Epidemiological characteristics of gastric and pancreatic cancers in Latin America: GASPAR (LACOG 0222) study.

R Renata D'Alpino Peixoto (BC Cancer, Vancouver, BC, Canada) V Victor Hugo Fonseca Jesus (Centro de Pesquisas Oncológicas (CEPON), Florianópolis, Brazil) D Diogo Bugano Diniz Gomes (Department of Oncology, Hospital Israelita Albert Einstein, São Paulo, Brazil; Hospital Municipal Vila Santa Catarina, São Paulo, Brazil) D David Yossen (Grupo Argentino de Investigación Clínica en Oncología (GAICO), Buenos Aires, Argentina) R Rui Fernando Weschenfelder (Hospital Moinhos de Vento (HMV), Porto Alegre, Brazil) T Tiago Cordeiro Felismino (A.C. Camargo Cancer Center, São Paulo, Brazil) F Federico Esteso (Instituto Alexander Fleming, Buenos Aires, Argentina) C Carlos Eduardo Bonilla (Gastrointestinal Cancer and Neuroendocrine Tumors Functional Unit, Cancer Treatment and Research Center (CTIC) Luis Carlos Sarmiento Angulo, Bogotá, Colombia) A Anelisa Kruschewsky Coutinho Araujo (ÉTICA - Clínica AMO (Assistência Multidisciplinar em Oncologia), Salvador, Brazil) A Antonio Soares Dias Jr (BP - A Beneficência Portuguesa de São Paulo, São Paulo, Brazil) B Berenice Freile (Instituto Alexander Fleming, Buenos Aires, Argentina) T Tainá Cabalheiro (Latin American Cooperative Oncology Group (LACOG), Porto Alegre, Brazil) G Gustavo Gössling (Latin American Cooperative Oncology Group (LACOG), Porto Alegre, Brazil) P Pablo Barrios (Dana-Farber Cancer Institute, Boston, MA)

Abstract

369 Background: Gastric (GC) and pancreatic cancer (PC) have poor prognosis representing major public health challenges, particularly in Latin America. Real-world data are limited. GASPAR (LACOG 0222) study addresses this gap by creating a multicenter database to analyze epidemiological, clinical, and pathological data, treatments, and outcomes for patients (pts) with GC and PC. Methods: This retrospective and prospective observational cohort study enrolled pts from 7 research sites in 3 LATAM countries with metastatic/locally advanced not amenable to curative intent GC (Cohort A) and PC (Cohort B) diagnosed from January 2019. Data were collected from medical records. ( NCT05924789 ). Results: 201 pts were included: 122 with GC (Cohort A) and 79 with PC (Cohort B). 150 (75%) from Brazil, 29 (14%) from Argentina, and 22 (11%) from Colombia. Median age at diagnosis was 69 years (IQR 57-78), 70 (35%) had history of tobacco use, and 153 (76%) were covered by private healthcare (Table). In Cohort A (GC), HER2 status was assessed in 105 (86%) pts, with 12 (11%) HER2-positive; PD-L1 was tested in 87 (71%): 55 (63%) had ≥1% expression and 28% had ≥10%; all 88 (72%) patients who had MMR tested had MMR proficient. First-line treatment was given to 107 (88%) pts: 78 (73%) chemotherapy (CT) alone (FOLFOX in 43 [40%]; FLOT in 16 [15%]); 23 (21%) CT + immunotherapy; and 7 (7%) CT + anti-HER2. Only 59 (48%) pts received second-line treatment and 31 (25%) third-line. With median follow-up (mFUP) of 29 months (CI95% 18.2-50.4), the median progression-free survival (mPFS) at first-line was 5.6 months (CI95% 4.2-6.3) and the median overall survival (mOS) was 11.2 months (CI95% 9.2-14.1). In Cohort B (PC), 67 (85%) pts received first-line treatment: 41 (61%) FOLFIRINOX and 14 (21%) gemcitabine-nab-paclitaxel. 27 (34%) pts received second-line treatment and 10 (13%) third-line. With mFUP of 21 months (CI95% 15.6-NR), the mPFS at first-line was 5.4 months (CI95%3.9-6.4) and the mOS was 10.2 months (CI95% 8.6-13.1). Conclusions: The GASPAR study provides valuable real-world data on GC and PC in Latin America. Notably, the mPFS in both cohorts was slightly lower than historical controls for first-line treatments, while the mOS was similar, suggesting earlier disease progression despite comparable overall survival. Improved therapeutic strategies and healthcare access are needed to enhance outcomes for these populations. Clinical trial information: NCT05924789 . Clinical characteristics. Characteristic GC (Cohort A)N=122 PC (Cohort B)N=79 Median age (IQR), yr 66 (51–78) 71.0 (61–79) Male – n. (%) 58 (56) 40 (51) Race – n. (%) White 67 (55) 71 (90) American Indian or Alaska Native 15 (12) 6 (8) Black 7 (6) 0 Other 7 (6) 0 Not reported 26 (21) 2 (2) Disease status at study entry Locally advanced disease 4 (3) 14 (18) Metastatic disease 118 (97) 65 (82) ECOG status in first-line advanced disease – n. (%) 0-1 75 (70) 45 (67) ≥ 2 13 (12) 3 (4.5) Not reported 19 (17.8) 19 (28.4)

Article Details

Volume / Issue Vol. 43, Issue 4_suppl
Published February 01, 2025
Pages 369-369
ISSN 0732-183X
Publisher Lippincott Williams & Wilkins

Journal Info

Journal of Clinical Oncology

Lippincott Williams & Wilkins

ISSN: 0732-183X Health Sciences

Authors (14)

R

Renata D'Alpino Peixoto

BC Cancer, Vancouver, BC, Canada

V

Victor Hugo Fonseca Jesus

Centro de Pesquisas Oncológicas (CEPON), Florianópolis, Brazil

D

Diogo Bugano Diniz Gomes

Department of Oncology, Hospital Israelita Albert Einstein, São Paulo, Brazil; Hospital Municipal Vila Santa Catarina, São Paulo, Brazil

D

David Yossen

Grupo Argentino de Investigación Clínica en Oncología (GAICO), Buenos Aires, Argentina

R

Rui Fernando Weschenfelder

Hospital Moinhos de Vento (HMV), Porto Alegre, Brazil

T

Tiago Cordeiro Felismino

A.C. Camargo Cancer Center, São Paulo, Brazil

F

Federico Esteso

Instituto Alexander Fleming, Buenos Aires, Argentina

C

Carlos Eduardo Bonilla

Gastrointestinal Cancer and Neuroendocrine Tumors Functional Unit, Cancer Treatment and Research Center (CTIC) Luis Carlos Sarmiento Angulo, Bogotá, Colombia

A

Anelisa Kruschewsky Coutinho Araujo

ÉTICA - Clínica AMO (Assistência Multidisciplinar em Oncologia), Salvador, Brazil

A

Antonio Soares Dias Jr

BP - A Beneficência Portuguesa de São Paulo, São Paulo, Brazil

B

Berenice Freile

Instituto Alexander Fleming, Buenos Aires, Argentina

T

Tainá Cabalheiro

Latin American Cooperative Oncology Group (LACOG), Porto Alegre, Brazil

G

Gustavo Gössling

Latin American Cooperative Oncology Group (LACOG), Porto Alegre, Brazil

P

Pablo Barrios

Dana-Farber Cancer Institute, Boston, MA