H. Lindman et al., Serum markers TPS, TPA and CA 15-3 as monitors of chemotherapy in patientswith metastatic breast cancer, J TUMOR M, 15(3), 2000, pp. 177-186
The serum markers TPS, TPA and CA 15-3 have been applied in monitoring the
clinical course of 63 patients with metastatic breast cancer. To evaluate t
he clinical usefulness of these markers, we investigated the relationship b
etween the initial marker levels and the changes of the marker levels durin
g chemotherapy. All three markers demonstrated high sensitivity for detecti
ng visceral and bone metastases (89-94%) compared to soft tissues and local
ly advanced disease in the patients (45-50%). The marker combination, TPS a
nd CA15-3, showed the highest sensitivity for detecting bone/visceral metas
tases (98%) and soft tissues/locally advanced metastases (75%).
The patients were followed for an extended time period and in total, 126 cl
inical events (CR, PR, SD, PD) were recorded. Median 7 serum samples per pa
tient were analyzed. TPA showed the highest sensitivity (85%) to the clinic
ally confirmed events PR/CR compared to TPS (68%) or CA 15-3 (54%). In the
case of clinical confirmed progressive disease (PD), TPS and TPA showed the
highest sensitivity with increased marker levels (>25%) in 77-78% of the e
vents compared to CA 15-3 (58%). On the other hand, in patients with increa
sed marker levels (>25%), the formal evaluation could verify a PD in 90% an
d 94% of the events for TPS and TPA compared to 78% for CA 15-3. Analogous
the correlation between decreasing (>50%) marker levels and clinical PR/CR
was 72% for CA 15-3 compared to 65-66% for the cytokeratin markers. Overall
, TPS and TPA tend to be superior to CA 15-3 for follow-up of metastatic br
east cancer patients. TPS, TPA and CA 15-3 marker increase preceded the cli
nical and/or radiological signs of PD in most of the patients; 1.5, 1.5 and
1.1 months, respectively.
The cytokeratin markers TPS and TPA tended to be the most useful tumor mark
ers for monitoring treatment and the simultaneous determination of two mark
ers provided additive diagnostic information in advanced breast cancer pati
ents.