Phase II trial with D-Trp-6-LH-RH in prostatic carcinoma: Comparison with other hormonal agents

Various approaches to hormonal treatment of prostate carcinoma are discussed. Eighty‐one patients with prostatic carcinoma, eight with stage B, nine with stage C, and 64 with stage D disease, were treated subcutaneously daily for 3 months with the LH‐RH agonist D‐Trp‐6‐LH‐RH (Decapeptyl) in order to...

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Veröffentlicht in:The Prostate 1986, Vol.9 (4), p.327-342
Hauptverfasser: Mathé, Georges, Schwarzenberg, Leon, Vovan, Marie L., Machover, David, Misset, Jean L., Court, Bernard, Bouchard, Philippe, Pappo, Edmond, Schally, Andrew V., Comaru-Schally, Ana M., Mauvernay, Roland Y., Duchier, Jacques, Morin, Philippe, Keiling, Roger, Kerbrat, Pierre, Achille, Emmanuel, Tronc, Jacques C., Fendler, Jean P., Metz, Roland, Prevot, Gilles
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container_end_page 342
container_issue 4
container_start_page 327
container_title The Prostate
container_volume 9
creator Mathé, Georges
Schwarzenberg, Leon
Vovan, Marie L.
Machover, David
Misset, Jean L.
Court, Bernard
Bouchard, Philippe
Pappo, Edmond
Schally, Andrew V.
Comaru-Schally, Ana M.
Mauvernay, Roland Y.
Duchier, Jacques
Morin, Philippe
Keiling, Roger
Kerbrat, Pierre
Achille, Emmanuel
Tronc, Jacques C.
Fendler, Jean P.
Metz, Roland
Prevot, Gilles
description Various approaches to hormonal treatment of prostate carcinoma are discussed. Eighty‐one patients with prostatic carcinoma, eight with stage B, nine with stage C, and 64 with stage D disease, were treated subcutaneously daily for 3 months with the LH‐RH agonist D‐Trp‐6‐LH‐RH (Decapeptyl) in order to evaluate the incidence of remissions according to WHO recommendations for oncologic trials. The findings were compared to those obtained with other hormonal therapies of prostatic carcinoma according to the statistical method of “expected response rate” as adapted by Lee and Wesley for phase II trials. Treatment with D‐Trp‐6‐LH‐RH greatly reduced serum LH and testosterone levels without raising serum prolactin. After 1‐2 weeks of therapy, there was relief of subjective symptoms and a reversal of the signs of prostatism as well as a marked decrease in bone pain. At 90 days 52 patients had complete relief of prostatism and 21 had only mild signs and symptoms. Seventy paitents were experiencing no bone pain and an additional six had only mild pain. Prostatic size, evaluated by rectal examination and transabdominal ultrasonography, reverted to normal in 26.4% of patients (complete remission) and was reduced by more than 50% in an additional 17.6% (partial remission), the overall rate of complete plus partial regression of prostatic enlargement being 44%. Scans showed a major improvement of bone lesions in 14.8% of cases. This response increased to 37% after more than 6 months of follow‐up. Prostatic acid phosphatase levels were decreased by more than 50% in 61% of the patients, but this test appears to be a less valid marker than the lipid‐associated sialic acid (LASA). The increase in LASA before treatment and a reduction after treatment can frequently be correlated with the objective volume of the neoplasms. No flare‐up of the disease was encountered, and there were no side effects except for impotence. Statistical analyses of results by the method of Lee and Wesley indicated that the incidence of complete and partial regression (CR and PR) observed with D‐Trp‐6‐LH‐RH was not significantly different from that recorded in previous studies for another LH‐RH analog, Buserelin. However, CR and PR obtained with D‐Trp‐6‐LH‐RH (44%) were significantly higher than with subcapsular orchiectomy (22%). Hormonal effects and some other actions of D‐Trp‐6‐LH‐RH were compared and contrasted with those produced by castration, estrogens, antiandrogens, and progestogens. The treat
doi_str_mv 10.1002/pros.2990090404
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Eighty‐one patients with prostatic carcinoma, eight with stage B, nine with stage C, and 64 with stage D disease, were treated subcutaneously daily for 3 months with the LH‐RH agonist D‐Trp‐6‐LH‐RH (Decapeptyl) in order to evaluate the incidence of remissions according to WHO recommendations for oncologic trials. The findings were compared to those obtained with other hormonal therapies of prostatic carcinoma according to the statistical method of “expected response rate” as adapted by Lee and Wesley for phase II trials. Treatment with D‐Trp‐6‐LH‐RH greatly reduced serum LH and testosterone levels without raising serum prolactin. After 1‐2 weeks of therapy, there was relief of subjective symptoms and a reversal of the signs of prostatism as well as a marked decrease in bone pain. At 90 days 52 patients had complete relief of prostatism and 21 had only mild signs and symptoms. Seventy paitents were experiencing no bone pain and an additional six had only mild pain. Prostatic size, evaluated by rectal examination and transabdominal ultrasonography, reverted to normal in 26.4% of patients (complete remission) and was reduced by more than 50% in an additional 17.6% (partial remission), the overall rate of complete plus partial regression of prostatic enlargement being 44%. Scans showed a major improvement of bone lesions in 14.8% of cases. This response increased to 37% after more than 6 months of follow‐up. Prostatic acid phosphatase levels were decreased by more than 50% in 61% of the patients, but this test appears to be a less valid marker than the lipid‐associated sialic acid (LASA). The increase in LASA before treatment and a reduction after treatment can frequently be correlated with the objective volume of the neoplasms. No flare‐up of the disease was encountered, and there were no side effects except for impotence. Statistical analyses of results by the method of Lee and Wesley indicated that the incidence of complete and partial regression (CR and PR) observed with D‐Trp‐6‐LH‐RH was not significantly different from that recorded in previous studies for another LH‐RH analog, Buserelin. However, CR and PR obtained with D‐Trp‐6‐LH‐RH (44%) were significantly higher than with subcapsular orchiectomy (22%). Hormonal effects and some other actions of D‐Trp‐6‐LH‐RH were compared and contrasted with those produced by castration, estrogens, antiandrogens, and progestogens. The treatment of prostatic carcinoma with D‐Trp‐6‐LH‐RH avoids the cardiovascular and mammotropic side effects of estrogens, hepatic effects of some antiandrogens, and psychological impact of orchiectomy. There is still no evidence that the combination of LH‐RH analogs and small doses of antiandrogens offers an advantage over the use of LH‐RH agonists alone. Our findings indicate that currently LH‐RH analogs may be the method of choice for the treatment of advanced prostatic carcinoma. We also suggest that hormonal therapy with LH‐RH agonists can be combined with chemotherapy, the intial response to which might be potentiated by an early and transitory increase in testosterone levels. Our results warrant continuation of large‐scale clinical trials with LHRH agonists to establish their long‐term efficacy.</description><identifier>ISSN: 0270-4137</identifier><identifier>EISSN: 1097-0045</identifier><identifier>DOI: 10.1002/pros.2990090404</identifier><identifier>PMID: 2947053</identifier><identifier>CODEN: PRSTDS</identifier><language>eng</language><publisher>New York: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Acid Phosphatase - metabolism ; Aged ; Aged, 80 and over ; Antineoplastic agents ; Biological and medical sciences ; Carcinoma - drug therapy ; Chemotherapy ; Drug Administration Schedule ; Drug Evaluation ; Gonadotropin-Releasing Hormone - administration &amp; dosage ; Gonadotropin-Releasing Hormone - analogs &amp; derivatives ; Gonadotropin-Releasing Hormone - therapeutic use ; Humans ; Luteinizing Hormone - blood ; Male ; Medical sciences ; Middle Aged ; Pharmacology. Drug treatments ; Prostatic Neoplasms - drug therapy ; Testosterone - blood ; Triptorelin Pamoate</subject><ispartof>The Prostate, 1986, Vol.9 (4), p.327-342</ispartof><rights>Copyright © 1986 Wiley‐Liss, Inc., A Wiley Company</rights><rights>1987 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4114-d9685ea990226102f05e7f68bc6323b99f2a4ba9860159b8b83e329be112925e3</citedby><cites>FETCH-LOGICAL-c4114-d9685ea990226102f05e7f68bc6323b99f2a4ba9860159b8b83e329be112925e3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fpros.2990090404$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fpros.2990090404$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,4010,27900,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=8235430$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/2947053$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Mathé, Georges</creatorcontrib><creatorcontrib>Schwarzenberg, Leon</creatorcontrib><creatorcontrib>Vovan, Marie L.</creatorcontrib><creatorcontrib>Machover, David</creatorcontrib><creatorcontrib>Misset, Jean L.</creatorcontrib><creatorcontrib>Court, Bernard</creatorcontrib><creatorcontrib>Bouchard, Philippe</creatorcontrib><creatorcontrib>Pappo, Edmond</creatorcontrib><creatorcontrib>Schally, Andrew V.</creatorcontrib><creatorcontrib>Comaru-Schally, Ana M.</creatorcontrib><creatorcontrib>Mauvernay, Roland Y.</creatorcontrib><creatorcontrib>Duchier, Jacques</creatorcontrib><creatorcontrib>Morin, Philippe</creatorcontrib><creatorcontrib>Keiling, Roger</creatorcontrib><creatorcontrib>Kerbrat, Pierre</creatorcontrib><creatorcontrib>Achille, Emmanuel</creatorcontrib><creatorcontrib>Tronc, Jacques C.</creatorcontrib><creatorcontrib>Fendler, Jean P.</creatorcontrib><creatorcontrib>Metz, Roland</creatorcontrib><creatorcontrib>Prevot, Gilles</creatorcontrib><title>Phase II trial with D-Trp-6-LH-RH in prostatic carcinoma: Comparison with other hormonal agents</title><title>The Prostate</title><addtitle>Prostate</addtitle><description>Various approaches to hormonal treatment of prostate carcinoma are discussed. Eighty‐one patients with prostatic carcinoma, eight with stage B, nine with stage C, and 64 with stage D disease, were treated subcutaneously daily for 3 months with the LH‐RH agonist D‐Trp‐6‐LH‐RH (Decapeptyl) in order to evaluate the incidence of remissions according to WHO recommendations for oncologic trials. The findings were compared to those obtained with other hormonal therapies of prostatic carcinoma according to the statistical method of “expected response rate” as adapted by Lee and Wesley for phase II trials. Treatment with D‐Trp‐6‐LH‐RH greatly reduced serum LH and testosterone levels without raising serum prolactin. After 1‐2 weeks of therapy, there was relief of subjective symptoms and a reversal of the signs of prostatism as well as a marked decrease in bone pain. At 90 days 52 patients had complete relief of prostatism and 21 had only mild signs and symptoms. Seventy paitents were experiencing no bone pain and an additional six had only mild pain. Prostatic size, evaluated by rectal examination and transabdominal ultrasonography, reverted to normal in 26.4% of patients (complete remission) and was reduced by more than 50% in an additional 17.6% (partial remission), the overall rate of complete plus partial regression of prostatic enlargement being 44%. Scans showed a major improvement of bone lesions in 14.8% of cases. This response increased to 37% after more than 6 months of follow‐up. Prostatic acid phosphatase levels were decreased by more than 50% in 61% of the patients, but this test appears to be a less valid marker than the lipid‐associated sialic acid (LASA). The increase in LASA before treatment and a reduction after treatment can frequently be correlated with the objective volume of the neoplasms. No flare‐up of the disease was encountered, and there were no side effects except for impotence. Statistical analyses of results by the method of Lee and Wesley indicated that the incidence of complete and partial regression (CR and PR) observed with D‐Trp‐6‐LH‐RH was not significantly different from that recorded in previous studies for another LH‐RH analog, Buserelin. However, CR and PR obtained with D‐Trp‐6‐LH‐RH (44%) were significantly higher than with subcapsular orchiectomy (22%). Hormonal effects and some other actions of D‐Trp‐6‐LH‐RH were compared and contrasted with those produced by castration, estrogens, antiandrogens, and progestogens. The treatment of prostatic carcinoma with D‐Trp‐6‐LH‐RH avoids the cardiovascular and mammotropic side effects of estrogens, hepatic effects of some antiandrogens, and psychological impact of orchiectomy. There is still no evidence that the combination of LH‐RH analogs and small doses of antiandrogens offers an advantage over the use of LH‐RH agonists alone. Our findings indicate that currently LH‐RH analogs may be the method of choice for the treatment of advanced prostatic carcinoma. We also suggest that hormonal therapy with LH‐RH agonists can be combined with chemotherapy, the intial response to which might be potentiated by an early and transitory increase in testosterone levels. Our results warrant continuation of large‐scale clinical trials with LHRH agonists to establish their long‐term efficacy.</description><subject>Acid Phosphatase - metabolism</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Antineoplastic agents</subject><subject>Biological and medical sciences</subject><subject>Carcinoma - drug therapy</subject><subject>Chemotherapy</subject><subject>Drug Administration Schedule</subject><subject>Drug Evaluation</subject><subject>Gonadotropin-Releasing Hormone - administration &amp; dosage</subject><subject>Gonadotropin-Releasing Hormone - analogs &amp; derivatives</subject><subject>Gonadotropin-Releasing Hormone - therapeutic use</subject><subject>Humans</subject><subject>Luteinizing Hormone - blood</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Pharmacology. 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Eighty‐one patients with prostatic carcinoma, eight with stage B, nine with stage C, and 64 with stage D disease, were treated subcutaneously daily for 3 months with the LH‐RH agonist D‐Trp‐6‐LH‐RH (Decapeptyl) in order to evaluate the incidence of remissions according to WHO recommendations for oncologic trials. The findings were compared to those obtained with other hormonal therapies of prostatic carcinoma according to the statistical method of “expected response rate” as adapted by Lee and Wesley for phase II trials. Treatment with D‐Trp‐6‐LH‐RH greatly reduced serum LH and testosterone levels without raising serum prolactin. After 1‐2 weeks of therapy, there was relief of subjective symptoms and a reversal of the signs of prostatism as well as a marked decrease in bone pain. At 90 days 52 patients had complete relief of prostatism and 21 had only mild signs and symptoms. Seventy paitents were experiencing no bone pain and an additional six had only mild pain. Prostatic size, evaluated by rectal examination and transabdominal ultrasonography, reverted to normal in 26.4% of patients (complete remission) and was reduced by more than 50% in an additional 17.6% (partial remission), the overall rate of complete plus partial regression of prostatic enlargement being 44%. Scans showed a major improvement of bone lesions in 14.8% of cases. This response increased to 37% after more than 6 months of follow‐up. Prostatic acid phosphatase levels were decreased by more than 50% in 61% of the patients, but this test appears to be a less valid marker than the lipid‐associated sialic acid (LASA). The increase in LASA before treatment and a reduction after treatment can frequently be correlated with the objective volume of the neoplasms. No flare‐up of the disease was encountered, and there were no side effects except for impotence. Statistical analyses of results by the method of Lee and Wesley indicated that the incidence of complete and partial regression (CR and PR) observed with D‐Trp‐6‐LH‐RH was not significantly different from that recorded in previous studies for another LH‐RH analog, Buserelin. However, CR and PR obtained with D‐Trp‐6‐LH‐RH (44%) were significantly higher than with subcapsular orchiectomy (22%). Hormonal effects and some other actions of D‐Trp‐6‐LH‐RH were compared and contrasted with those produced by castration, estrogens, antiandrogens, and progestogens. The treatment of prostatic carcinoma with D‐Trp‐6‐LH‐RH avoids the cardiovascular and mammotropic side effects of estrogens, hepatic effects of some antiandrogens, and psychological impact of orchiectomy. There is still no evidence that the combination of LH‐RH analogs and small doses of antiandrogens offers an advantage over the use of LH‐RH agonists alone. Our findings indicate that currently LH‐RH analogs may be the method of choice for the treatment of advanced prostatic carcinoma. We also suggest that hormonal therapy with LH‐RH agonists can be combined with chemotherapy, the intial response to which might be potentiated by an early and transitory increase in testosterone levels. Our results warrant continuation of large‐scale clinical trials with LHRH agonists to establish their long‐term efficacy.</abstract><cop>New York</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>2947053</pmid><doi>10.1002/pros.2990090404</doi><tpages>16</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0270-4137
ispartof The Prostate, 1986, Vol.9 (4), p.327-342
issn 0270-4137
1097-0045
language eng
recordid cdi_proquest_miscellaneous_77182074
source Wiley-Blackwell Journals; MEDLINE
subjects Acid Phosphatase - metabolism
Aged
Aged, 80 and over
Antineoplastic agents
Biological and medical sciences
Carcinoma - drug therapy
Chemotherapy
Drug Administration Schedule
Drug Evaluation
Gonadotropin-Releasing Hormone - administration & dosage
Gonadotropin-Releasing Hormone - analogs & derivatives
Gonadotropin-Releasing Hormone - therapeutic use
Humans
Luteinizing Hormone - blood
Male
Medical sciences
Middle Aged
Pharmacology. Drug treatments
Prostatic Neoplasms - drug therapy
Testosterone - blood
Triptorelin Pamoate
title Phase II trial with D-Trp-6-LH-RH in prostatic carcinoma: Comparison with other hormonal agents
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