History of cancer chemotherapy

The first efforts (1940–1950)

The beginnings of the modern era of cancer chemotherapy can be traced directly to the discovery of nitrogen mustard, a chemical warfare agent, as an effective treatment for cancer. Two pharmacologists, Louis S. Goodman and Alfred Gilman were recruited by the United States Department of Defense to investigate potential therapeutic applications of nitrogen mustard anticancer chemotherapeutic), into a patient with non-Hodgkin's lymphoma. They observed a dramatic reduction in the patient's tumour masses. Although this effect lasted only a few weeks, this was the first step to the realization that cancer could be treated by pharmacological agents (Goodman et al 1946).

Another leap forward - The antifolates

Shortly after World War II, a second approach to drug therapy of cancer began. Sidney Farber, a pathologist at Harvard Medical School, studied the effects of amethopterin (now methotrexate) were antagonistic to folic acid, and blocked the function of folate-requiring enzymes. When administered to children with ALL in the late 1940s, these agents became the first drugs to induce remission in children with ALL. Remissions were brief, but the principle was clear — antifolates could suppress proliferation of malignant cells, and could thereby re-establish normal bone-marrow function. It is worth noting that Farber met resistance to conducting his studies at a time when the commonly held medical belief was that leukemia was incurable, and that the children should be allowed to die in peace. Afterwards, Farber's 1948 report in the New England Journal of Medicine was met with incredulity and ridicule.

Remarkably, a decade later at the National Cancer Institute, Roy Hertz and Min Chiu Li discovered that methotrexate treatment alone could cure choriocarcinoma (1958), a germ-cell malignancy that originates in trophoblastic cells of the placenta. This was the first solid tumour to be cured by chemotherapy.

6-MP, vinca alkaloids and a National Treatment Effort by the US

Joseph Burchenal, at Memorial Sloan-Kettering Cancer Center in New York, with Farber's help, started his own methotrexate study and found the same effects. He then decided to try and develop anti-metabolites in the same way as Farber, by making small changes in a metabolite needed by a cell to divide. With the help of 6-mercaptopurine (6-MP), which was subsequently shown to be a highly active antileukemic drug.

The microtubule polymerization, and therefore cell division.

The United States Congress created a National Cancer Chemotherapy Service Center (NCCSC) at the NCI in 1955 in response to early successes. This was the first federal programme to promote drug discovery for cancer - unlike now, most pharmaceutical companies were not yet interested in developing anticancer drugs. The NCCSC developed the methodologies and crucial tools (like cell lines and animal models) for chemotherapeutic development.

Combination chemotherapy

  In 1965, a major break-through in cancer therapy occurred. James Holland, Emil Freireich, and Emil Frei hypothesized that cancer chemotherapy should follow the strategy of antibiotic therapy for tuberculosis with combinations of drugs, each with a different mechanism of action. Cancer cells could conceivably mutate to become resistant to a single agent, but by using different drugs concurrently it would be more difficult for the tumor to develop resistance to the combination. Holland, Freireich, and Frei simultaneously administered prednisone — together referred to as the POMP regimen — and induced long-term remissions in children with acute lymphoblastic leukaemia (ALL). With incremental refinements of original regimens, using randomized clinical studies by St. Jude Children's Research Hospital, the Medical Research Council in the UK (UKALL protocols) and German Berlin-Frankfurt-Münster clinical trials group (ALL-BFM protocols), ALL in children has become a largely curable disease.

This approach was extended to the lymphomas in 1963 by Vincent T. DeVita and George Canellos at the NCI, who ultimately proved in the late 1960s that nitrogen mustard, vincristine, procarbazine and prednisone — known as the MOPP regimen — could cure patients with Hodgkin's and non-Hodgkin's lymphoma. Currently, nearly all successful cancer chemotherapy regimens use this paridigm of multiple drugs given simultaneously.

Adjuvant therapy

As predicted by studies in animal models, drugs were most effective when used in patients with tumours of smaller volume. Another important strategy developed from this - if the tumour burden could be reduced first by surgery, then chemotherapy may be able to clear away any remaining malignant cells, even if it would not have been potent enough to destroy the tumor in its entirety. This approach was termed "adjuvant therapy".

Emil Frei first demonstrated this effect - high doses of methotrexate prevented recurrence of osteosarcoma following surgical removal of the primary tumour. 5-fluorouracil, an inhibitor of DNA synthesis, was later shown to improve survival when used as an adjuvant to surgery in treating patients with colon cancer. Similarly, the landmark trials of Bernard Fisher, chair of the National Surgical Adjuvant Breast and Bowel Project, and of Gianni Bonadonna, working in the Istituto Nazionale Tumori di Milano, Italy, proved that adjuvant chemotherapy after complete surgical resection of breast tumours significantly extended survival — particularly in more advanced cancer.

Drug Discovery at the NCI and elsewhere

Zubrod's initiatives

  In 1956, C. Gordon Zubrod, who had formerly led the development of antimalarial agents for the United States Army, took over the Division of Cancer Treatment of the NCI and guided development of new drugs. In the two decades that followed the establishment of the NCCSC, a large network of cooperative clinical trial groups evolved under the auspices of the NCI to test anticancer agents. Zubrod had a particular interest in natural products, and established a broad programme for collecting and testing plant and marine sources, a controversial programme that led to the discovery of taxanes (in 1964) and camptothecins (in 1966). Both classes of drug were isolated and characterized by the laboratory of Monroe Wall at the Research Triangle Institute.

The taxanes

Bristol-Myers Squibb, was exclusively marketed by BMS who went on to make over a billion dollars profit from Taxol, despite the bulk of the initial work being funded by US taxpayers.^[POV]

The camptothecins

Another drug class originating from the NCI was the camptothecins. Food and Drug Administration (FDA) approval for the treatment of colon cancer. Later, this agent would also be used to treat lung and ovarian cancers.

Platinum-based agents

carboplatin, a cisplatin derivative with broad antitumour activity and comparatively less nephrotoxicity.

Nitrosoureas

A second group with an NCI contract, led by John Montgomery at the Southern Research Institute, synthesized nitrosoureas, an alkylating agent which cross-links DNA. Fludarabine phosphate, a purine analogue which has become a mainstay in treatment of patients with chronic lymphocytic leukaemia, was another similar development by Montgomery.

Anthracyclines and epipodophyllotoxins

Other effective molecules also came from industry during the period of 1970 to 1990, including DNA synthesis.

Supportive care during chemotherapy

As is obvious from their origins, the above cancer chemotherapies are essentially poisons. Patients receiving these agents experienced severe side-effects that limited the doses which could be administered, and hence limited the beneficial effects. Clinical investigators realized that the ability to manage these toxicities was crucial to the success of cancer chemotherapy.

Several examples are noteworthy. Many chemotherapeutic agents cause profound suppression of the bone marrow. This is reversible, but takes time to recover. Support with antibiotics in case of infection during this period is crucial to allow the patient to recover.

Several practical factors are also worth mentioning. Most of these agents caused very severe nausea (termed chemotherapy-induced nausea and vomiting (CINV) in the literature) which, while not directly causing patient deaths, was unbearable at higher doses. The development of new drugs to prevent nausea (the prototype of which was ondansetron) was of great practical use, as was the design of indwelling intravenous catheters (e.g. Hickman lines and PICC lines) which allowed safe administration of chemotherapy as well as supportive therapy.

A period of quiet

With the successes of combination chemotherapy and the discovery of many new agents, there was a feeling at this time that all cancers could be treated, if only one could administer the correct combination of drugs, at the correct doses and at the correct intervals. A search continued, with the pharmaceutical industry screening for new compounds and clinical scientists performing elaborate clinical trials with ever more complex combinations and higher doses.

One important contribution during this period was the discovery of a means that allowed the administration of previously lethal doses of chemotherapy. The patient's bone marrow was first harvested, the chemotherapy administered, and the harvested marrow then returned to patient a few days later. This approach, termed autologous bone marrow transplantation, was initially thought to be of benefit to a wide group of patients, including those with advanced breast cancer. However, rigorous studies have failed to confirm this benefit, and autologous transplantation is no longer widely used for solid tumors. The proven curative benefits of high doses of chemotherapy afforded by autologous bone marrow rescue are limited to Hodgkins disease patients who had failed therapy with conventional combination chemotherapy. However, autologous transplantation continues to be used as a component of therapy for a number of hematologic malignancies.

The hormonal contribution to several categories of breast cancer subtypes was recognized during this time, leading to the development of pharmacological modulators (e.g. of tamoxifen.

Although clinical oncologists appeared to have hit a wall at this point in terms of results, under the surface something extraordinary was happening: namely, elucidation of the mechanisms underlying cancer. Understanding of the machinery of the cell and advances in techniques to probe perturbations in its function allowed researchers to understand the genetic nature of cancer. It is important to realize that prior to this point, chemotherapeutic agents had been discovered essentially by chance, or by inhibiting the metabolic pathways crucial to cell division, but none were particularly specific to the cancer cell.

Targeted therapy

 

Molecular and genetic approaches to understanding cell biology uncovered entirely new signalling networks that regulate cellular activities such as proliferation and survival. Many of these networks were found to be radically altered in cancer cells, and these alterations had a genetic basis caused by a chance somatic mutation.

Tyrosine kinase inhibitors

The classic example of targeted development is imatinib was found to have the most promise in laboratory experiments. First Druker and then other groups worldwide demonstrated that when this small molecule is used to treat patients with chronic-phase CML, 90% achieve complete haematological remission. It is hoped that molecular targeting of similar defects in other cancers will have the same effect.

Monoclonal antibodies

Another branch in targeted therapy is the increasing use of Rituximab, a drug used to treat lymphomas, is a prime example.

Concluding Comments

The discovery that certain toxic chemicals administered in combination can cure certain cancers ranks as one of the greatest in modern medicine. Childhood ALL, testicular cancer, and Hodgkins disease, previously universally fatal, are now generally curable diseases. The early revolution in cancer therapy was largely a North American experience, powered by an optimistic and forward-looking United States Federal government, which funded the NCI with the same "big-idea" philosophy as the Apollo Program. In fact, it was only later that the pharmaceutical industry became heavily involved.

Conventional cytotoxic chemotherapy has shown the ability to cure some cancers, including testicular cancer, Hodgkin disease, non-Hodgkin lymphoma, and some leukemias. It has also proven effective in the adjuvant setting, in reducing the risk of recurrence after surgery for high-risk breast cancer, colon cancer, and lung cancer, among others. However, the hopes created by the dramatic initial success of cancer chemotherapy were not fully borne out, as conventional cytotoxic chemotherapy has fallen short of the high expectations of curing the most common cancers.

The overall impact of chemotherapy on cancer survival can be difficult to estimate, since improved cancer screening, prevention (e.g. anti-smoking campaigns), and detection all influence statistics on cancer incidence and mortality. In the United States, overall cancer incidence rates were stable from 1995 through 1999, while cancer death rates decreased steadily from 1993 through 1999.^[1] Again, this likely reflects the combined impact of improved screening, prevention, and treatment. Nonetheless, cancer remains a major cause of illness and death, and conventional cytotoxic chemotherapy has proven unable to cure most cancers after they have metastasized.

New knowledge about the molecular biology of cancer and new tools to specifically target aberrant proteins are opening up new possibilities. The next two decades will see two competing strategies of cancer therapy: small molecular inhibitors and adoptive immunotherapy with re-programmed effector cells will match strengths in an attempt to finally cure cancer.

References

1. ^ Abeloff: Clinical Oncology, 3rd ed. Churchill Livingston, 2004. Pp 408-413.

• Goodman LS, Wintrobe MM, Dameshek W, Goodman MJ, Gilman A and McLennan MT. Nitrogen mustard therapy. Use of methyl-bis(beta-chloroethyl)amine hydrochloride and tris(beta-chloroethyl)amine hydrochloride for Hodgkin's disease, lymphosarcoma, leukemia, and certain allied and miscellaneous disorders. J Am Med Assoc 1946;105:475-476. Reprinted in JAMA 1984;251:2255-61. PMID 6368885.
• Papac RJ. Origins of cancer therapy. Yale J Biol Med 2001;74:391-8. PMID 11922186.
• Gilman A. The initial clinical trial of nitrogen mustard. Am J Surg 1963;105:574-8. PMID 13947966.
• Gilman A. The biological actions and therapeutic applications of the B-chloroethyl amines and sulfides. Science 1946;103:409–436.
• Farber S, Diamond LK, Mercer RD, Sylvester RF, Wolff JA. Temporary remissions in acute leukemia in children produced by folic antagonist, 4-aminopteroylglutamic acid (aminopterin). N Engl J Med 1948;238:787–793.
• Bonadonna G, Brusamolino E, Valagussa P, Rossi A, Brugnatelli L, Brambilla C, De Lena M, Tancini G, Bajetta E, Musumeci R, Veronesi U. Combination chemotherapy as an adjuvant treatment in operable breast cancer. N Engl J Med 1976;294:405-10. PMID 1246307.
• Li MC, Hertz R, Bergenstal DM. Therapy of choriocarcinoma and related trophoblastic tumors with folic acid and purine antagonists. N Engl J Med 1958;259:66–74. PMID 13566422.
• Jaffe N, Link MP, Cohen D, Traggis D, Frei E 3rd, Watts H, Beardsley GP, Abelson HT. High-dose methotrexate in osteogenic sarcoma. Natl Cancer Inst Monogr 1981;:201-6. PMID 6975438.
• Corbin AS, Buchdunger E, Pascal F, Druker BJ. Analysis of the structural basis of specificity of inhibition of the Abl kinase by STI571. J Biol Chem 2002;277:32214-32219. PMID 12077114.
• O'Brien SG, Guilhot F, Larson RA, Gathmann I, Baccarani M, Cervantes F, Cornelissen JJ, Fischer T, Hochhaus A, Hughes T, Lechner K, Nielsen JL, Rousselot P, Reiffers J, Saglio G, Shepherd J, Simonsson B, Gratwohl A, Goldman JM, Kantarjian H, Taylor K, Verhoef G, Bolton AE, Capdeville R, Druker BJ. Imatinib compared with interferon and low-dose cytarabine for newly diagnosed chronic-phase chronic myeloid leukemia. N Engl J Med 2003;348:994-1004. PMID 12637609.

External links

• http://www.laskerfoundation.org/reports/pdf/devita/combination_chemotherapy_hodgkins_disease_1970.pdf
• http://www.laskerfoundation.org/reports/pdf/devita/medical_progress_1973.pdf
• http://www.laskerfoundation.org/reports/pdf/devita/therapeutic_implications_new_biology_2000.pdf
• Cancer chemotherapy history