Nr. Abu-rustum et al., Compliance with and acute hematologic toxic effects of chemoradiation in indigent women with cervical cancer, GYNECOL ONC, 81(1), 2001, pp. 88-91
Objectives. The goals of this work were to describe the compliance with and
acute hematologic toxic effects of chemoradiation for cervical cancer in i
ndigent women and to explore the likelihood that chemoradiation is effectiv
e outside research settings. We hypothesized that if compliance and toxicit
y are not limiting in this high-risk group of patients, the effectiveness o
f chemoradiation for cervical cancer in community settings is likely to mir
ror the efficacy demonstrated in clinical trials.
Methods. This study is a retrospective review of prospectively maintained d
ata on women with newly diagnosed cervical cancer treated with chemoradiati
on between August 1998 and August 2000. Cisplatin was given weekly at 40 mg
/m(2) to a maximum of six courses. A WBC count < 3000/mm(3) resulted in can
celation of cisplatin but not radiation, and patients were transfused for h
emoglobin <9 g/dl. Statistical analysis was performed using the t test, <ch
i>(2) test, and Fisher's exact test.
Results. In all, 19 of 65 patients treated (29.2%) missed at least one chem
otherapy cycle, with 10 (15.4%) due to missed appointments, 8 (12.3%) due t
o a low WBC count, and 1 due to increased creatinine. Nineteen patients (29
.2%) received RBC transfusion during chemoradiation, and two (3%) had plate
lets < 75,000/mm(3). Noncompliant patients had a lower mean total point A d
ose (7986 cGy vs 8413 cGy, P = 0.04) and longer overall treatment duration
(79 days vs 51 days, P < 0.001). No patient had a fatal hematologic complic
ation.
Conclusion. Nearly a third of the indigent women treated with chemoradiatio
n for cervical cancer do not complete the prescribed treatment, and a simil
ar number require blood transfusions. In indigent and minority women, the e
ffectiveness of chemoradiation protocols may not mirror the efficacy obtain
ed in clinical trials. (C) 2001 Academic Press.