| Id |
Subject |
Object |
Predicate |
Lexical cue |
| TextSentencer_T1 |
0-183 |
Sentence |
denotes |
A phase I dose-finding study of combined treatment with an antisense Bcl-2 oligonucleotide (Genasense) and mitoxantrone in patients with metastatic hormone-refractory prostate cancer. |
| T1 |
0-183 |
Sentence |
denotes |
A phase I dose-finding study of combined treatment with an antisense Bcl-2 oligonucleotide (Genasense) and mitoxantrone in patients with metastatic hormone-refractory prostate cancer. |
| TextSentencer_T2 |
184-192 |
Sentence |
denotes |
PURPOSE: |
| T2 |
184-192 |
Sentence |
denotes |
PURPOSE: |
| TextSentencer_T3 |
193-401 |
Sentence |
denotes |
Bcl-2 is a negative prognostic indicator in prostate cancer, implicated in the development of androgen independence and treatment resistance, and is overexpressed in hormone-refractory prostate cancer (HRPC). |
| T3 |
193-401 |
Sentence |
denotes |
Bcl-2 is a negative prognostic indicator in prostate cancer, implicated in the development of androgen independence and treatment resistance, and is overexpressed in hormone-refractory prostate cancer (HRPC). |
| TextSentencer_T4 |
402-704 |
Sentence |
denotes |
Genasense is a phosphorothioate antisense oligonucleotide complementary to the bcl-2 mRNA open reading frame that in preclinical studies has shown significant activity in inhibiting expression of Bcl-2, delaying androgen independence, and improving chemosensitivity in prostate and other cancer models. |
| T4 |
402-704 |
Sentence |
denotes |
Genasense is a phosphorothioate antisense oligonucleotide complementary to the bcl-2 mRNA open reading frame that in preclinical studies has shown significant activity in inhibiting expression of Bcl-2, delaying androgen independence, and improving chemosensitivity in prostate and other cancer models. |
| TextSentencer_T5 |
705-843 |
Sentence |
denotes |
In this dose escalation study, we evaluated the combination of Genasense and mitoxantrone, a standard chemotherapy for patients with HRPC. |
| T5 |
705-843 |
Sentence |
denotes |
In this dose escalation study, we evaluated the combination of Genasense and mitoxantrone, a standard chemotherapy for patients with HRPC. |
| TextSentencer_T6 |
844-851 |
Sentence |
denotes |
DESIGN: |
| T6 |
844-851 |
Sentence |
denotes |
DESIGN: |
| TextSentencer_T7 |
852-1026 |
Sentence |
denotes |
Twenty-six patients with HRPC were treated at seven dose levels receiving Genasense at a dose ranging from 0.6 to 5.0 mg/kg/day and mitoxantrone from 4 mg/m(2) to 12 mg/m(2). |
| T7 |
852-1026 |
Sentence |
denotes |
Twenty-six patients with HRPC were treated at seven dose levels receiving Genasense at a dose ranging from 0.6 to 5.0 mg/kg/day and mitoxantrone from 4 mg/m(2) to 12 mg/m(2). |
| TextSentencer_T8 |
1027-1155 |
Sentence |
denotes |
Genasense was administered as a 14-day i.v. continuous infusion every 28 days with mitoxantrone given as an i.v. bolus on day 8. |
| T8 |
1027-1155 |
Sentence |
denotes |
Genasense was administered as a 14-day i.v. continuous infusion every 28 days with mitoxantrone given as an i.v. bolus on day 8. |
| TextSentencer_T9 |
1156-1164 |
Sentence |
denotes |
RESULTS: |
| T9 |
1156-1164 |
Sentence |
denotes |
RESULTS: |
| TextSentencer_T10 |
1165-1207 |
Sentence |
denotes |
No dose-limiting toxicities were observed. |
| T10 |
1165-1207 |
Sentence |
denotes |
No dose-limiting toxicities were observed. |
| TextSentencer_T11 |
1208-1308 |
Sentence |
denotes |
Hematological toxicities were transient and included neutropenia, thrombocytopenia, and lymphopenia. |
| T11 |
1208-1308 |
Sentence |
denotes |
Hematological toxicities were transient and included neutropenia, thrombocytopenia, and lymphopenia. |
| TextSentencer_T12 |
1309-1465 |
Sentence |
denotes |
Nonhematological toxicities included fatigue, fever, nausea, arthralgias, myalgias, and transient elevations in serum creatinine, none of which were severe. |
| T12 |
1309-1465 |
Sentence |
denotes |
Nonhematological toxicities included fatigue, fever, nausea, arthralgias, myalgias, and transient elevations in serum creatinine, none of which were severe. |
| TextSentencer_T13 |
1466-1528 |
Sentence |
denotes |
Two patients had >50% reductions in prostate-specific antigen. |
| T13 |
1466-1528 |
Sentence |
denotes |
Two patients had >50% reductions in prostate-specific antigen. |
| TextSentencer_T14 |
1529-1686 |
Sentence |
denotes |
One patient, who received six cycles of Genasense at 1.2 mg/kg/day and a low dose (4 mg/m(2)) of mitoxantrone, also had symptomatic improvement in bone pain. |
| T14 |
1529-1686 |
Sentence |
denotes |
One patient, who received six cycles of Genasense at 1.2 mg/kg/day and a low dose (4 mg/m(2)) of mitoxantrone, also had symptomatic improvement in bone pain. |
| TextSentencer_T15 |
1687-1882 |
Sentence |
denotes |
Peripheral blood lymphocyte Bcl-2 protein expression decreased in five of five patients given Genasense at 5mg/kg/day (mean change from baseline, -12.8%; SD, 16.4%) as assessed by flow cytometry. |
| T15 |
1687-1882 |
Sentence |
denotes |
Peripheral blood lymphocyte Bcl-2 protein expression decreased in five of five patients given Genasense at 5mg/kg/day (mean change from baseline, -12.8%; SD, 16.4%) as assessed by flow cytometry. |
| TextSentencer_T16 |
1883-1981 |
Sentence |
denotes |
Serum concentrations of Genasense given at doses of 3 mg/kg/day and greater, exceeded 1 microg/ml. |
| T16 |
1883-1981 |
Sentence |
denotes |
Serum concentrations of Genasense given at doses of 3 mg/kg/day and greater, exceeded 1 microg/ml. |
| TextSentencer_T17 |
1982-1994 |
Sentence |
denotes |
CONCLUSIONS: |
| T17 |
1982-1994 |
Sentence |
denotes |
CONCLUSIONS: |
| TextSentencer_T18 |
1995-2194 |
Sentence |
denotes |
Genasense and mitoxantrone are well tolerated in combination, and mitoxantrone can be delivered at a standard dose with biologically active doses of Genasense without significant additional toxicity. |
| T18 |
1995-2194 |
Sentence |
denotes |
Genasense and mitoxantrone are well tolerated in combination, and mitoxantrone can be delivered at a standard dose with biologically active doses of Genasense without significant additional toxicity. |
| TextSentencer_T19 |
2195-2343 |
Sentence |
denotes |
This observation allays concerns about trials that combine Genasense with full doses of other cytotoxic agents seeking greater evidence of activity. |
| T19 |
2195-2343 |
Sentence |
denotes |
This observation allays concerns about trials that combine Genasense with full doses of other cytotoxic agents seeking greater evidence of activity. |