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It is important that patients and their loved ones stay hopeful during the ovarian cancer journey. We asked attendees of the 2018 NOCC Annual Conference how they keep positive.

What Gives Patients and Loved Ones Hope?

Professor Richard Scolyer, a top doctor and leading melanoma pathologist, was diagnosed with Glioblastoma (GBM) brain cancer in July of 2023 and told he had only a few months to live. However, Richard didn't give up. Using everything he knew about melanoma science, Richard and his team used pre-surgery combined immunotherapy and a personalized cancer vaccine, the first in the world to do so.

Patients like Richard need your support in order to access the specialists, advanced treatments, and devices they need. Give today to support the End Brain Cancer Initiative's (EBCI’s) mission and help patients and families. Learn more about Richard's story at https://www.youtube.com/watch?app=desktop&v=2D9_mlLZPdI.

Support from individuals is vital for the End Brain Cancer Initiative to continue helping patients and families facing brain cancer, brain tumors, and metastatic disease to the brain. Gifts will support free access to DIRECT support from EBCI, a wealth of resources through the EBCI Website and the EBCI Disease Education Mobile App, and patient disease education online events. People can help EBCI reach their goal of $20,000 dollars raised for GiveBIG 2025 by giving at endbraincancer.org/donate.

Gifts to EBCI for GiveBIG will also fuel the nonprofit’s advocacy efforts, giving EBCI the ability to advocate for policies that increase patient access to specialists, advanced treatments, and devices. One such policy is the Bolstering Research And Innovation Now (BRAIN) Act (H.R.2767/ S.1330), which aims to advance the quest to defeat brain tumors, once and for all, by increasing research funding, fostering collaboration, promoting critical awareness efforts, and supporting innovations in and access to care.

GiveBIG 2025 is all about that good feeling we get when we show up for others, whether it’s a family member, a neighbor, or a local nonprofit we care about. People can make good things happen at the End Brain Cancer Initiative by giving to help patients and families facing brain cancer, brain tumors, and metastatic disease to the brain.

The End Brain Cancer Initiative is a 501(c)3 non-profit patient organization focused on disease education, awareness, outreach and increasing patient access. The End Brain Cancer Initiative, formerly known as the Chris Elliott Fund, is dedicated to ensuring that all patients diagnosed with brain cancer, a brain tumor, or metastatic disease to the brain have equal access to advanced diagnostics, treatments, specialists, and clinical trial participation. We believe that IMMEDIATE ACCESS to these options provides this patient community with the best HOPE for survival and sustained quality of life. We partner with industry, patients, researchers, advocacy groups, medical teams, hospital networks and others to educate patients and their caregivers so they can have empowered conversations with medical teams. Learn more about and support the End Brain Cancer Initiative’s work and mission at EndBrainCancer.org.

Professor Richard Scolyer, a renowned melanoma pathologist, was diagnosed with Glioblastoma in 2023. Despite a grim prognosis, he utilized his expertise to undergo innovative treatments, including pre-surgery combined immunotherapy and a personalized cancer vaccine. The End Brain Cancer Initiative (EBCI) supports patients like Richard by providing access to specialists, treatments, and resources. Donations to EBCI aid in advocacy efforts, such as the BRAIN Act, and help achieve fundraising goals like GiveBIG 2025. EBCI is committed to ensuring equal access to advanced care for brain cancer patients.

People can help EBCI reach their goal of $20,000 dollars raised for GiveBIG 2025 by giving at endbraincancer.org/donate.

NOINDEX

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Tumor

Support Patient Access and Education with the End Brain Cancer Initiative for GiveBIG 2025

The End Brain Cancer Initiative (EBCI) is currently seeking Primary Central Nervous System Lymphoma (PCNSL) patients and care partners to participate in an online roundtable discussion on April 11, 2025, from 11AM to 12:30PM Pacific Time.

The PCNSL Online Roundtable will help further resources and education provided to this patient population by doing a deep dive into the results of their recent PCNSL patient and care partner survey. The roundtable, sponsored by Ono Pharmaceutical, will be moderated by Dellann Elliott Mydland, President and CEO of the End Brain Cancer Initiative.

Patients and care partners interested in participating in this discussion should fill out the interest form at endbraincancer.org/pcnsl before March 31, 2025. Qualifying participants will be compensated $75 for their time.

Ono Pharmaceutical Co., Ltd., headquartered in Osaka, is an R&D-oriented pharmaceutical company committed to creating innovative medicines in specific areas. Ono focuses its research on oncology, immunology, neurology, and specialty area with high medical needs as priority areas for discovery and development of innovative medicines. For further information, please visit the company’s website at https://www.ono-pharma.com/en.

To support/donate to the End Brain Cancer Initiative’s increased access and health delivery for patients, mission, services and programs, please visit EndBrainCancer.org

The End Brain Cancer Initiative (EBCI) is a 501(c)3 non-profit patient advocacy organization focused on disease education, awareness, outreach, increasing patient access and improving Standard of Care. The End Brain Cancer Initiative, formerly known as the Chris Elliott Fund (CEF), is dedicated to ensuring that all patients diagnosed with brain cancer, a brain tumor, or metastatic disease to the brain have equal access to advanced diagnostics, treatments, specialists, and clinical trial participation. We believe that IMMEDIATE ACCESS to these options provides this patient community with the best HOPE for survival and sustained quality of life. We partner with industry, patients, researchers, advocacy groups, medical teams, hospital networks and others to educate patients and their caregivers so they can have empowered conversations with their medical teams. Learn more about the End Brain Cancer Initiative at EndBrainCancer.org.

The End Brain Cancer Initiative (EBCI) is organizing an online roundtable for Primary Central Nervous System Lymphoma (PCNSL) patients and care partners on April 11, 2025. This event aims to enhance resources and education for this patient group by analyzing recent survey results. Sponsored by Ono Pharmaceutical, the roundtable will be moderated by EBCI's President, Dellann Elliott Mydland. Participants will receive $75 for their involvement. EBCI is a non-profit focused on improving access to advanced diagnostics and treatments for brain cancer patients.

Primary Central Nervous System Lymphoma Patient and Care Partner Roundtable Hosted by the End Brain Cancer Initiative

Registration is now open for the 2025 Know All Your Treatment Options (KAYTO25) online patient disease education event/webinar

Registration is now open for the 2025 Know All Your Treatment Options (KAYTO25) online patient disease education event/webinar, hosted by the End Brain Cancer Initiative (EBCI), on Friday, May 16th, 2025, from 11 AM to 2 PM Pacific Time.

This free annual online event is designed specifically for members of the brain tumor, brain cancer, and metastasized brain tumor community to hear directly from top specialists, including researchers, in the field about advanced and FDA approved treatment options, clinical trials, devices, diagnostics, etc. that they may not have heard about and to “DIRECTLY CONNECT” this patient population to many of these specialists. The event is free to attend due to corporate sponsorships, but pre-registration is required: endbraincancer.org/know-all-your-treatment-options-2025/.

KAYTO attendees will hear from multiple presenters, including a representative from Telix Pharmaceuticals, one of the presenting sponsors of this event. Telix is at the forefront of developing advanced imaging agents to improve the diagnosis and management of brain cancers, particularly gliomas. Telix’s brain cancer program comprises an investigational therapy and an investigational PET imaging agent – both small molecule-based. The company aims to provide clearer and more specific imaging results, aiding in the accurate differentiation between tumor progression and treatment-related changes.

Visit endbraincancer.org/know-all-your-treatment-options-2025/ to learn more about sponsorship opportunities to support this patient disease education online event.

Telix is a biopharmaceutical company focused on the development and commercialization of therapeutic and diagnostic radiopharmaceuticals and associated medical technologies. Telix is developing a portfolio of clinical and commercial stage products that aims to address significant unmet medical needs in oncology and rare diseases. Visit http://www.telixpharma.com/ for further information.

The 2025 Know All Your Treatment Options (KAYTO25) online event, hosted by the End Brain Cancer Initiative, will take place on May 16th, 2025. This free event aims to educate the brain tumor community about advanced treatment options and connect them with specialists. Sponsored by companies like Telix Pharmaceuticals, the event will feature presentations on innovative imaging agents for brain cancer management. The End Brain Cancer Initiative, a non-profit organization, focuses on improving patient access to diagnostics, treatments, and clinical trials, enhancing survival and quality of life.

Registration Open for the 2025 Know All Your Treatment Options Webinar Hosted by the End Brain Cancer Initiative

Each May, for over a decade, the End Brain Cancer Initiative (EBCI) has presented the National HOPE Award to a brain cancer patient who deeply inspires us with their courage and story. EBCI established this patient disease education initiative and award to highlight exceptional people who have done exceptional things during their brain cancer journey, all while inspiring others.

The deadline for submitting HOPE Award nominations is April 16th, 2025. To submit a nomination, people can visit https://endbraincancer.org/hope-award-nomination/. 

Patrick “Paddy” O'Donnell is the 2024 National HOPE Award recipient. Paddy was a 20-year-old collegiate ice hockey goaltender at the University of Utah when he had a seizure. He woke up in the Neuro ICU connected to tubes and monitors wondering what happened. A biopsy revealed he had Glioblastoma (GBM) and three tumors. Paddy was nominated by his mother, Anne O'Donnell. "Paddy had to create his own HOPE and sought answers and second opinions about his treatment," she said. "End Brain Cancer Initiative was vital in our search, at the most critical time, availing us of options and direct contact with experts in the field whom Dellann knew personally."

The 2025 HOPE Award recipient will be announced during the End Brain Cancer Initiative's Know All Your Treatment Options (KAYTO25) online patient disease education event/webinar on May 16th, 2025. This free annual online event is designed specifically for members of the brain tumor, brain cancer, and metastasized brain tumor community to hear directly from top specialists, including researchers, in the field about advanced and FDA approved treatment options, clinical trials, devices, diagnostics, etc. that they may not have heard about and to “DIRECTLY CONNECT” this patient population to many of these specialists. The event is free to attend due to corporate sponsorships, but pre-registration is required: endbraincancer.org/know-all- your-treatment-options-2025/.

To support/donate to the End Brain Cancer Initiative’s increased access and health delivery for patients, mission, services and programs, please visit EndBrainCancer.org. 

The End Brain Cancer Initiative (EBCI) annually presents the National HOPE Award to a brain cancer patient who inspires with their courage and story. The 2024 recipient is Patrick “Paddy” O'Donnell, a collegiate ice hockey goaltender diagnosed with Glioblastoma. The 2025 recipient will be announced at the KAYTO25 event, which connects patients with specialists and provides information on advanced treatments. EBCI, a non-profit organization, focuses on disease education, awareness, and increasing patient access to advanced diagnostics and treatments, aiming to improve survival and quality of life.

Nominations Open for the End Brain Cancer Initiative’s 2025 National Patient Disease Education Initiative and HOPE Award

In March 2025, the FDA approved neoadjuvant treatment with Imfinzi (durvalumab) plus gemcitabine and cisplatin, followed by single-agent, adjuvant Imfinzi following radical cystectomy in muscle invasive bladder cancer, according to a news release from the United States Food and Drug Administration (FDA).

Notably, the efficacy of the now-FDA-approved approach was evaluated in the randomized, open-label, multicenter, 

. In the study, the investigative combination demonstrated a statistically significant improvement in event-free survival and overall survival for patients with muscle invasive bladder cancer who were candidates for radical cystectomy (surgery to remove the urinary bladder).

In an interview with CURE, Dr. Matthew Galsky sat down to discuss the significance 

 and key takeaways for patients within this population.

“The most important takeaway [message] is that there has been a slow but steady improvement in our ability to treat muscle-invasive bladder cancer,” Galsky explained in the interview. “I think we are at a tipping point in the next few years, where the convergence of better therapies and better technologies — specifically, our ability to measure small amounts of cancer with increased precision using better testing — will all come together and potentially completely change the way we treat bladder cancer moving forward.”

Galsky is professor of Medicine (Hematology and Medical Oncology), director of Genitourinary Medical Oncology, co-director of the Center of Excellence for Bladder Cancer, and associate director for Translational Research, all located at The Tisch Cancer Institute, the Mount Sinai Health System, in New York, New York.

CURE: To begin, what makes this approval significant for patients and providers managing muscle-invasive bladder cancer?

: A standard treatment for muscle-invasive bladder cancer is the surgical removal of the bladder. We know that after the bladder is removed, a subset of individuals will experience the cancer reappearing elsewhere in the body, developing metastatic recurrence, typically months to years later.

For decades, doctors attempted to combine chemotherapy with surgery to eradicate any microscopic cancer cells that might be present, aiming to reduce the risk of metastatic recurrence. When chemotherapy is administered before surgery, it's called neoadjuvant therapy. This concept of giving chemotherapy prior to surgery to treat potential microscopic spread of cancer is used in various solid tumors. When chemotherapy is given after surgery, it's known as adjuvant therapy.

For decades, the only neoadjuvant therapy proved beneficial in muscle-invasive bladder cancer was a combination of chemotherapy drugs, including cisplatin. This truly represented the standard treatment approach for many years because nothing had been shown to be superior.

Finally, after several decades, the NIAGARA trial demonstrated that integrating immunotherapy in the pre-surgical and post-surgical periods decreases the risk of metastatic disease development and improves longevity for patients.

The NIAGARA trial demonstrated a 32% reduction in the risk of recurrence and a 25% reduction in the risk of death. How do these results compare with historical outcomes using neoadjuvant chemotherapy alone?

The historical outcomes for patients with muscle-invasive bladder cancer treated with chemotherapy followed by surgery are really mirrored by the control arm of this study, as that was the control arm. Now, patients in this study fared slightly better than what we typically observe historically, likely because our treatment and supportive care have evolved.

However, we know that beyond that standard of care, the addition of immune checkpoint blockade, or [Imfinzi (durvalumab)] — both in the pre-surgical and post-surgical periods — improves our ability to prevent cancer recurrence and allows patients to live longer, even exceeding what we consider the contemporary and historical standard treatment.

What can patients expect during treatment with this combination of immunotherapy and chemotherapy — both in terms of the timeline and potential side effects?

Immune checkpoint blockade involves drugs that we call PD-1 or PDL-1 inhibitors, and Imfinzi is a PDL-1 inhibitor. These drugs have been used alone in various indications and also combined with chemotherapy for a variety of different indications across various solid tumors. So, oncologists are quite accustomed to administering these combinations at this point.

Our extensive experience thus far indicates that when you give immunotherapy with chemotherapy, it does not seem to worsen the side effects of the chemotherapy, nor does the chemotherapy seem to worsen the side effects of the immunotherapy. That said, when you administer two classes of drugs simultaneously, there's a higher overall risk for side effects because you have the potential side effects of each component, but they don't amplify each other.

Regarding side effects, those that can occur with cisplatin-based chemotherapy, in particular, are the ones many people associate with chemotherapy. These can include fatigue, nausea, vomiting, hair loss, an impact on kidney function and neuropathy, such as numbness and tingling in the fingers and toes. Fortunately, many of these side effects are transient and reversible with chemotherapy. Immune checkpoint blockade, or immunotherapy, has a very different side effect profile; many patients experience few to no side effects with it. However, a subset of patients will develop side effects that we refer to as immune-related [side effects].

These involve inflammation of different parts of the body and really mimic what we think of as autoimmune diseases, except usually, when these side effects occur, they affect one organ in an individual rather than multiple organs. For example, one individual might develop inflammation of the skin, called dermatitis, which manifests as a rash or itching. Another person might get inflammation of the bowel, called colitis, which manifests as diarrhea. When these side effects occur, if they're mild, immunotherapy is held. If they're more severe, they are typically treated with steroid medication.

When we give chemotherapy with immunotherapy prior to surgery, in the neoadjuvant setting, it's administered in three-week cycles. During each three-week cycle, treatment is given twice, once in the first week and once in the second week. These three-week cycles are repeated four times, and then surgery is performed. After surgery, the immunotherapy is generally given once a month to complete eight more months of treatment.

What follow-up research or real-world data are needed to further validate the role of this regimen?

There are several other trials testing a similar concept: should we integrate immune checkpoint blockade with cisplatin-based chemotherapy in the perioperative setting, meaning both before and after surgery?

The results of these trials collectively will, of course, enhance our understanding of the full context regarding what is being achieved with these regimens. However, as a standalone trial, NIAGARA led to FDA approval of this regimen and is now an accepted standard of care for use in patients with muscle-invasive bladder cancer.

Transcript has been edited for clarity and conciseness.

For more news on cancer updates, research and education, don’t forget to 

The FDA approved a neoadjuvant treatment regimen combining Imfinzi (durvalumab) with gemcitabine and cisplatin, followed by adjuvant Imfinzi, for muscle-invasive bladder cancer. This approval is based on the NIAGARA trial, which showed significant improvements in event-free and overall survival. The integration of immunotherapy in pre- and post-surgical periods reduces metastatic disease risk and enhances patient longevity. The treatment involves immune checkpoint blockade, with manageable side effects. Ongoing trials will further elucidate the regimen's efficacy, but it is now a standard of care.

Dr. Matthew Galsky discusses the FDA approval of Imfinzi and chemo before and after surgery for muscle-invasive bladder cancer, based on the NIAGARA trial.

Imfinzi Combination Shows Efficacy in Bladder Cancer Treatment

Imdelltra (tarlatamab-dlle) has shown statistically significant and clinically meaningful improvement in overall survival compared to local standard-of-care chemotherapy among patients with small cell lung cancer (SCLC) whose disease has progressed on or after a single line of platinum-based chemotherapy, it has been announced.

Amgen announced the development that Imdelltra had met its primary endpoint at a planned interim analysis of the global phase 3 DeLLphi-304 clinical trial in a news release.

“Small cell lung cancer is one of the most aggressive malignancies, with a high unmet need for more effective therapies,” said Dr. Jay Bradner, executive vice president, Research and Development, at Amgen. “The topline results from DeLLphi-304 demonstrate overwhelming clinical benefit for people living with this devastating disease and affirm Imdelltra as standard of care.”

A type of immunotherapy drug known as a bispecific T-cell engager, or BiTE, Imdelltra works by bringing healthy T cells, part of the body’s immune system, and lung cancer cells closer together so that the T cells can more effectively kill the lung cancer cells, as the National Cancer Institute explained on its website. It does so by binding to the protein CD3 on healthy T cells and the protein DLL3 on small cell lung cancer cells.

“It essentially forces an interaction between the tumor and the T cells that are otherwise repelling or ignoring one another,” says Dr. Carl Gay of the Department of Thoracic/Head and Neck Medical Oncology in the Division of Cancer Medicine at The University of Texas MD Anderson Cancer Center in Houston 

. “In doing so, the T cells finally gain access to the tumor, and seemingly recognize they’ve been sleeping on the job, and go about their expected role of attacking the tumor and eliminating at least a portion, if not, in some cases, nearly all of the tumor in some of the patients that have received this therapy.”

 from the U.S. Food and Drug Administration in May 2024 for patients with extensive-stage small cell lung cancer with disease progression on or after platinum-based chemotherapy was based on phase 2 results from the 

The FDA reported at the time that the most common side effects, experienced by more than 20% of patients, were cytokine release syndrome, fatigue, pyrexia, dysgeusia, decreased appetite, musculoskeletal pain, constipation, anemia and nausea.

The safety profile of Imdelltra, Amgen noted in the recent press release, was consistent with the drug’s known safety profile. Detailed data from DeLLphi-304, the company stated, will be presented at an upcoming medical congress.

With 509 patients enrolled, the currently active DeLLphi-304 clinical trial is being held at 223 locations around the world, according to its listing on clinicaltrials.gov. The trial, according to the listing, is estimated to be completed on July 31, 2027.

Small cell lung cancer, Amgen detailed in the news release, has a 5% to 10% five-year relative survival rate across all stages combined, and comprises approximately 15% of the more than 2.4 million patients who receive a diagnosis of lung cancer worldwide annually. And, according to the news release, despite initial high response rates to first-line platinum-based chemotherapy, most patients relapse within months and require further treatment.

Imdelltra (tarlatamab-dlle) has demonstrated significant improvement in overall survival for small cell lung cancer (SCLC) patients who progressed after platinum-based chemotherapy. This bispecific T-cell engager (BiTE) immunotherapy binds to CD3 on T cells and DLL3 on cancer cells, enhancing T cell-mediated tumor destruction. The phase 3 DeLLphi-304 trial confirmed its efficacy, leading to accelerated FDA approval. Common side effects include cytokine release syndrome and fatigue. The trial, involving 509 patients across 223 global sites, is expected to conclude in 2027.

Imdelltra is associated with improvement in overall survival compared to local standard-of-care chemotherapy among patients with small cell lung cancer.

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