Ovarian Cancer

Ovarian Cancer

Advances in treatment and an improved understanding of ovarian cancer have led to longer lives and better quality of life for women with the disease.

The breakthrough discovery that specific gene mutations – in the BRCA 1 and 2 genes – increase a woman's risk for ovarian and breast cancer has led to important risk-reducing strategies. Additionally, recent studies have shown that ovarian cancer is not one disease, but a spectrum of related diseases with unique genetic characteristics, creating the potential for developing more effective, personalized treatment regimens. 

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1999

FDA approves liposomal doxorubicin for advanced ovarian cancer

FDA approves liposomal doxorubicin for advanced ovarian cancer

Liposomal doxorubicin (Doxil) receives accelerated FDA approval to treat advanced ovarian cancer that has progressed after prior treatment. The drug is unique because the active chemotherapy agent is encased in a microscopic fat bubble that releases the drug at the tumor site, delivering more of the chemotherapy directly to the tumor and less to other parts of the body, thereby limiting side effects. Full approval is granted in 2005 based on follow-up studies showing that the drug shrinks ovarian tumors and extends survival compared to standard topotecan (Hycamptin) chemotherapy. By the end of the 1990s, patients with advanced ovarian cancer have a growing number of chemotherapy options to select from.

1996

New chemotherapy drug for advanced ovarian cancer

1994

BRCA1 and BRCA2 gene mutations linked to increased breast cancer risk

BRCA1 and BRCA2 gene mutations linked to increased breast cancer risk

Badge indicating that research was paid for using federal funds

Researchers discover that women who have mutations in the genes known as BRCA1 and BRCA2 have a 50 to 85 percent increased risk of developing breast and ovarian cancers. These mutations are found to be particularly common among women of Ashkenazi Jewish descent. The identification of this important genetic cancer risk factor enables women with these mutations to undergo more frequent screening, and in some cases to undergo preventive surgical removal of the breasts, ovaries or both. Preventive use of tamoxifen (Novaldex) or raloxifene (Evista) becomes an additional option after the drugs are proven effective for this purpose in the following years.

1992

Taxanes emerge as vital chemotherapy option for ovarian, breast cancer

Taxanes emerge as vital chemotherapy option for ovarian, breast cancer

Badge indicating that research was paid for using federal funds

A new family of treatments debuts with the FDA approval of paclitaxel (Taxol) for advanced ovarian cancer. The drug receives one of the fastest-ever approvals, on the heels of data showing it shrinks ovarian tumors by more than half in many women who had stopped responding to all other therapies. Later studies show it extends survival by over a year when used as an initial therapy for advanced ovarian cancer, along with the chemotherapy drug cisplatin. This approach is later replaced by a regimen involving paclitaxel and another chemotherapy drug, called carboplatin (Paraplatin, Paraplat), which results in fewer side effects.

Over the next decade, paclitaxel also proves effective for all stages of breast cancer – both extending lives and delaying disease progression compared to existing therapies. The drug is derived from the bark of a yew tree, and is the product of a field of research exploring 'natural' products for a range of diseases. Until drugmakers discovered a synthetic method for producing the drug, there was widespread concern that the natural resources needed to produce the drug would not meet demand.

1989

FDA approves carboplatin for ovarian cancer

FDA approves carboplatin for ovarian cancer

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The chemotherapy drug carboplatin (Paraplatin, Paraplat) becomes available as a second line of therapy for ovarian cancer, after research shows that it promotes tumor shrinkage. It becomes available as an initial therapy two years later, after being shown to increase survival. This approval offers an effective treatment alternative for patients who cannot tolerate the standard chemotherapy drug, cisplatin, which carries significant side effects. It later becomes the preferred initial chemotherapy, after studies show it is as effective as cisplatin but causes fewer side effects.

1984

Scientists discover "biomarker" tied to ovarian cancer – CA-125

Scientists discover "biomarker" tied to ovarian cancer – CA-125

Researchers determine that levels of a specific protein in the blood, CA-125, are linked to ovarian cancer. The test soon becomes routinely used in women with ovarian cancer to track their response to treatment and to monitor for recurrence. However, efforts to use CA125 testing for early detection or to screen for ovarian cancer in healthy women have proven difficult, because CA-125 levels can rise for reasons unrelated to ovarian cancer (such as liver cirrhosis, menstruation and pregnancy). Large-scale studies on the appropriate use of this marker continue today.

1981

Oral contraceptives found to cut ovarian cancer risk

Oral contraceptives found to cut ovarian cancer risk

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Studies first begin suggesting that oral contraceptive use lowers the risk of developing ovarian cancer. Evidence continues to accumulate over the coming years, and in 2008, a review of 45 published studies concludes that "the pill" lowers ovarian cancer risk by 20 percent for every five years it is used. Authors of the 2008 study estimate that oral contraceptives had prevented some 200,000 ovarian cancers and 100,000 deaths worldwide in the 50 years since oral contraceptives were introduced, and may currently prevent 30,000 new cases of ovarian cancer each year.

1978

Cisplatin approved for advanced ovarian cancer

Cisplatin approved for advanced ovarian cancer

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The chemotherapy drug cisplatin becomes available as a treatment for newly-diagnosed ovarian cancer, as well as ovarian cancer that persists after initial therapy, after trials show the drug decreases the size of patients' tumors. Later research leads to the development of new and more effective combination chemotherapy regimens that utilize cisplatin, such as cyclophosphamide (Cytoxan) plus cisplatin and a regimen called CHAP, which combines the drugs doxorubicin (Adriamycin), hexamethylmelamine, cyclophosphamide and cisplatin.

First effective combination chemotherapy regimen for ovarian cancer

First effective combination chemotherapy regimen for ovarian cancer

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Researchers led by Robert Young develop a combination chemotherapy regimen for advanced ovarian cancer, known as HEXACAF. This regimen combines the drugs hexamethylmelamine, cyclophosphamide (Cytoxan), methotrexate and 5-fluorouracil, each of which was already known to have an effect on ovarian cancer tumors. The combined regimen is found to benefit more patients, cause greater tumor shrinkage and extend survival by more than 12 months over single-drug chemotherapy with melphalan (Alkeran), an earlier drug commonly used to treat advanced ovarian cancer. However, this new combination regimen causes significantly more side effects.