GH/IGF-I normalization and tumor shrinkage during long-term treatment of acromegaly by lanreotide

被引:19
作者
Attanasio, R [1 ]
Barausse, M [1 ]
Cozzi, R [1 ]
机构
[1] Niguarda Hosp, Div Endocrinol, Milan, Italy
关键词
acromegaly; lanreotide; somatostatin analogs; tumor shrinkage; GH; IGF-I;
D O I
10.1007/BF03343849
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
New depot somatostatin analogs such as lanreotide-slow release (LAN) represent a significant improvement in the medical treatment of acromegaly. Seventy-three consecutive acromegalic patients, treated by LAN, were evaluated in a retrospective monocentric study. Sixteen were excluded from further evaluation due to combined treatment with dopamine agonist drugs, early LAN withdrawal for persistence of headache, or gastrointestinal side-effects. Fifty-seven patients (aged 20-82 years, 16 males) were thus evaluated. Thirty-two patients had been previously treated by neurosurgery (Tx) and/or radiotherapy (Rx). After washout, LAN (30 mg) was administered im at 10-14-day intervals. Time intervals between injections were then individually tailored to normalize IGF-I levels. LAN was administered for 12(6-36) [median (range)] months. GH and IGF-I levels decreased from 13 (7-20) [median (interquartile)] mug/l to 3.2 (1.7-6.2) mug/l (p <0.0001) and from 780 (596-1000) mug/l to 264 (180-530) mug/l (p <0.000001), respectively. Seven patients were resistant to treatment. Among the 50 sensitive patients, GH levels fell below 2.5 mug/l in 52% (and below 1 mug/l in 18%), IGF-I levels normalized in 72% and both results were obtained in 46%. IGF-I values normalized in 87% of patients treated every 14 days, in 100% every 21-28 days, in 69% every 10 days and in 22% every 7 days. No different control of GH/IGF-I hypersecretion was evidenced between patients previously treated or not by Tx and/or Rx. Patients with the lowest basal hormonal levels and those over 55 years showed greater responsiveness (both p <0.05). The maintenance of LAN schedule up to 18 months determined a further suppression (p=0.04 for IGF-I). A reduction of tumor size was shown in 60% of evaluated patients (6/10), HbA(1c) slightly increased in 42% of patients and gallstones were observed in 16%. LAN is a very effective tool in the treatment of acromegaly: its chronic administration normalizes GH/IGF-I levels in most patients, shrinks the tumor in a high percentage of patients and seems to control hormonal hypersecretion as primary treatment as well as neurosurgery. ((C))2001, Editrice Kurtis.
引用
收藏
页码:209 / 216
页数:8
相关论文
共 26 条
[11]   SMS-201-995 INDUCES A CONTINUOUS DECLINE IN CIRCULATING GROWTH-HORMONE AND SOMATOMEDIN-C LEVELS DURING THERAPY OF ACROMEGALIC PATIENTS FOR OVER 2 YEARS [J].
LAMBERTS, SWJ ;
UITTERLINDEN, P ;
DELPOZO, E .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1987, 65 (04) :703-710
[12]   Sandostatin(R) LAR(R): A promising therapeutic tool in the management of acromegalic patients [J].
Lancranjan, I ;
Bruns, C ;
Grass, P ;
Jaquet, P ;
Jervell, J ;
KendallTaylor, P ;
Lamberts, SWJ ;
Marbach, P ;
Orskov, H ;
Pagani, G ;
Sheppard, M ;
Simionescu, L .
METABOLISM-CLINICAL AND EXPERIMENTAL, 1996, 45 (08) :67-71
[13]   LONG-TERM TREATMENT OF ACROMEGALY WITH THE SLOW-RELEASE SOMATOSTATIN ANALOG LANREOTIDE [J].
MAREK, J ;
HANA, V ;
KRSEK, M ;
JUSTOVA, V ;
CATUS, F ;
THOMAS, F .
EUROPEAN JOURNAL OF ENDOCRINOLOGY, 1994, 131 (01) :20-26
[14]   Current treatment guidelines for acromegaly [J].
Melmed, S ;
Jackson, I ;
Kleinberg, D ;
Klibanski, A .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1998, 83 (08) :2646-2652
[15]   SLOW-RELEASE LANREOTIDE TREATMENT IN ACROMEGALIC PATIENTS PREVIOUSLY NORMALIZED BY OCTREOTIDE [J].
MORANGE, I ;
DEBOISVILLIERS, F ;
CHANSON, P ;
LUCAS, B ;
DEWAILLY, D ;
CATUS, F ;
THOMAS, F ;
JAQUET, P .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1994, 79 (01) :145-151
[16]   Octreotide as primary therapy for acromegaly [J].
Newman, CB ;
Melmed, S ;
George, A ;
Torigian, D ;
Duhaney, M ;
Snyder, P ;
Young, W ;
Klibanski, A ;
Molitch, ME ;
Gagel, R ;
Sheeler, L ;
Cook, D ;
Malarkey, W ;
Jackson, I ;
Vance, ML ;
Barkan, A ;
Frohman, L ;
Kleinberg, DL .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1998, 83 (09) :3034-3040
[17]   DETERMINANTS OF CLINICAL OUTCOME AND SURVIVAL IN ACROMEGALY [J].
RAJASOORYA, C ;
HOLDAWAY, IM ;
WRIGHTSON, P ;
SCOTT, DJ ;
IBBERTSON, HK .
CLINICAL ENDOCRINOLOGY, 1994, 41 (01) :95-102
[18]   THE GROWTH-HORMONE RESPONSES TO OCTREOTIDE IN ACROMEGALY CORRELATE WITH ADENOMA SOMATOSTATIN RECEPTOR STATUS [J].
REUBI, JC ;
LANDOLT, AM .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1989, 68 (04) :844-850
[19]   Depot somatostatin analogs - A new first line therapy for acromegaly [J].
Robbins, RJ .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1997, 82 (01) :15-17
[20]   OCTREOTIDE TREATMENT IN ACROMEGALY - A COMPARISON BETWEEN PEN-TREATED AND PUMP-TREATED PATIENTS IN A CROSS-OVER STUDY [J].
ROELFSEMA, F ;
FROLICH, M ;
DEBOER, H ;
HARRIS, AG .
ACTA ENDOCRINOLOGICA, 1991, 125 (01) :43-48