Related Experiment Video
Updated: May 13, 2025

Testing Targeted Therapies in Cancer using Structural DNA Alteration Analysis and Patient-Derived Xenografts
Published on: July 25, 2020
Designing Clinical Trials for Patients With Rare Cancers: Connecting the Zebras
Vivek Subbiah1, Megan Othus2,3, Jim Palma4
1Sarah Cannon Research Institute, Nashville, TN.
Abstract:
The field of rare cancer research is rapidly transforming, marked by significant progress in clinical trials and treatment strategies. Rare cancers, as defined by the National Cancer Institute, occur in fewer than 150 cases per million people each year, yet they collectively represent a significant portion of all cancer diagnoses. Because of their infrequency, these cancers pose distinct challenges for clinical trials, including limited patient populations, geographical dispersion, and a general lack of awareness of treatment options. Economic limitations further complicate drug development, making initiatives such as the Orphan Drug Act essential for incentivizing research. The advent of next-generation sequencing (NGS) and precision medicine has been instrumental in identifying actionable genetic alterations in parallel with an explosion in the development of genomically targeted therapies, immunotherapies, and antibody drug conjugates. Advances in clinical NGS, precision medicine, and tumor-agnostic therapies have become central to the progress in rare cancer research. The development and approval of tumor-agnostic drugs, such as BRAF, NTRK, and RET inhibitors, and immunotherapy for mismatch repair deficient/microsatellite instability-high status cancers highlight the potential of personalized treatments across diverse cancer types and across the age spectrum. Collaborative trials from cooperative groups including SWOG DART, ASCO TAPUR, NCI-MATCH, pediatric COG-match, DRUP, IMPRESS, and innovative registrational basket and platform trials (eg, VE-Basket, ROAR, LIBRETTO-001, ARROW), along with patient advocacy group-run trials like TRACK, are enhancing access to clinical trials. In addition, artificial intelligence has the potential to improve the trial matching process. An integrated approach, combining these innovations in collaboration with multiple stakeholders, is crucial for advancing rare cancer research, offering hope for better patient outcomes and quality of life.
Insights
Rare cancer research is advancing rapidly through precision medicine and targeted therapies. Innovations in clinical trials and collaborative efforts are improving treatment options and patient outcomes for rare diseases.
Area of Science:
- Oncology
- Genetics
- Clinical Trials
Background:
- Rare cancers affect fewer than 150 people per million annually, posing unique challenges for research and treatment due to small patient populations and limited awareness.
- Economic factors and logistical hurdles complicate drug development for rare cancers, necessitating supportive legislation like the Orphan Drug Act.
Purpose of the Study:
- To review the transformative progress in rare cancer research, focusing on advancements in clinical trials, precision medicine, and targeted therapies.
- To highlight the impact of next-generation sequencing (NGS) and novel treatment modalities on rare cancer treatment strategies.
Main Methods:
- Review of recent clinical trials, including collaborative efforts (e.g., SWOG DART, NCI-MATCH) and innovative trial designs (basket, platform trials).
- Analysis of the role of next-generation sequencing (NGS), precision medicine, and tumor-agnostic therapies in identifying and treating rare cancers.
- Exploration of emerging therapeutic approaches like targeted therapies, immunotherapies, and antibody drug conjugates.
Main Results:
- Tumor-agnostic drugs (e.g., BRAF, NTRK, RET inhibitors) and immunotherapy demonstrate efficacy across diverse rare cancer types.
- Collaborative and innovative clinical trials are increasing patient access and accelerating research for rare malignancies.
- Artificial intelligence shows promise in optimizing clinical trial matching for rare cancer patients.
Conclusions:
- Integrated approaches combining NGS, precision medicine, tumor-agnostic therapies, and collaborative trials are crucial for advancing rare cancer research.
- These advancements offer significant hope for improved patient outcomes and quality of life in rare cancer populations.
- Continued collaboration among researchers, clinicians, industry, and patient advocacy groups is essential for future progress.
More Related Videos
00:04A Clinical Trial Assessing the Safety, Efficacy, and Delivery of Olive-Oil-Based Three-Chamber Bags for Parenteral Nutrition
Published on: September 20, 2019
06:20Irradiator Commissioning and Dosimetry for Assessment of LQ α and β Parameters, Radiation Dosing Schema, and in vivo Dose Deposition
Published on: March 11, 2021
Related Concept Videos
Combination Therapies and Personalized Medicine
The combination of the drug acetazolamide and sulforaphane is a good example of combination therapy to treat cancer. The cells in the interior of a large tumor often die due to the hypoxic and...
Targeted Cancer Therapies
There are several types of targeted therapies against...