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FDG-PET Predicts Neoadjuvant Therapy Response and Survival in Borderline Resectable/Locally Advanced Pancreatic Adenocarcinoma.
Abdelrahman, Amro M; Goenka, Ajit H; Alva-Ruiz, Roberto; Yonkus, Jennifer A; Leiting, Jennifer L; Graham, Rondell P; Merrell, Kenneth W; Thiels, Cornelius A; Hallemeier, Christopher L; Warner, Susanne G; Haddock, Michael G; Grotz, Travis E; Tran, Nguyen H; Smoot, Rory L; Ma, Wen Wee; Cleary, Sean P; McWilliams, Robert R; Nagorney, David M; Halfdanarson, Thorvardur R; Kendrick, Michael L; Truty, Mark J.
Afiliação
  • Abdelrahman AM; Division of Hepatobiliary and Pancreas Surgery, Department of Surgery.
  • Goenka AH; Division of Nuclear Medicine Radiology, Department of Radiology.
  • Alva-Ruiz R; Division of Hepatobiliary and Pancreas Surgery, Department of Surgery.
  • Yonkus JA; Division of Hepatobiliary and Pancreas Surgery, Department of Surgery.
  • Leiting JL; Division of Hepatobiliary and Pancreas Surgery, Department of Surgery.
  • Graham RP; Division of Anatomic Pathology, Department of Laboratory Medicine and Pathology.
  • Merrell KW; Department of Radiation Oncology; and.
  • Thiels CA; Division of Hepatobiliary and Pancreas Surgery, Department of Surgery.
  • Hallemeier CL; Department of Radiation Oncology; and.
  • Warner SG; Division of Hepatobiliary and Pancreas Surgery, Department of Surgery.
  • Haddock MG; Department of Radiation Oncology; and.
  • Grotz TE; Division of Hepatobiliary and Pancreas Surgery, Department of Surgery.
  • Tran NH; Division of Medical Oncology, Department of Oncology, Mayo Clinic, Rochester, Minnesota.
  • Smoot RL; Division of Hepatobiliary and Pancreas Surgery, Department of Surgery.
  • Ma WW; Division of Medical Oncology, Department of Oncology, Mayo Clinic, Rochester, Minnesota.
  • Cleary SP; Division of Hepatobiliary and Pancreas Surgery, Department of Surgery.
  • McWilliams RR; Division of Medical Oncology, Department of Oncology, Mayo Clinic, Rochester, Minnesota.
  • Nagorney DM; Division of Hepatobiliary and Pancreas Surgery, Department of Surgery.
  • Halfdanarson TR; Division of Medical Oncology, Department of Oncology, Mayo Clinic, Rochester, Minnesota.
  • Kendrick ML; Division of Hepatobiliary and Pancreas Surgery, Department of Surgery.
  • Truty MJ; Division of Hepatobiliary and Pancreas Surgery, Department of Surgery.
J Natl Compr Canc Netw ; 20(9): 1023-1032.e3, 2022 09.
Article em En | MEDLINE | ID: mdl-36075389
BACKGROUND: Neoadjuvant therapy (NAT) is used in borderline resectable/locally advanced (BR/LA) pancreatic ductal adenocarcinoma (PDAC). Anatomic imaging (CT/MRI) poorly predicts response, and biochemical (CA 19-9) markers are not useful (nonsecretors/nonelevated) in many patients. Pathologic response highly predicts survival post-NAT, but is only known postoperatively. Because metabolic imaging (FDG-PET) reveals primary tumor viability, this study aimed to evaluate our experience with preoperative FDG-PET in patients with BR/LA PDAC in predicting NAT response and survival. METHODS: We reviewed all patients with resected BR/LA PDAC who underwent NAT with FDG-PET within 60 days of resection. Pre- and post-NAT metabolic (FDG-PET) and biochemical (CA 19-9) responses were dichotomized in addition to pathologic responses. We compared post-NAT metabolic and biochemical responses as preoperative predictors of pathologic responses and recurrence-free survival (RFS) and overall survival (OS). RESULTS: We identified 202 eligible patients. Post-NAT, 58% of patients had optimization of CA 19-9 levels. Major metabolic and pathologic responses were present in 51% and 38% of patients, respectively. Median RFS and OS times were 21 and 48.7 months, respectively. Metabolic response was superior to biochemical response in predicting pathologic response (area under the curve, 0.86 vs 0.75; P<.001). Metabolic response was the only univariate preoperative predictor of OS (odds ratio, 0.25; 95% CI, 0.13-0.40), and was highly correlated (P=.001) with pathologic response as opposed to biochemical response alone. After multivariate adjustment, metabolic response was the single largest independent preoperative predictor (P<.001) for pathologic response (odds ratio, 43.2; 95% CI, 16.9-153.2), RFS (hazard ratio, 0.37; 95% CI, 0.2-0.6), and OS (hazard ratio, 0.21; 95% CI, 0.1-0.4). CONCLUSIONS: Among patients with post-NAT resected BR/LA PDAC, FDG-PET highly predicts pathologic response and survival, superior to biochemical responses alone. Given the poor ability of anatomic imaging or biochemical markers to assess NAT responses in these patients, FDG-PET is a preoperative metric of NAT efficacy, thereby allowing potential therapeutic alterations and surgical treatment decisions. We suggest that FDG-PET should be an adjunct and recommended modality during the NAT phase of care for these patients.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Pancreáticas / Adenocarcinoma / Carcinoma Ductal Pancreático Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Revista: J Natl Compr Canc Netw Assunto da revista: NEOPLASIAS Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Pancreáticas / Adenocarcinoma / Carcinoma Ductal Pancreático Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Revista: J Natl Compr Canc Netw Assunto da revista: NEOPLASIAS Ano de publicação: 2022 Tipo de documento: Article