Benign persistent elevation of alphafoetoprotein (AFP) after curative treatment for germ-cell tumors.

S Solenn Barraud (Department of Medical Oncology, Gustave Roussy, Villejuif, France) N Natacha Naoun (Department of Medical Oncology, Gustave Roussy, Villejuif, France) C Clement Dumont (Hopital Saint Louis, Paris, France) D Damien Pouessel (Medical Oncology Department, Oncopole Claudius Regaud, IUCT-Oncopole, Toulouse, France) L Loic Mourey (Institut Claudius Regaud, IUCT-Oncopole, Toulouse, France) M Marine Gross-Goupil (University Hospital of Bordeaux, Bordeaux, France) B Brigitte Laguerre (Department of Medical Oncology, Centre Eugene—Marquis, Rennes, France) M Mathilde Guerin (Institut Paoli-Calmettes, Marseille, France) F Florence Joly G Gwenn Le Gall (Francois Baclesse Cancer Center, Caen, France) Z Zahra Castel-Ajgal (Curie Institute, Paris, France) C Cyril Roussel-Simonin (Hôpital Universitaire Pitié Salpêtrière, Paris, France) A Aude Fléchon (Oncology Department, Centre Léon Bérard, Lyon, France) K Karim Fizazi (Centre Oscar Lambret, University of Paris-Saclay, Lille, France)

Abstract

598 Background: Follow-up of patients with germ-cell tumours (GCT) relies on monitoring serum markers (SM) including alpha-fetoprotein (AFP), human chorionic gonadotropin (hCG), and lactate dehydrogenase (LDH). Instances of benign, non-GCT related elevation of AFP have been reported as case reports. Identifying such occurrences is crucial to prevent misdiagnosis of residual disease and subsequent overtreatment, which may lead to increased morbidity. Methods: We conducted a national retrospective study in nine GETUG institutions. Patients with isolated persistent elevation of AFP levels above the normal range after receiving curative treatment for GCT without detectable disease on CT scan imaging were identified. Data on patient characteristics, treatment response, changes in SM values over time, and serum AFP levels from first- and second-degree relatives were collected. Familial AFP elevation was defined as AFP levels above the normal range in at least one first- or second-degree relative. Results: From June 1990 to April 2024, 31 patients were identified. Median age was 35 years (range, 19 to 49 years). 15 patients (48%) had pure seminoma, and 16 (52%) had non-seminomatous GCT. Overall, 19 patients (61%) had a clinical stage I disease, 17 (23%) had stage II, and 5 (16%) had stage III. No patient had a history of chronic alcoholism or consumption of medications with hepatic toxicity. Median AFP level after curative treatment was 12 ng/mL (range, 8.8 to 36 ng/mL). No evidence of disease was found on CT scan. An ultrasound examination of the contralateral testis and an FDG-PET/CT were performed in 15 (48%) and 7 patients (23%), respectively, also showing no evidence of disease. Serum AFP levels from family relatives were obtained for 14 patients (45%), with a family elevation identified for 10/14 patients (71%). After a median follow-up of 35 months (range: 7-253 months), AFP levels remained elevated in all 31 patients without documented disease relapse. Conclusions: Benign and often familial elevations of serum AFP levels are rare occurrences, which can be a chance finding following curative treatment for GCT. Ultrasound examination of the contralateral testis and AFP measurement in family members are recommended. Surveillance alone is appropriate.

Article Details

Volume / Issue Vol. 44, Issue 7_suppl
Published March 01, 2026
Pages 598-598
ISSN 0732-183X
Publisher Lippincott Williams & Wilkins

Journal Info

Journal of Clinical Oncology

Lippincott Williams & Wilkins

ISSN: 0732-183X Health Sciences

Authors (14)

S

Solenn Barraud

Department of Medical Oncology, Gustave Roussy, Villejuif, France

N

Natacha Naoun

Department of Medical Oncology, Gustave Roussy, Villejuif, France

C

Clement Dumont

Hopital Saint Louis, Paris, France

D

Damien Pouessel

Medical Oncology Department, Oncopole Claudius Regaud, IUCT-Oncopole, Toulouse, France

L

Loic Mourey

Institut Claudius Regaud, IUCT-Oncopole, Toulouse, France

M

Marine Gross-Goupil

University Hospital of Bordeaux, Bordeaux, France

B

Brigitte Laguerre

Department of Medical Oncology, Centre Eugene—Marquis, Rennes, France

M

Mathilde Guerin

Institut Paoli-Calmettes, Marseille, France

F

Florence Joly

G

Gwenn Le Gall

Francois Baclesse Cancer Center, Caen, France

Z

Zahra Castel-Ajgal

Curie Institute, Paris, France

C

Cyril Roussel-Simonin

Hôpital Universitaire Pitié Salpêtrière, Paris, France

A

Aude Fléchon

Oncology Department, Centre Léon Bérard, Lyon, France

K

Karim Fizazi

Centre Oscar Lambret, University of Paris-Saclay, Lille, France