Current Projects:
Translation of UCSF 500 Cancer Gene Panel Test for Pediatric Cancers in Mexico
UCSF Investigators: Alejandro Sweet-Cordero, MD; Roberto Ruiz-Cordero, MD
Mexico Investigator: Alejandro Mohar Betancourt, MD, ScD, Commissioner of the National Institutes of Health and High Specialty Hospitals of Mexico
UCSF 500 provides genomic sequencing for nearly 500 different genes, including the majority of known cancer genes, and it compares tumor cells and non-tumor cells to understand genetic variants in cancer. The results of this test are used at UCSF to clarify diagnoses and identify appropriate targeted therapies and clinical trials, thus improving patients’ cancer treatment. UCSF has partnered with Instituto Nacional de Medicina Genómica (INMEGEN) to develop an abbreviated gene panel test for pediatric cancers for Mexico. The gene panel for Mexico will test approximately 50 different genes.
Feasibility of a Colorectal Cancer Screening Program in Mexico City
UCSF Investigator: Michael Potter, MD
Mexico Investigator: Martin Lajous, MD, ScD, Instituto Nacional de Salud Pública
Colorectal cancer is the fourth most common cause of cancer mortality in Mexico, with the mortality rate rapidly increasing, especially in urban areas where there havebeen marked epidemiologal and nutritional transitions. Colorectal cancer is often preventable with screening and early detection, but in the absence of effective screening programs, colorectal cancer is usually diagnosed at advanced stage and associated with poor ourcomes. Growing availability of screening, diagnostic, and treatment resouces in Mexico confers an opportunity to develop Mexico's first colorectal cancer screening program. UCSF, INSP, and INCan have partnered to evaluate the feasibility of a colorectal cancer screening program in Mexico City. This project aims to determine the current capacity in Mexico City to provide colorectal cancer screening, identify potential barriers and facilitators to colorectal cancer screening, and evaluate the feasibility and scalability of incorporating mobile health technology for patient navigation to support completion of a colorectal cancer screening protocol.
The California-Mexico-Puerto Rico (CAMPO) Consortium for Prevention of HPV-related Cancer in Populations Living with HIV
UCSF Investigator: Joel Palefsky, MD
Mexico Investigator: Jorge Salmeron, MD DrSc, Instituto Nacional de Salud Pública
Puerto Rico Investigator: Ana Ortiz, PhD, University of Puerto Rico Comprehensive Cancer Center
Human papillomavirus (HPV)-associated cancers are major causes of morbidity and mortality in the Latin American and Caribbean region. The Global Cancer Program at HDFCCC received a U54 award for a partnership with Mexico and Puerto Rico to reduce the risk of HPV-associated cancers in people living with HIV in Latin America. The Global Cancer Program will partner with the Instituto Nacional de Cancerlogia and Instituto Nacional de Salud Pública in Mexico and the University of Puerto Rico, to establish The CAlifornia-Mexico-Puerto RicO (“CAMPO”) Collaboration for Prevention of HPV-related cancer in people living with HIV (PLWH).
Beyond universal HPV vaccination programs, cost-effective strategies are needed to enhance early detection and improve non-invasive management of precancerous lesions among PLWH. Little is known about the performance of newer screening technologies in women living with HIV (WLWH) in Latin America. The California-Mexico-Puerto Rico (CAMPO) Consortium will perform three clinical research studies focused on the prevention of cervical cancer among WLWH in Mexico and Puerto Rico. Study 1 will examine new screening algorithms for cervical high-grade squamous intraepithelial lesions (HSIL) in 4000 WLWH in Mexico and Puerto Rico. This study will evaluate triage strategies that include liquid-based cytology, point-of-care genotyping for high-risk HPV DNA, E6/7 oncoprotein expression, and viral and host methylation to detect cervical HSIL among WLWH. We hypothesize that a test with high sensitivity, followed by a test with high specificity, will provide for optimal sensitivity, specificity and predictive value for cervical HSIL in this population. We will also screen 1000 men who have sex with men (MSM) living with HIV for anal HSIL to identify men with anal HSIL for our HSIL treatment studies (Studies 2 and 3) and evaluate anal HSIL screening algorithms using the same tests as those being done in the cervix. Through the cases of cervical and anal HSIL identified in these screening studies, the CAMPO Consortium will also develop and implement two randomized placebo-controlled treatment studies for HSIL. Study 2 will evaluate the impact of anogenital probiotic use on anal and cervical microbiota profiles and the relationship to anal and cervical HSIL regression in 600 HIV-positive PLWH as well as reduction of high-risk HPV DNA persistence among those with no lesions. Study 3 will evaluate the safety and efficacy of a multivalent replication-defective adenovirus-based therapeutic HPV vaccine to treat cervical and anal HSIL in 300 PLWH and identify immune response correlates of HSIL regression. Together, CAMPO Collaboration will examine innovative approaches to cervical and anal cancer prevention among people living with HIV in hopes of advancing the field as quickly as possible. This U54 award is part of the National Cancer Institute Division of Cancer Prevention’s US-Latin American-Caribbean Clinical Trials Network (ULACNet) for Prevention of HPV-related Cancers in People Living with HIV.