E. Frei et al., The interval between courses of high-dose chemotherapy with stem cell rescue: therapeutic hypotheses, BONE MAR TR, 24(9), 1999, pp. 939-945
Citations number
48
Categorie Soggetti
Hematology,"Medical Research Diagnosis & Treatment
The interval between courses of chemotherapy have classically been kept to
a minimum in order to maximize dose intensity. Certain clinical observation
s suggest that longer intervals, particularly in the high-dose setting, may
be more effective. This is based in part on the evidence that resistance i
s reversible over time and that the interval should be sufficient to allow
for such a reversal. Clinical evidence for such reversibility include the f
ollowing. In metastatic breast cancer, double or double high-dose stem cell
rescue (HD-SCR) studies involving a minimal interval, have not, at least a
s yet, been shown to be superior to single HD-SCR, In Hodgkin's disease, re
sponse after relapse correlates directly with duration of time to relapse.
Tn a comparative study of metastatic breast cancer, early HD-SCR preceded b
y daunorubicin induction was inferior to delayed HD-SCR, The latter was not
preceded by induction chemotherapy, In a comparative study of childhood AL
L, patients randomized to delayed (4 month interval) intensification had a
significantly; superior survival as compared to patients randomized to imme
diate (1 month interval) intensification. Taken together, these clinical ob
servations indicate that resistance is reversible and that optimization of
the interval must take this into account. Cytokinetic modeling of those cli
nical studies also found that delayed HD-SCR could result in a superior eff
ect. Cytokinetic models of minimal residual tumor which were also examined
included the Skipper exponential model, the Norton-Simon model which emphas
izes the Gompertzian effect, the clonal evolution model, and the Retsky-Dem
isheli model which derives from a bimodal relapse pattern above, Biological
and clinical data have resulted in a clinical protocol in the CALGB wherei
n patients with metastatic breast cancer are randomly allocated to (1) a si
ngle HD-SCR arm; (2) a double HD-SCR with a 5-week interval; and (3) a doub
le HD-SCR arm with a 16 week interval.