TY - JOUR
T1 - Recurrence-Free Survival Analysis in Locally Advanced Pheochromocytoma
T2 - First Appraisal
AU - Moog, Sophie
AU - Castinetti, Frédéric
AU - Docao, Christine
AU - Amar, Laurence
AU - Hadoux, Julien
AU - Lussey-Lepoutre, Charlotte
AU - Borson-Chazot, Françoise
AU - Vezzosi, Delphine
AU - Drui, Delphine
AU - Laboureau, Sandrine
AU - Raffin Sanson, Marie Laure
AU - Lamartina, Livia
AU - Pierre, Peggy
AU - Batisse Ligner, Marie
AU - Hescot, Ségolène
AU - Al Ghuzlan, Abir
AU - Renaudin, Karine
AU - Libé, Rosella
AU - Laroche, Suzanne
AU - Deniziaut, Gabrielle
AU - Gimenez-Roqueplo, Anne Paule
AU - Jannin, Arnaud
AU - Leboulleux, Sophie
AU - Guerin, Carole
AU - Faron, Matthieu
AU - Baudin, Eric
N1 - Publisher Copyright:
© 2021 The Author(s). Published by Oxford University Press on behalf of the Endocrine Society. All rights reserved.
PY - 2021/9/1
Y1 - 2021/9/1
N2 - Context: The behavior of locally advanced pheochromocytoma (LAP) remains unknown. Objective: We characterized the population with LAP and recurrence-free survival (RFS). Methods: This retrospective multicentric study was run within the ENDOCAN-COMETE network and French Group of Endocrine Tumors (GTE) from 2003 to 2018, including patients from 11 French referral centers with LAP as defined by capsular invasion, vascular invasion, adipose tissue invasion, and/or positive locoregional lymph nodes at diagnosis without evidence of distant metastasis. The main outcome measure was recurrence, defined as tumor reappearance, including local site and/or distant metastasis. The primary endpoint was RFS analysis; secondary endpoints were characterization, overall survival (OS), and prognostic factors of recurrence. Results: Among 950 patients, 90 (9%) exhibited LAP criteria and 55 met inclusion criteria (median age, 53 years; 61% males; 14% with germline mutation; 84% with catecholamine excess). LAP was defined by 31 (56%) capsular invasions, 27 (49%) fat invasions, 6 (11%) positive lymph nodes, and 22 (40%) vascular invasions. After median follow-up of 54 months (range, 6-180), 12 patients (22%) had recurrences and 3 (5%) died of metastatic disease. Median RFS was 115 months (range, 6-168). Recurrences were local in 2 patients, distant in 2, and both local and distant in 8 patients. Median OS of patients was not reached. Size above 6.5 cm (P = 0.019) and Ki-67 > 2% (P = 0.028) were identified as independent significant prognostic factors in multivariate analysis. Conclusion: LAP represents 9% of pheochromocytoma's population and has a metastatic behavior. This study paves the way for future pathological TNM classification.
AB - Context: The behavior of locally advanced pheochromocytoma (LAP) remains unknown. Objective: We characterized the population with LAP and recurrence-free survival (RFS). Methods: This retrospective multicentric study was run within the ENDOCAN-COMETE network and French Group of Endocrine Tumors (GTE) from 2003 to 2018, including patients from 11 French referral centers with LAP as defined by capsular invasion, vascular invasion, adipose tissue invasion, and/or positive locoregional lymph nodes at diagnosis without evidence of distant metastasis. The main outcome measure was recurrence, defined as tumor reappearance, including local site and/or distant metastasis. The primary endpoint was RFS analysis; secondary endpoints were characterization, overall survival (OS), and prognostic factors of recurrence. Results: Among 950 patients, 90 (9%) exhibited LAP criteria and 55 met inclusion criteria (median age, 53 years; 61% males; 14% with germline mutation; 84% with catecholamine excess). LAP was defined by 31 (56%) capsular invasions, 27 (49%) fat invasions, 6 (11%) positive lymph nodes, and 22 (40%) vascular invasions. After median follow-up of 54 months (range, 6-180), 12 patients (22%) had recurrences and 3 (5%) died of metastatic disease. Median RFS was 115 months (range, 6-168). Recurrences were local in 2 patients, distant in 2, and both local and distant in 8 patients. Median OS of patients was not reached. Size above 6.5 cm (P = 0.019) and Ki-67 > 2% (P = 0.028) were identified as independent significant prognostic factors in multivariate analysis. Conclusion: LAP represents 9% of pheochromocytoma's population and has a metastatic behavior. This study paves the way for future pathological TNM classification.
KW - locally advanced pheochromocytoma
KW - metastatic pheochromocytoma
KW - prognostic factor
KW - recurrence-free survival
UR - http://www.scopus.com/inward/record.url?scp=85114303649&partnerID=8YFLogxK
U2 - 10.1210/clinem/dgab202
DO - 10.1210/clinem/dgab202
M3 - Article
C2 - 33782697
AN - SCOPUS:85114303649
SN - 0021-972X
VL - 106
SP - 2726
EP - 2737
JO - Journal of Clinical Endocrinology and Metabolism
JF - Journal of Clinical Endocrinology and Metabolism
IS - 9
ER -