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Draft of Edits for History of the Treatment
editHigh-dose chemotherapy (HDC) with autologous bone marrow transplant (ABMT) was a treatment for advanced breast cancer developed in the 1980s[1], but the idea for HDC/ABMT was based on a previous leukemia treatment that emerged in the 1950s when E. Donnall Thomas had shown that bone marrow could be harvested from a person and transplanted into the same or another person.[2] The treatment of high-dose chemotherapy with autologous bone marrow transplant had serious side effects for the patient, including cardiac toxicity, sepsis, pulmonary failure, and nephrotoxicity, among others. Chronic consequences of the treatment included development of leukemias and lymphomas and heightened vulnerability to infections soon after the transplant. Randomized clinical trials reported treatment-mortality rates from 0% to 7% for women who received the HDC/BMT treatment, versus no such deaths within the control groups that received the typical chemotherapy regimen. [3]
In HDC, the bone marrow transplantation was used to maximise chemotherapeutic dosage. By harvesting and freezing bone marrow, then implanting the marrow after HDC, doctors were theoretically able to break through the frontier of toxicity; the so-called "red ceiling". Early proponents of the technique were George Canellos and Emil Frei of the Dana–Farber Cancer Institute, and William Peters, whom Frei had recruited to the institute in 1982.[4] Howard Skipper and Frank Schabel demonstrated efficacy in mouse models for megadose therapy in 1983.[5]
Frei and Peters developed the Solid Tumor Autologous Marrow Program (STAMP) regimen. Researchers in the National Cancer Institute (NCI) did not believe that the treatment would be effective and were wary of the consequences of this treatment. For example, George Canellos, one of the original members of the NCI, had noticed that a long-term side effect of megadose chemotherapy regimens was myelodysplasia, a condition that tended to progress to leukemia.[5] During the early stages of the STAMP clinical trial, the first patients were those who were hopeless cases — women with advanced, metastatic breast cancer that had already received, and did not respond to, existing treatments. However, about halfway through the trial, a previously untreated woman with metastatic breast cancer enrolled in the STAMP program, and many of Peters's colleagues began to take notice. The results of her treatment were unprecedented — her tumor and metastatic deposits had shrunk significantly. From then until the end of this preliminary clinical trial, Peters had transplanted and treated more cases and also obtained significant remissions similar to that of this woman's. They then believed that STAMP produced more durable remissions than those by conventional chemotherapy, and so Peters left to set up a randomized clinical trial at Duke University. [5]
By December 1984, 32 women had completed the Phase I study of the regimen, designed to investigate safety. The researchers proceeded with Phase II trials, which showed very promising results. However, only women who were healthier and responded better to conventional chemotherapy were eligible for the Phase II studies. The problem with Phase II studies was explained thus:
If you have a hundred patients and you give them a treatment applicable to all 100, and two are alive after 10 years, that is a 2% absolute survival rate. If you have 100 patients and you have a treatment applicable to 20 of the 100, and 20% of those 20 are alive after 10 years, that's only a 4% absolute survival rate, not a 20% survival rate.
— Gabriel N. Hortobagyi, M.D., Journal of the National Cancer Institute, July 5, 1995[6]
This selection bias makes the treatment look better, because candidates who would have fared better under any condition were selected. To belabour the point further Hortobagyi, using data from the University of Texas M. D. Anderson Cancer Center in Houston, reported in May 1995 that those eligible for high-dose chemotherapy survived 65% longer on conventional chemotherapy than those who would not have been eligible for the protocol.[6] Subsequent research on doxorubicin-containing protocols for the treatment of metastatic breast cancer, found that median progression-free survival (PFS) was 16 and 8 months and median overall survival (OS) was 30 and 17 months, respectively for women who met eligibility criteria versus those who did not, when all received the conventional treatment.[7]
Stage III randomised controlled trials were needed to confirm the benefit of HDC/BMT.[6] In 1985, William Peters left the National Cancer Institute to set up the trial at Duke University in North Carolina. He persuaded the Cancer and Leukemia Group B (CALGB) to sponsor a multicenter, randomised controlled trial.[5]
Clinical use of this treatment was driven by women with breast cancer and advocacy groups, such as ACT UP; they believed that the FDA treatment approval process was too slow.[5] Health Net's denial of Nelene Fox's transplant — a case involving insurance coverage of HDC/ABMT — ignited a public reaction and prompted change in access to treatment. [5] Unlike new drugs, which are evaluated and approved by the Food and Drug Administration (FDA), medical procedures are not officially regulated by any agency nor does there exist any statutory requirement to serve a similar function.[8] Around 30,000 women received the HDC/ABMT procedure in the 1989-2002 period; the medical profession was divided in its commitment to clinical trials and sanctioned the procedure as better than existing treatment before there was proof from the scientific community — of the women who received the procedure, only about 1000 of them were enrolled in randomized clinical trials in the United States.[9] In contrast, repeated assessments concluded that existing data did not support claims of the effectiveness of HDC/ABMT, leading to the high-priority phase 3 clinical trials in 1990-1991, which were supported by the effort of the National Cancer Institute (NCI), skeptical scientists, health insurance companies, and cancer groups.[10]
The results of clinical trials ended up showing that HDC/BMT for breast cancer was not an effective treatment and did not increase survival rates compared to existing treatment. These conclusions were drawn from a combination of studies, including that of Peters and a large study executed by the Netherlands Cancer Institute, both of which drew the conclusion that HDC/BMT was not superior to standard breast cancer treatment. Another study, done by researcher Werner Bezwoda, reached the conclusion that the treatment was effective, but his study was later discredited due to scientific misconduct, including the falsification of data. [11] The treatment was discontinued for breast cancer, although it is still used to combat other types of cancers, like leukemias and lymphomas. [12]
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Draft of Edits for Funding mechanisms and litigation
editWith the rise in popularity of this treatment, more and more women with breast cancer wanted it to be available to the public — not just offered in clinical trials. Inspired by HIV/AIDS activism, several cancer advocacy groups began to lobby for the general availability of HDC/BMT. This drew potential patients away from clinical trials, such as that of Peters. As a result, by the late 1980s, most hospitals and private clinics had transplant wards to provide HDC/BMT to those women who sought it. [5]
Treatment remained exclusive of most women due to high cost; $50,000 to $400,000 per patient. As long as HMOs regarded the regime as experimental or investigational, there was no contractual obligation to cover it. While, in the mid-1980s, fewer than 100 bone marrow transplants a year were performed on breast cancer patients,[13] the uptake of HDC/BMT increased six-fold between January 1, 1989 and June 30, 1995. Between those dates 19,291 autotransplants were reported to the Autologous Blood and Marrow Transplant Registry; 5,886 were for breast cancer. After 1992, breast cancer was the most common indication for autotransplant. Only 11% of women with stage 2/3 disease and less than one percent of those with stage 4 disease participated in randomized trials.[14] The International Bone Marrow Transplant Registry estimated that at least 4,000 women were treated with HDC/BMT, from 1989 through 1993, with fewer than 10% doing so within trials. Based on the unsubstantiated belief in the success of HDC/BMT, women refused to be randomised to conventional treatment conditions, and doctors were not reimbursed for additional time spent administering protocols.[6] Simultaneously, the treatment was highly profitable for hospitals who, by 1995, were billing the procedure at $80,000 to $100,000, at a cost to the hospital of less than $60,000.[13] Hospitals, like Beth Israel in Boston, devoted entire floors to transplant units.[5]
In 1993, a landmark court case, Fox v. Health Net.[5] changed the existing policy of HMOs toward paying for the treatment. A public-school teacher named Nelene Hiepler Fox (January 9, 1953 – April 22, 1993) was diagnosed with breast cancer in 1991.[15]: 74 She requested her HMO to pay for High-Dose Chemotherapy and Bone Marrow Transplant (HDC/BMT) to treat her cancer. Her health maintenance organization, Health Net, declined her request, stating this therapy was an unproven, experimental therapy. Fox's brother, Mark Hiepler, took her HMO, Health Net, to court to force them to pay for HDC/BMT, which they had refused to do. Despite raising $220,000 herself and receiving the treatment regime, Fox died on April 22, 1993. Mark Hiepler sought damages from Health Net for delaying his sister's treatment. On December 28, Fox's family was awarded $89 million by a Californian jury, including $12.1 for bad faith and reckless infliction of emotional distress, and $77 million in punitive damages.[13] Jim Fox and the estate of Nelene Fox v. Health Net is considered a watershed case in that most health insurers subsequently began approving HDC/BMT for advanced breast cancer.[5]
Between 1988 and 2002, 86 cases were filed to force HMOs to pay for transplants, of which 47 were successful.[5] The legislatures of Massachusetts, New Hampshire, Virginia, and Minnesota mandated insurance coverage for all high-dose chemotherapy with ABMT or peripheral blood stem cell (PBSCT) transplant for women with breast cancer.[6]
The media, both newspapers and television, played an important role in promoting HDC/ABMT to people, especially through their portrayals of women with breast cancer, which ignited public protests and prompted legislative change that mandated insurance coverage of HDC/ABMT. For example, the Boston Globe published a story regarding Charlotte Turner, a woman with breast cancer whose HMO would not pay for her treatment, which spurred the lobbying of the Massachusetts state legislature. In response to the lobbying and public pressure generated by the story, the Massachusetts state legislature passed legislation requiring HMOs to cover the HDC/BMT treatment in late 1993.[16] Journalists portrayed HDC/ABMT as a miracle treatment, with patients playing the victims, doctors the saviors, and breast cancer and health insurers the villains.[17] Most articles made three major points: one, HDC was logical because if a little chemotherapy could treat early cases, then more chemotherapy was clearly needed for more advanced cases; two, HDC/ABMT was the only hope for someone an advanced breast cancer; three, the main barrier between someone and their potential cure was money, which health insurance companies did not want to spend to cover the treatment.[18] This led to many people having the wrong impression of HDC/ABMT, which in reality, was a treatment that was not supported by clinical trials. As a result, patients pushed for the treatment to be administered more widely and to be covered by insurance companies. [19]
The reluctance of insurance organizations to pay for the HDC/BMT treatment stemmed from the difference in patients'/doctors' and researchers' opinions of the treatment. [20] Academic researchers wanted to wait for the results of the clinical trials, while breast cancer oncologists and bone marrow transplanters supported the procedure. [21]At the time, the clinical trials on the effectiveness and benefits of this treatment diverged greatly: the trials by Peters in the U.S. and other large research hospitals in Europe reached the conclusion that the treatment had at most modest results — even negative results – regarding the superiority of this high-dose chemotherapy with autologous bone marrow transplant. However, a study by the researcher Werner Bezwoda showed promising benefits of this treatment – although his study was later confirmed to have falsified data. In addition, there was already a lot of positive publicity surrounding the treatment, and 79% of oncologists believed that HDC/BMT was an appropriate treatment for women with locally advanced breast cancer. In fact, the number of women who received this treatment increased by about 8000 between 1990 and 1999. [22] This disparity was one of the reasons HMOs held back from covering high-dose chemotherapy with autologous bone marrow transplant; if a treatment is expensive and not clinically proven to be beneficial, health organizations can decline to pay for the treatment, regardless of patient protests.
General strategies for plaintiffs included arguing that HDC/BMT was the patient's only chance for survival, patient choice from a physician's recommendation, and portraying the HMO in unfavorable terms to the jury. General strategies for the defendant, or insurer, included stating that the coverage plans did not believe HDC/BMT was in the patient's best interests because of the high mortality rates and reduced quality of life; stating that the treatment had not been clinically proven to be beneficial and more effective than existing treatments – the results of the clinical trials had not yet been reported. [23]
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Draft of Edits for Status in breast cancer
editUtilization of HDC/ABMT for breast cancer decreased sharply after the negative reports revealed at the ASCO meeting in 1999.[24] In addition, a mixture of wins and losses from litigation lawsuits over health insurance corporations' coverage of the treatment influenced the decline of the treatment, because technology assessments exhibited in court had concluded that the data did not support claims that HDC/ABMT was better than conventional therapy. [25] Due to the decreased quality of life during and following HDC/BMT compared to that of conventional breast cancer treatment as well as the minimal extension of life, many physicians and the majority of people believe that the treatment is ineffective and too toxic. [26] In addition, the finding that the Bezwoda study was false further drove the point that the treatment was not of significant benefit compared to standard treatment, because it was the only study that suggested a degree of recurrence-free survival benefit from HDC/BMT. The other randomized trials performed in the Netherlands and the United States, for example, all supported the opposite point: that this treatment is not a significant improvement over then-current conventional breast cancer treatment. [26] High-dose therapy is also associated with an increase in second malignancies, including myelodysplastic syndromes and leukemias.[5] When reflecting on the story of HDC/ABMT, especially on the widespread treatment and the lack of scientific data, many researchers and medical professionals stated that HDC/ABMT should have never been made accessible to the public without sound scientific data and conclusions; they view it as a period of shame for cancer medicine. [27]
A 2011 overview of six randomized trials concluded:
Overall survival of patients with metastatic breast cancer in the six randomized trials was not significantly improved by high-dose chemotherapy; any benefit from high doses was small. No identifiable subset of patients seems to benefit from high-dose chemotherapy.
— Berry et al., Journal of Clinical Oncology, August 20, 2011[28]
While HDC/ABMT has been discontinued, a rising therapy for cancer that is similar to HDC/BMT is CAR-T cell therapy, which is a type of immunotherapy.[29] CAR T therapy collects the patient's own immune cells to treat their cancer, which is a similar idea to that behind HDC/BMT. Currently, there exist FDA-approved CAR T-cell therapies for children with acute lymphoblastic leukemia and adults with advanced lymphomas, but clinical trials are still in development as to whether CAR T-cell therapy can be effective against solid tumor cancers, like breast cancer. [30] In a similar way to HDC/BMT, the treatment was first introduced for people for whom all other treatments have stopped working. [31] The first women to participate in Peters's clinical trial were also those who had advanced breast cancer and for whom other treatments had stopped working.[5]
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Draft High-dose chemotherapy and bone marrow transplant for other cancers
editWhile the high-dose chemotherapy and bone marrow transplant treatment is known for its impact on breast cancer, the treatment is presently used to treat other types of cancer, including testicular cancer, neuroblastoma, multiple myeloma, and various types of leukemias and lymphomas, like Hodgkin and non-Hodgkin Lymphoma. [32]
There are two types of stem cell (bone marrow) transplants: autologous stem cell transplant, where the person's own stem cells are collected, frozen, and stored before the chemotherapy regimen and transfused back into their body by IV after chemotherapy, and allogeneic stem cell transplant, where the stem cells come from a donor that matches the person's HLA type to prevent the risk of graft-versus-host disease.
Autologous stem cell transplants are used more often to treat lymphoma, but this may not be an option if the person's lymphoma has metastasized to their bone marrow or blood. Allogeneic stem cell transplants have side effects that can make it hard for the patient to tolerate the treatment.[33] In addition, since the bone marrow produces cells that are needed by the immune system to fight off infection, people who undergo the treatment are advised to take precautions regarding sanitation and are often placed in private hospital rooms with special air filters to reduce possibility of infection. Soon after treatment, patients have low red and white blood cell counts, and are thus usually placed on antibiotics to keep them from getting infections. Side effects of the treatment include heart, lung, stomach, kidney, or liver problems, among others. [34]
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High-dose chemotherapy and bone marrow transplant Article
editWe have studied this as "autologous bone marrow transplantation". I plan to focus on how this was used in breast cancer, like we talked about in class, and possibly on how it is used in other diseases, specifically cancer. I am hoping to add content about why this treatment for breast cancer surfaced (because doctors wanted to up the dose of chemotherapy without it being fatal to stem cells), the clinical trials that followed, who pioneered the treatment, and the results of the treatment. In addition, I may touch on how this treatment is used to treat blood cancers, i.e. lymphoma. Working List of Sources: Mukherjee, Siddhartha. The Emperor of All Maladies: A Biography of Cancer. New York: Scribner, 2010. Print. https://www.cancer.org/cancer/non-hodgkin-lymphoma/treating/bone-marrow-stem-cell.html https://www.mskcc.org/cancer-care/diagnosis-treatment/cancer-treatments/blood-stem-cell-transplantation/autologous https://www.cancer.gov/about-cancer/treatment/types/stem-cell-transplant/stem-cell-fact-sheet https://www.cancer.org/treatment/treatments-and-side-effects/treatment-types/stem-cell-transplant/process.html http://med.stanford.edu/news/all-news/2011/07/survival-of-stage-iv-breast-cancer-patients-improves-with-stem-cell-treatment-study-finds.html https://www.healthaffairs.org/doi/abs/10.1377/hlthaff.20.5.101
Article Evaluation
editI chose to evaluate the Wikipedia article on the Hallmarks of Cancer. While reading this article, I noticed that all the information in the article is relevant to the subject, and that all important conclusions are statements are cited. This article is also neutral; the authors do not express their opinions, but do reference criticism from credible scientific journals like Nature Reviews Cancer. The "bias" given by the "Criticism" section is consistently cited and mentioned as a direct conclusion from a credible source. There is not much information on popular criticism or praise, but both are referenced: the Wikipedia article talks about how the original Hallmarks of Cancer article was published and that as of March 2011, was Cell's most cited article. The links to the citations I checked all direct me to legitimate scientific articles. The sources for the citations I read all supported the claims in the article. The last time this article was edited was in November 2017, but this was a minor edit. In addition, all of the talk in the Talk page is from 2011. Thus, I believe that information can be added about present viewpoints on the Hallmarks of Cancer — including new criticisms and/or praise from credible scientific journals, and new information that has arisen on this subject and its implications for the modern perspective on how cancer works. The Wikipedia article on the Hallmarks of Cancer is similar to what we discussed in class, but it would perhaps benefit the length and depth of the article if more scientific background were added to each hallmark.
Content Gap Discussion
editA content gap is when people look for information (on Wikipedia) and do not find it. These content gaps often include academic topics, and are most likely not "Featured" or "Good" articles on Wikipedia, which are articles that the community has already vetted — they come from a reliable set of sources and usually meet at high standards of writing. A reason a content gap may arise is that the subject or information is controversial and does not have reliable and unbiased sources, so the information was not able to be published. Another reason is that the information may be so new that not many outside sources have published about it (which leads to lack of citations) or that the volunteers writing the article do not yet have enough of an established understanding of the information to summarize it on Wikipedia. Wikipedia is written by volunteers, who try to improve articles on areas they are interested in. They should be unbiased – or at least write without bias – and reference all information to a credible source. To be unbiased on Wikipedia means that the written information is subjective and encompasses all possible viewpoints from reliable sources. The information should not have any of the writer's opinion in it, nor should it only reflect one point of view (even if cited). This is similar to my definition of bias, which is when a person's viewpoint on an area influences how they view information relating to that subject or on how they talk about the subject.
- ^ Cite error: The named reference
Weiss
was invoked but never defined (see the help page). - ^ Thomas ED, Lochte HL, Lu WC, Ferrebee JW (12 September 1957). "Intravenous infusion of bone marrow in patients receiving radiation and chemotherapy". The New England Journal of Medicine. 257: 491–496. doi:10.1056/NEJM195709122571102. PMID 13464965.
- ^ Mello, Michelle; Brennan, Troyen (September 2001). "The Controversy Over High-Dose Chemotherapy With Autologous Bone Marrow Transplant for Breast Cancer". Health Affairs. 20 (5). PMID 11558695.
{{cite journal}}
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(help) - ^ Hayes, Daniel (6 September 2007). "False Hope: Bone Marrow Transplantation for Breast Cancer". The New England Journal of Medicine. 357: 1059–1060. doi:10.1056/NEJMbkrev58584. Retrieved 23 December 2012.
- ^ a b c d e f g h i j k l m Mukherjee, Siddhartha (2011). The Emperor of All Maladies. HarperCollins Publishers. ISBN 9780007435814.
- ^ a b c d e Smigel, Kara (5 July 1995). "Women flock to ABMT for breast cancer without final proof". Journal of the National Cancer Institute. 87 (13): 953–5. doi:10.1093/jnci/87.13.952. Retrieved 24 December 2012.
- ^ Rahman, Z. U.; D. K. Frye; A. U. Buzdar; T. L. Smith; L. Asmar; R. E. Champlin; G. N. Hortobagyi (October 1997). "Impact of selection process on response rate and long-term survival of potential high-dose chemotherapy candidates treated with standard-dose doxorubicin-containing chemotherapy in women with metastatic breast cancer". Journal of Clinical Psychology. 15 (10): 3171–3177. doi:10.1200/jco.1997.15.10.3171. PMID 9336352. Retrieved 24 December 2012.
- ^ Rettig, Richard (2007). False Hope: Bone Marrow Transplantation for Breast Cancer. New York: Oxford University Press.
- ^ Rettig, Richard (2007). False Hope: Bone Marrow Transplantation for Breast Cancer. New York: Oxford University Press.
- ^ Rettig, Richard (2007). False Hope: Bone Marrow Transplantation for Breast Cancer. New York: Oxford University Press.
- ^ Mello, Michelle; Brennan, Troyen (September 2001). "The Controversy Over High-Dose Chemotherapy With Autologous Bone Marrow Transplant for Breast Cancer". Health Affairs. 20 (5). PMID 11558695.
{{cite journal}}
:|access-date=
requires|url=
(help) - ^ "Blood-Forming Stem Cell Transplants". National Cancer Institute. National Cancer Institute. Retrieved March 2, 2018.
- ^ a b c Brownlee, Shannon; Winters, Dan (1 August 2002). "Bad Science and Breast Cancer". Discover Magazine. Retrieved 24 December 2012.
- ^ Antman KH, Rowlings PA, Vaughan WP, Pelz CJ, Fay JW, Fields KK, Freytes CO, Gale RP, Hillner BE, Holland HK, Kennedy MJ, Klein JP, Lazarus HM, McCarthy PL, Saez R, Spitzer G, Stadtmauer EA, Williams SF, Wolff S, Sobocinski KA, Armitage JO, Horowitz MM (May 1997). "High-dose chemotherapy with autologous hematopoietic stem-cell support for breast cancer in North America". Journal of Clinical Oncology. 15 (5): 1870–1879. doi:10.1200/JCO.1997.15.5.1870. Retrieved 23 December 2012.
- ^ Cite error: The named reference
Rettig
was invoked but never defined (see the help page). - ^ Mello, Michelle; Brennan, Troyen (September 2001). "The Controversy Over High-Dose Chemotherapy With Autologous Bone Marrow Transplant for Breast Cancer". Health Affairs. 20 (5). PMID 11558695.
{{cite journal}}
:|access-date=
requires|url=
(help) - ^ Rettig, Richard (2007). False Hope: Bone Marrow Transplantation for Breast Cancer. New York: Oxford University Press.
- ^ Rettig, Richard (2007). False Hope: Bone Marrow Transplantation for Breast Cancer. New York: Oxford University Press.
- ^ Rettig, Richard (2007). False Hope: Bone Marrow Transplantation for Breast Cancer. New York: Oxford University Press.
- ^ Mello, Michelle; Brennan, Troyen (September 2001). "The Controversy Over High-Dose Chemotherapy With Autologous Bone Marrow Transplant for Breast Cancer". Health Affairs. 20 (5). PMID 11558695.
{{cite journal}}
:|access-date=
requires|url=
(help) - ^ Rettig, Richard (2007). False Hope: Bone Marrow Transplantation for Breast Cancer. New York: Oxford University Press.
- ^ Mello, Michelle; Brennan, Troyen (September 2001). "The Controversy Over High-Dose Chemotherapy With Autologous Bone Marrow Transplant for Breast Cancer". Health Affairs. 20 (5). PMID 11558695.
{{cite journal}}
:|access-date=
requires|url=
(help) - ^ Rettig, Richard (2007). False Hope: Bone Marrow Transplantation for Breast Cancer. New York: Oxford University Press.
- ^ Rettig, Richard (2007). False Hope: Bone Marrow Transplantation for Breast Cancer. New York: Oxford University Press.
- ^ Rettig, Richard (2007). False Hope: Bone Marrow Transplantation for Breast Cancer. New York: Oxford University Press.
- ^ a b Rodenhuis, S. (October 2000). "The Status of High-Dose Chemotherapy in Breast Cancer". The Oncologist. 5 (5): 369–375. doi:10.1634/theoncologist.5-5-369. Retrieved 26 December 2012.
- ^ Rettig, Richard (2007). False Hope: Bone Marrow Transplantation for Breast Cancer. New York: Oxford University Press.
- ^ Berry, D. A.; Ueno, N. T.; Johnson, M. M.; Lei, X.; Caputo, J.; Smith, D. A.; Yancey, L. J.; Crump, M.; Stadtmauer, E. A.; Biron, P.; Crown, J. P.; Schmid, P.; Lotz, J.-P.; Rosti, G.; Bregni, M.; Demirer, T. (20 August 2011). "High-Dose Chemotherapy With Autologous Hematopoietic Stem-Cell Transplantation in Metastatic Breast Cancer: Overview of Six Randomized Trials". Journal of Clinical Oncology. 29 (24): 3224–3231. doi:10.1200/JCO.2010.32.5936. PMC 4322116. PMID 21768454. Retrieved 26 December 2012.
- ^ "CAR T Cells: Engineering Patients' Immune Cells to Treat Their Cancers". National Cancer Institute. National Institutes of Health. Retrieved April 7, 2018.
- ^ "CAR T Cells: Engineering Patients' Immune Cells to Treat Their Cancers". National Cancer Institute. National Institutes of Health. Retrieved April 7, 2018.
- ^ "CAR T Cells: Engineering Patients' Immune Cells to Treat Their Cancers". National Cancer Institute. National Institutes of Health. Retrieved April 7, 2018.
- ^ "Blood-Forming Stem Cell Transplants". National Cancer Institute. National Cancer Institute. Retrieved March 2, 2018.
- ^ "High-Dose Chemotherapy and Stem-Cell Transplant for Non-Hodgkin Lymphoma". American Cancer Society. American Cancer Society. Retrieved March 2, 2018.
- ^ "What's It Like to Get a Stem Cell Transplant?". Stem Cell Transplant for Cancer. American Cancer Society. Retrieved March 2, 2018.