Reliable results require careful design
“The most important part of the biostatistician’s role is to be involved at the early stages of designing a study in order to get convincing results at the end. It might not be the result the researchers wanted, but it will be a reliable answer,” said Tangen.
For example, for this study, the early steps included Tangen talking with principal investigator Seth P. Lerner, MD, of Baylor College of Medicine Medical Center, in 2009, to define his study question. Next, she got to work coming up with a sample size and power calculations — essentially determining how many patients would need to enroll to achieve the number of events (such as relapse or death) that would allow the team to answer the primary objective. The biostatistics team also designed tools for collecting surgical quality control and complication data.
“This can be an iterative process between the biostatisticians and others involved in designing the trial, to come up with a study that’s both scientifically meaningful and feasible to run," said Tangen. "You need a clear road map and then have to follow it."
Which is better? Comparing medicine combinations
The study on classic Hodgkin lymphoma compared outcomes for adolescents and adults with newly diagnosed stage 3 or 4 disease receiving initial treatment with nivolumab plus AVD chemotherapy (N+AVD) to outcomes for patients receiving brentuximab vedotin plus AVD, a standard combination. AVD stands for the chemotherapy drugs doxorubicin/Adriamycin, vinblastine and dacarbazine.
“This study is unusual because there aren’t many phase 3 studies in which we have a significant cohort of kids along with adults — multiple ages being treated essentially the same way,” said LeBlanc. Researchers enrolled 970 patients, some as young as 12 years old, at 256 sites in the U.S. and Canada. The study chair was Alex Herrera, MD, from City of Hope.
Patients on the investigational therapy had significantly lower risk of disease progression or death compared to those on the standard regimen. Treatment with nivolumab was also better tolerated by patients. After formal interim analysis, the SWOG Data and Safety Monitoring Committee recommended releasing the trial data, which showed positive results, in 2023. Now, a follow-up analysis has confirmed the findings. LeBlanc noted that successful conduct and analyses for the trial would not have been possible without Fred Hutch staff statistical colleague, Hongli Li, MS, also an author on the paper.
Based on the results, N+AVD should be a strong candidate for primary treatment in adolescent and adult populations with stage 3 or 4 Hodgkin lymphoma, according to the published report. Spurred by the promising findings, the maker of nivolumab, Bristol-Myers Squibb, intends to request approval from the U.S. Food and Drug Administration to use nivolumab in this clinical setting.
Like Tangen, LeBlanc champions the role of biostatisticians in careful study design.
“We try to limit the data points we’re bringing in, focusing on the key things we need in order to answer the questions for that study,” he said. “We want to do studies that have impact, so our goal is to keep the data ‘lean and mean.’”
LeBlanc has been with Fred Hutch for 30 years — not as long as the SWOG SDMC has been here, but long enough to have witnessed the center’s evolution.
“One of the accomplishments we’re quite proud of is that we adopted standards across diseases that we’ve used for a long time now, such as how the team codes for disease progression. While ‘progression’ for each disease, such as lymphoma versus leukemia versus melanoma, may have its own definition, progression appears in our database in a standard way. Standardized reporting mechanisms and tools help to ensure that the results of studies are reproducible — that following the same procedures will lead to the same answer,” he said, such as whether a particular treatment regimen is more effective in a certain type of patient and situation.
Teamwork underpins each successful study
Together, the SWOG SDMC at Fred Hutch and CRAB have more than 100 staff members who contribute to SWOG research in a variety of ways. Along with faculty biostatisticians, there are statistical research associates, statistical unit assistants, data coordinators, administrators, applications developers, information technology specialists and more. Both LeBlanc and Tangen stress that when their names appear on published manuscripts in the New England Journal of Medicine or elsewhere, they represent a multitude of staff members who’ve put in hours of meticulous work on both the statistical science and data management of the trials.
“So many people are part of the team," said Tangen. "I’m a general for a huge army behind me."
The bladder cancer study was supported by grants from the NCI and the Canadian Cancer Society.
The Hodgkin lymphoma study was funded by the NCI, with additional support provided by Bristol-Myers Squibb (BMS) through a cooperative research and development agreement between NCI and BMS. Brentuximab vedotin was provided by Seagen. This research was also supported by the Leukemia and Lymphoma Society, the Lymphoma Research Foundation, the V Foundation for Cancer Research and the Miller Family Fund.