Predictive value of the early response to chemotherapy in high‐risk stages II and III Hodgkin's disease

A series of 60 patients with “high risk” Stage II and III Hodgkin's disease (B symptoms, or large mediastinal mass, or E lung disease) were staged without laparotomy and treated with combined modality treatment: mechlorethamine, vincristine, procarbazine, and prednisone (6 MOPP) plus radiotherapy. Patients were restaged after the first three courses of MOPP and the status of response to therapy at that time was called early response to chemotherapy (ERC). The rate of nitrogen mustard and procarbazine delivery (MRD) during the first three cycles of chemotherapy also was assessed. At the completion of the therapy patients were restaged and the final response was assessed. Fifty‐two (86.7%) patients entered complete remission (CR). Forty‐eight percent of the complete respondent achieved CR in the first three courses of MOPP. Eight‐year survival and disease‐free survival (DFS) rates of the patients achieving CR were 71% and 73%, respectively. Survival and DFS were significantly better for the patients who achieved CR in the first three cycles of chemotherapy than for patients who entered CR at a later stage of therapy: 8‐year survival 90% versus 55% (P = 0.00); 8‐year DFS 87% versus 59% (P = 0.01). The attainment of a complete ERC was adversely affected by lymphocyte depletion (LD) histologic type (P = 0.01) and MRD less than 65% (P = 0.04). However, when a multivariate regression analysis was used, ERC was the only significant prognostic variable for survival and DFS and its predictive value was confirmed even after correction by MRD. These data suggest that the rapidity of response to chemotherapy could be an important prognostic factor in high‐risk Stage II and III Hodgkin's disease.

[1]  D. Weisenburger,et al.  Chemotherapy for diffuse large-cell lymphoma--rapidly responding patients have more durable remissions. , 1986, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

[2]  F. Cavalli,et al.  Malignant Lymphomas and Hodgkin’s Disease: Experimental and Therapeutic Advances , 2011, Developments in Oncology.

[3]  J. Connors,et al.  MOPP/ABV hybrid program: combination chemotherapy based on early introduction of seven effective drugs for advanced Hodgkin's disease. , 1985, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

[4]  D. Rosenthal,et al.  Stage III Hodgkin's disease: improved survival with combined modality therapy as compared with radiation therapy alone. , 1985, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

[5]  F. Frassoni,et al.  High‐dose chemotherapy and non‐frozen autologous bone marrow transplantation in relapsed advanced lymphomas or those resistant to conventional chemotherapy , 1984, Cancer.

[6]  R. Makuch,et al.  Second malignant neoplasms complicating Hodgkin's disease: the National Cancer Institute experience. , 1984, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

[7]  R. Mertelsmann,et al.  Treatment of advanced Hodgkin's disease with chemotherapy and irradiation. Controlled trial of two versus three alternating, potentially non-cross-resistant drug combinations. , 1984, American Journal of Medicine.

[8]  F. Freiha,et al.  Prognostic significance of a decline in serum human chorionic gonadotropin levels after initial chemotherapy for advanced germ-cell carcinoma. , 1984, Annals of internal medicine.

[9]  G. Curt,et al.  Drug resistance in cancer. , 1984, Cancer treatment reports.

[10]  M. Imbert,et al.  Early response to chemotherapy as a prognostic factor in Hodgkin's disease , 1983, Cancer.

[11]  S. Rosenberg,et al.  A dose and time response analysis of the treatment of Hodgkin's disease with MOPP chemotherapy. , 1983, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

[12]  W. Ph,et al.  Hodgkin's disease with direct extension into pulmonary parenchyma from a mediastinal mass: a presentation requiring special therapeutic considerations. , 1982 .

[13]  Coltman Ca,et al.  Second malignancies complicating Hodgkin's disease: a Southwest Oncology Group 10-year followup. , 1982 .

[14]  C. Bloomfield,et al.  Chemotherapy and combined modality therapy for Hodgkin's disease: a progress report on Cancer and Leukemia Group B studies. , 1982, Cancer treatment reports.

[15]  D. Rosenthal,et al.  Anatomic substages of stage IIIA Hodgkin's disease: followup of a collaborative study. , 1982, Cancer treatment reports.

[16]  S. Hellman,et al.  Influence of mediastinal adenopathy on site and frequency of relapse in patients with Hodgkin's disease. , 1982, Cancer treatment reports.

[17]  A. Santoro,et al.  Alternating drug combinations in the treatment of advanced Hodgkin's disease. , 1982, The New England journal of medicine.

[18]  J. Bertino,et al.  Combined modality therapy for advanced Hodgkin's disease: long-term followup data. , 1982, Cancer treatment reports.

[19]  A. Santoro,et al.  Salvage chemotherapy with ABVD in MOPP-resistant Hodgkin's disease. , 1982, Annals of internal medicine.

[20]  N. Breslow Covariance analysis of censored survival data. , 1974, Biometrics.

[21]  V. Devita,et al.  Combination chemotherapy in the treatment of advanced Hodgkin's disease. , 1970, Annals of internal medicine.

[22]  E. Kaplan,et al.  Nonparametric Estimation from Incomplete Observations , 1958 .