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New frontline treatments needed for Hodgkin lymphoma

With these complications in mind, stabilizing the effects between improved efficacy and minimizing the toxicities associated with current frontline treatments needs to be a focus as new therapies are developed.

For young patients specifically, minimizing toxicities is crucial, as many will have a lifetime ahead of them after Hodgkin lymphoma and will want to avoid the risks associated with current treatments including lung disease, heart disease and infertility.8-10,12-15,22

Treating elderly patients can also be challenging due to their reduced ability to tolerate aggressive frontline treatment and multi-agent chemotherapy, which causes inferior survival outcomes when compared to younger patients.23-25 These secondary effects can affect a patient’s quality of life8-9,12,14-15,22,26-28  and exacerbate preexisting conditions commonly experienced by those undergoing treatment, including long-term fatigue, chronic medical and psychosocial complications, and general deterioration in physical well-being.22

Studies have shown that most relapses after ASCT typically occur within 2 years.29 After a relapse, the patient may endure a substantial physical and psychological burden due to the need for additional treatment, impacting quality of life for both the patient and their caregiver.22,26,30

 Goals of clinical research

Despite its recognition as a highly treatable cancer, newly diagnosed Hodgkin lymphoma remains incurable in up to 30% of patients with advanced disease.7-10 Though current therapies seek to achieve remission and extend the lives of patients, it is often at the cost of treatment-related toxicities and side effects that can significantly reduce quality of life.

Moving forward, it is critical that these gaps in treatment are addressed in new frontline treatments that aim to benefit patients, including those with advanced stage disease, while reducing short-term and long-term toxicities. 

 Acknowledgements: The author would like to acknowledge the W2O Group for their writing support, which was funded by Millennium Pharmaceuticals Inc., a wholly owned subsidiary of Takeda Pharmaceutical Company Limited.

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1American Cancer Society. What Are the Key Statistics About Hodgkin Disease? https://www.cancer.org/cancer/hodgkin-lymphoma/about/key-statistics.html. Accessed February 16, 2017.

2Ries LAG, Young JL, Keel GE, Eisner MP, Lin YD, Horner M-J (editors). SEER Survival Monograph: Cancer Survival Among Adults: U.S. SEER Program, 1988-2001, Patient and Tumor Characteristics. National Cancer Institute, SEER Program, NIH Pub. No. 07-6215, Bethesda, MD, 2007.

3American Cancer Society. Survival Rates for Hodgkin Disease by Stage. https://www.cancer.org/cancer/hodgkin-lymphoma/detection-diagnosis-staging/survival-rates.html. Accessed February 16, 2017.

4Fermé C, et al. New Engl J Med, 2007.357:1916–27.

5Sureda A, et al. Ann Oncol, 2005;16: 625–633.

6Majhail NS, et al. Biol Blood Marrow Transplant, 2006;12:1065–1072.

7Gordon LI, et al. J Clin Oncol, 2013;31:684-691.

8Carde P, et al. J Clin Oncol, 2016;34(17):2028-2036.

9Engert A, et al. J Clin Oncol, 2009;27(27):4548-4554

10Viviani S, et al. New Engl J Med, 2011;365(3):203-212.

11Sklar C, et al. J Endocrinology & Metabolism, 2000;85(9):3227-3232

12Behringer K, et al. J Clin Oncol, 2013;31:231-239.

13Borchmann P, et al. J Clin Oncol, 2011;29(32):4234-4242.

14Duggan DB, et al. J Clin Oncol, 2003;21(4):607-614.

15Johnson P, McKenzie H. Blood, 2015;125(11):1717-1723.

16Maddi RN, et al. Indian J Medical and Paediatric Oncology, 2015;36(4):255-260

17Ansell SM. American Journal of Hematology, 2014;89: 771–779.

18Merli F, et al. J Clin Oncol, 34:1175-1181.

19Johnson P, et al. N Engl J Med. 2016;3‌74:24‌19‑24‌29

20American Cancer Society. Treating Hodgkin Disease: Radiation Therapy for Hodgkin Disease. https://www.cancer.org/cancer/hodgkin-lymphoma/treating/radiation.html. Accessed January 30, 2017.

21Adams MJ, et al. J Clin Oncol, 2004; 22: 3139–48.

22Khimani N, et al. Ann Oncol, 2013;24(1):226-230.

23Engert A, et al. J Clin Oncol, 2005;23(22):5052-60.

24Evens AM, et al. Br J Haematol, 2013;161: 76–86.

25Janssen-Heijnen ML, et al. Br J Haematol, 2005;129:597-606.

26Ganz PA et al. J Clin Oncol, 2003;21(18):3512-3519.