Skip to main content

Advertisement

Log in

Body weight changes in patients undergoing chemotherapy for ovarian cancer influence progression-free and overall survival

  • Original Article
  • Published:
Supportive Care in Cancer Aims and scope Submit manuscript

Abstract

Purpose

The aim of this study was to evaluate whether body weight changes in patients undergoing chemotherapy for epithelial ovarian cancer (EOC) influence progression-free survival (PFS) and overall survival (OS).

Methods

An analysis of 190 patients diagnosed with ovarian cancer after first-line chemotherapy was conducted. Changes in body weight were assessed by comparing measurements at baseline to those of the third and sixth cycles of chemotherapy. PFS and OS were calculated with the Kaplan–Meier method and multivariate Cox model.

Results

Significant reduction in body weight in advanced EOC was observed with no changes in early EOC. Significant differences in PFS were observed in advanced EOC patients that lost more than 5 % of their body weight (6 months), maintained weight (13 months), or gained more than 5 % of their body weight (15 months). Similarly, significant differences in OS were noted in advanced EOC at the following time points: 24.3, 42.4, and 66.2 months. No effect was reported for early EOC patients. The multivariate Cox analysis showed significant body weight changes from the first to the sixth chemotherapy cycle for PFS (HR = 0.97; 95 % CI 0.95–0.99) and OS (HR = 0.94; 95 % CI 0.91–0.97) as well as from the first to the third chemotherapy cycle for OS (HR = 0.93; 95 % CI 0.88–0.98).

Conclusions

Body weight changes can be recognized as a prognostic factor for PFS and OS in advanced EOC patients undergoing chemotherapy. Weight loss is associated with poorer survival while weight gain improved outcomes.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2
Fig. 3
Fig. 4

Similar content being viewed by others

References

  1. Reynolds EA, Moller KA (2006) A review and an update on the screening of epithelial ovarian cancer. Curr Probl Cancer 30:203–232

    Article  PubMed  Google Scholar 

  2. Kearney N, Miller M, Maguire R, Dolan S, MacDonald R, McLeod J, Maher L, Sinclair L, Norrie J, Wengström Y (2008) WISECARE+: results of a European study of a nursing intervention for the management of chemotherapy-related symptoms. Eur J Oncol Nurs 12(5):443–448

    Article  PubMed  Google Scholar 

  3. Hall M, Gourley C, McNeish I, Ledermann J, Gore M, Jayson G, Perren T, Rustin G, Kaye S (2013) Targeted anti-vascular therapies for ovarian cancer: current evidence. Br J Cancer 108(2):250–258

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  4. Bandera EV, Kushi LH, Rodriguez-Rodriguez L (2009) Nutritional factors in ovarian cancer survival. Nutr Cancer 61:580–586

    Article  PubMed  Google Scholar 

  5. Collaborative Group on Epidemiological Studies of Ovarian Cancer (2012) Ovarian cancer and body size: individual participant meta-analysis including 25,157 women with ovarian cancer from 47 epidemiological studies. PLoS medicine 9:e1001200

    Article  PubMed Central  Google Scholar 

  6. Barrett SV, Paul J, Hay A, Vasey PA, Kaye SB, Glasspool RM, Scottish Gynaecological Cancer Trials Group (2008) Does body mass index affect progression-free or overall survival in patients with ovarian cancer? Results from SCOTROC I trial. Ann Oncol 19:898–902

    Article  CAS  PubMed  Google Scholar 

  7. Hess LM, Barakat R, Tian C, Ozols RF, Alberts DS (2007) Weight change during chemotherapy as a potential prognostic factor for stage III epithelial ovarian carcinoma: a gynecologic oncology group study. Gynecol Oncol 107:260–265

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  8. Ataseven B, Harter P, Grimm C, Heitz F, Heikaus S, Traut A, Kahl A, Kurzeder C, Prader S, du Bois A (2016) The revised 2014 FIGO staging system for epithelial ovarian cancer: is a subclassification into FIGO stage IVA and IVB justified? Gynecol Oncol. doi:10.1016/j.ygyno.2016.05.021

    Google Scholar 

  9. WHO (1995) Physical status: the use and interpretation of anthropometry. Report of a WHO Expert Committee. WHO Technical Report Series 854. Geneva: World Health Organization

  10. Protani MM, Nagle CM, Webb PM (2012) Obesity and ovarian cancer survival: a systematic review and meta-analysis. Cancer Prev Res 5:901–910

    Article  Google Scholar 

  11. Zorlini R, Akemi Abe Cairo A, Salete Costa Gurgel M (2008) Nutritional status of patients with gynecologic and breast cancer. Nutr Hosp 23(6):577–583

    CAS  PubMed  Google Scholar 

  12. Laky B, Janda M, Cleghorn G, Obermair (2008) A comparison of different nutritional assessments and body-composition measurements in detecting malnutrition among gynecologic cancer patients. Am J Clin Nutr 87(6):1678–1685

    CAS  PubMed  Google Scholar 

  13. Davies M (2005) Nutritional screening and assessment in cancer-associated malnutrition. Eur J Oncol Nurs Suppl 2:S64–S73

    Article  Google Scholar 

  14. Malihi Z, Kandiah M, Chan YM, Esfandbod M, Vakili M, Hosseinzadeh M, Zarif Yeganeh M (2015) The effect of dietary intake changes on nutritional status in acute leukaemia patients after first induction chemotherapy. Eur J Cancer Care 24(4):542–552

    Article  CAS  Google Scholar 

  15. Gil KM, Frasure HE, Hopkins MP, Jenison EL, von Gruenigen VE (2006) Body weight and composition changes in ovarian cancer patients during adjuvant chemotherapy. Gynecol Oncol 103:247–252

    Article  PubMed  Google Scholar 

  16. Hutton JL, Baracos VE, Wismer WV (2007) Chemosensory dysfunction is a primary factor in the evolution of declining nutritional status and quality of life in patients with advanced cancer. J Pain Symptom Manag 33(2):156–165

    Article  Google Scholar 

  17. Enig B, Petersen HN, Smith DF, Larsen B (1987) Food preferences, nutrient intake and nutritional status in cancer patients. Acta Oncol 26(4):301–315

    Article  CAS  PubMed  Google Scholar 

  18. Dell Antone P (2012) Energy metabolism in cancer cells: how to explain the Warburg and Crabtree effects? Med Hypotheses 79(3):388–392

    Article  CAS  Google Scholar 

  19. Ravasco P, Monteiro-Grillo I, Vidal PM, Camilo ME (2004) Cancer: disease and nutrition are key determinants of patients’ quality of life. Support Care Cancer 12(4):246–252

    Article  PubMed  Google Scholar 

  20. Ansell SM, Rapoport BL, Falkson G, Raats JI, Moeken CM (1993) Survival determinants in patients with advanced ovarian cancer. Gynecol Oncol 50:215–220

    Article  CAS  PubMed  Google Scholar 

  21. Kim SI, Kim HS, Kim TH, Suh DH, Kim K, No JH, Chung HH, Kim YB, Song YS (2014) Impact of underweight after treatment on prognosis of advanced-stage ovarian cancer. J Immunol Res 349546

  22. Rutten IJ, van Dijk DP, Kruitwagen RF, Beets-Tan RG, Olde Damink SW, van Gorp T (2016) Loss of skeletal muscle during neoadjuvant chemotherapy is related to decreased survival in ovarian cancer patients. J Cachexia Sarcopenia Muscle. doi:10.1002/jcsm.12107

    PubMed  PubMed Central  Google Scholar 

  23. Mardas M, Jamka M, Mądry R, Walkowiak J, Krótkopad M, Stelmach-Mardas M (2015) Dietary habits changes and quality of life in patients undergoing chemotherapy for epithelial ovarian cancer. Support Care Cancer 23:1015–1023

    Article  PubMed  Google Scholar 

  24. Salminen EK, Lagström HK, Heikkilä S, Salminen S (2000) Does breast cancer change patients’ dietary habits? Eur J Clin Nutr 54:844–848

    Article  CAS  PubMed  Google Scholar 

  25. Van Loon K, Wigler D, Niedzwiecki D, Venook AP, Fuchs C, Blanke C, Saltz L, Goldberg RM, Meyerhardt JA (2013) Comparison of dietary and lifestyle habits among stage III and metastatic colorectal cancer patients: findings from CALGB 89803 and CALGB 80405. Clin Colorectal Cancer 12:95–102

    Article  PubMed  PubMed Central  Google Scholar 

  26. Stephenson LE, Bebb DG, Reimer RA, Culos-Reed SN (2009) Physical activity and diet behaviour in colorectal cancer patients receiving chemotherapy: associations with quality of life. BMC Gastroenterol 9:60–69

    Article  PubMed  PubMed Central  Google Scholar 

  27. Zhou Y, Chlebowski R, LaMonte MJ, Bea JW, Qi L, Wallace R, Lavasani S, Walsh BW, Anderson G, Vitolins M, Sarto G, Irwin ML (2014) Body mass index, physical activity, and mortality in women diagnosed with ovarian cancer: results from the Women’s Health Initiative. Gynecol Oncol 133:4–10

    Article  PubMed  PubMed Central  Google Scholar 

  28. Backes FJ, Nagel CI, Bussewitz E, Donner J, Hade E, Salani R (2011) The impact of body weight on ovarian cancer outcomes. Int J Gynecol Cancer 21:1601–1605

    Article  PubMed  PubMed Central  Google Scholar 

  29. Ravasco P, Monteiro-Grillo I, Vidal PM, Camilo ME (2005) Dietary counseling improves patient outcomes: a prospective, randomized, controlled trial in colorectal cancer patients undergoing radiotherapy. J Clin Oncol 23(7):1431–1438

    Article  PubMed  Google Scholar 

  30. Ravasco P, Monteiro Grillo I, Camilo M (2007) Cancer wasting and quality of life react to early individualized nutritional counseling. Clin Nutr 26(1):7–15

    Article  PubMed  Google Scholar 

  31. Isenring EA, Capra S, Bauer JD (2004) Nutrition intervention is beneficial in oncology outpatients receiving radiotherapy to the gastrointestinal or head and neck area. Br J Cancer 91(3):447–452

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  32. De Waele E, Mattens S, Honoré PM, Spapen H, De Grève J, Pen JJ (2015) Nutrition therapy in cachectic cancer patients. The Tight Caloric Control (TiCaCo) pilot trial. Appetite 91:298–301

    Article  PubMed  Google Scholar 

Download references

Acknowledgments

The authors are grateful to Dr. Robert Tower for the English correction of the manuscript.

Author’s contributions

MM was responsible for the data collection, data analysis, and writing the manuscript. MSM was responsible for the data analysis and writing the manuscript. RM was responsible for the data collection and critically reviewed the manuscript.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Marta Stelmach-Mardas.

Ethics declarations

The protocol of the study was approved by the local Bioethical Committee, which is associated with Poznan University of Medical Sciences (nr 399/15).

Conflict of interest

The authors declare that they have no conflict of interest.

Electronic supplementary material

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Mardas, M., Stelmach-Mardas, M. & Madry, R. Body weight changes in patients undergoing chemotherapy for ovarian cancer influence progression-free and overall survival. Support Care Cancer 25, 795–800 (2017). https://doi.org/10.1007/s00520-016-3462-1

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s00520-016-3462-1

Keywords

Navigation