Literature DB >> 3219273

Treatment of bone metastases from breast cancer with (3-amino-1-hydroxypropylidene)-1,1-bisphosphonate (APD).

R E Coleman1, P J Woll, M Miles, W Scrivener, R D Rubens.   

Abstract

Twenty-eight patients with progressive symptomatic bone metastases from breast cancer received (3-amino-1-hydroxypropylidene)-1,1-bisphosphonate (APD) 30 mg in 500 ml of 0.9% saline infused over 2 h every 14 days. No other systemic therapy for breast cancer was prescribed. All patients had progressed on at least one previous systemic treatment. APD was continued until the disease progressed. Patients were assessed for objective response by the UICC criteria. In addition, subjective response was determined by a pain questionnaire. Radiological evidence of bone healing with sclerosis of lytic disease (UICC partial response) was seen in 4 patients. The median duration of response was 10 months. Eleven patients had stable disease for at least 3 months (median 5 months) and 9 progressed. Symptomatic response occurred in 9 patients and 12 reported an improvement in quality of life. Treatment was tolerated well with no significant toxicity. In conclusion, long-term inhibition of bone destruction is possible with APD therapy alone and both subjective and objective responses are seen.

Entities:  

Mesh:

Substances:

Year:  1988        PMID: 3219273      PMCID: PMC2246822          DOI: 10.1038/bjc.1988.272

Source DB:  PubMed          Journal:  Br J Cancer        ISSN: 0007-0920            Impact factor:   7.640


  19 in total

1.  Mechanisms of bone destruction in the development of skeletal metastases.

Authors:  C S Galasko
Journal:  Nature       Date:  1976-10-07       Impact factor: 49.962

2.  Diphosphonates for osteolytic metastases.

Authors:  I Elomaa; C Blomqvist; L Porkka; T Holmström; T Taube; C Lamberg-Allardt; G H Borgström
Journal:  Lancet       Date:  1985-05-18       Impact factor: 79.321

3.  Inhibition by diphosphonates of bone resorption induced by the Walker tumor of the rat.

Authors:  A Jung; J Bornand; B Mermillod; C Edouard; P J Meunier
Journal:  Cancer Res       Date:  1984-07       Impact factor: 12.701

4.  Characteristics and bisphosphonate treatment of a patient with juvenile osteoporosis.

Authors:  K Hoekman; S E Papapoulos; A C Peters; O L Bijvoet
Journal:  J Clin Endocrinol Metab       Date:  1985-11       Impact factor: 5.958

5.  New biochemical marker for bone metabolism. Measurement by radioimmunoassay of bone GLA protein in the plasma of normal subjects and patients with bone disease.

Authors:  P A Price; J G Parthemore; L J Deftos
Journal:  J Clin Invest       Date:  1980-11       Impact factor: 14.808

6.  Comparison of intravenous (3-amino-1-hydroxypropylidene)-1, 1-bisphosphonate and volume repletion in tumour-induced hypercalcaemia.

Authors:  H P Sleeboom; O L Bijvoet; A T van Oosterom; J H Gleed; J L O'Riordan
Journal:  Lancet       Date:  1983-07-30       Impact factor: 79.321

7.  Long-term controlled trial with diphosphonate in patients with osteolytic bone metastases.

Authors:  I Elomaa; C Blomqvist; P Gröhn; L Porkka; A L Kairento; K Selander; C Lamberg-Allardt; T Holmström
Journal:  Lancet       Date:  1983-01-22       Impact factor: 79.321

8.  Two modes of action of bisphosphonates on osteoclastic resorption of mineralized matrix.

Authors:  P M Boonekamp; L J van der Wee-Pals; M M van Wijk-van Lennep; C W Thesing; O L Bijvoet
Journal:  Bone Miner       Date:  1986-02

9.  Influence of treatment with APD-bisphosphonate on the bone lesions in the mouse 5T2 multiple myeloma.

Authors:  J Radl; J W Croese; C Zurcher; M H van den Enden-Vieveen; R J Brondijk; M Kazil; J J Haaijman; P H Reitsma; O L Bijvoet
Journal:  Cancer       Date:  1985-03-01       Impact factor: 6.860

10.  Kinetic studies of bone and mineral metabolism during treatment with (3-amino-1-hydroxypropylidene)-1,1-bisphosphonate (APD) in rats.

Authors:  P H Reitsma; O L Bijvoet; H Verlinden-Ooms; L J van der Wee-Pals
Journal:  Calcif Tissue Int       Date:  1980       Impact factor: 4.333

View more
  22 in total

1.  Treating bony metastases.

Authors:  D Dodwell; A Howell
Journal:  BMJ       Date:  1991-08-24

Review 2.  Bisphosphonates. Pharmacology and use in the treatment of tumour-induced hypercalcaemic and metastatic bone disease.

Authors:  H Fleisch
Journal:  Drugs       Date:  1991-12       Impact factor: 9.546

Review 3.  Strategies for management of prostate cancer-related bone pain.

Authors:  R C Pelger; V Soerdjbalie-Maikoe; N A Hamdy
Journal:  Drugs Aging       Date:  2001       Impact factor: 3.923

4.  Pamidronate in patients with painful bone metastases, who failed initial treatment with hormones and/or chemotherapy.

Authors:  S Cascinu; V Casadei; E Del Ferro; P Alessandroni; G Catalano
Journal:  Support Care Cancer       Date:  1996-01       Impact factor: 3.603

Review 5.  Causes and treatment of bone pain of malignant origin.

Authors:  B Thürlimann; N D de Stoutz
Journal:  Drugs       Date:  1996-03       Impact factor: 9.546

Review 6.  Clinical and economic issues in the treatment of advanced breast cancer with bisphosphonates.

Authors:  Nicola Lucio Liberato; Monia Marchetti; Giovanni Barosi
Journal:  Drugs Aging       Date:  2003       Impact factor: 3.923

7.  Sclerosis of lytic metastatic bone lesions during treatment with pamidronate in a patient with adenocarcinoma of unknown primary site.

Authors:  M Tanaka; H Fushimi; T Fuji; J M Ford
Journal:  Eur Spine J       Date:  1996       Impact factor: 3.134

Review 8.  Medical treatment of tumor-induced hypercalcemia and tumor-induced osteolysis: challenges for future research.

Authors:  J J Body
Journal:  Support Care Cancer       Date:  1993-01       Impact factor: 3.603

Review 9.  Postmenopausal breast cancer. Drug therapy in the 1990s.

Authors:  C I Falkson; G Falkson; H C Falkson
Journal:  Drugs Aging       Date:  1993 Mar-Apr       Impact factor: 3.923

Review 10.  Bisphosphonate treatment of lytic bone metastases.

Authors:  A Lipton; J R Berenson
Journal:  Drugs Aging       Date:  1999-04       Impact factor: 3.923

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.