Wednesday, June 22, 2005

IMF Newsletter: Chemo Advice: Tea, Porridge and OTC Options

We've continued gathering chemo advice and once again have a wonderful collection of tips to share. Every cancer patient faces the challenge of keeping a good quality of life as treatment decisions come along. Sometimes they seem overwhelming, so we're hopeful that the advice shared here helps you or someone you know feel a little less alone and a little better educated on what to expect when facing the prospect of cancer treatment.

"I am 63 and chemo still makes me sick even with my meds. But my friend got me some peppermint tea and I got over being sick, so I drink about two cups a day. What a difference it makes!"

"During my Chemo cycles involving 40 pills a day for 3 days, each cycle my savior was to take homemade thick porridge with milk and sugar and take the pills either before, during or after, all according to the instructions. As a result I felt fine considering, had no stomach problems and managed to get to work almost without a break. I hope others find this useful."

"I found that I would become extremely constipated within 3-5 days of chemo. A nurse in the oncology department suggested I take magnesium citrate. I found the product at my local pharmacy and started using it immediately. It has now become my chemo partner. From then on, on my second day of chemo, I would drink mag-citrate over ice each day. What a relief."

Saturday, June 18, 2005

The Road to Proteasome Inhibitor Discovery

Early 1970s
Experiments show the breakdown of a cell’s proteins requires energy.

1975
The label that “tags” a protein for degradation is isolated. Because ubiquitin exists in numerous tissues and organisms, its name is based on the Latin word ubique, meaning “everywhere.”

Late 1970s
Protein degradation in cells shown to take place in a series of steps that involves labeling proteins for destruction.

1980
Avram Hershko, MD, PhD, Aaron Ciechanover, MD, and Irwin Rose, PhD (all of whom won the 2004 Nobel Prize in Chemistry for their findings), publish research demonstrating the function and action of ubiquitin.

1981-1983
Drs. Hershko, Ciechanover and Rose develop the multistep ubiquitin-tagging hypothesis based on three newly discovered classes of enzymes they term E1, E2 and E3. These enzymes bind to a ubiquitin chain, transport it and attach it to a protein, thus tagging it for destruction.

1986
Alfred Goldberg, PhD, and Martin Rechsteiner, PhD, discover the proteasome.

1995
ProScript (which was later acquired by Millennium Pharmaceuticals in 1999) discovers a drug that blocks the proteasome. The National Cancer Institute agrees to fund clinical trials for the drug PS-341 (known today as Velcade).

1998
First clinical trial testing Velcade initiated at M. D. Anderson Cancer Center in Houston.

May 13, 2003
Velcade is the first proteasome inhibitor to be approved by the Food and Drug Administration for the treatment of multiple myeloma.

2004
Velcade currently being tested in numerous cancers, including lymphoma, lung and prostate.

http://www.curetoday.com/

Friday, June 17, 2005

Jensmiles

Jennifer Machajewski has a walking goal for 2005 - she will walk an average of 8 miles a day and raise $100,000 for the Multiple Myeloma Research Foundation (MMRF). That is the cost of one research grant, which she hopes will benefit multiple myeloma patients.

The distance over the year, 2800 miles, is approximately the same distance as walking across the width of the United States. Supporters can pledge or donate money for her effort on the Jensmiles website. This project is endosed by the Multiple Myeloma Research Foundation.

http://www.jensmiles.com/

Thursday, June 16, 2005

Bortezomib vs. Dex - New England Journal of Medicine

Background This study compared bortezomib with high-dose dexamethasone in patients with relapsed multiple myeloma who had received one to three previous therapies.

Methods We randomly assigned 669 patients with relapsed myeloma to receive either an intravenous bolus of bortezomib (1.3 mg per square meter of body-surface area) on days 1, 4, 8, and 11 for eight three-week cycles, followed by treatment on days 1, 8, 15, and 22 for three five-week cycles, or high-dose dexamethasone (40 mg orally) on days 1 through 4, 9 through 12, and 17 through 20 for four five-week cycles, followed by treatment on days 1 through 4 for five four-week cycles. Patients who were assigned to receive dexamethasone were permitted to cross over to receive bortezomib in a companion study after disease progression.

Results Patients treated with bortezomib had higher response rates, a longer time to progression (the primary end point), and a longer survival than patients treated with dexamethasone. The combined complete and partial response rates were 38 percent for bortezomib and 18 percent for dexamethasone (P<0.001), and the complete response rates were 6 percent and less than 1 percent, respectively (P<0.001).> in the bortezomib and dexamethasone groups were 6.22 months (189 days) and 3.49 months (106 days), respectively (hazard ratio, 0.55; P<0.001).> percent among patients taking bortezomib and 66 percent among patients taking dexamethasone (P=0.003), and the hazard ratio for overall survival with bortezomib was 0.57 (P=0.001). Grade 3 or 4 adverse events were reported in 75 percent of patients treated with bortezomib and in 60 percent of those treated with dexamethasone.

Conclusions Bortezomib is superior to high-dose dexamethasone for the treatment of patients with multiple myeloma who have had a relapse after one to three previous therapies.

New England Journal of Medicine: Volume 352:2487-2498 June 16, 2005

Wednesday, June 15, 2005

GCS-100 new compound studied to treat Myeloma

GlycoGenesys, Inc. is a biotechnology company focused on carbohydrate-based drug development. The Company currently is conducting a Phase I dose escalation trial of GCS-100LE, a unique compound to treat cancer, in patients with solid tumors. In addition, the Company is conducting a Phase I/II dose escalation trial of GCS-100LE in multiple myeloma at the Dana-Farber Cancer Institute in Boston, Massachusetts. Further clinical trials are planned for 2005. Additional information is available on GlycoGenesys' web site: www.glycogenesys.com.

Farnesyltransferase inhibitor R115777 (Zarnestra, Tipifarnib) synergizes with paclitaxel to fight Myeloma cells

From the Drug Discovery Program, the Experimental Therapeutics Program and Immunology Program, Biostatistics Core, H. Lee Moffitt Cancer Center & Research Institute and the Department of Interdisciplinary Oncology, University of South Florida College of Medicine, Tampa, FL; the Department of Microbiology and Immunology, Sylvester Comprehensive Cancer Center, University of Miami, Miami, FL; and Yale University, Department of Chemistry, New Haven, CT.

Recently we have found that disease stabilization was achieved in 64% of patients with advanced MM treated with the farnesyltransferase inhibitor R115777 (Zarnestra) in a phase 2 clinical trial. In order to enhance R115777 antitumor activity in MM, we examined the combination of this novel agent with other anticancer drugs in MM cell lines. In this study, R115777 was found to synergize with paclitaxel and docetaxel, but not with other chemotherapy agents, including doxorubicin, 5-fluorouracil, cisplastin, melphalan, mitoxantrone, and dexamethasone. R115777 synergized with paclitaxel to inhibit MM cell proliferation and to induce apoptosis. Synergism in the induction of apoptosis was accompanied by increase in cytochrome c release and caspase-3 activation. Furthermore, flow cytometry analysis also showed that paclitaxel and R115777 synergized to induce G2/M cell-cycle arrest. Importantly, synergism was observed in taxane- and R115777-resistant MM cells. In the human severe combined immunodeficient (SCID-hu) bone model of myeloma growth, the ability of paclitaxel to inhibit tumor growth in vivo was enhanced by R115777. Combination of paclitaxel or docetaxel with R115777 in the treatment of MM cells from patients with multiple myeloma was more beneficial than treatment with single agents. Our results provide the basis for combination therapy clinical trials with paclitaxel or docetaxel with R115777 in MM patients.

(Blood. 2005;105:4759-4766)
Blood, 15 June 2005, Vol. 105, No. 12, pp. 4759-4766

Tuesday, June 14, 2005

MMRC Tissue Bank

If you are being treated for multiple myeloma at one the following MMRC Member Institutions, the MMRC encourages you to provide tissue to the MMRC Tissue Bank.
  • Dana-Farber Cancer Institute
  • H. Lee Moffitt Cancer Center & Research Institute
  • Mayo Clinic Cancer Center
  • University Health Network (Princess Margaret Hospital)
If you are interested in participating, please email Alicia Sable-Hunt, RN at sablehunt@themmrc.org

Monday, June 13, 2005

MMRF Research: Targeting ERAD and UPR in myeloma

From the Summer 2005 Newsletter of the Multiple Myeloma Research Foundation.

Allan M. Weissman, MD, Center for Cancer Research, NCI-Frederick
Project Title: Targeting ERAD and UPR in multiple myeloma

Abstract: Dr. Weissman's research will investigate endoplasmaic reticulum-associated degradation (ERAD), a process by which myeloma cells destroy excess antibodies and proteins in order to survive. By blocking this process, Dr. Weissman believes myeloma cell death can occur, as has happened in studies of mice. He will use this funding to apply these findings to human myeloma as a step toward new therapeutics for treatment.

Sunday, June 12, 2005

MMRF Research: Immunoproteasome as a target for Myeloma therapy

From the Summer 2005 Newsletter of the Multiple Myeloma Research Foundation.

Robert Z. Orlowski, MD, PhD, University of North Carolina at Chapel Hill
Project Title: The Immunoproteasome as a target for multiple myeloma therapy

Abstract: Dr. Orlowski has identified a novel inhibitor of a specific myeloma proteasome called the immunoproteasome, which prevents the removal of unwanted and damaged proteins needed for myeloma cell death and remission. This agent killed myeloma cells but spared other cells in laboratory studies, while non-specific inhibitors like bortezomib caused death in all of them. These and other findings suggest that the immunoproteasome is a novel, distinct therapeutic target whose inhibition could help patients with myeloma while causing fewer side effects. Dr. Orlowski's new funding will examine the utility of this new class of drugs.

Saturday, June 11, 2005

New cancer-causing agent revealed

Scientists have pinpointed a new cancer-causing agent - tiny pieces of genetic material called microRNAs. Studies in the journal Nature suggest identifying the fragments may help detect even hard-to-diagnose cancer.

New York's Cold Spring Harbor Laboratory found raised levels of microRNA activity were linked to aggressive forms of blood cancer.

A second study found different cancers can be identified by their highly distinct patterns of microRNA activity.

It is thought the discovery could lead to an overhaul of the way cancers are classified, diagnosed and treated.

Dr Paul Meltzer, of the US National Human Genome Research Institute, said: "These studies change the landscape of cancer genetics."

MicroRNAs appear to regulate a broad array of physiological and developmental processes. However, they are so tiny, and prone to subtle variation that it has proved difficult to pin down their exact role. More than 200 different microRNAs have been identified - but the function of only a handful has been established.

New technology

Despite this scientists suspected they are implicated in cancer because of their role in embryonic development.

The New York laboratory team tested the theory by examining blood cancer (lymphoma) cells.

The cells showed increased levels of activity in a genetic segment containing a cluster of microRNAs called mir-17-92.

An analysis of tumour samples taken from patients produced similar results.

The researchers next bred mice with increased activity in the key cluster area. They developed lymphoma tumours more quickly than normal animals, and the tumours were more aggressive, killing all the animals within three months.

The researchers believe the microRNA activity may block the usual pattern of programmed cell death within a tumour, speeding up its growth and making it highly malignant.

Researcher Dr Gregory Hannon said: "This is by no means a final answer about the role of microRNAs in cancer. But it's the first really definitive link where we can show with biological experiments that microRNAs can act as an oncogene [cancer gene]."

Distinctive patterns

In separate research, a team led by Dr Todd Golub, of the Dana-Farber Cancer Institute, developed a sophisticated colour-coding technique which enabled them to analyse microRNAs more effectively than has previously been possible.

They examined different types of cancer cells to determine whether they showed distinct patterns of microRNA activity.

The patterns proved to be so distinctive that the researchers were able to use them to distinguish between not only normal cells and cancer cells, but different types of cancer, and even different subtypes of the same cancer.

The technique proved particularly useful in identifying cancers than can be difficult to distinguish from other forms because they look so similar under the microscope.

Henry Scowcroft, of the charity Cancer Research UK, said RNA had often been thought of as the "disposable" sister molecule of DNA - but recent research suggested it was nothing of the sort.

"Although at a very early stage, the research may open up a whole new world of discovery for cancer researchers. If microRNAs are as important in the everyday workings of cells as this research suggests, then exploiting them could play a role in almost every aspect of cancer medicine, from screening and diagnosis, to prediction of treatment outcomes, to cancer treatment itself."

http://news.bbc.co.uk/go/pr/fr/-/1/hi/health/4072368.stm

© BBC MMV

Friday, June 10, 2005

MMRF Research: Selective Inhibition of HDAC6

From the Summer 2005 Newsletter of the Multiple Myeloma Research Foundation.

James E. Bradner, MD, Broad Institute of Harvard and MIT Project Title: Selective inhibition of HDAC6 in the treatment of Multiple Myeloma.

Abstract: Dr. Bradner's research will investigate how to block HDAC6, a gatekeeper that allows elimination of toxic proteins and prevents the permanent death of myeloma cells in patients on bortezomib (Velcade). His lab discovered the only drug against HDAC6, called tubacin, and has recently proved that this drug kills myeloma cells in Petri dishes and that when tubacin and bortezomib are combined, myeloma cells are killed more effectively. Dr. Bradner will use his funding to invoestigate over 10 more potent versions of tubacin that he has identified and bring the best candidate into the clinic.

Thursday, June 09, 2005

Myeloma bone disease: pathophysiology and management

Bone disease is a major feature of multiple myeloma. Myeloma-induced bone destruction is the result of an increased activity of osteoclasts, which is not accompanied by a comparable increase of osteoblast function. Recent studies have revealed that new molecules such as the receptor activator of nuclear factor-kappa B (RANK), its ligand (RANKL), osteoprotegerin (OPG), and macrophage inflammatory protein-1alpha are implicated in osteoclast activation and differentiation, while proteins such as dickkopf-1 inhibit osteoblastic bone formation. These new molecules seem to interfere not only with the biology of myeloma bone destruction but also with tumour growth and survival, creating novel targets for the development of new antimyeloma treatment. Currently, bisphosphonates play a major role in the management of myeloma bone disease. Clodronate, pamidronate and zoledronic acid are the most effective bisphosphonates in symptomatic myeloma patients. Biochemical markers of bone remodeling have been used in an attempt to identify patients more likely to benefit from early treatment with bisphosphonates. Furthermore, using microarray techniques, myeloma patients may be subdivided into molecular subgroups with certain clinical characteristics, such as propensity for lytic lesions that may need early prophylactic treatment. Recent phase I studies with recombinant OPG and monoclonal antibodies to RANKL appear promising.

Department of Hematology, 251 General Airforce Hospital, Athens, Greece; Department of Hematology, Faculty of Medicine Imperial College London, Hammersmith Hospital, London, UK.

http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract&list_uids=15928069&query_hl=8

Wednesday, June 08, 2005

Velcade as Front Line Therapy

Two phase II studies with Bortezomib ( Velcade ) showed very high response rates in front-line multiple myeloma. Overall response rates ranged from 88 to 95 percent with complete and near complete responses ranging from 25 to 29 percent. Use of Bortezomib in the front-line setting allowed for successful stem cell transplants for these patients.

A complete and near complete response rate of 57 percent was reported following single stem cell transplant preceded by induction with Bortezomib, Doxorubicin and Dexamethasone (PAD). This response rate was similar to the complete and very good partial response rates previously published for tandem transplants.

"These data indicate that earlier use of Bortezomib may improve overall response outcomes for multiple myeloma patients," said James Cavenagh, principal investigator of the PAD study at St. Bartholomew's Hospital, West Smithfield, London.

Bortezomib for injection alone and in combination with Dexamethasone

The multicenter phase II study, led by Sundar Jagannath, assessed the efficacy and safety of Bortezomib as a single agent and in combination with standard therapy Dexamethasone in patients with previously untreated, symptomatic multiple myeloma.

Patients were treated for up to six cycles with Bortezomib. Dexamethasone was administered the day of and the day after Bortezomib if less than a partial response (PR) after cycle two or less than a complete response (CR) after cycle four was achieved. Patients received a median of six cycles. Response was assessed according to the European Group for Blood and Marrow Transplantation criteria (EBMT). Results from 32 evaluable patients included:

  • Overall response rate (CR+PR) for Bortezomib alone or in combination with Dexamethasone was 88 percent with a complete and near complete response rate of 25 percent;
  • After two cycles of therapy, single agent Bortezomib achieved a response rate of 40 percent;
  • Six of eight patients who achieved complete or near complete responses did so on Bortezomib alone;
  • Survival at one year was 87 percent with a median followup of 5.5 months; and
  • Improved response after the addition of Dexamethasone was observed in 68 percent of patients who received Dexamethasone.

Stem cell harvesting and engraftment was successful for all transplant patients in this study. Adverse events were reported to be manageable and included gastrointestinal events, neuropathy, myalgia, fatigue, and hematologic toxicities.

PAD induction therapy prior to Stem Cell Transplant

The multicenter phase I/II study, led by Cavenagh, assessed Bortezomib in combination with Doxorubicin and Dexamethasone (PAD) as induction therapy prior to stem cell transplant in previously untreated multiple myeloma patients.

Four cycles of PAD therapy were administered to patients. Thereafter, patients underwent stem cell mobilization, and the ability to adequately harvest peripheral blood stem cells was evaluated. High-dose Melphalan was administered, peripheral blood stem cells were infused, and the rate of hematologic recovery was assessed. Response, based on EBMT criteria, was measured after each cycle of PAD and three months after transplantation. Results from the 21 patients included:

  • Overall response rate (CR+PR) was 95 percent with a complete and near complete response rate of 29 percent;
  • Stem cell collection was adequate in 20 of 21 patients;
  • Eighteen of 20 patients were successfully transplanted as two patients declined transplant;
  • Post-transplantation, the overall response rate at three months was 95 percent with a 57 percent complete and near complete response rate; and
  • No dose limiting toxicities occurred and adverse events included infections, hyperglycemia, peripheral neuropathy, postural hypotension, gastrointestinal events and atrial fibrillation.

The works have been published in the British Journal of Haematology.

Bortezomib is contraindicated in patients with hypersensitivity to Bortezomib, boron, or mannitol. Risks associated with Bortezomib therapy include new or worsening peripheral neuropathy, hypotension, cardiac disorders, gastrointestinal adverse events, thrombocytopenia and tumor lysis syndrome. Women of childbearing potential should avoid becoming pregnant while being treated with Bortezomib.

http://www.xagena.it/news/medicinenews_net_news/33abffcedac43a654ac7f501856bf700.html

Tuesday, June 07, 2005

Drug CEO's Business Becomes Personal

(Reduced from the original LA Times article) As his staff raced to test a cancer medicine that might save his life, an executive negotiated a merger that could have halted the experiments.

Michael Crockett rushed through the door at the Sunnyvale, Calif., laboratory of Scios Inc. toting an Igloo cooler. Packed inside, beneath a layer of ice, was a vial of human bone marrow. The marrow was needed to test a tantalizing hypothesis: that Scios' experimental rheumatoid arthritis pill, SCIO-469, might also treat cancer. As Crockett, manager of the company's drug projects, delivered the bone marrow to Scios researchers in February 2003, he knew there was more at stake than product development. His boss, Scios Chief Executive Richard B. Brewer, donated the marrow. Brewer had multiple myeloma.

But scientists had to work fast. The firm's board of directors was preparing to sell the unprofitable biotech to drug giant Johnson & Johnson. And there were no guarantees that the SCIO-469 cancer project would continue under new ownership. J&J saw enormous potential in SCIO-469 — perhaps a billion dollars a year — but as a pill for rheumatoid arthritis. Brewer hoped to persuade his new bosses to also test the pill in cancer patients. "I'm hoping [other patients] won't have to go through what I went through," Brewer said.

Those at Scios who had watched Brewer battle his illness believed they were on a mission. "When someone you know and respect gets a disease, you get angry," said Scios' top scientist, George F. Schreiner. "We hated myeloma…. We wanted to tear it down, plow it under the ground and put enough salt in so it never comes back."

A top priority at Scios was developing a drug to neutralize p38, an enzyme believed to spur inflammation in rheumatoid arthritis patients. Using sophisticated computer programs, Scios researchers designed molecules that looked like they might block the activity of p38, and neutralize it. Guided by the computer models, chemists then mixed one compound after another in search of a usable drug. By the end of 2000, Scios was ready to test its pill in patients with rheumatoid arthritis.

Meanwhile, Brewer faced his own struggle. The first sign of trouble came in May 2000, when Brewer felt a twinge in his back. At first, he thought he had strained a muscle when he loaded his dog, a 70-pound boxer, into the back of his SUV. But the pain worsened, so Brewer went to a doctor, who told him he had a compressed disk. His condition didn't improve with rest. By spring 2001, Brewer could not stand upright and had to sleep in a chair to avoid intense pain.

Brewer kept up a grueling schedule, which was also taking its toll. Brewer steadily lost weight and the pain got worse, despite visits to a chiropractor. Aspirin didn't help. Damage to his spine had shaved an inch off his 6-foot 4-inch height. The scientists on Scios' executive team were alarmed by their boss' worsening condition. Chief Medical Officer Darlene Horton, a physician, feared she was watching Brewer die. She warned him that he might have cancer.

"This is not normal back pain," Horton recalled telling him. "You don't need massages, you don't need a chiropractor. You need an MRI — now." But Brewer told her his bone scans, another sort of imaging test, showed no sign of disease. Finally, at the recommendation of his doctor, Brewer had a surgeon inject plastic into his spine to cushion the damaged disk. During the procedure, the surgeon took a bone marrow biopsy.

The executive learned he had myeloma, a cancer he had never heard of. In late summer 2001, Brewer started high doses of chemotherapy at City of Hope National Medical Center in
Duarte. Six months later, he underwent a risky bone marrow transplant to restore damaged tissue. "It was the worst experience I could have imagined," he said. "Every cell in your body has been turned upside down and backwards. It changes you."

Brewer was back at work in April 2002. His cancer was in remission, but because myeloma is incurable, Brewer did not know how long he would remain cancer-free. His doctor at City of Hope, Stephen Forman, said remissions could last more than five years, or as little as one.

By mid-December, two firms, including Johnson & Johnson, said they wanted to buy Scios. With Scios' permission, the suitors started reviewing confidential documents in preparation for a bid. Then, in January 2003, Brewer spotted an article in a newsletter about a study that linked the p38 enzyme — the target of SCIO-469 — to myeloma. The researcher was Kenneth Anderson of the Dana-Farber Cancer Institute in
Boston, an authority on the disease.

Brewer contacted Anderson, who was surprised by the call. He was used to hearing from industry scientists but seldom talked shop with CEOs. He explained to Brewer that p38 releases chemicals that spur the growth of cancerous myeloma cells. In theory, if a drug blocks p38, the tumor can't survive. Brewer turned the article over to one of his top researchers, Linda Higgins, and asked her to dig deeper. After a week of intense research, Higgins told her boss: "I think we have a shot."

Higgins needed healthy cells from human bone marrow for her experiments, so Brewer volunteered. The first anniversary of Brewer's bone marrow transplant was approaching, and he was scheduled for a full day of medical tests at City of Hope. The CEO arranged to have marrow taken for Scios at the hospital.

Higgins isolated very specific cells, called stromal cells, from Brewer's tissue. In healthy people, stromal cells form the scaffolding that supports the blood-forming cells in the marrow. In patients with myeloma, stromal cells become "brainwashed" by cancerous plasma cells to produce nourishing chemicals, called cytokines. While stromal cells do the bidding of cancer cells, they remain healthy and don't become malignant.

Four days after his trip to City of Hope, Brewer voted with the rest of Scios' directors to accept a $2.4-billion offer for the company from J&J. Brewer had not wanted to sell the company. Scios, after a decade of disappointment, had finally tasted success. Its heart drug had been approved, and the company appeared close to potential breakthroughs in arthritis and cancer. But as a director accountable to shareholders, Brewer said he could not turn down J&J's offer.

During negotiations with J&J, Brewer made a case for continuing the myeloma project after the merger. To J&J pharmaceutical group president Joseph Scodari, the research sounded plausible, but sketchy. "It was obvious to us that Dick not only saw this as a business opportunity but had a great personal interest in this," he recalled. Brewer knew the transition to new ownership would take several months, time Scios could use to build a case for the drug. "We decided to go full blast," Brewer said.

One of his first steps was to recruit expert advisors, including Anderson of the Dana-Farber institute. Anderson flew to California in late February and came away impressed with the small company's science and inspired by its CEO. “The circumstances that brought us together were very rare," Anderson said. "One has to believe there must be a reason."

Still, many at Scios worried about scientists at the company losing objectivity on a project so dear to them — and their CEO. So the myeloma team held open forums, allowing other scientists to grill them. Brewer resolved to stay out of his scientists' way.

Higgins wrote a detailed plan to test SCIO-469. She coaxed the healthy stromal cells from Brewer's marrow to secrete the chemicals that fed tumors. Then she added SCIO-469 to the mix. With a team of junior scientists, Higgins repeated each step three times with the same encouraging result: The flow of nourishing chemicals slowed. Much work remained before the pill would be ready to test in cancer patients.

By mid-June 2003, Higgins completed her work. Thirty people — Scios scientists, their academic advisors and representatives of J&J — gathered to review all the data. Higgins told the group that myeloma cells in a lab dish became weaker when SCIO-469 was added. The healthy stromal cells were unharmed.

Higgins' work suggested that long-term use of SCIO-469 would lead to the death of myeloma cells. At the very least, the experts believed, the pill would spare patients the severe bone pain and damage that Brewer had experienced. By the end of the meeting, the experts had devised a plan for testing SCIO-469 in cancer patients. "That is when our p38 inhibitor became a full development oncology project," Crockett said.

Several dozen cancer patients have taken SCIO-469 as part of a clinical trial, scheduled to end by early summer. They took the pill alone for a while, then in combination with a cancer drug called Velcade, which J&J shares the rights to market. If the results are promising, Scios plans a bigger test with more patients.

Today, three years after his bone marrow transplant, Brewer remains in remission. Brewer is not in the clear, however, and his treatments haven't ended: He receives regular infusions of a drug to rebuild his bones.

"What I am hoping is that patients will be able to take two pills a day and live with their cancer," he said. "That would be Valhalla for us."

Copyright 2005 Los Angeles Times

http://www.latimes.com/business/la-fi-scios1jun01,0,544936.story?coll=la-home-headlines

Monday, June 06, 2005

Phase I Clinical Trial for CHIR-258

Chiron Corporation (Nasdaq:CHIR) and the Multiple Myeloma Research Consortium (MMRC) announced the initiation of a Phase I clinical trial of CHIR-258 in multiple myeloma. CHIR-258, an orally available kinase inhibitor developed by Chiron, is the first drug candidate to undergo clinical study through the MMRC, a non-profit organization that integrates leading academic institutions with the goal of accelerating drug development in multiple myeloma.

This Phase I trial of CHIR-258 in multiple myeloma is designed to evaluate the safety, tolerability, and pharmacokinetic and pharmacodynamic profiles of CHIR-258 in these patients.

Unlike many kinase inhibitors that only target vascular endothelial growth factor (VEGF), CHIR-258 inhibits receptors in the fibroblast growth factor (FGF) pathway, as well as VEGF and platelet-derived growth factor (PDGF). FGF receptor tyrosine kinase inhibition is potentially of therapeutic significance to a group of myeloma patients whose cancer cells express high levels of surface FGF receptors.

CHIR-258 is a novel, orally available tyrosine kinase inhibitor. Preclinical data show that CHIR-258 works to inhibit multiple kinases associated with different cancers, including acute myeloid leukemia (AML) and multiple myeloma.

http://home.businesswire.com/portal/site/google/index.jsp?ndmViewId=news_view&newsId=20050602005242&newsLang=en

Sunday, June 05, 2005

New powerful combination: Velcade and Tubacin

A novel strategy devised by Dana-Farber Cancer Institute scientists has proved highly effective in killing drug-resistant multiple myeloma cells in the laboratory and could open a new form of attack on the deadly blood cancer, they report.

Highly encouraged by the findings, the researchers hope to move rapidly to clinical trials of the therapy, a combination of the drug Velcade and an experimental compound that was designed by researchers at the Broad Institute of Massachusetts Institute of Technology and Harvard University.

The report, which will be posted online this week by the Proceedings of the National Academy of Sciences (http://www.pnas.org/papbyrecent.shtml), demonstrates that the combination was more than twice as effective as either drug alone in killing resistant cells from patients' bone marrow.

The promise is particularly exciting, scientists say, because many patients don't respond to Velcade, a drug approved just two years ago that's been an important new therapy for multiple myeloma.

"This is not just another drug, this is a whole new approach to treating multiple myeloma," said Kenneth Anderson, MD, senior author of the paper, whose lead author is Teru Hideshima, MD, also of Dana-Farber. Others include Stuart L. Schreiber, PhD, of Harvard University and the Broad Institute, and Jay Bradner, MD, of Dana-Farber and the Broad Institute.

Velcade is the first in a class of so-called proteasome inhibitors, which cause lethal stress in cancer cells by blocking the proteasome, a disposal mechanism that rids the cell of abnormal proteins. Cells in which the proteasome is jammed eventually commit suicide, triggered by the accumulation of proteins, explains Anderson, who is also the Kraft Family Professor of Medicine at Harvard Medical School.

However, many cancer cells are resistant to proteasome inhibitors like Velcade. Recent studies have revealed an alternative protein-disposal complex, the aggresome, that may take over enough of the job when the proteasome falters to allow the cells to survive.

Therefore, the Dana-Farber researchers suggested that blocking both protein disposals at once might get around this resistance mechanism. Scientists led by Schreiber at the Broad Institute designed a drug, tubacin, that blocks histone deacetylase 6, an enzyme that is critical to the aggresome's ability to function.

These highly promising results, wrote the researchers, "provide the framework for clinical trials designed to enhance sensitivity and overcome resistance to bortezomib [Velcade], thereby improving patient outcome in multiple myeloma.

Saturday, June 04, 2005

Hepatitis C link to Myeloma

People infected with the hepatitis C virus (HCV) have a higher risk of developing non-Hodgkin's lymphoma and multiple myeloma, according to a recent study of the Swedish population.

Previous studies have shown that people with HCV have a higher risk of developing cirrhosis and liver cancer. In Sweden, a cluster of four cases of non-Hodgkin's lymphoma in 554 HCV patients raised the question of an association between those two diseases and other related cancers.

To evaluate this possibility, researchers gathered data to examine the incidence of non-Hodgkin's lymphoma, multiple myeloma, chronic lymphatic leukemia, acute lymphatic leukemia, Hodgkin's lymphoma and thyroid cancer in the country's entire cohort of HCV patients.

For 27,150 HCV patients, the researchers modelled the date of HCV infection based on age and mode of transmission. They then collected data on the relevant cancer diagnoses among these patients from 1990 to 2000. Lastly, they performed statistical analyses to compare these patients' cancer rates to those of the entire Swedish population.

They found that the risk of both non-Hodgkin's lymphoma and multiple myeloma were significantly higher compared to the general population - 1.99 and 2.54 times higher, respectively. "The majority of the non-Hodgkin's lymphoma and multiple myeloma patients were estimated to have been infected more than 15 years, which is consistent with the theory that lymphomagenesis is a slow process and non-Hodgkin's lymphoma develops after a long influence," say the authors. They suggest that the risk for HCV-related malignancy increases with time of HCV infection.

In conclusion, "this is the first study of the incidence of non-Hodgkin's lymphoma, multiple myeloma, chronic lymphatic leukemia, acute lymphatic leukemia, Hodgkin's lymphoma and thyroid cancer in a nationwide cohort of HCV-infected persons," the authors report. "Although the delayed diagnosis of hepatitis C most probably has made us underestimate the risk, this study showed that the risk of B-cell non-Hodgkin's lymphoma and multiple myeloma were significantly increased."

http://www.interscience.wiley.com/journal/hepatology

Friday, June 03, 2005

Celgene Update

Celgene, an offshoot of chemical maker Celanese Corp., is expanding its drug portfolio. Over the next 12 months, it's expected to win approval from the FDA for two new drugs. Future sales from those drugs could quickly grow the company's revenues and reduce its dependence on Thalomid, the successor to Thalidomide.

Celgene was started in 1986 by scientists developing technology to use enzymes to "eat" pollution in water. When they found it wasn't economically feasible, they moved on to study Thalidomide, a morning-sickness drug that caused grievous birth defects before being banned in 1962. Research showed Thalidomide can stimulate or suppress the immune system, giving it potential to treat many disorders, and it can prevent growth of blood vessels that feed tumors.

Redeveloped as Thalomid, the drug's steady revenues have helped Celgene grow into one of the ten largest biotech companies in the world and bankrolled its research on treatments for cancer and other disorders. The company's stock price has climbed steadily for the past three years. Those financial results could improve if the FDA grants approval to two Celgene drugs in the pipeline.

Celgene is awaiting a decision on Focalin XR, an extended-release drug for ADHD. Another Celgene drug, Revlimid, is up for two FDA approvals, to treat the bone cancer multiple myeloma and a rare form of the bone marrow disease myelodysplastic syndrome.

Thursday, June 02, 2005

Shingles Vaccine - New England Journal of Medicine

Background The incidence and severity of herpes zoster and postherpetic neuralgia increase with age. We tested the hypothesis that vaccination would decrease the incidence, severity, or both of herpes zoster and postherpetic neuralgia among older adults.

Methods We enrolled 38,546 adults 60 years of age or older in a randomized, double-blind, placebo-controlled trial of an investigational "zoster vaccine". Herpes zoster was diagnosed according to clinical and laboratory criteria. The pain and discomfort associated with herpes zoster were measured repeatedly for six months. The primary end point was the burden of illness due to herpes zoster, a measure affected by the incidence, severity, and duration of the associated pain and discomfort. The secondary end point was the incidence of postherpetic neuralgia.

Results
More than 95% of the subjects continued in the study to its completion, with a median of 3.12 years of surveillance for herpes zoster. A total of 957 confirmed cases of herpes zoster (315 among vaccine recipients and 642 among placebo recipients) and 107 cases of postherpetic neuralgia (27 among vaccine recipients and 80 among placebo recipients) were included in the efficacy analysis. The use of the zoster vaccine reduced the burden of illness due to herpes zoster by 61.1%, the incidence of postherpetic neuralgia by 66.5%, and reduced the incidence of herpes zoster by 51.3%. Reactions at the injection site were more frequent among vaccine recipients but were generally mild.

Conclusions
The zoster vaccine markedly reduced morbidity from herpes zoster and postherpetic neuralgia among older adults.

New England Journal of Medicine, Volume 352:2271-2284, June 2, 2005, Number 22

Wednesday, June 01, 2005

Carrot, Celery, Fennel, Parsley, Parsnip Cytotoxic Activities

Extracts of roots and bulbs of carrots, celery, fennel, parsley, and parsnip were investigated for their content of polyacetylenes. All five species contained polyacetylenes, although carrots and fennel only in minor amounts.

Carrots, celery, fennel, parsley, and parsnip, are widely cultivated vegetables in temperate regions. Despite their wide usage as foodstuff, little is known about nonpolar secondary metabolites from celery bulbs, fennel bulbs, and parsnip roots.

Polyacetylenes possess a great number of beneficial as well as potential detrimental bioactivities for the human consumer. Polyacetylenes are potent antifungal and antibacterial compounds. They are also known to be inhibitors of a number of enzymes such as diacylglycerol acyltransferase, inducible nitric oxide synthase, and cholesteryl ester transfer protein as well as microsomal and mitochondrial enzymes. In vitro experiments indicate that some polyacetylenes might exhibit antiallergenic and anti-inflammatory activities. In addition, polyacetylenes have proven to be cytotoxic against a number of solid and leukemic cancer cell lines and to potentiate cytotoxicity of other anti-cancer drugs. For example, panaxytriol has been shown to rapidly inhibit cellular respiration in B16 melanoma cells transplanted to mice.

A medicinal usage of pure polyacetylenes is not feasible because of their pronounced chemical instability and their ability to induce allergic reactions. However, consumption of food containing polyacetylenes might have a chemopreventive benefit.

A dose-dependent biphasic effect of falcarinol from carrots on epithelial cells has been demonstrated recently. Low concentrations of falcarinol stimulated growth of these cells; in contrast, higher concentrations had an inhibitory effect. This is in line with the assumption that bioactive secondary metabolites contribute to the beneficial effects of a diet rich in fruits and vegetables against cancer and cardiovascular disease. Bioavailability of falcarinol from carrots in humans was demonstrated recently in biologically relevant concentrations. It was also demonstrated that dietary falcarinol intake inhibited cancerous lesions in mice.

Adverse effects due to an excessive intake of polyacetylenes with the human diet are not to be expected, because polyacetylenes have a bitter off-taste in higher concentrations and are one of the main compounds contributing to the bitter taste of stored carrots.

The present study has investigated the isolation and structure of polyacetylenes from celery, the contents of these compounds in celery and other vegetables from the Apiaceae family, and the in vitro cytotoxicity of four polyacetylenes isolated from celery against different human cancer cell lines.

All investigated polyacetylenes showed medium-level cytotoxicity against the investigated leukemia, lymphoma, and myeloma cell lines.

Consumption of celery, parsley, and parsnip is expected to lead to an uptake of polyacetylenes in quantities where biological effects (e.g., chemopreventive effects) are occurring. The average amount of polyacetylenes contained in umbelliferous vegetables might be subject to considerable variation due to different cultural varieties present and effects of processing and storage on the content of polyacetylenes in these plants.

Another point to be kept in mind is the frequency and amount of vegetables taken in by human consumers. Here carrots play a dominant role. Therefore, polyacetylenes from carrots will contribute the largest amount of polyacetylenes to the human diet, though our investigations indicate that other vegetables from the Apiaceae family may contain higher concentrations of these bioactive food constituents.

The so far unexplained paradox that high contents of natural carotenes in blood correlate with a low incidence of several types of cancer, while carotenes taken as food supplements do not have a positive effect, was linked with the fact that carrots are the major source of carotenes in Europe and North America and that carrots are also the only known major food items that contain the bioactive polyacetylene falcarinol. These authors concluded that the content of polyacetylenes in carrots and facarinol in particular might be responsible for the beneficial effects of carrot consumption. This implies that the observed negative correlation of low cancer risk with high intake of natural carotene is coincidental and produced by the co-occurrence of carotenes and polyacetylenes in carrots. If these findings can be verified, celery, parsley, and parsnip, which contain high amounts of bioactive polyacetylenes, will become promising ingredients of a diet aimed at cancer prevention.

Edited from: Cytotoxic Polyacetylenes from Apiaceae Vegetables J. Agric. Food Chem., Vol. 53, No. 7, 2005 2523

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