Acromegaly
ICD-10 E22.0 · ICD-11 5A60.0

Acromegaly Treatment When Transsphenoidal Surgery Has Not Achieved Remission

Transsphenoidal surgery is the primary treatment approach for acromegaly. When it does not achieve biochemical remission, a structured second-line strategy is required. This protocol addresses that specific clinical situation.

Scenario

The patient has undergone transsphenoidal surgery as primary therapy for acromegaly — performed via the transsphenoidal route using either the operating microscope or the operating endoscope with microsurgical technique — and biochemical remission was not achieved.

When Surgery Did Not Succeed

Prior therapy: Transsphenoidal surgery

Goals not reached: Surgical remission requires a normalized serum IGF-1 and a random serum GH below 1 µg/L (GH below 0.14 µg/L is taken as a marker of surgical remission), assessed at 12 weeks after surgery. Failure to meet these thresholds indicates the need for adjuvant medical therapy.

Next Step: Adjuvant Medical Therapy

Initial adjuvant medical therapy involves a somatostatin receptor ligand (SRL) or an alternative medical agent — the specific choice, formulation, and full management algorithm are detailed in the complete protocol.

Complete agent selection, regimen, and individualisation criteria available via the link below.

Biochemical Targets

Treatment success is defined by an age-normalized serum IGF-1 value and a random GH below 1.0 µg/L. Both markers are measured at 12 weeks, just prior to the next dose.

References

DOI: 10.1210/jc.2014-2700

  • In a patient with significant disease (ie, with moderate-to-severe signs and symptoms of GH excess and without local mass effects), we suggest use of either a SRL or pegvisomant as the initial adjuvant medical therapy.
  • There are two equally effective long-acting available preparations: im octreotide long-acting release (LAR), and deep sc lanreotide depot/autogel.
  • We suggest a biochemical target goal of an age-normalized serum IGF-1 value, which signifies control of acromegaly.
  • We suggest using a random GH < 1.0 µg/L as a therapeutic goal, as this correlates with control of acromegaly.
  • Effectiveness of treatment is based on measurement of serum IGF-1 and GH, which should be measured after 12 weeks just prior to the next dose.
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