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21. |
Comparison of Current Alkylating Agents with a Homo-aza-Steroidal Ester for Antineoplastic Activity |
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Oncology,
Volume 51,
Issue 1,
1994,
Page 74-78
Panayotis Catsoulacos,
Athanasios Papageorgiou,
Elizabeth Margarity,
Dionysis Mourelatos,
Eleftheria Mioglou,
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摘要:
The modified steroidal alkylating agent, 17β-hydroxy-3-aza-A-homo-4α-androsten-4-one-p-bis(2-chloroethyl)aminophenoxyacetate has been tested against L1210 and P388 leukemias, and Lewis lung cancer, on DNA synthesis of EAT, L1210, P388, and BHK cell cultures, and on the induction of sister chromatid exchange. Comparable studies in vivo and in vitro were also done with p-bis(2-chloroethyl)aminophenoxyacetic acid, cyclophosphamide, melphalan, and chlorambuci
ISSN:0030-2414
DOI:10.1159/000227314
出版商:S. Karger AG
年代:1994
数据来源: Karger
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22. |
High-Dose (480 mg/day) Tamoxifen with Etoposide: A Study of a Potential Multi-Drug Resistance Modulator |
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Oncology,
Volume 51,
Issue 1,
1994,
Page 79-83
Michael J. Millward,
Ernst A. Lien,
Angela Robinson,
Brian M.J. Cantwell,
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摘要:
Tamoxifen and its principle metabolite N-desmethyltamoxifen can modulate multi-drug resistance in vitro. Tamoxifen 480 mg/day was given for 6 days with oral etoposide on days 4-6 to 17 patients with advanced solid tumours. Venous thrombosis (2 patients), reversible neurological toxicity (1 patient), and WHO grade III nausea/vomiting (3 patients) related to tamoxifen were observed but overall toxicity was manageable. One partial response occurred in 15 assessable patients. Mean plasma concentrations of tamoxifen and N-desmethyltamoxifen increased to 4.3 μmol/l and 2.7 μmol/l, respectively, by day 6. Plasma concentrations corresponding to active in vitro levels were attained by most patient
ISSN:0030-2414
DOI:10.1159/000227315
出版商:S. Karger AG
年代:1994
数据来源: Karger
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23. |
13-cis-Retinoic Acid Plus Interferon-α: A Phase II Clinical Study in Squamous Cell Carcinoma of the Lung and the Head and Neck |
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Oncology,
Volume 51,
Issue 1,
1994,
Page 84-86
Arnaud D. Roth,
Reto Abele,
Pierre Alberto,
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摘要:
Retinoids and interferon-α (IFN-α) have been shown to have a synergetic antiproliferative and differentiative effect on many cell lines, and in combination they have already been tested with some success in the treatment of some tumors. We investigated the tolerance and efficacy of high dose 13-cis-retinoic acid (2 mg/kg/day) and IFN-α in the treatment of advanced squamous cell carcinoma of the lung and of the head and neck. No partial or complete response was observed in the 10 patients treated. The toxicity was unusual and mild to moderate considering the dose of retinoid given. This observation leads us to suspect that IFN-α may alleviate some of the side effects of the retinoid, and is of interest in the design of future clinical tri
ISSN:0030-2414
DOI:10.1159/000227316
出版商:S. Karger AG
年代:1994
数据来源: Karger
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24. |
Treatment of Advanced Primary Lung Cancer Associated with Malignant Pleural Effusion by the Combination of Immunotherapy and Chemotherapy |
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Oncology,
Volume 51,
Issue 1,
1994,
Page 87-94
Hiromi Miyao,
Takaaki Chou,
Kazuhiko Ito,
Hiroyuki Moriyama,
Satoshi Mitsuma,
Masaya Wakabayashi,
Hirohisa Yoshizawa,
Masaaki Arakawa,
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摘要:
Twelve patients with advanced primary lung cancers associated with malignant pleural effusion were treated with intrathoracic instillation of recombinant interleukin-2 with or without in-vitro-sensitized cells. Two cases achieved complete response, and 7 partial response. The adverse effects seen in the protocol were marginal, and the protocol was well-tolerated and feasible. Furthermore, 4 cases were treated with the combination of systemic chemotherapy and adoptive immunotherapy. Of these, 3 cases responded well to the therapy and have shown a complete response for more than 20 months, indicating that adoptive immunotherapy together with chemotherapy might be a beneficial treatment for advanced lung cancer patients.
ISSN:0030-2414
DOI:10.1159/000227317
出版商:S. Karger AG
年代:1994
数据来源: Karger
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25. |
Therapeutic and Endocrine Effects of Decapeptyl®, Synthetic LH-RH Agonistic Analogue in Premenopausal Women with Metastatic Breast Cancer |
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Oncology,
Volume 51,
Issue 1,
1994,
Page 95-101
Zora B. Nešković-Konstantinović,
Labuda B. Vuletić,
Ljubinka I. Nikolić-Stanojević,
Snežana V. Šušnjar,
Svetislav B. Jelić,
Mirjana V. Branković-Magić,
Siniša S. Radulović,
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PDF (1649KB)
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摘要:
Twelve premenopausal patients with advanced breast cancer were entered into pilot phase II study to assess efficacy, toxicity and influence of the synthetic LH-RH agonistic analogue D-Trp6-LH-RH (Decapeptyl®) on the patients’ hormonal status. The patients, aged 33-50, with newly diagnosed stage IV or recurrent breast cancer were not previously treated by any kind of endocrine therapy. Steroid receptor status was known in 9 patients. Decapeptyl was applied monthly at a dose of 3.75 mg i.m. until progression. The therapeutic response was evaluated in 11/12 patients. Partial remission was achieved in 5, stabilization in 3, and 3 consecutive patients failed to respond. The best therapeutic response was obtained in patients with pleuropulmonal and soft-tissue involvement, aged 41-45, including those with incomplete ovarian suppression, and regardless of steroid receptor status. The mean serum gonadotropins and estradiol levels were suppressed. The treatment was free of any side effects, except hot flushes in 7 patien
ISSN:0030-2414
DOI:10.1159/000227318
出版商:S. Karger AG
年代:1994
数据来源: Karger
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26. |
Treatment of Gastric Adenocarcinoma with the Combination of Etoposide, Adriamycin and Cisplatin (EAP): Comparison between Two Schedules |
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Oncology,
Volume 51,
Issue 1,
1994,
Page 102-107
Nissim Haim,
Medy Tsalik,
Eliezer Robinson,
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摘要:
The results of two schedules of the combination of etoposide, doxorubicin, and cisplatin (EAP) in gastric cancer are reported. EAP-1 was administered as originally reported and consisted of i.v. doxorubicin (adriamycin) 20 mg/m2 on days 1 and 7, i.v. cisplatin 40 mg/m2 on days 2 and 8 and i.v. etoposide (VP-16) 120 mg/m2 (100 mg/m2 in patients aged 60-65) on days 4-6. EAP-2 consisted of i.v. adriamycin 40 mg/m2 on day 1, i.v. cisplatin 80 mg/m2 (total dose per cycle) given in 3 divided doses on days 1-3 and i.v. VP-16 100 mg/m2 on days 1-3. Cycles of the two regimens were repeated on day 22. Drug doses were reduced in patients over 65 years of age. Twenty patients were treated with EAP-1 and 43 with EAP-2. Forty-five of the 63 patients included in this study had advanced gastric carcinoma, 16 had radically resected stage III disease, and 2 had metastatic signet ring cell carcinoma of unknown primary origin. Thirty-eight patients with advanced gastric adenocarcinoma were evaluable for response. The response rate for EAP-1 (6/13, 46%) was similar to that of EAP-2 (13/25, 52%). The median duration of response was 8 months for EAP-1 and 6.5 months for EAP-2. Myelotoxicity of EAP-1 was much more severe than that of EAP-2. Hospitalization due to granulocytopenic fever was required in 15/78 (19%) EAP-1 versus 20/215 (9%) EAP-2 courses. Toxic deaths occurred in 3/20 treated with EAP-1 and in 1/45 treated with EAP-2. The difference in toxicity between the two regimens could not be attributed to differences in patients’ characteristics or to dose intensity. We conclude that the modified EAP regimen (EAP-2) is effective in the treatment of gastric cancer and is less toxic than the original EA
ISSN:0030-2414
DOI:10.1159/000227319
出版商:S. Karger AG
年代:1994
数据来源: Karger
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27. |
Azaphilones Inhibit Tumor Promotion by 12-O-Tetradecanoylphorbol-13-Acetate in Two-Stage Carcinogenesis in Mice |
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Oncology,
Volume 51,
Issue 1,
1994,
Page 108-112
Ken Yasukawa,
Masanao Takahashi,
Shinsaku Natori,
Ken-ichi Kawai,
Mikio Yamazaki,
Mieko Takeuchi,
Michio Takido,
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摘要:
Monascorubrin (an azaphilone derivative) was isolated from Monascus anka, ‘Monascus pigment’, a natural pigment of food additivies, was extracted from Monasucs spp., and chaetoviridin A, one of the azaphilones, was isolated from Chaetomium globosum var. flavo-viridae. Application of 1 ug of 12-O-tetradecanoylphorbol-13-acetate (TPA), a tumor promoting agent, to the mouse ear resulted in induction of inflammation. Among monascorubrin and related compounds assayed, monascorubrin, chaetoviridin A and its related compounds inhibited the inflammatory activity of TPA in mice. The 50% inhibitory dose of these compounds for TPA-induced inflammation was 0.4-1.5 μmol. Furthermore, monascorubrin (2 μmol), chaetoviridin A (2 μmol) and Monascus pigment (1 mg) markedly suppressed the promoting effect of TPA (1 μg) on skin tumor formation in mice initiated with 7,12-dimethylbenz[a]an-thracene (50 μg). It is assumed that the inhibition of tumor promotion by monascorubrin, chaetoviridin A and Monascus pigment is due to anti-inflammatory
ISSN:0030-2414
DOI:10.1159/000227320
出版商:S. Karger AG
年代:1994
数据来源: Karger
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28. |
Ondansetron Compared with Granisetron in the Prophylaxis of Cisplatin-lnduced Acute Emesis: A Multicentre Double-Blind, Randomised, Parallel-Group Study |
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Oncology,
Volume 51,
Issue 1,
1994,
Page 113-118
P. Ruff,
W. Paska,
L. Goedhals,
R. Pouillart,
A. Rivière,
D. Vorobiof,
B. Bloch,
A. Jones,
C. Martin,
R. Brunet,
M. Butcher,
J. Forster,
B. McQuade,
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摘要:
This is the first international, multi-centre, double-blind, randomised, parallel group study to directly compare the efficacy and safety profile of a single intravenous dose of ondansetron (8 or 32 mg) with granisetron (3 mg) in the control of cisplatin-induced acute emesis. A total of 496 patients were randomised to receive one of three anti-emetic treatments prior to cisplatin chemotherapy (≥50 mg/m2). Of these, 165 and 162 patients received 8 and 32 mg of ondansetron, respectively, and 169 patients received 3 mg of granisetron. Complete control of emesis (0 emetic episodes) over 24 h was reported in 59% of patients in the 8-mg ondansetron group, 51% of patients in the 32-mg ondansetron group and 56% of patients in the granisetron group. Complete or major control (≤2 emetic episodes) was achieved in 76 and 74% of patients in the 8- and 32-mg ondansetron group, respectively, compared with 78% of patients in the granisetron group. Nausea graded none or mild 24 h after the start of cisplatin infusion was reported in 71 and 69% of patients in the 8- and 32-mg ondansetron groups, respectively, and in 73% of patients in the granisetron group. There were no significant differences between the treatment groups when global satisfaction scores were compared. Logistic regression models were fitted to assess any interaction between treatments and prognostic factors (age, gender, alcohol use, cisplatin dose or concomitant chemotherapy) on complete or major response, but there was no evidence of interaction for any factor. All three anti-emetic treatments were well tolerated and no severe or unexpected drug-related adverse events were observed with ondansetron or granisetron. Headache, the most reported drug-related adverse event for all three treatment groups, occurred in 9% of all patients. In summary, no significant difference was observed between any of the treatment groups with respect to emesis, nausea or drug-related adverse eve
ISSN:0030-2414
DOI:10.1159/000227321
出版商:S. Karger AG
年代:1994
数据来源: Karger
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29. |
Contents, Vol. 51, Supplement 1, 1994 |
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Oncology,
Volume 51,
Issue 1,
1994,
Page -
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PDF (459KB)
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ISSN:0030-2414
DOI:10.1159/000227409
出版商:S. Karger AG
年代:1994
数据来源: Karger
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