Background: Continuous measurement of perfusate leakage into the systemic c
irculation is of the utmost importance and can be performed with the help o
f radioactive tracers. The purpose of this study was to assess changes in t
he perfusion leakage rate between two periods: 1977-1990 and 1991-2000, and
to determine the factors responsible for these changes.
Methods: During the 1991-2000 period. 119 patients underwent HILP mainly fo
r locally recurrent melanoma or Locally advanced soft tissue sarcoma. HILP
was performed with melphalan (33%) or in combination with TNF alpha (65%).
There were 67 iliacal, 12 femoral, 25 popliteal, and 15 axillary perfusions
performed. Leakage into the systemic circulation was monitored continuousl
y with the help of I-131-albumin and a stationary scintillation detector pl
aced above the heart.
Results: The median maximum leakage was 2.7% {range 0%-21%) which is signif
icantly less than the previous period (1977-1990) where leakage of 8% (rang
e 0%-30%) was reposed (P <.05). A statistical difference in leakage was det
ected among perfusion locations where the iliac and femoral vessels showed
more leakage than the axillary and popliteal vessels (P <.05). Furthermore,
there appeared to be significantly less leakage when TNF alpha was used th
an when melphalan was the sole drug (P <.05).
Conclusions: Nowadays leakage from isolated perfusions into the systemic ci
rculation is further minimized compared with the days when me1phalos was th
e sole drug used. Increased awareness about TNF<alpha> leakage, continuous
external monitoring with I-131-albumin as the main isotope, flow rate regul
ation in the perfusion circuit, and regulation of the patient's systemic bl
ood pressure have all been major contributors to this improvement.