prospective multi-institutional study of TORS for HPV+ oropharynx cancer followed by risk-adjusted adjuvant therapy. The primary endpoint was two-year progression-free survival in patients determined to be at intermediate risk after surgical excision.

"The tissue samples and imaging studies collected in the course of this trial are a rich resource for studying the biology of intermediate- and high-risk disease, in work that is ongoing," said ECOG-ACRIN Head and Neck Committee Chair, Barbara A. Burtness, MD, Professor of Medicine, and Co-Leader, Developmental Therapeutics Program, Yale Cancer Center and Yale School of Medicine (pictured). "ECOG-ACRIN plans to pursue the current data with a randomized phase three trial of TORS-based treatment deintensification compared with conventional chemoradiation."

A lump in the neck and a sore throat are the most common signs of oropharynx cancer, a disease in which cancer cells form in the tissues of the oropharynx–the middle part of the throat (pharynx), at the base of the tongue and tonsils. About 60% of oropharynx cancers are associated with HPV infection. The incidence has been increasing in recent years, especially in individuals under the age of 45. This change is attributed to the increasing prevalence of HPV infection in developed countries, the practice of oral sex, and the rising number of sexual partners.

While surgeons and patients widely favor the organ-preservation approach of transoral robotic surgery, there remain serious concerns about both short- and long-term toxicities associated with chemotherapy. Besides, given the potential long-term consequences of radiation therapy for a younger population, re-evaluation of adjuvant treatment intensity is needed.

Upstate professor lands federal grant to continue kidney cancer research

On May 13, 2020 An Upstate Medical University urology professor reported that it has been awarded a grant from the Department of Defense (DOD) to continue and advance his research on kidney cancer (Press release, SUNY Upstate, MAY 13, 2020, View Source [SID1234557898]).

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The grant will support work by Mehdi Mollapour, PhD, vice chair for translational research for the department of urology, and his lab as it continues a decade-long research project into understanding kidney cancer biology and to develop novel therapeutic strategies to treat patients. Mollapour, professor of urology, molecular biology and biochemistry, is also the director of kidney cancer biology at Upstate.

His work, published in high-impact-factor journals (Dushukyan et al, 2017, Cell Reports & Oberoi et al, Proceedings of the National Academy of Sciences, 2016) identified a prosurvival role for PP5 protein in kidney cancer. Mollapour’s lab is currently funded by several grants from the National Institutes of Health and the National Cancer Institute. He applied for this DOD grant last fall and was notified of the award this spring.

"It’s always exciting when any grant is funded," he said. "From small amounts to big amounts, to have the funds to be able to continue our work and pay students and pay researchers is exciting."

About 74,000 Americans will be diagnosed with kidney cancer in 2020, according to the American Cancer Society. The disease is more common in men and kills nearly 15,000 people in the U.S. each year, according to the ACS.

In the application for the DOD grant, Mollapour’s lab cites a higher risk for developing kidney cancer among military families because of environmental exposures. The application also talks about what a difficult disease it can be to treat, highlighting the need to seek biomarkers for early detection and new therapies like those being developed in Mollapour’s lab. Traditional radiation and chemotherapies are ineffective in patients with kidney cancer and when presenting with large or locally advanced tumors, about 50 percent develop metastatic disease, for whom the five-year survival rate is less than 20 percent, according to the application.

The most recent grant – Mollapour’s first from the DOD – will propel the lab’s work and continue to open doors for additional funding.

"The grant allows us to better understand this disease and new ways of treating it. Naturally, data generated here will enable us to obtain further funding," he said. The $400,000 grant will support research staff, including students, working in the lab for two years. He and his staff are actively applying for additional funding from the National Institutes of Health.

Mollapour credits the work of everyone in his lab for obtaining this grant. After learning the good news about the DOD funding, Mollapour said he does what he always does when he is notified of new grant funding – he calls Upstate Chair of Urology Gennady Bratslavsky, MD, on the phone and plays the song "We Are The Champions," by Queen over the phone.

"When he hears that he knows what happened," Mollapour said laughing. "We have a secret code and Bratslavsky gets equally excited because he appreciates the importance of research and that is why he is fully committed in supporting research."

Mollapour and Bratslavsky worked together before coming to Upstate.

"Dr. Mollapour is a brilliant scientist and I take great pride in being able to recruit him from the National Cancer Institute where we both worked in urologic oncology studying kidney cancer," Bratslavsky said. "I respect Dr. Mollapour’s talent in research, his perseverance and his ability to be a mentor for many of my students and residents."

Mollapour said this grant is exciting and important because of its direct connection to patient care and its potential to extend the lives of kidney cancer patients.

"I know whatever we are going to do in terms of research will directly impact the kidney cancer patient," he said. "This is not one of those types of research that is 10 steps away from helping the patient. This is so gratifying and very exciting. The patient is always on my mind. It might be cliché but I really think we will help the patients with this. We are going to make it happen one way or another."

Arvinas Announces Updated Phase 1 Data Demonstrating Clinical Activity of PROTAC® Protein Degrader ARV-110 in Patients with Refractory Prostate Cancer

On May 13, 2020 Arvinas, Inc. (Nasdaq: ARVN), a clinical-stage biotechnology company creating a new class of drugs based on targeted protein degradation, reported updated safety and initial efficacy data contained in an abstract scheduled as an oral presentation at the 2020 American Society of Clinical Oncology (ASCO) (Free ASCO Whitepaper) Annual Meeting, to be held May 29–31, 2020 (Press release, Arvinas, MAY 13, 2020, View Source [SID1234557897]). The presentation will share updated data from the dose escalation portion of Arvinas’ Phase 1/2 clinical trial of ARV-110 in men with metastatic castration-resistant prostate cancer. The abstract describes two patients with ongoing confirmed prostate-specific antigen (PSA) responses, including one with an unconfirmed partial tumor response.

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"We are thrilled to present the first evidence that our PROTAC protein degrader, ARV-110, can provide clinical efficacy," said John Houston, Ph.D., President and Chief Executive Officer at Arvinas. "This is a significant milestone for our technology platform and for the field of targeted protein degradation."

"While still early, we are pleased to see a safety profile to date for ARV-110 that continues to support dose escalation," added Ron Peck, M.D., Chief Medical Officer at Arvinas. "Our trial of ARV-110 has enrolled a particularly heavily pre-treated population of patients who have exhausted most available treatment options. Most patients received both enzalutamide and abiraterone as well as prior chemotherapy. Despite this, ARV-110 demonstrated the first evidence of antitumor activity in this difficult-to-treat patient population."

The presentation will include data collected since the abstract submission date. Dose escalation continues, with enrollment initiated above the previously disclosed daily dose of 280 milligrams.

Abstract details are as follows:
Presentation Title: First-in-human phase I study of ARV-110, an androgen receptor PROTAC degrader in patients with metastatic castrate-resistant prostate cancer following enzalutamide and/or abiraterone
Abstract Number: 3500
Session Type: Oral Abstract Session
Session Track: Development Therapeutics – Molecularly Targeted Agents and Tumor Biology

For a copy of the abstract, please visit ASCO (Free ASCO Whitepaper)’s official website.

About ARV-110
ARV-110 is an orally bioavailable PROTAC protein degrader designed to selectively target and degrade the androgen receptor (AR). ARV-110 is being developed as a potential treatment for men with metastatic castration-resistant prostate cancer.

ARV-110 has demonstrated activity in preclinical models of AR mutation or overexpression, both common mechanisms of resistance to currently available AR-targeted therapies.

About Metastatic Castration-Resistant Prostate Cancer (mCRPC)
In the United States, prostate cancer is both the second most prevalent cancer in men and the second leading cause of cancer death in men. The American Cancer Society predicts that one in nine men will be diagnosed with prostate cancer in his lifetime. Metastatic castration-resistant prostate cancer (mCRPC) is defined by disease progression despite androgen deprivation therapy and is often correlated with rising levels of prostate-specific antigen (PSA).

Current AR-targeted standard of care treatments for mCRPC are less effective in patients whose disease has increased levels of androgen production, AR gene or gene enhancer amplification, or AR point mutations. Up to 25 percent of patients do not respond to second-generation hormone therapies like abiraterone and enzalutamide, and the vast majority of responsive patients will ultimately become resistant, resulting in poor prognoses for men diagnosed with this devastating condition.

AMERICAN SOCIETY OF CLINICAL ONCOLOGY (ASCO) ABSTRACT REPORTS INITIAL ALLO-501 ALPHA PHASE 1 DATA IN RELAPSED/REFRACTORY NON-HODGKIN LYMPHOMA

On May 13, 2020 Allogene Therapeutics, Inc. (Nasdaq: ALLO), a clinical-stage biotechnology company pioneering the development of allogeneic CAR T (AlloCAR T) therapies for cancer, in collaboration with its development partner Servier, an independent international pharmaceutical company, reported the release of the abstract related to an upcoming oral presentation at the American Society of Clinical Oncology (ASCO) (Free ASCO Whitepaper) Annual Meeting (Press release, Allogene, MAY 13, 2020, View Source [SID1234557896]). This will be the first data from Allogene’s Phase 1 dose escalation ALPHA study of ALLO-501 in relapsed/refractory non-Hodgkin lymphoma (NHL). This study utilizes ALLO-647, Allogene’s anti-CD52 monoclonal antibody (mAb), as a part of its differentiated lymphodepletion regimen.

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"As we look ahead to the end of the month to the virtual ASCO (Free ASCO Whitepaper) meeting, we are excited to present initial clinical data from our first-in-human study of ALLO-501 and ALLO-647," said Rafael G. Amado, M.D., Executive Vice President of Research & Development and Chief Medical Officer of Allogene. "These findings will provide an early glimpse into the potential of our AlloCAR T pipeline and ALLO-647 based lymphodepletion strategy, which we believe will be foundational in driving the future success and broad applicability of AlloCAR T therapies."

The ASCO (Free ASCO Whitepaper) abstract includes preliminary data on the first nine patients treated with escalating doses of ALLO-501 and lower dose (39mg) ALLO-647. No dose limiting toxicities or graft-vs-host disease (GvHD) was observed. The most common Grade (Gr) ≥ 3 adverse events were neutropenia (55.6%), leukopenia (33.3%) and anemia (22.2%). Two patients (22.2%) developed cytokine release syndrome (one Gr1 and one Gr2) that resolved within 72 hours without steroids or tocilizumab. One patient developed Gr1 neurotoxicity that resolved without treatment. One patient developed upper respiratory tract infection (Gr2), CMV (Gr3) and EBV viremia (Gr1), which all resolved. One patient had a Gr2 infusion reaction to ALLO-647 which resolved with antihistamines.

In this limited dataset with a small number of patients, the overall response rate (ORR) was 78% (95% exact CI: 40%, 97%) with three complete responses (CR) and four partial responses (PR). As of the January 2020 data cutoff, there was a median follow up of 2.7 months with four patients in ongoing response and three patients having progressed at 2, 4 and 6 months.

The virtual presentation will include data on 11 patients across ALLO-501 cell dose cohorts and the lower dose (39mg) of ALLO-647, as well as additional patients treated with ALLO-501 and the higher dose (90mg) of ALLO-647. The Phase 1 ALPHA study continues to enroll patients with higher dose ALLO-647 in an effort to optimize lymphodepletion.

This virtual presentation will be available on demand when ASCO (Free ASCO Whitepaper) releases pre-recorded presentations on May 29, 2020 at 5:00 a.m. PT/8:00 a.m. ET. Allogene will also host a conference call on May 29th following the release of the presentation.

Oral Abstract Session: Hematologic Malignancies – Lymphoma and Chronic Lymphocytic Leukemia
Abstract #8002
Title: First-in-Human Data of ALLO-501 and ALLO-647 in Relapsed/Refractory Large B-cell or Follicular Lymphoma (R/R LBCL/FL): ALPHA Study.
Presenter: Sattva S. Neelapu, MD, The University of Texas MD Anderson Cancer Center, Department of Lymphoma/Myeloma, Houston, TX
Session Release Date & Time: May 29, 2020 at 5:00 a.m. PT/8:00 a.m. ET
Location: On demand virtual presentation

Allogene is the sponsor of this Phase 1 trial which is designed to assess the safety and tolerability at increasing dose levels of ALLO-501 and ALLO-647 in patients with relapsed/refractory diffuse large B-cell lymphoma and follicular lymphoma.

Allogene expects to initiate enrollment in ALPHA2, a Phase 1 trial with abbreviated dose escalation of ALLO-501A, in Q2 2020. ALLO-501A is the next generation of ALLO-501, which eliminates the rituximab recognition domains, and it is intended for Phase 2 development.

About ALLO-501 (Allogene Sponsored)
Allogene’s AlloCAR T programs utilize Cellectis technologies. ALLO-501 is an anti-CD19 allogeneic CAR T (AlloCAR T) therapy being jointly developed under a collaboration agreement between Servier and Allogene based on an exclusive license granted by Cellectis to Servier. Servier grants to Allogene exclusive rights to ALLO-501 in the U.S. while Servier retains exclusive rights for all other countries.

Maryland’s Immunomic Therapeutics Exceeds Fundraising Goal, Envisions Future IPO

On May 13, 2020 Immunomic Therapeutics Incorporated (ITI), located in Rockville, Maryland reported that it had closed on $61.3M in financing, exceeding its initial fundraising projections by over $11M (Press release, Immunomic Therapeutics, MAY 13, 2020, View Source [SID1234557895]). The Korean investment group HLB Co., LTD led the financing round, which is just the latest accomplishment for the clinical-stage biotechnology company that launched in 2006.

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ITI, and its founder and CEO Bill Hearl, chose the proverbial road "less traveled" to get to where it is today — a leading, privately-held biotechnology company pioneering the study of nucleic acid immunotherapy platforms. Hearl and the Immunomic team’s trust in their gut instincts and willingness to buck conventional wisdom has transformed what was once a fledgling startup into a BioHealth Capital Region company to reckon with.

"You need to trust your instincts. Every so often things that seem like a bad idea to everybody else may seem like a really good idea to you — sometimes that is worth pursuing," stated Hearl.

At a pivotal point in ITI’s history, the company was pursuing R&D in the allergy space. Advisors, life science colleagues and investors told Hearl this was a mistake and that the company should move into oncology. Hearl trusted his gut, stuck to his belief that the allergy space was where ITI needed to be and forged ahead.

In 2015, Hearl’s bold, unconventional decision paid off in a watershed moment for ITI: The company struck a licensing deal with Astellas Pharma Inc. for its LAMP-vax products for the treatment or prevention of any and all allergic diseases in humans. The deal paid ITI $300M upfront with a double-digit royalty agreement while preserving ITI’s right to use the platform for other indications, including cancer immunotherapy.

The Astellas Pharma worldwide licensing agreement was a game changer for ITI. Up until that point, ITI had been a lean and mean operation that had raised around $17M in angel financing across several fundraising rounds. True to form, Hearl avoided diluting ownership of ITI by constructing the angel round based on a dividend model, which eventually paid off big for the angel investors after the Astellas agreement was consummated.

ITI also raised approximately $6M in 2016, but the company has generally funded operations independently over the years. The Astellas upfront payment, subsequent milestones and license fees have played a big role in funding ITI operations up until the recent $61.3M financing round. The unconventional decision to stick with its allergy approach early also empowered the company to get into the immuno-oncology space.

The HLB Co., LTD led fundraising round that exceeded ITI’s original goal of $50M is based around ITI’s lead product candidate, ITI-1000, which is a promising cell therapy treatment for glioblastoma, a highly deadly form of brain cancer.

ITI-1000 is nearing Phase II trials and is based on the company’s UNITE (Universal Intracellular Targeted Expression) technology platform. UNITE is the evolution of ITI’s LAMP-vax platform, which was licensed from Johns Hopkins University in 2006. ITI’s science remains firmly rooted in its Lysosomal Associated Membrane Protein (LAMP) vaccine technology; the current UNITE platform is an improved version of the original LAMP-vax.
"The core of the technology is our ability to activate the immune system. When we first started working with this, there was a phrase in a lot of academic papers that referred to ‘professional antigen presenting cells.’ I wondered ‘Who were the amateur antigen presenting cells?’ What they were talking about were immune cells whose specific job it is to teach other cells about foreign entities," stated Hearl.

"In the UNITE platform, we’ve found a way to have immune cells teach the rest of the immune system what doesn’t belong. It doesn’t matter if it’s an allergen, a cancer protein or a viral protein, your body follows the same basic mechanism of using white blood cells to educate the immune system about what’s foreign and then eliminating it from your body. We believe we’ve found the best way to teach the immune system about a foreign entity and use that to get rid of it," he added.

The genesis of ITI-1000 began with Dr. John Sampson at Duke University and Dr. Duane Mitchell at the University of Florida. Sampson and Mitchell discovered that tumor tissue was co-infected with cytomegalovirus; their research also showed that the cytomegalovirus pp65 protein was expressed on a high percentage of glioblastoma biopsies. Hearl was floored when he saw Sampson and Mitchell’s work in 2014 and then went about acquiring rights to the necessary IP over the next several years. ITI also made investments in funding Mitchell’s studies and provided a 5-year, $5M commitment to the University of Florida’s ReMission Alliance.

The pp65 protein was eventually coupled with the UNITE technology for a Phase I trial, called ATTAC-I. The first study was small, but the results showed an overall survival of over 40 months, which was a vast improvement over the 14-16 month survival typically seen with the normal standard of care. The ATTAC-II or Phase II study is larger with 120 patients and is a randomized, blind and placebo-controlled study deploying the most current version of the UNITE platform.

Since 2016, 100 patients have been under study and ITI expects some interim data towards the end of 2020.

"Frankly, I feel like this is my personal mission to bring this treatment to brain cancer patients in the near future. If we can do that, it’s a game changer for everyone with brain cancer," stated Hearl.

"One of the challenges of this study is that it’s for newly diagnosed glioblastoma patients so we have to see patients before chemotherapy. A lot of times patients have an overly optimistic view of their survival chances; unfortunately, they don’t realize they have to do something important to save their lives. They follow the standard of care and then it comes back," stated Hearl.

"We’re trying to get the word out that it’s important to get into the study site as soon as possible," he added.

ITI has always been a patient-focused company. The organization created a traveler fund that pays those enrolled in its study for travel, lodging and per diem costs associated with getting to the study site no matter where a participant might live in the U.S. This fund helps encourage enrollment and relieves some of the financial burdens placed on patients and families battling the disease.
Hearl’s wider vision for brain cancer treatment includes establishing brain cancer centers on the east and west coasts of the U.S., as well as in Seoul, South Korea. Hearl feels that ITI’s partnership with HLB will help propel the company toward achieving this long-term goal.

"I’m very excited about the idea of creating brain cancer centers around the world…When we first started talking with HLB, part of the discussion was about creating a Korean center to treat brain cancer patients in Seoul," Hearl stated. "This is a big part of our future."

"The people at HLB have been fantastic. They are looking to build a dynamic biopharma business. I’m very excited to be working with them," he added.

The $61.3M funding round, led by HLB, will primarily be used to continue the clinical development of ITI-1000 and to build out ITI’s commercial manufacturing capabilities. Currently, ITI can treat about 10-15 patients a month. This new round of funding will enable ITI to treat approximately 100 patients per month.

While ITI is intent on progressing its ITI-1000 program into Phase III trials and advancing other promising product candidates along its pipeline, including a cell-free version of the glioblastoma therapy called ITI-1001, it is simultaneously deploying the UNITE technology to develop a COVID-19 vaccine.

In the past, the UNITE platform has been widely applied to create vaccine candidates for rabies, yellow fever, Dengue fever, hepatitis C and another coronavirus, SARS, so Hearl and his team felt confident that their platform could help solve the COVID-19 problem. ITI has partnered with Epivax to develop the design for the vaccine and Pharmajet to deliver the COVID-19 vaccine via its needle-free injection technology if the vaccine is approved.

"Going back to the starting days of ITI, our scientific founder was Tom August. He was a brilliant scientist that developed the LAMP concept and his background was primarily in infectious disease…He did work in HIV, Dengue fever and West Nile, SARS and MERS…For a while, we were focused on other areas of interest, but when COVID-19 hit it was the right time in our lifecycle. We had the partners and the right technology to try to solve this problem," Hearl stated.

"For COVID-19 we can hit multiple targets on the virus, not just the spike protein. We can pull these together and create a vaccine design that will generate a better, more robust response," said Hearl.

"We have materials prepared and are conducting mouse experiments. Once we have proof of concept in an animal model we can really start looking at human safety studies for our COVID-19 vaccine hopefully later this year," he added.

What does the future hold for ITI? Hearl sees an IPO as the logical next step for the company.
"I think we will command a good valuation and be able to raise the funds we need to get our glioblastoma product commercialized. We’ve had investors with us for 14 years. I think they’d like to see that and I think it’s a smart way forward," Hearl said with a smile.

The hard choice to take the road "less travelled" early in the company’s history could lead ITI to a transformative IPO that could potentially make all the difference to patients and families battling COVID-19, glioblastoma, other cancers and allergies.

Along this less traveled road to whatever the future holds, Hearl and his team will continue to steadfastly follow their instincts, trust in their science, remain transparent and stay focused on helping patients in need.

To hear more from Hearl and about ITI, check out his recent appearance on BioHealth Innovation’s BioTalk Podcast with Rich Bendis.