EARLY HEMATOLOGICAL TOXICITY OF ADJUVANT PERIOPERATIVE INTRAPORTAL AND INTRAVENOUS CHEMOTHERAPY WITH FLUOROURACIL, MITOMYCIN AND HEPARIN INCOLORECTAL-CANCER
W. Weber et al., EARLY HEMATOLOGICAL TOXICITY OF ADJUVANT PERIOPERATIVE INTRAPORTAL AND INTRAVENOUS CHEMOTHERAPY WITH FLUOROURACIL, MITOMYCIN AND HEPARIN INCOLORECTAL-CANCER, Anticancer research, 15(5), 1995, pp. 2197-2200
Background: From 1987 to 1993 the Swiss Group for Clinical Cancer Rese
arch (SAKK) performed a randomized phase III adjuvant trial in patient
s with colorectal adenocarcinoma with the objective of comparing intra
portal versus intravenous perioperative chemotherapy. Patients and met
hods: Patients younger than 75 years had a curative en bloc resection
of their cancer and were then randomized into three arms: 1. adjuvant
perioperative portal liver infusion with fluorouracil, mitomycin and h
eparin, 2. adjuvant subclavian intravenous infusion with the same regi
men and 3. no adjuvant treatment. The hematological toxicity was evalu
ated by hemoglobin determination and leucocyte and thrombocyte countin
g before and during ten days after surgery. Results: Hemoglobin showed
a median decrease of 22% in the control group. This decrease is aggra
vated significantly by 3% through the chemotherapy. Leucocytes showed
a median decrease of 7% in the control group. Perioperative chemothera
py caused a significantly higher median drop: 23% when given into the
liver through a subclavian catheter. Thrombocytes revealed a median de
crease of 25% in the control group. Chemotherapy was not associated wi
th a significant additional drop. Conclusions: Adjuvant perioperative
chemotherapy with fluorouracil, mitomycin and Heparin as given in this
study is associated with a significant mild drop in hemoglobin and le
ucocytes during the first 10 postoperative days. If drug dose increase
s are planned in future trials the addition of hematopoietic growth fa
ctors might be considered.