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Who cares for adolescents and young adults with cancer in Brazil? Please cite this article as: Martins HT, Balmant NV, Silva NP, Santos MO, Reis RS, Camargo B. Who cares for adolescents and young adults with cancer in Brazil? J Pediatr (Rio J). 2018;94:440-5.

Abstract

Objective:

Approximately 6% of all cancers arise in adolescents and young adults. Currently, the ward type best placed to treat this patient group remains controversial. The aim of this study was to evaluate exactly where adolescents and young adults with cancer are treated in Brazil.

Methods:

Data were extracted from 271 Brazilian hospital-based cancer registries (2007-2011), including all five national regions (North, Northeast, Midwest, South, and Southeast). Variables included gender, age, ethnicity, National Code of Health Establishment, hospital unit state, and region. Tumors were classified according to the World Health Organization classification for adolescents and young adults with cancer. Odds ratios with 95% confidence intervals were computed by unconditional logistic regression.

Results:

Most patients were managed on medical oncology wards, followed by pediatric oncology and then by non-specialist wards. Of patients aged 15-19 years, 49% were managed on pediatric wards; most of the older patients (96%; aged 20-24) were managed on adult wards. Patients were more likely to be seen in medical oncology wards as their age increased (OR = 2.03 [1.98-2.09]), or if they were based in the South (OR = 1.50 [1.29-1.73]). Conversely, bone tumors were less likely to be treated (decreased OR) on medical oncology wards, regardless of age, gender, and region.

Conclusion:

An elevated risk of treatment on medical oncology wards was observed for older patients and those treated in the South. Bone tumors were generally treated in pediatric oncology wards, while skin cancers were treated in medical oncology wards, regardless of age, gender, and region.

KEYWORDS
Adolescents and young adults; Cancer; Site of care

Resumo

Objetivo:

Aproximadamente 6% de todos os cânceres surgem em adolescentes e adultos jovens. Atualmente, o melhor tipo de enfermaria para tratar esse grupo de pacientes continua sendo controverso. O objetivo deste estudo foi avaliar exatamente onde os adolescentes e adultos jovens com câncer são tratados no Brasil.

Métodos:

Foram coletados dados de 271 registros de câncer de base hospitalar (2007-2011), inclusive de todas as cinco regiões nacionais (Norte, Nordeste, Centro-Oeste, Sul e Sudeste). As variáveis incluíram sexo, idade, etnia, o Código Nacional de Estabelecimento de Saúde e o estado e a região da unidade hospitalar. Os tumores foram classificados de acordo com a classificação da Organização Mundial de Saúde para adolescentes e adultos jovens com câncer. As razões de chance com intervalos de confiança de 95% foram calculadas por regressão logística incondicional.

Resultados:

A maioria dos pacientes foi tratada em enfermaria de oncologia médica, seguido da enfermaria de oncologia pediátrica e, então, a enfermaria sem especialidade. 49% dos pacientes entre 15-19 anos foram tratados em enfermarias pediátricas; os pacientes mais velhos (96%, entre 20-24) foram tratados em enfermarias de adultos. Os pacientes apresentaram maior propensão a serem vistos em enfermarias de oncologia conforme mais velhos (RC = 2,03 [1,98-2,09]) ou caso morassem na região Sul (RC = 1,50 [1,29-1,73]). Por outro lado, os tumores ósseos mostraram menor propensão a tratamento (redução da RC) em enfermarias de oncologia, independentemente da idade, sexo e região.

Conclusão:

Foi visto um risco elevado de tratamento, em enfermarias de oncologia, de pacientes mais velhos e os tratados na Região Sul. Os tumores ósseos foram, em geral, tratados em enfermarias de oncologia pediátrica, ao passo que os cânceres de pele foram tratados em enfermarias de oncologia médica, independentemente de idade, sexo e região.

PALAVRAS-CHAVE
Adolescentes e adultos jovens; Câncer; Local de atendimento

Introduction

Currently, no clear age definition exists in the literature for the patient group comprising adolescents and young adults (AYA). The World Health Organization (WHO) defines adolescence as the age bracket of 10-19 years, whereas the United Nations (UN) uses 15-24 years of age to define adolescence, using the term “young adult” to refer to those aged 20 and over.11 World Health Organization (WHO). Report of a WHO Study Group on Young People and Health for All. Geneva: WHO; 1986. The Brazilian Children and Adolescents Statute defines adolescence as 12-18 years of age.22 Eisenstein E. Adolescência: definições, conceitos e critérios. Adolesc Saude. 2005;2:6-7.

The incidence of cancer in the AYA group has increased when compared with other age groups. Approximately 6% of all cancers now arise in AYA patients (aged 15-29 years); this incidence is 2.7-fold greater than in younger patients (aged < 15 years.).33 Bleyer A, O’Leary M, Barr R, Ries LA. Cancer epidemiology in older adolescents and young adults 15 to 29 years of age, including SEER incidence and survival: 1975-2000 [monograph]. Bethesda, MD: National Cancer Institute (NIH); 2006. In Brazil, the median incidence of cancer in this population is 218 cases per million for male patients, and 232 cases per million in female patients; the majority of cases is diagnosed as carcinomas, lymphomas, and leukemias.44 Balmant NV, de Souza Reis R, Pinto Oliveira JF, Ferman S, de Oliveira Santos M, de Camargo B. Cancer incidence among adolescents and young adults (15 to 29 years) in Brazil. J Pediatr Hematol Oncol. 2016;38:88-96.

The AYA age group lies at the boundary of pediatric and medical oncology, and manifests unique biological and clinical characteristics. Pediatric tumors are mostly embryonic, while tumors in older adults tend to originate from epithelial tissue. The spectrum of cancer type therefore differs when comparing younger children and adults, which reflects the different pathologic mechanisms involved, as well as tolerance and response to therapy. Consequently, there is a growing awareness of the need for specialist adolescent treatment units within pediatric wards.

One of the considerable challenges with regard to cancer treatment for the AYA population is in determining where best to treat these patients, given the heterogeneity in biological/clinical behavior when comparing pediatric and medical oncology. Dedicated units specialized in treating AYA patients are needed, especially given the lack of any improvement in survival for this group when compared with children or adults aged 29 years of age and above.55 Bleyer A. Young adult oncology: the patients and their survival challenges. CA Cancer J Clin. 2007;57:242-55. This disappointing failure to improve therapy for the AYA patient group may reflect a poor recognition of, and a lack of specialist attention to, the unique pathobiology exhibited by these patients, together with inadequate support for their psychosocial needs.66 Desandes E, Bonnay S, Berger C, Brugieres L, Demeocq F, Laurence V, et al. Pathways of care for adolescent patients with cancer in France from 2006 to 2007. Pediatr Blood Cancer. 2012;58:924-9.

7 Zebrack B, Bleyer A, Albritton K, Medearis S, Tang J. Assessing the health care needs of adolescents and young adults cancer patients and survival. Cancer. 2006;107:2915-23.

8 Pollock BH, Birch JM. Registration and classification of adolescent and young adult cancer cases. Pediatr Blood Cancer. 2008;50:1090-3.
-99 Bleyer A, Barr R. Cancer in young adults 20 to 39 years of age: overview. Semin Oncol. 2009;36:194-206.

The optimal treatment site for AYA patients remains controversial.1010 Stock W, La M, Sanford B, Bloomfield CD, Vardiman JW, Gaynon P, et al. What determines the outcomes for adolescents and young adults with acute lymphoblastic leukemia treated on cooperative group protocols? A comparison of Children's Cancer Group and Cancer and Leukemia Group B studies. Blood. 2008;112:1646-54.

11 Ram R, Wolach O, Vidal L, Gafter-Gvili A, Shpilberg O, Raanani P. Adolescents and young adults with a acute lymphoblastic leukemia have a better outcome when treated with pediatric-inspired regimens: systematic review and meta-analysis. Am J Hematol. 2012;87:472-8.

12 Pole JD, Alibhai SM, Ethier MC, Teuffel O, Portwine C, Zelcer S, et al. Adolescents with acute lymphoblastic leukemia treated at pediatric versus adult hospitals. Ann Oncol. 2013;24:801-6.
-1313 Parsons HM, Harlan LC, Schmidt S, Keegan TH, Lynch CF, Kent EE, et al. Who treats adolescents and young adults with cancer? A report from the AYA HOPE Study. J Adolesc Young Adult Oncol. 2015;4:141-50. Referral to pediatric wards appears to be associated with age, type of cancer, and the distance to pediatric oncology centers.1414 Albritton KH, Wiggins CH, Nelson HE, Weeks JC. Site of oncologic specialty care for older adolescents in Utah. J Clin Oncol. 2007;25:4616-21.

15 Bleyer A. The quid pro quo of pediatric versus adult services for older adolescent cancer patients. Pediatr Blood Cancer. 2010;54:238-41.
-1616 Downs-Canner S, Shaw PH. A comparison of clinical trial enrollment between adolescent and young adult (AYA) oncology patients treated at affiliated adult and pediatric oncology centers. J Pediatr Hematol Oncol. 2009;31:927-9. Ideally a specialist adolescent cancer unit would be used. In Brazil, data on where AYA patients are treated is lacking. This shortcoming hampers the improvement of institutional practice and the development of specific treatment protocols.1313 Parsons HM, Harlan LC, Schmidt S, Keegan TH, Lynch CF, Kent EE, et al. Who treats adolescents and young adults with cancer? A report from the AYA HOPE Study. J Adolesc Young Adult Oncol. 2015;4:141-50.

The aim of this study was to determine where the oncologic care for AYA patients takes place in Brazil.

Materials and methods

Data sources

Data were extracted from thirteen thousand four hundred and seventeen cases of cancer in AYA patients aged 15 to 24 years from 271 Brazilian hospital-based cancer registries (BHCR; 2007-2011) across the five main regions of Brazil (North, Northeast, Southeast, South, and Midwest; data extracted from the Integrator System [IS - http://www.inca.gov.br]). Patient information from each registry included: gender, age, National Code of Health Establishment (NCHE), type of hospital unit, and geographic region. Tumors were classified according to the WHO AYA cancer classification.1717 Barr RD, Holowaty EJ, Birch JM. Classification scheme for tumors diagnosed in adolescents and young adults. Cancer. 2006;106:1425-30. Data collection was by telephone contact with each hospital unit to determine the presence (or not) of a pediatric oncology ward, as well as the age group admitted by the ward.

Statistical analyses

All variables were subject to descriptive analyses. Crude and adjusted odds ratios (OR) with 95% confidence intervals (CI) were obtained by logistic regression analyses with gender, region, and AYA classification included as categorical variables. Patient age was included as a continuous variable (per year of age increase). Reference categories for variables were female, the Southeast region, and leukemia. All analyses were conducted using SPSS (IBM SPSS Statistics for Windows, version 20.0, NY, USA).

This study was approved by the Research Ethics Committee of Instituto Nacional de Câncer José Alencar Gomes da Silva (INCA).

Results

Sociodemographic and tumor characteristics for this patient cohort are presented in Table 1. The majority of patients were diagnosed with carcinomas, then lymphomas, and leukemias. Most patients were managed in medical oncology wards (n = 9399), followed by pediatric oncology wards (n = 2907), and then by non-specialist wards (n = 146). The Southeast region had the highest number of hospital units with pediatric oncology wards (n = 37/28%), most specifically in São Paulo. The North and Northeast regions had the highest proportion of pediatric oncology wards, in 50% of their hospital units (Fig. 1). In 81 of 94 pediatric oncology wards, patients were aged 0-18 years (n = 37/81; 45.7%). For patients aged 15-19 years, 49.6% of cases were managed in pediatric wards, while for those aged 20-24 years, the majority (96.1%) were referred to adult wards. For those aged 15-19, bone tumors (61%), central nervous system tumors (55.8%), and leukemias (53%) were managed, in general, in pediatric wards. In contrast, approximately 56% of carcinomas were managed in medical oncology wards.

Table 1
Sociodemographic and tumor characteristics of adolescent and young adult (AYA) patients in Brazilian cancer hospital registries (2007–2011).

Figure 1
Distribution of specialized wards according to Brazilian regions, 2007-2011.

Table 2 shows the crude and adjusted ORs with 95% CIs for the site of patient treatment in terms of gender, age, region, and tumor type. Age, used as a continuous variable, showed (per year of increase) an independent association with medical oncology ward (OR = 2.02 [95% CI: 1.97-2.07]). Bone tumors revealed a decreased chance of treatment on a medical oncology ward irrespective of gender, age, and region (OR = 0.72 ([95% CI: 0.59-0.88]). Among patients from the South (region) of Brazil, there was an increased risk of being treated on a medical oncology ward (OR = 1.50 [95% CI: 1.29-1.73]) while patients from the North (OR = 0.66 [95% CI: 0.52-0.85]) were more likely to be treated on a pediatric oncology ward regardless of tumor type, age, or gender.

Table 2
Risk estimate for treatment on a medical oncology ward by sociodemographic and tumor characteristics (data retrieved from Brazilian cancer hospital registries for 2007–2011).

Discussion

The incidence of cancer in the AYA patient group is higher than for children aged less than 15 years,33 Bleyer A, O’Leary M, Barr R, Ries LA. Cancer epidemiology in older adolescents and young adults 15 to 29 years of age, including SEER incidence and survival: 1975-2000 [monograph]. Bethesda, MD: National Cancer Institute (NIH); 2006. with carcinomas, lymphomas, and leukemias being the most frequent tumor types in Brazil.44 Balmant NV, de Souza Reis R, Pinto Oliveira JF, Ferman S, de Oliveira Santos M, de Camargo B. Cancer incidence among adolescents and young adults (15 to 29 years) in Brazil. J Pediatr Hematol Oncol. 2016;38:88-96. How and where these patients are treated remain controversial issues that are further confused by the lack of clarity in defining this patient population. With these problems in mind, the authors sought to collate data for how this patient group is diagnosed and treated in Brazil.

The tumors most frequently registered in the BHCRs were similar to those described in population-based cancer registries, and consisted of carcinomas, lymphomas, and leukemias. Thyroid and cervical carcinoma were the most frequent in the AYA age group, with the latter tumor type predominant in young Brazilian women. The median incidence rate of cervical carcinoma in the AYA patient group, according to Brazilian population-based data, was 2.11 cases per 100,000 women aged 20-24 years.1818 Viana LS. Incidence and mortality trends in cervix cancer in adolescents and young adults in Brazil, 2015 [monograph]. Rio de Janeiro: National Institute of Cancer (INCA); 2015. Thyroid tumors, which occur more frequently in female patients, showed a median incidence rate of 13.7 cases per million.44 Balmant NV, de Souza Reis R, Pinto Oliveira JF, Ferman S, de Oliveira Santos M, de Camargo B. Cancer incidence among adolescents and young adults (15 to 29 years) in Brazil. J Pediatr Hematol Oncol. 2016;38:88-96.

The present data revealed that the majority of AYAs aged 15-24 years were managed on medical oncology wards; increasing age was shown to be a significant risk factor for being treated on this type of ward. The confusion wrought by the varying age definitions for the AYA patient group is reflected by a lack of standardization among the different hospital units. One limitation of this study is that there is no information on whether a patient admitted to an adult ward is always followed by an adult oncologist, mainly in hospital units that have both services (pediatric and adult oncology). Accordingly, some authors report that most AYAs with a cancer diagnosis are treated by non-pediatric oncologists.1313 Parsons HM, Harlan LC, Schmidt S, Keegan TH, Lynch CF, Kent EE, et al. Who treats adolescents and young adults with cancer? A report from the AYA HOPE Study. J Adolesc Young Adult Oncol. 2015;4:141-50.,1919 Cash T, Qayed M, Ward KC, Mertens AC, Rapkin L. Comparison of survival at adult versus pediatric treatment centers for rare pediatric tumors in an adolescent and young adult (AYA) population in the state of Georgia. Pediatr Blood Cancer. 2015;62:456-62.

The medical, physical, psychological, and emotional needs vary for different patient groups, which poses a distinct challenge when deciding where AYA patients should be treated. Consequently, a multidisciplinary team is mandatory, and an oncologist with medical and psychosocial expertise relevant to this age group should be involved. Standardizing the site and type of care available to AYA patients with a cancer diagnosis may help to improve outcomes for this patient group, given that the spectrum of cancers for AYA and pediatric patients differs. Further, it is recognized that pediatric and adult cancers are best treated with protocols and centers dedicated to those patient groups. In the present population, pediatric tumor types such as bone and leukemia were more likely to be managed on a pediatric ward, while carcinomas and lymphomas were managed on adult wards.

The biological characteristics of tumors diagnosed in AYA patients present heterogeneous responses to different protocols; it is suggested that adherence to treatment is improved when patients are treated on pediatric wards. However, the lack of participation and exposure of AYA patients to clinical trials and protocols2020 Bleyer A, Viny A, Barr R. Cancer in 15- to 29-year-olds by primary site. Oncologist. 2006;11:590-601.

21 Fern L, Davies S, Eden T, Feltbower R, Grant R, Hawkins M, et al. Rates of inclusion of teenagers and young adults in England into National Cancer Research Network clinical trials: report from the National Cancer Research Institute (NCRI) Teenage and Young Adult Clinical Studies Development Group. Br J Cancer. 2008;99:1967-74.
-2222 McTiernan A. Issues surrounding the participation of adolescents with cancer in clinical trials in the UK. Eur J Cancer Care. 2003;12:233-9. may explain, in part, the limited treatment options available for this age group, as improved protocols and therapies generally require trial participation and the subsequent development of well-established multidisciplinary protocols.1616 Downs-Canner S, Shaw PH. A comparison of clinical trial enrollment between adolescent and young adult (AYA) oncology patients treated at affiliated adult and pediatric oncology centers. J Pediatr Hematol Oncol. 2009;31:927-9.,1919 Cash T, Qayed M, Ward KC, Mertens AC, Rapkin L. Comparison of survival at adult versus pediatric treatment centers for rare pediatric tumors in an adolescent and young adult (AYA) population in the state of Georgia. Pediatr Blood Cancer. 2015;62:456-62.

The majority of reports observed improved results when treatment is performed on a pediatric oncology ward when compared with adult wards.2323 Wood WA, Lee SJ. Malignant hematologic diseases in adolescents and young adults. Blood. 2011;117:5803-15. A meta-analysis performed in 2012 assessing 11 publications revealed that AYAs treated with pediatric protocols achieved superior outcomes than those treated with adult protocols.1010 Stock W, La M, Sanford B, Bloomfield CD, Vardiman JW, Gaynon P, et al. What determines the outcomes for adolescents and young adults with acute lymphoblastic leukemia treated on cooperative group protocols? A comparison of Children's Cancer Group and Cancer and Leukemia Group B studies. Blood. 2008;112:1646-54. Previous studies performed in different countries (United States, United Kingdom, and the Netherlands) demonstrated that in the setting of AYA patients with Acute Lymphoblastic Leukemia (ALL), treatment according to pediatric protocols showed a superior outcome compared to adult protocols.1010 Stock W, La M, Sanford B, Bloomfield CD, Vardiman JW, Gaynon P, et al. What determines the outcomes for adolescents and young adults with acute lymphoblastic leukemia treated on cooperative group protocols? A comparison of Children's Cancer Group and Cancer and Leukemia Group B studies. Blood. 2008;112:1646-54.,2424 Boissel N, Auclerc MF, Lhéritier V, Perel Y, Thomas X, Leblanc T, et al. Should adolescents with acute lymphoblastic leukemia be treated as old children or young adults? Comparison of the French FRALLE-93 and LALA-94 trials. J Clin Oncol. 2003;21:774-80.

25 De Bont JM, Holt Bv, Dekker AW, van der Does-van den Berg A, Sonneveld P, Pieters R, et al. Significant difference in outcome for adolescents with acute lymphoblastic leukemia treated on pediatric vs. adult protocols in the Netherlands. Leukemia. 2004;18:2032-53.
-2626 Ramanujachar R, Richards S, Hann I, Goldstone A, Mitchell C, Vora A, et al. Adolescents with acute lymphoblastic leukemia: outcome on UK National Paediatric (ALL 97) and Adult (UKALLXII/E2993) trials. Pediatr Blood Cancer. 2007;48:254-61. Regarding the treatment of other tumors, such as Ewing's sarcoma, it was also demonstrated that adolescents older than 15 years of age treated in pediatric wards presented an improved survival when compared with those treated on non-pediatric wards, despite receiving the same treatment protocol.2727 Paulussen M, Ahrens S, Juergens HF. Cure rates in Ewing tumor patients aged over 15 years are better in pediatric oncology units. Results of the GPOH CESS/EICESS studies. Proc Am Soc Clin Oncol. 2003;22:3279. The underlying reasons for these disparate outcomes remain unclear. However, a definitive association between medical specialty and outcome for adolescents with cancer has been demonstrated, despite the fact that the present study did not evaluate responses to specific treatments or protocols.

Confusingly, some studies have shown no differences in survival rates for specialized wards, as well as improved survival rates for AYA patients treated on adult oncology wards.1919 Cash T, Qayed M, Ward KC, Mertens AC, Rapkin L. Comparison of survival at adult versus pediatric treatment centers for rare pediatric tumors in an adolescent and young adult (AYA) population in the state of Georgia. Pediatr Blood Cancer. 2015;62:456-62.,2828 Howell DL, Ward KC, Austin HD. Access to pediatric cancer care by age, race, and diagnosis, and outcomes of cancer treatment in pediatric and adolescent patients in the state of Georgia. J Clin Oncol. 2007;25:4610-5. The authors believe that these discrepancies may relate to the histological type of tumor. For example, carcinomas and skin tumors are more specific to adults and are best handled on medical oncology wards. In turn, bone tumors, as a tumor type, have also been shown to be a protective factor in terms of referral to medical oncology wards. According to GLOBOCAN (International Agency for Research on Cancer), this histological group of tumors comprises 5% of all neoplasias in the population aged 0-19 years. In other words, bone tumors are strongly associated with younger patients and therefore tend to be treated in pediatric wards, as shown by the present data.

A lower risk for management in medical wards was found for the Northeast region, which has a high proportion of hospitals with pediatric oncology wards. These data could imply a “geographic” protection factor in terms of management on medical wards.

While the literature remains controversial, most international findings demonstrate the importance of a pediatric oncologist in the prognosis and treatment of tumors for AYA patients. Pediatric oncology wards in Brazil care for children and adolescents until 18 years of age, as dictated by the Brazilian Children and Adolescent Statute, which defines adolescence as the age bracket of 12-18 years of age. However, currently, in Brazil, there is a lack of data for the effectiveness of specific treatments or protocols for AYA cases.

Clinical programs with appropriately trained healthcare professionals, as well as improved communication and collaboration between adult and pediatric oncologists are vital if the care provision for AYA patients with cancer is to be optimized. Several countries such as the United Kingdom, United States, Australia, and Germany have established collaborative care programs, although the development of a comparable AYA oncology program in Brazil remains a challenge.2929 Rogers PC, De Pauw S, Schacter B, Barr RD. A process for change in the care of adolescents and young adults with cancer in Canada. J Adolesc Young Adult Oncol. 2013;2:72-6.,3030 Ramphal R, Aubin S, Czaykowski P, De Pauw S, Johnson A, McKillop S, et al. Adolescent and young adult cancer: principles of care. Curr Oncol. 2016;23:204-9.

Further work is now needed in terms of evaluating treatment outcomes for the AYA patient age group in Brazil. With this in mind, the focus now should be on evaluating treatment response, protocols, and outcomes according to tumor type and site of care.

  • Funding
    HTGM and NVB were awarded scholarships from the Nacional Cancer Institute post-graduation program, and BDC receives a scholar grant from the National Council for Scientific and Technological Development (Conselho Nacional de Desenvolvimento Científico e Tecnológico, CNPq, Brasília; #306291/2014-2) and from the Foundation for Support of Research in the State of Rio de Janeiro (Fundação de Amparo à Pesquisa do Estado do Rio de Janeiro, FAPERJ, Rio de Janeiro; #212989-2016).
  • Please cite this article as: Martins HT, Balmant NV, Silva NP, Santos MO, Reis RS, Camargo B. Who cares for adolescents and young adults with cancer in Brazil? J Pediatr (Rio J). 2018;94:440-5.

Acknowledgements

The authors would like to thank all the BHCR coordinators in Brazil that contributed the datasets that made this work possible.

References

  • 1
    World Health Organization (WHO). Report of a WHO Study Group on Young People and Health for All. Geneva: WHO; 1986.
  • 2
    Eisenstein E. Adolescência: definições, conceitos e critérios. Adolesc Saude. 2005;2:6-7.
  • 3
    Bleyer A, O’Leary M, Barr R, Ries LA. Cancer epidemiology in older adolescents and young adults 15 to 29 years of age, including SEER incidence and survival: 1975-2000 [monograph]. Bethesda, MD: National Cancer Institute (NIH); 2006.
  • 4
    Balmant NV, de Souza Reis R, Pinto Oliveira JF, Ferman S, de Oliveira Santos M, de Camargo B. Cancer incidence among adolescents and young adults (15 to 29 years) in Brazil. J Pediatr Hematol Oncol. 2016;38:88-96.
  • 5
    Bleyer A. Young adult oncology: the patients and their survival challenges. CA Cancer J Clin. 2007;57:242-55.
  • 6
    Desandes E, Bonnay S, Berger C, Brugieres L, Demeocq F, Laurence V, et al. Pathways of care for adolescent patients with cancer in France from 2006 to 2007. Pediatr Blood Cancer. 2012;58:924-9.
  • 7
    Zebrack B, Bleyer A, Albritton K, Medearis S, Tang J. Assessing the health care needs of adolescents and young adults cancer patients and survival. Cancer. 2006;107:2915-23.
  • 8
    Pollock BH, Birch JM. Registration and classification of adolescent and young adult cancer cases. Pediatr Blood Cancer. 2008;50:1090-3.
  • 9
    Bleyer A, Barr R. Cancer in young adults 20 to 39 years of age: overview. Semin Oncol. 2009;36:194-206.
  • 10
    Stock W, La M, Sanford B, Bloomfield CD, Vardiman JW, Gaynon P, et al. What determines the outcomes for adolescents and young adults with acute lymphoblastic leukemia treated on cooperative group protocols? A comparison of Children's Cancer Group and Cancer and Leukemia Group B studies. Blood. 2008;112:1646-54.
  • 11
    Ram R, Wolach O, Vidal L, Gafter-Gvili A, Shpilberg O, Raanani P. Adolescents and young adults with a acute lymphoblastic leukemia have a better outcome when treated with pediatric-inspired regimens: systematic review and meta-analysis. Am J Hematol. 2012;87:472-8.
  • 12
    Pole JD, Alibhai SM, Ethier MC, Teuffel O, Portwine C, Zelcer S, et al. Adolescents with acute lymphoblastic leukemia treated at pediatric versus adult hospitals. Ann Oncol. 2013;24:801-6.
  • 13
    Parsons HM, Harlan LC, Schmidt S, Keegan TH, Lynch CF, Kent EE, et al. Who treats adolescents and young adults with cancer? A report from the AYA HOPE Study. J Adolesc Young Adult Oncol. 2015;4:141-50.
  • 14
    Albritton KH, Wiggins CH, Nelson HE, Weeks JC. Site of oncologic specialty care for older adolescents in Utah. J Clin Oncol. 2007;25:4616-21.
  • 15
    Bleyer A. The quid pro quo of pediatric versus adult services for older adolescent cancer patients. Pediatr Blood Cancer. 2010;54:238-41.
  • 16
    Downs-Canner S, Shaw PH. A comparison of clinical trial enrollment between adolescent and young adult (AYA) oncology patients treated at affiliated adult and pediatric oncology centers. J Pediatr Hematol Oncol. 2009;31:927-9.
  • 17
    Barr RD, Holowaty EJ, Birch JM. Classification scheme for tumors diagnosed in adolescents and young adults. Cancer. 2006;106:1425-30.
  • 18
    Viana LS. Incidence and mortality trends in cervix cancer in adolescents and young adults in Brazil, 2015 [monograph]. Rio de Janeiro: National Institute of Cancer (INCA); 2015.
  • 19
    Cash T, Qayed M, Ward KC, Mertens AC, Rapkin L. Comparison of survival at adult versus pediatric treatment centers for rare pediatric tumors in an adolescent and young adult (AYA) population in the state of Georgia. Pediatr Blood Cancer. 2015;62:456-62.
  • 20
    Bleyer A, Viny A, Barr R. Cancer in 15- to 29-year-olds by primary site. Oncologist. 2006;11:590-601.
  • 21
    Fern L, Davies S, Eden T, Feltbower R, Grant R, Hawkins M, et al. Rates of inclusion of teenagers and young adults in England into National Cancer Research Network clinical trials: report from the National Cancer Research Institute (NCRI) Teenage and Young Adult Clinical Studies Development Group. Br J Cancer. 2008;99:1967-74.
  • 22
    McTiernan A. Issues surrounding the participation of adolescents with cancer in clinical trials in the UK. Eur J Cancer Care. 2003;12:233-9.
  • 23
    Wood WA, Lee SJ. Malignant hematologic diseases in adolescents and young adults. Blood. 2011;117:5803-15.
  • 24
    Boissel N, Auclerc MF, Lhéritier V, Perel Y, Thomas X, Leblanc T, et al. Should adolescents with acute lymphoblastic leukemia be treated as old children or young adults? Comparison of the French FRALLE-93 and LALA-94 trials. J Clin Oncol. 2003;21:774-80.
  • 25
    De Bont JM, Holt Bv, Dekker AW, van der Does-van den Berg A, Sonneveld P, Pieters R, et al. Significant difference in outcome for adolescents with acute lymphoblastic leukemia treated on pediatric vs adult protocols in the Netherlands. Leukemia. 2004;18:2032-53.
  • 26
    Ramanujachar R, Richards S, Hann I, Goldstone A, Mitchell C, Vora A, et al. Adolescents with acute lymphoblastic leukemia: outcome on UK National Paediatric (ALL 97) and Adult (UKALLXII/E2993) trials. Pediatr Blood Cancer. 2007;48:254-61.
  • 27
    Paulussen M, Ahrens S, Juergens HF. Cure rates in Ewing tumor patients aged over 15 years are better in pediatric oncology units. Results of the GPOH CESS/EICESS studies. Proc Am Soc Clin Oncol. 2003;22:3279.
  • 28
    Howell DL, Ward KC, Austin HD. Access to pediatric cancer care by age, race, and diagnosis, and outcomes of cancer treatment in pediatric and adolescent patients in the state of Georgia. J Clin Oncol. 2007;25:4610-5.
  • 29
    Rogers PC, De Pauw S, Schacter B, Barr RD. A process for change in the care of adolescents and young adults with cancer in Canada. J Adolesc Young Adult Oncol. 2013;2:72-6.
  • 30
    Ramphal R, Aubin S, Czaykowski P, De Pauw S, Johnson A, McKillop S, et al. Adolescent and young adult cancer: principles of care. Curr Oncol. 2016;23:204-9.

Publication Dates

  • Publication in this collection
    Jul-Aug 2018

History

  • Received
    8 Feb 2017
  • Accepted
    14 June 2017
  • Published
    06 Sept 2017
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