1.Phase II Study of Low-dose Paclitaxel and Cisplatin as a Second-line Therapy after 5-Fluorouracil/Platinum Chemotherapy in Gastric Cancer.
Keun Wook LEE ; Jee Hyun KIM ; Tak YUN ; Eun Kee SONG ; Im Il NA ; Hyunchoon SHIN ; So Yeon OH ; In Sil CHOI ; Do Youn OH ; Dong Wan KIM ; Seock Ah IM ; Tae You KIM ; Jong Seok LEE ; Dae Seog HEO ; Yung Jue BANG ; Noe Kyeong KIM
Journal of Korean Medical Science 2007;22(Suppl):S115-S121
This study was performed to evaluate the efficacy and toxicity of low-dose paclitaxel/cisplatin chemotherapy in patients with metastatic or recurrent gastric cancer that had failed 5-fluorouracil/platinum-based chemotherapy. Thirty-two patients with documented progression on or within 6 months after discontinuing 5-fluorouracil/platinum-based chemotherapy were enrolled. As a second-line treatment, paclitaxel (145 mg/m2) and cisplatin (60 mg/m2) was administered on day 1 every 3 weeks. Among 32 patients enrolled, 8 (25%) responded partially to paclitaxel/cisplatin, 8 (25%) had stable disease, and 14 (44%) had progressive disease. Two patients (6%) were not evaluable. The median time to progression (TTP) and overall survival for all patients were 2.9 months and 9.1 months, respectively. The most common hematologic toxicity was anemia (47%). Grade 3 neutropenia developed in three patients (9%), but no other grade 3/4 hematologic toxicity occurred. The most common non-hematologic toxicities were emesis (31%) and peripheral neuropathy (38%). Three cases (9%) of grade 3/4 emesis and 2 cases (6%) of grade 3 peripheral neuropathy developed. In conclusion, low-dose paclitaxel and cisplatin chemotherapy showed moderate activity with favorable toxicity profiles. However, relatively short TTP of this regimen warrants the development of more effective paclitaxel-based regimens other than combination with cisplatin in these patients as second-line therapies.
Adenocarcinoma/*drug therapy
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Adult
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Aged
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Antineoplastic Combined Chemotherapy Protocols/*administration & dosage/adverse
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Cisplatin/administration & dosage/adverse effects
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Female
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Fluorouracil/administration & dosage/adverse effects
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Humans
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Leucovorin/administration & dosage/adverse effects
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Male
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Middle Aged
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Organoplatinum Compounds/administration & dosage/adverse effects
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Paclitaxel/administration & dosage/adverse effects
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Stomach Neoplasms/*drug therapy/mortality
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Survival Rate
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Treatment Failure
2.A Pilot Study of Bortezomib in Korean Patients with Relapsed or Refractory Myeloma.
Keun Wook LEE ; Tak YUN ; Eun Kee SONG ; Im Il NA ; Hyunchoon SHIN ; Soo Mee BANG ; Jae Hoon LEE ; Seung Tae LEE ; Jee Hyun KIM ; Sung Soo YOON ; Jong Seok LEE ; Seonyang PARK ; Byoung Kook KIM ; Noe Kyeong KIM
Journal of Korean Medical Science 2005;20(4):598-602
Recent clinical trials showed that bortezomib, a novel proteasome inhibitor, had therapeutic activity in multiple myeloma. However, there was no data about the feasibility of bortezomib in Korean patients. We performed a pilot study of bortezomib in patients with relapsed or refractory myeloma (1.3 mg/m2 twice weekly for 2 week in a 3-week cycle). Seven patients were enrolled. The median age of patients was 59 yr. All patients previously received VAD (vincristine, doxorubicin and dexamethasone) and thalidomide chemotherapy. Three patients previously received alkylator-containing chemotherapy and 4 patients, autologous stem cell transplantation. Bortezomib monotherapy resulted in 3 partial remissions (43%), 3 no changes (43%) and 1 progressive disease (14%). One patient who had no response to bortezomib monotherapy experienced partial remission after addition of dexamethasone to bortezomib. The most common serious toxicity was thrombocytopenia (grade 3/4, 10 of 20 cycles (50%)) and grade 3 peripheral neuropathy was developed in 2 of 20 cycles (10%). Drug-related adverse event led to discontinuation of bortezomib in 1 patient. There was no treatment related mortality. Overall, bortezomib seems to be effective and feasible. Conduction of larger clinical studies on Korean patients is necessary to characterize clinical efficacy and safety of bortezomib more precisely.
Aged
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Antineoplastic Agents/administration & dosage/adverse effects/*therapeutic use
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Antineoplastic Combined Chemotherapy Protocols/adverse effects/therapeutic use
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Boronic Acids/administration & dosage/adverse effects/*therapeutic use
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Dexamethasone/administration & dosage/adverse effects
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Disease Progression
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Drug Resistance, Neoplasm
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Female
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Humans
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Korea
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Male
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Middle Aged
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Multiple Myeloma/*drug therapy
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Neoplasm Recurrence, Local
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Pilot Projects
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Pyrazines/administration & dosage/adverse effects/*therapeutic use
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Research Support, Non-U.S. Gov't
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Survival Analysis
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Thrombocytopenia/chemically induced
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Time Factors
3.Graft-Versus-Host Disease after Allogeneic Hematopoietic Stem Cell Transplantation with Non-Myeloablative Conditioning: Experiences at a Single Center.
Im Il NA ; Hyunchoon SHIN ; Eun Kee SONG ; Keun Wook LEE ; Tak YUN ; Jee Hyun KIM ; Sung Soo YOON ; Jong Seok LEE ; Seonyang PARK ; Byoung Kook KIM
Korean Journal of Hematology 2006;41(2):92-98
BACKGROUND: The use of non-myeloablative stem cell transplantation (NST) has recently been increasing for treating the patients who cannot tolerate ablative hematopoietic stem cell transplantation (HSCT). Although graft-versus-host disease (GVHD) is one of the greatest problems in HSCT, the clinical effect of GVHD following NST is not clear. We undertook this study to evaluate the clinical manifestations of GVHD and the outcomes after NST. METHODS: From October 2000 to October 2004, 61 patients underwent NST with a fludarabine-based conditioning regimen. The cumulative incidence of GVHD and the survival rates were obtained from the Kaplan-Meier curves. RESULTS: With a median follow-up of 195 days, the estimate for overall three-year survival was 32%. The cumulative incidences of grades II~IV acute GVHD and chronic GVHD were 33% (18/53) and 78% (29/37), respectively. The response rates for acute and chronic GVHD were 33% and 89%, respectively. The survival rates of patients with acute and chronic GVHD were 27% and 89%, respectively. The median survival time was 6.5 months CONCLUSION: The incidence of GVHD after NST did not differ from that after ablative HSCT. This study suggests that the aggressive treatment of acute GVHD should be considered to improve the overall survival after NST.
Follow-Up Studies
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Graft vs Host Disease*
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Hematopoietic Stem Cell Transplantation*
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Hematopoietic Stem Cells*
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Humans
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Incidence
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Stem Cell Transplantation
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Survival Rate