Lung cancer news

For nearly a decade, Sandi Walraven has brought people affected by lung cancer together to share experiences, find support, and build lasting friendships. What began as the first cancer support group at Northeast Georgia Health System has grown into a close-knit community that Sandi lovingly describes as her “labor of love.”

In recognition of her extraordinary dedication, GO2 for Lung Cancer is proud to honor Sandi with the 2026 Lung Cancer Support Group Facilitator Award.

Established in 2009, the Lung Cancer Support Group Facilitator Award recognizes individuals who go above and beyond to create welcoming, supportive spaces for people affected by lung cancer. The award celebrates the often-unseen work of building and sustaining a support group, and the facilitators who help people find connection, encouragement, and a sense of belonging.

Sandi embodies everything this award was created to recognize.

A career dedicated to caring for others

For more than 30 years, Sandi has provided compassionate, patient-centered oncology care. Her career has taken her through many aspects of cancer care, including radiation, infusion, nurse navigation, and hospice.

Along the way, she helped establish her health system's navigation program, which has guided hundreds of newly diagnosed patients through the challenges of understanding their diagnosis, making treatment decisions, and finding the support and resources they need.

In 2016, Sandi saw a chance to offer something more. With the help of a grant and facilitator training from GO2 for Lung Cancer, she established the Lung Cancer Support Group at Northeast Georgia Health System, the first cancer support group of any kind within the health system.

What began as a place for people living with lung cancer to connect has become something much more.

More than a support group

A few years after establishing the group, Sandi's responsibilities at work changed. The group's regular meeting time now fell on her day off, and her colleagues assumed she would pass the responsibility to someone else. But Sandi had other ideas.  

She told them they'd have to arm wrestle her for it.

She kept the group, and nearly a decade after starting it, she continues to lead its meeting on her own time.  

Under Sandi's care, the group has become a family. Members gather each month to share a meal, talk about their experiences, and enjoy one another's company. Sandi even provides gas cards to help ensure that transportation costs don't prevent people from attending.

She also finds ways to keep meetings engaging, inviting professional speakers, incorporating chair yoga, and organizing activities like board games. But the most important part of the group isn't any particular activity. It's the relationships that have grown over time.

Remarkably, 4 members have been part of the group since its very beginning. Together, members have navigated illness, loss, and difficult moments. They've also celebrated birthdays, clear scans, new babies, and countless other milestones.

Through it all, Sandi has helped create a space where people can show up exactly as they are, knowing they'll find others who understand what they're going through.

The lasting impact of connection

Living with lung cancer can be isolating. Even with the support of family, friends, and a dedicated healthcare team, it can be difficult to find people who truly understand the experience.

Support groups help bridge that gap. They offer opportunities to share concerns, exchange information, celebrate good news, and build relationships with others navigating similar challenges.

But a successful support group doesn't happen on its own. It takes someone willing to bring people together, make them feel welcome, and keep showing up, month after month and year after year.

For Sandi, that commitment has never wavered. Her group is a testament to the difference one dedicated person can make by providing information and resources, while also helping people build a community they can count on.

GO2 for Lung Cancer is grateful to the many facilitators across our Lung Cancer Support Group Network who devote their time, energy, and compassion to supporting others. Their work makes a meaningful difference in the lives of people affected by lung cancer every day.

This year, we are especially proud to recognize Sandi Walraven for 10 years of extraordinary dedication, kindness, and commitment to the lung cancer community.

Congratulations, Sandi, and thank you for turning your labor of love into a source of connection and support for so many.

Explore GO2's Lung Cancer Support Group Network to find opportunities for connection and support.

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‍Annual San Francisco event recognizes progress in lung cancer care and raises critical funds to improve outcomes for people impacted by the disease

GO2 for Lung Cancer (GO2) will honor Lilly at the organization’s annual “Simply the Best” Gala on Saturday, November 14, at the Fairmont San Francisco. Lilly will receive the GO2 Excellence Award in Advancing Innovative Precision Medicine, recognizing the company’s leadership in precision medicine and its unwavering commitment to advancing biomarker testing and delivering targeted treatments to people with lung cancer at every stage of their journey.

“Precision medicine has fundamentally changed what is possible for people with lung cancer, but innovation only matters if it reaches the people who need it,” said GO2 for Lung Cancer CEO David Benson. “Lilly is a leader in advancing precision medicine, and we are proud to recognize its contributions to improving care for people with lung cancer.”

Each year, the Simply the Best Gala brings together industry partners, researchers, doctors, nurses, survivors, advocates, funders, and individual supporters who share a commitment to improving outcomes for people impacted by lung cancer. The evening recognizes important advances across the lung cancer community while raising critical funds to support GO2’s work.

Lung cancer remains the leading cause of cancer death in the United States. Advances in comprehensive biomarker testing and precision medicine have transformed care, allowing treatment decisions to be increasingly informed by the unique characteristics of an individual’s cancer. Continued research, innovation, and access to these advances are critical to improving survival.

For more than two decades, the Simply the Best Gala has brought the lung cancer community together in San Francisco to celebrate progress and look ahead to what is still possible. Proceeds support GO2’s work to advance patient-centered research, expand access to screening and high-quality care, provide personalized support and navigation, and advocate for policies and funding that accelerate progress.

To learn more about the 2026 Simply the Best Gala, purchase tickets, or support the event, visit go2.org/gala.

A rare inherited mutation in the Epidermal Growth Factor Receptor (EGFR) gene is associated with a 25-fold increased risk of lung cancer, according to a study by investigators at Dana-Farber Cancer Institute and 23andMe Research Institute. The findings included de-identified, aggregated genetic data from more than 3.3 million 23andMe research-consented participants.

Among people who never smoked, carriers of the mutation were more than 60 times as likely to develop lung cancer as people without it. Researchers identified EGFR T790M as one of the strongest inherited risk factors for lung cancer discovered to date. This could have important implications for genetic testing and future lung cancer screening strategies for people who carry the mutation.  

The findings were published in Science.

"Today, lung cancer screening is driven almost entirely by smoking history,” says Jaclyn LoPiccolo, M.D., Ph.D., attending physician and lung cancer researcher at Dana-Farber Cancer Institute, who co-led the study. “Our findings raise the possibility that, in the future, screening could also be dictated by inherited genetic risk. If further studies confirm the benefit, people with EGFR T790M could be identified through genetic testing and offered personalized CT screening to identify lung cancers when they are at their most curable stage."

Although most lung cancers are associated with tobacco use or exposure, the proportion diagnosed in people who have never smoked has been rising. Yet the genetic factors underlying these cancers, particularly the role of inherited risk, aren’t well understood.

In 2005, researchers identified a rare inherited mutation called EGFR T790M in a European family with multiple cases of lung cancer. Since then, the mutation has been reported in other families with unusually high rates of the disease.

"For years we've known that some families inherit a markedly increased risk of lung cancer, but because this variant is so rare, we've never been able to accurately measure that risk,” said co-senior author Pasi A. Jänne, M.D., Ph.D., Senior Vice President for Translational Research and a lung cancer specialist at Dana-Farber. “By studying more than three million people, we were able to demonstrate just how strongly this inherited mutation is associated with lung cancer."

Comparing people with lung cancer to those without the disease, the researchers examined whether EGFR T790M was more common among those who had developed lung cancer. They also analyzed people who had never smoked separately to determine whether the association persisted in the absence of tobacco use. Additional data supporting the association came from participants in the INHERIT Study (NCT05587439), led at Dana-Farber by Drs. LoPiccolo and Jänne, in partnership with GO2 for Lung Cancer (GO2) and the Addario Lung Cancer Medical Institute (ALCMI).

The researchers expected EGFR T790M to increase lung cancer risk, but they had not anticipated the magnitude of the increased risk.

“One of the remarkable findings here is just how strong an effect a single mutation can have,” said co-senior author Alexander Gusev, Ph.D., a quantitative geneticist at Dana-Farber. Dr. Gusev continued, “To my knowledge it's one of the strongest, if not the strongest, cancer risk increasing mutations that has ever been found.”

Among people who smoked, carriers of the mutation were about 10 times as likely to develop lung cancer as noncarriers. Among people who never smoked, carriers were more than 60 times as likely to develop lung cancer. This relative risk does not mean smoking is protective, the researchers explained. Because smoking already greatly increases lung cancer risk, the mutation’s effect appears smaller by comparison.

“Smoking is bad for lung cancer. This mutation is bad for lung cancer. When you do both, your risk is the sum of those two risks,” Dr. Gusev said. “So, you definitely don't want to smoke.”

The mutation was not linked to any of 17 other common cancers studied, suggesting that its effects may be largely limited to lung cancer.

Dr. LoPiccolo noted that the prevalence of the mutation in the U.S. population is about 1 in 15,000. But in certain areas of the Southeastern U.S., it can be as frequent as 1 in 2,000 people.

“We found that the vast majority of carriers inherited the mutation from the same ancestral lineage,” she said. “We could trace that lineage to British and Irish settlers in the United States and show that the mutation became enriched after a founder event and genetic bottleneck in Southern Appalachia about 200 years ago. It's a fascinating example of how human migration and genealogy can shape disease risk, generations later.”

The researchers recommend that people with several family members who have had lung cancer, multiple lung nodules, multifocal lung cancers, or ancestral roots in areas of the southeastern U.S., where the variant is more common, consult a genetic counselor. A counselor can help determine whether genetic testing and regular lung cancer screening may be appropriate.

23andMe members who participate in research were essential in driving these discoveries. The size and scale of the 23andMe database allowed researchers the opportunity to analyze data from more than 10 million 23andMe research-consented participants. They then focused on 3.3 million participants for whom both genetic and lung cancer data were available.

“We’ve built a research community where millions of people consent to take part and answer questions about their health year after year to accelerate meaningful discoveries,” said Joyce Tung, Ph.D., Vice President of Research at 23andMe. “Finding a variant this rare, measuring what it does, and tracing where it came from are three different scientific challenges, and addressing all three takes genetic and health information in one place, at scale. We're grateful for what our participants made possible here.”

“This groundbreaking discovery builds on a body of research into inherited lung cancer risk that GO2 and ALCMI helped advance,” said David Benson, Chief Executive Officer of GO2. “The more we understand about inherited risk, the more knowledge patients, families, and clinicians have to make informed decisions. For people with a family history of lung cancer, that knowledge can be incredibly powerful. We are excited to see this science continue to grow and open new possibilities for earlier detection and, ultimately, saving lives.”

As next steps, researchers hope to learn why some EGFR T790M carriers develop lung cancer while others do not, why the mutation increases the risk of lung cancer but not other common cancers, and how environmental exposures and additional genetic changes influence risk. Future studies will include more diverse populations and investigate other inherited EGFR mutations that may predispose people to lung cancer. Meanwhile, Drs. LoPiccolo and Jänne are continuing to recruit participants for the INHERIT Study to further understand the genetic risk and predispositions for developing lung cancer.

Data analyzed in the study includes participants in the Lung Cancer Genetics Study, which is funded by the Susan Wojcicki Foundation and powered by 23andMe. The Susan Wojcicki Foundation is continuing to recruit for the Lung Cancer Genetics Study, which investigates how genetics, environment, and other factors impact lung cancer risk and disease progression. Enrollment is open to anyone in the US aged 18 or older who has been diagnosed with lung cancer.

Funding for this study was provided by the LUNGevity Foundation (Career Development Award to J.L.); the Elaine & Gerald Schuster Fund for Lung Cancer Research (J.L.); the National Institutes of Health (NIH grant R01 HG012133 to A.G., NIH/National Cancer Institute grant U01 CA209414 to D.C., and NIH grant R35 CA220497 to P.A.J.); the American Cancer Society (grant CRP-17-111-01-CDD to P.A.J.); the Chen-Huang Center for EGFR-Mutant Lung Cancers (J.L. and P.A.J.); GO2 for Lung Cancer (INHERIT Study); the Addario Family; Sam and Janet Bain; the Burns Family; the Jain and Patkar Family; David Lefkowitz and Julie Persily; the Smita and Pankaj Patel Family; SITA Foundation; The Van Auken Private Foundation; the Ray B. Marglous Family Foundation in memory of Lindsey Rae Marglous; the Michele Simeone Abrecht Memorial Fund, established by Charlotte and Clifford Abrecht; the Cammarata Family Foundation Research Fund; the Zhen-Quan Xu and Lin Yuan Fund for Lung Cancer Research; and the Gohl Family Lung Cancer Research Fund.

‍Research highlights real-world opportunities to improve equitable screening, biomarker testing, and clinical trial access

GO2 for Lung Cancer (GO2) presented 10 research studies at the IASLC 2026 World Conference on Lung Cancer hosted by the International Association for the Study of Lung Cancer, taking place September 12-15 in Seoul, Republic of Korea. The research reflects GO2’s collaborative, cross-departmental approach to identifying real-world barriers and developing practical solutions across lung cancer screening, diagnosis, treatment, smoking cessation, clinical trial participation, patient education, and psychosocial support.

The portfolio includes findings generated through GO2's Centers of Excellence network, LungMATCH program, and community-based initiatives, as well as a shared decision-making study conducted with Fred Hutch Cancer Center and the University of Washington. Together, the posters elevate the perspectives of patients, health care professionals, and community partners and point to actionable ways to make high-quality lung cancer care more accessible and equitable.

“Research matters most when it changes what people experience,” said GO2 For Lung Cancer CEO David Benson. “These studies identify barriers that prevent people from receiving the care they need and benefiting from scientific advances. More importantly, they offer practical solutions for overcoming those barriers and improving outcomes.”

GO2 research presented at WCLC 2026:

Integrating Restorative Practices to Enhance Shared Decision-Making and Lung Cancer Screening Uptake in Black Communities

Led by GO2 in partnership with Fred Hutch Cancer Center and the University of Washington, this 12-month equity grant study assesses the feasibility and acceptability of “SDM Circles,” a restorative justice-informed, community-engaged model designed to make lung cancer screening conversations opportunities for trust-building, healing and empowerment. Findings will inform a scalable, community-informed model to reduce structural barriers to early detection. Lead GO2 authors include Joelle Fathi and Cyndi Lemery.

Monitoring Stage Shift in a National Network of Screening Programs: Successes and Challenges in Real-World Implementation

Using data from GO2's Centers of Excellence Benchmarking and Practice Variation Survey, researchers found that 68% of responding screening programs tracked lung cancer diagnosis rates, but more than half did not track stage breakdown. Even among programs that tracked stage, 34% of reported diagnoses had an unknown stage, underscoring the need for stronger documentation and information-sharing across clinical departments. Angela Barry is the lead author.

A Revealing Snapshot into Implementation of Smoking Cessation Services Across Academic and Community-Based Facilities

Using data from GO2’s Centers of Excellence network, researchers examined how smoking cessation services are implemented across academic and community-based lung cancer programs. The findings reveal variation in how patients are identified, referred to services, and supported in quitting, highlighting opportunities to better integrate evidence-based cessation care into routine practice and ensure more people receive consistent support. Joelle Fathi is the lead author.

Real World Assessment of Biomarker Testing Turn Around Time Impacts in US-Based Lung Cancer Treatment Programs

A survey of 82 U.S. facilities in GO2's Centers of Excellence network found that most treatment teams would likely begin first-line therapy before biomarker results were available if turnaround exceeded two weeks. Nearly all respondents used send-out testing, and reflex-testing workflows varied widely. The findings point to the potential for standardized protocols and adequately resourced reflex testing to support more timely treatment decisions. Andrew Ciupek is the lead author.

Reality Check: Identifying Real-World Barriers to Clinical Trial Engagement

Drawing on patient-reported data from 300 LungMATCH participants and clinician-reported data from GO2's Centers of Excellence network, the analysis found a gap between screening patients for trial eligibility and enrollment: responding centers reported screening all potential patients, yet median enrollment was only 5%. Both patients and providers identified stringent eligibility criteria as a leading barrier. The authors call for earlier, shared decision-making conversations and greater patient and frontline provider input in trial design. Brittney Nichols is the corresponding author; Andrew Ciupek is the lead author.

Community-Based Biomarker Education Improves Clinical Trial Readiness in Black Communities

Developed and delivered with a community advisory board and local partners in Broward County, Florida, this culturally tailored education program reached 296 adults, 80.5% of whom identified as Black or African American. Participants showed significant gains in biomarker-testing knowledge and confidence discussing testing with a provider, while phase-specific education increased willingness to consider clinical trials. The work was conducted through Ready Lung, a partner-funded program that concluded at the end of 2025. Shanada Monestime is the lead author.

From Community Outreach to Lung Cancer Screening: A Navigation Model for Black Communities

This community-based model used independent pharmacies in Washington, D.C., and a mobile health unit in Baton Rouge, Louisiana, to identify screening-eligible adults and connect them with navigation and low-dose CT screening. Among 450 people assessed, 80 enrolled in navigation and 21 completed screening. The findings identify appointment scheduling as the largest point of drop-off and suggest that virtual shared decision-making and screening offered at the point of interest may reduce barriers. The work was conducted through Program Connect, a partner-funded program that concluded at the end of 2025. Shanada Monestime is the lead author.

Hidden Barriers, Real Conversations: Health Literacy and Health Equity Insights from the Lung Cancer Living Room®

A review of Lung Cancer Living Room sessions from the previous year identified recurring barriers involving screening awareness, stigma in conversations about smoking history, communication about clinical trials and access to specialty care. The findings show how a community-centered hybrid forum can surface real-world gaps and inform strategies that use plain language, expand access to early detection and strengthen clinical trial navigation. Chaya Estrin-Lebovic is the author.

Who Needs Another Podcast? You Do! Creating the Coping with Lung Cancer Podcast

Developed by GO2 and the Roy Castle Lung Cancer Foundation as part of a broader international collaboration, the Coping with Lung Cancer podcast addresses a gap in information about psychosocial programs and services for people affected by lung cancer. The series grew from expert interviews and a project focused on coping-related needs, resources, and best practices, demonstrating how collaboration can make proven support strategies more accessible worldwide. GO2's Maureen Rigney is the lead author.

Education and Connection: What the Small Cell Community Wants

A national GO2 survey of 106 people affected by small cell lung cancer found strong interest in peer-led advice, treatment options, clinical trials and side-effect management. Respondents also prioritized information and resource connections, help identifying clinical trials and opportunities to connect with others who share similar experiences. GO2 is using the findings to shape small cell lung cancer education, navigation and peer-support offerings. Maureen Rigney is the lead author.

Learn more about WCLC 2026 at wclc.iaslc.org.  

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Did you know? HER2 is a gene found in cells that are important for cell growth and survival. You may also sometimes see HER2 referred to as ERBB-2. In some people, the HER2 gene begins to mutate or change, which can be a driving cause of cancer. HER2 mutations occur in about 2 out of every 100 cases (2%) of non-small cell lung cancers (NSCLC).

On September 9, 2026, the U.S. Food and Drug Administration (FDA) granted accelerated approval to Hyrnuo (sevabertinib) for people with locally advanced or metastatic, non-squamous NSCLC whose tumors have a HER2 (ERBB-2) activating mutation.  

This approval expands the FDA’s previous approval of Hyrnuo (sevabertinib) from November 2025 by making it a first-line treatment option for people with HER2-positive NSCLC.

This latest approval is based on the results of the SOHO-01 study, which looked at how safe and effective Hyrnuo (sevabertinib) is for people with locally advanced or metastatic, non-squamous NSCLC whose tumors have a HER2 activating mutation. Study participants who had not yet received systemic treatment received Hyrnuo (sevabertinib). They experienced both a promising response rate and benefits that lasted for a meaningful time period in those who responded to treatment.

This is an exciting update from the FDA because it gives people with locally advanced or metastatic, non-squamous NSCLC whose tumors have a HER2 activating mutation another first-line therapy treatment option.

Please speak with your healthcare team for more information about Hyrnuo (sevabertinib) and to see if it may be an option for you. If you have questions about treatment, trials, or biomarker testing, contact our LungMATCH team at support@go2.org or 1-800-298-2436.  

Read the  full FDA announcement.  

‍Nonprofit leader with nearly three decades of experience will guide GO2 for Lung Cancer as it continues to improve outcomes for people affected by lung cancer

GO2 for Lung Cancer (GO2), a national nonprofit dedicated to improving outcomes for people at risk for and living with lung cancer, today announced the appointment of David Benson as its new chief executive officer.

Benson brings more than 27 years of executive leadership experience advancing patient-centered cancer care through innovation, philanthropy, strategic partnerships, and organizational transformation. As chief executive officer, he will build on GO2's strong momentum by ensuring people affected by lung cancer remain at the center of the organization's work while advancing research, strengthening advocacy, expanding access to lung cancer screening and high-quality care, and providing the support and resources patients and families need.

Prior to joining GO2, Benson served as executive vice president of the American Cancer Society, where he led one of the organization's largest regional operations, overseeing fundraising, operations, and volunteer engagement across 17 states. Under his leadership, the organization strengthened corporate alliances, expanded fundraising initiatives, and secured major philanthropic investments that generated hundreds of millions of dollars to support patients, caregivers, research, advocacy, and cancer prevention efforts.

Throughout his tenure, Benson partnered closely with volunteers, corporate leaders, philanthropists, healthcare organizations, and community partners to expand patient support programs, accelerate research, and drive significant growth in charitable giving. His leadership is widely recognized for building high-performing teams, fostering trusted relationships, and bringing people together around a common vision to create lasting impact.

"David is an exceptional leader with a deep commitment to improving the lives of people affected by cancer," said GO2 Board President Rick Sherlock. "His collaborative leadership style, strategic vision, and ability to build meaningful partnerships make him the right person to lead GO2 into our next chapter. David has a proven ability to unite volunteers, donors, healthcare leaders, and community partners around a shared purpose, and his deep understanding of the cancer landscape will help accelerate GO2's work to improve survival and quality of life for everyone impacted by lung cancer. The Board is excited to welcome David and looks forward to working alongside him as we continue building on GO2's momentum."

Benson earned a Master of Business Administration from the University of St. Thomas and bachelor's degrees in political science and religion from St. Olaf College.

"I am honored to join GO2 for Lung Cancer," said Benson. "I was drawn to GO2 because of its extraordinary impact and unwavering commitment to improving the lives of people affected by lung cancer. The organization has earned a reputation for turning compassion into action through research, advocacy, patient support, and efforts to expand access to screening and high-quality care. I look forward to building on that strong foundation as we continue expanding our reach and ensuring every person affected by lung cancer has the support and resources they need."

Did you know? ROS1 is a gene found in healthy cells that plays an important role in cell growth and development. In some people, the ROS1 gene joins, or fuses, with another gene. This fusion can cause cells to grow out of control, which may lead to cancer. When this happens in the lung, it is called ROS1-positive non-small cell lung cancer (NSCLC), which occurs in about 2 out of every 100 cases (2%) of lung cancer.

On July 22, 2026, the U.S. Food and Drug Administration (FDA) granted accelerated approval for Jideytro (zidesamtinib) for people with locally advanced or metastatic ROS1-positive NSCLC  whose cancer progressed after treatment with a ROS1 targeted therapy. ROS1 targeted therapies work by blocking the abnormal ROS1 protein that can help cancer cells grow.

This latest approval is based on the results of the ARROS-1 trial, which evaluated the safety and effectiveness of Jideytro (zidesamtinib) in people with locally advanced or metastatic ROS1-positive NSCLC who had previously received a ROS1-targeted therapy. The study showed that some participants experienced a response to treatment, and for those who responded, the benefits lasted for a meaningful period of time. It also showed promising results for people whose cancer had spread to the brain (brain metastases) or whose cancer had developed changes called resistance mutations that may cause a ROS1-targeted therapy to stop working.

This approval provides a new treatment option for people with ROS1-positive NSCLC whose cancer has progressed after a ROS1-targeted therapy, including people with brain metastases or resistance mutations.

Please speak with your healthcare team for more information about Jideytro (zidesamtinib) and to see if it may be an option for you. If you have questions about treatment, trials, or biomarker testing, contact our LungMATCH team at support@go2.org or 1-800-298-2436.  

Read the full FDA announcement.  

GO2 for Lung Cancer (GO2) and the Addario Lung Cancer Medical Institute (ALCMI) are proud to announce that Christine M. Lovly, MD, PhD, FASCO, professor of medical oncology and chief of thoracic medical oncology at City of Hope®, one of the largest and most advanced cancer research and treatment organizations in the United States, has been selected as the 2026 recipient of the Bonnie J. Addario Lectureship Award. The award recognizes Dr. Lovly's extraordinary contributions to advancing precision medicine, accelerating lung cancer research, and championing compassionate, personalized care for every person affected by the disease.

An internationally recognized physician-scientist and leader in precision oncology, Dr. Lovly has transformed the understanding and treatment of lung cancer through pioneering research in biomarker-driven therapies, precision medicine, and liquid biopsy technologies. Her work has expanded treatment options for patients worldwide while advancing a more personalized approach to care that improves both outcomes and quality of life.

Named in honor of Bonnie J. Addario, a lung cancer survivor, advocate, and co-founder of both GO2 and ALCMI, the Bonnie J. Addario Lectureship Award celebrates individuals whose work has profoundly influenced the field of lung cancer. This year marks the 19th annual Bonnie J. Addario Lectureship Award, and Dr. Lovly joins an esteemed group of leaders whose scientific innovation, clinical excellence, and commitment to patients have advanced progress against lung cancer.

"Dr. Lovly exemplifies everything this award represents," said Danielle Hicks, co-interim CEO of GO2 for Lung Cancer and daughter of Addario. "She has helped redefine what is possible through precision medicine while never losing sight of the individual behind every diagnosis. Her commitment to pairing groundbreaking science with compassionate, personalized care reflects the vision my mother championed. Every person with lung cancer deserves hope, innovation, and access to the right care for them, at the right time."

"I am deeply honored to receive the Bonnie J. Addario Lectureship Award," said Dr. Lovly. "The remarkable progress we've made in lung cancer has only been possible because of the partnership among researchers, clinicians, advocates, patients, and families. While innovation continues to move the field forward at an extraordinary pace, our responsibility is to ensure that every person has access to the advances that can improve both the length and quality of their lives. It is a privilege to contribute to that shared mission."

"We support investigator-initiated clinical trials as our core mission because we get to collaborate with innovative researchers like Dr. Lovly to push forward lung cancer science," said Richard Erwin, chief operating officer and executive director of ALCMI. "We are proud to call her both a colleague and a friend, and it is a privilege to recognize her with this year's Bonnie J. Addario Lectureship Award."

Beyond her research accomplishments, Dr. Lovly is a leading voice for ensuring that advances in lung cancer care reach every patient. She has emphasized that while innovation in targeted therapies, immunotherapy, and diagnostics continues to accelerate, improving access to biomarker testing, lung cancer screening, clinical trials, and expert care remains essential to translating scientific progress into better outcomes. Her leadership across national guideline committees, scientific organizations, and patient advocacy partnerships continues to help shape the future of lung cancer care worldwide.

Since 2008, the Bonnie J. Addario Lectureship Award has recognized individuals whose leadership has significantly advanced lung cancer research, treatment, and patient care. Dr. Lovly will formally receive the award and deliver the keynote lecture, "Precision Oncology in Lung Cancer: Progress, Pitfalls, and Promise," at the 27th Annual International Lung Cancer Conference in Huntington Beach, CA.

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Did you know? RET is a gene found in healthy cells that is important for their growth and survival. In some people, the RET gene joins, or fuses with a different gene. This causes the cells to grow out of control, causing cancer. When this happens in the lung, it is called RET-positive non-small cell lung cancer (NSCLC), which occurs in about 2 out of every 100 cases (2%) of lung cancer.

On July 14, 2026, the U.S. Food and Drug Administration (FDA) updated its accelerated approval of Retevmo (selpercatinib) to a traditional approval. Retevmo (selpercatinib) is now approved for people with locally advanced or metastatic solid tumors, including NSCLC, with a RET gene fusion, following prior systemic treatment such as chemotherapy.

Retevmo (selpercatinib) received accelerated approval for this population in May 2020. Updating the drug to “traditional” approval means that the FDA is satisfied the drug's previously predicted clinical benefit has been verified by further studies. The update does not change Retevmo’s (selpercatinib’s) availability or day-to-day usage.

This latest approval is based on the results of the LIBRETTO-001 study, which looked at how safe and effective Retevmo (selpercatinib) is for people with locally advanced or metastatic solid tumors with a RET gene fusion, following prior systemic treatment such as chemotherapy. The study showed participants in the trial experienced both a promising response rate and benefits lasted for a meaningful time period in those who responded.  

This is an exciting update, as Retevmo (selpercatinib) verified clinical benefit may help to inform discussions with your healthcare team about which RET-targeting treatment may be best for you.

Please speak with your healthcare team for more information about Retevmo (selpercatinib) and to see if it may be an option for you. If you have questions about treatment, trials, or biomarker testing, contact our LungMATCH team at support@go2.org or 1-800-298-2436.  

Read the full FDA announcement.  

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