Impact on survival of surgically defined favorable responses to salvage intraperitoneal chemotherapy in small-volume residual ovarian cancer Journal Article


Authors: Markman, M.; Reichman, B.; Hakes, T.; Lewis, J. L. Jr; Jones, W.; Rubin, S.; Barakat, R.; Curtin, J.; Almadrones, L.; Hoskins, W.
Article Title: Impact on survival of surgically defined favorable responses to salvage intraperitoneal chemotherapy in small-volume residual ovarian cancer
Abstract: Purpose: To evaluate the impact on survival of the attainment of surgically defined favorable responses (S-R) to salvage intraperitoneal (IP) chemotherapy after initial systemic cytotoxic drug delivery. Patients and Methods: We examined the survival of patients who were treated on one of three phase II IP trials that were conducted at the Memorial Sloan-Kettering Cancer Center. A total of 58 patients whose largest residual tumor masses measured ≤ 0.5 cm in maximum diameter at the initiation of this salvage therapy were assessable for response, 28 of whom (48%) demonstrated a S-R, which included 19 (33%) who achieved a surgically defined complete response (S-CR). Results: With a median follow-up of 43+ months (range, 33+ to 58+ months) from the initiation of IP therapy, 12 of 19 (63%) have recurred. The median duration of S-CR for the 10 patients with microscopic residual disease was 32 months compared with 15 months for the nine patients with macroscopic residual disease (largest tumor mass ≤ 0.5 cm; P > .1). For patients with microscopic residual disease who experienced a S-CR (n = 10) after salvage IP therapy, the median overall survival from the initiation of therapy has not been reached, but will exceed 4 years compared with a 25-month median survival for the nonresponding patients (n = 13; P = .004). The median survival for the 18 patients with small-volume macroscopic disease who responded to therapy was 40 months compared with 19 months for the nonresponders (P = .009). Conclusion: Although the results of this evaluation are encouraging and suggest that the attainment of a S-R, particularly a S-CR, after IP chemotherapy may result in a clinically meaningful favorable impact on survival, a randomized controlled trial will be required to address definitively this important issue. © 1992 by American Society of Clinical Oncology.
Keywords: cancer chemotherapy; cancer survival; treatment outcome; survival analysis; major clinical study; cancer recurrence; salvage therapy; cisplatin; cytarabine; ovarian neoplasms; ovary cancer; tumor volume; etoposide; antineoplastic combined chemotherapy protocols; recurrence; cancer regression; mitoxantrone; infusions, parenteral; intraperitoneal drug administration; prognosis; human; female; priority journal; article; support, non-u.s. gov't; support, u.s. gov't, p.h.s.
Journal Title: Journal of Clinical Oncology
Volume: 10
Issue: 9
ISSN: 0732-183X
Publisher: American Society of Clinical Oncology  
Date Published: 1992-09-01
Start Page: 1479
End Page: 1484
Language: English
DOI: 10.1200/jco.1992.10.9.1479
PUBMED: 1517791
PROVIDER: scopus
DOI/URL:
Notes: Article -- Source: Scopus
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MSK Authors
  1. William Hoskins
    255 Hoskins
  2. Richard R Barakat
    629 Barakat
  3. John P Curtin
    112 Curtin
  4. Lois Ann Cassidy
    72 Cassidy
  5. Thomas B Hakes
    115 Hakes
  6. Walter   Jones
    95 Jones
  7. John   Lewis
    132 Lewis
  8. Maurie Markman
    124 Markman
  9. Stephen C. Rubin
    112 Rubin