PUBLISHER: Mordor Intelligence | PRODUCT CODE: 2154720
PUBLISHER: Mordor Intelligence | PRODUCT CODE: 2154720
According to Mordor Intelligence, the South America pancreatic cancer therapeutics and Diagnostics Market size was valued at USD 0.38 billion in 2025 and is estimated to grow from USD 0.41 billion in 2026 to reach USD 0.56 billion by 2031, at a CAGR of 6.5% during the forecast period (2026-2031).

The rising pancreatic cancer burden supported demand in the South American pancreatic cancer therapeutics and diagnostics market. A January 2025 analysis reported that Brazil's age-standardized incidence increased by 0.7% annually from 1990 to 2019 for both sexes, while Peru recorded the region's sharpest increase, at 3.0% to 3.9% annually. Brazil's annual case volume rose from 4,431 in 1990 to 14,430 in 2019, while Argentina recorded incidence rates of 12.7 per 100,000 men and 10.5 per 100,000 women, with rising mortality trends. INCA projected 10,980 new pancreatic cancer cases annually in Brazil during the 2023-2025 estimation period, highlighting the need to expand treatment capacity beyond metropolitan hospitals.
Advanced diagnostics expanded beyond a limited number of metropolitan laboratories in the South American pancreatic cancer therapeutics and diagnostics market. Greater adoption of molecular testing linked diagnostic demand with targeted therapy approvals, as each treatment target required reliable patient identification before prescribing decisions. Companion diagnostics became increasingly integral to treatment access rather than a standalone laboratory service. Centralized laboratory models improved sample logistics and reporting capabilities for hospitals outside major cancer centers, supporting diagnostic revenue growth through biomarker selection and genomic profiling.
High treatment and testing costs restricted the addressable patient population in the South American pancreatic cancer therapeutics and diagnostics market. An ISPOR Europe 2025 analysis reported annual oncology treatment costs of USD 50,054 in Brazil and USD 1,992 in Argentina, compared with USD 134,933 in the United States. Public procurement limits and purchasing-power constraints reduced prices but did not ensure access to advanced therapies or molecular tests. Guardant360 was available through reference laboratories, including Diagnosticos do Brasil, but limited coverage mandates kept uptake concentrated among private-pay and supplemental-insurance patients.
Other drivers and restraints analyzed in the detailed report include:
For complete list of drivers and restraints, kindly check the Table Of Contents.
Diagnostic modalities are the fastest-growing product category in the South America pancreatic cancer therapeutics and diagnostics market, with a CAGR of 7.55% during 2026-2031. Therapeutics remains the larger revenue-generating category due to the widespread use of systemic treatment in advanced disease management. CT, MRI, and PET remain the highest-volume tools for staging and treatment monitoring, while high-volume centers in Sao Paulo, Buenos Aires, and Bogota increasingly use endoscopic ultrasound. Biomarker testing and molecular diagnostics are expanding as treatment selection relies more heavily on genomic information; the February 2025 DNBSEQ-G400 deployment supported 1,000 somatic and germline samples per month.
The diagnostics segment benefits from the wider adoption of centralized testing services and trial-led liquid biopsy development. The mirPANC 2 and BLENTI studies in Brazil supported liquid biopsy evidence generation, while the Panuri study began in June 2026 to assess a urine proteolytic-enzyme test for pancreatic ductal adenocarcinoma detection. Therapeutic demand remains anchored in FOLFIRINOX and gemcitabine plus nab-paclitaxel, while olaparib is relevant for the 4%-7% of patients with germline BRCA mutations and pembrolizumab for the rare MSI-H subset. Immunotherapy remains limited by the immunosuppressive pancreatic tumor microenvironment, while radiotherapy is constrained by limited stereotactic body radiotherapy capacity outside major academic centers; ImmunityBio updated its Phase 1 neoadjuvant chemoimmunotherapy protocol in April 2026.