Robert L. Ferris, MD, PhD • 2024 SITC Election

Robert L. Ferris, MD, PhD

Robert L. Ferris, MD, PhD

Robert L. Ferris, MD, PhD
UPMC Hillman Cancer Center

Biography

Robert Ferris is an internationally recognized expert in immunotherapy of H&N cancer who received his MD and PhD degrees at Johns Hopkins, followed by training in head and neck oncologic surgery, also at Hopkins. He moved to the University of Pittsburgh in 2001. As an active head and neck surgical oncologist and NIH funded translational tumor immunologist, Dr. Ferris’s lab and clinical trials investigate the efficacy and mechanisms of anti-tumor immunity in the tumor microenvironment (TME) as well as tumor cell escape.

For over 15 years, his group driven integration of perioperative cancer immunotherapy using neoadjuvant “window of opportunity” trials, analyzing pre- and post-treatment specimens with high-dimensional, single cell transcriptomic and spatial technologies, for resistance to approved agents and to test alternative, novel therapeutic targets. Other projects have focused on adoptive cellular therapies and vaccines, as well as intralesional therapies (oncolytic viral therapy, TLR agonists). He has led phase I, II and III clinical trials, targeting PD-(L)1, CTLA-4, and LAG-3 as well as correlative studies in the serum and TME. These include the phase III Checkmate-141 trial, leading to the FDA approval of nivolumab for HNSCC in 2016. Ongoing trials are studying optimal sequencing of PD-1 therapy with chemo- and radiation therapy. In 2012, he obtained UPMC resources to establish the Tumor Microenvironment Center. Since 2017, these roles and collaborations include leadership of the UPMC Hillman Cancer Center, which enables him to support the growth of cancer immunotherapy at UPMC and the University of Pittsburgh.

Dr. Ferris has been a dedicated SITC member for 20+ years, serving as an at-large SITC Board member (2015-2018). He is founding section editor of JITC’s Guidelines/Consensus Statements Section, and serves on many other editorial boards. He has participated in many strategic planning retreats for SITC, and co-leads the H&N cancer immunotherapy practice guidelines (CPG), the most highly cited CPG for JITC to date. He helped design and lead the committee which created the 8-module Certificate in Cancer Immunotherapy program, which has been completed by hundreds of SITC members. Dr. Ferris has co-chaired and participated on multiple SITC committees/taskforces, including Communications, Membership, Regulatory, and fellowship awards. He has co-authored over 400 manuscripts (h-index 110), which have been cited over 50,000 times. He co-founded two spinoff companies and collaborates with biotech and large pharma.

Dr. Ferris has recruited and mentored many trainees, as well as young, mid-career, and senior faculty, particularly female investigators and others typically under-represented in science and medicine, to develop successful careers in cancer immunotherapy and contribute impactfully to the SITC mission. He is passionate about developing the next generation of scientists and leaders. Realizing the key time and effort commitment of the SITC Vice President, Dr. Ferris is prepared to allocate adequate time to fully devote to SITC’s important activities, which demand the presence and engagement of this key SITC role in guiding the future of the society. 

SITC Election Platform Statement

What are the two or three critical issues facing the field of cancer immunotherapy?

I see three of the most important challenges facing cancer immunotherapy to be 1) Increasing IO responsiveness and biomarker development for selection of appropriate patients and combinations, 2) Ensuring that SITC remains the leading organization driving immunotherapies, and 3) Extending deep and durable responses to more patients.

1. Increasing clinical responsiveness with personalized immunotherapy. Neoadjuvant trials are becoming mainstream in many tumor types and provide dynamic insights into biology and follow the adaptive and innate immune response to immunotherapies. SITC should promote neoadjuvant “window” trials to deepen our understanding of individual patient responses and their cancer biology. Newly developed single-cell and spatial technologies now permit highly refined understanding of the TME during therapy and novel combinations, which will be the basis for personalized immunotherapy. Moreover, combinatorial approaches must be guided by science and adaptive designs. Moving IO into earlier lines of therapy, including preoperatively and in cancer immunoprevention, will keep SITC at the forefront of the field. This also requires elucidating the interactions with chemotherapies, radiotherapies, theranostics and novel combinations. SITC should promote the tools for gathering and integrating this information and developing the infrastructure for supporting personalized cancer immunotherapy, which is a key priority for the field. This strategy will help prioritize the most promising agents and combinations to test, facilitating nimble and effective drug development. SITC should promote both grant writing and trial design tools for trainees to enhance biomarker selection and novel discovery efforts.

2. Ensuring that SITC remains the leading organization driving the future of immunotherapy. Given the increasing integration of cancer immunotherapy into other important societies like ASCO, AACR, ASTRO, ESMO etc., SITC should refine and maintain its unique niche as a society driving immuno-oncology. No other society has done what SITC has, and it will need to strategically partner while maintaining its unique identity and contributions. Its recently increased membership size also makes it crucial to broaden the regional meetings that provide important education and collegiality for certain attendees and topics – the ACI program is an ideal example of taking IO to the oncology and scientific community, beyond large once-a-year annual meetings. Through its many educational programs, SITC’s effort should also include non-immunologists who manage adverse events, refer patients for cancer immunotherapy, or may have begun integrating this new type of therapy into their oncology practice. Continuing to integrate and coordinate the stakeholders from diverse disciplines in academia, early phase discovery, biotech/pharma, and regulatory agencies is essential, to drive novel approaches like neoadjuvant therapies, single-cell and AI technologies to harness the evolving immune response to cancer immunotherapy.

3. Expanding patients with deep and durable responses to cancer immunotherapy. With success of CAR T cells for blood cancers and now recently approved TIL product for melanoma, the cost and availability of these therapies is a challenge SITC can help overcome. Broader and cost-effective uptake will expand these therapies to more patients. There are many agents in development, and these are often quite expensive once approved. Developing innovative models for assessment of “value” and methods of reimbursement will also be critical for the optimal application and establishment of cancer immunotherapy strategies in the clinic. We must continue to develop consensus guidelines for optimally implementing cancer immunotherapy in patients, as the efficacy of immunotherapy extends to additional tumor types. This includes developing novel endpoints for drug approval that reflect the unique mechanisms of action and patterns of response, and building new, integrated models for scientific, clinical, regulatory, and payor collaboration in therapeutic development for dissemination into practice. SITC should continue to assemble broad groups of stakeholders, such as bioengineers, immunologists, regulatory agencies and industry, to synergize efforts and devise creative methods to lower costs and enhance the efficiency of delivery for these treatments, to allow more patients to receive these treatments. 


What is Your Vision for SITC?

Several key issues exist for SITC to approach during this pivotal time for cancer immunotherapy. Moving immuno-oncology (IO) into earlier lines of therapy including pre-operatively and in cancer immunoprevention, will keep SITC at the forefront of the field. This requires elucidating the interactions with chemotherapies, radiotherapies, and novel combinations. SITC must continue to promote development of new biological understanding and target discovery, as well as rational combinations and biomarkers. The potential to cure a subset (minority) of previously incurable cancer patients is transformative, but the field needs continued focus on biology and greater understanding of the TME. Indeed, these are very exciting times for our field, which SITC must anticipate and lead, tightly linking biomarker-driven trial design. SITC is a unique organization, interdigitating with academics, industry, regulatory and educational societies, advancing the field of immunotherapy in these exciting but challenging times of today’s NCI funding environment and medical practice. SITC should focus on expanding the Forward Fund with member and external donations to promote the next generation of SITC scientists, particularly for female investigators and other groups typically under-represented in science and medicine. As an active surgeon-scientist, I would like to help SITC develop the next generation of similar individuals to be successful in this exciting career path. At our cancer center, I also started a Taskforce on Female Faculty in 2017 and am a strong supporter of the SITC Women in Cancer Immunotherapy Network (WIN), which should expand its activities in mentoring, education and career development.

Given the increasing integration of cancer immunotherapy into other societies/meetings like ASCO, AACR, ASTRO, ESMO etc. SITC should define its unique niche and identity, while promoting collaborative relationships with these societies. SITC must remain an innovative and progressive organization, focus on cancer health equity, recognizing that immuno-oncology agents may not work in all populations of ethnicities and races equally, and must be studied collaboratively in all populations. Real world datasets can be facilitated, like the Immunoscore project, to complement large registrational trials to enhance diversity of populations, which would benefit all groups eventually treated with IO therapies. Accelerating progress in immuno-oncology will require continued attention to the most critical issues facing our field today.