Eva van Loo1, Klara Mosterd2, Gertruud A M Krekels3, Marieke H Roozeboom2, Judith U Ostertag4, Carmen D Dirksen5, Peter M Steijlen6, H A Martino Neumann7, Patty J Nelemans8, Nicole W J Kelleners-Smeets9. 1. Maastricht University FHML, P.O. Box 616, 6200 MD Maastricht, Netherlands. 2. Department of Dermatology, Maastricht University Medical Centre, P.O. Box 5800, 6202 AZ Maastricht, Netherlands; GROW Research Institute for Oncology and Developmental Biology, Maastricht University, P.O. Box 616, 6200 MD Maastricht, Netherlands. 3. Department of Dermatology, Maastricht University Medical Centre, P.O. Box 5800, 6202 AZ Maastricht, Netherlands; MohsA, Expertise Centre for Mohs Micrographic Surgery, Buitenlust 35, 5803 AZ Venray, Netherlands. 4. Department of Dermatology, Maastricht University Medical Centre, P.O. Box 5800, 6202 AZ Maastricht, Netherlands; Mohsklinieken, Winston Churchilllaan 85, 5623 KW Eindhoven, Netherlands. 5. Department of Clinical Epidemiology and Medical Technology Assessment, Maastricht University Medical Centre, P.O. Box 616, 6200 MD Maastricht, Netherlands. 6. Department of Dermatology, Maastricht University Medical Centre, P.O. Box 5800, 6202 AZ Maastricht, Netherlands; GROW Research Institute for Oncology and Developmental Biology, Maastricht University, P.O. Box 616, 6200 MD Maastricht, Netherlands; Department of Dermatology, Catharina Hospital, Michelangelolaan 2, 5623 EJ Eindhoven, Netherlands. 7. Department of Dermatology, Maastricht University Medical Centre, P.O. Box 5800, 6202 AZ Maastricht, Netherlands; Department of Dermatology, Erasmus Medical Centre, P.O. Box 2040, 3000 CA Rotterdam, Netherlands. 8. Department of Epidemiology, Maastricht University Medical Centre, P.O. Box 616, 6200 MD Maastricht, Netherlands. 9. Department of Dermatology, Maastricht University Medical Centre, P.O. Box 5800, 6202 AZ Maastricht, Netherlands; GROW Research Institute for Oncology and Developmental Biology, Maastricht University, P.O. Box 616, 6200 MD Maastricht, Netherlands; Department of Dermatology, Catharina Hospital, Michelangelolaan 2, 5623 EJ Eindhoven, Netherlands. Electronic address: n.kelleners.smeets@mumc.nl.
Abstract
BACKGROUND:Basal cell carcinoma (BCC) is the most common form of cancer among Caucasians and its incidence continues to rise. Surgical excision (SE) is considered standard treatment, though randomised trials with long-term follow-up are rare. We now report the long-term results of a randomised trial comparing surgical excision with Mohs' micrographic surgery (MMS) for facial BCC. METHODS:408 facial, high risk (diameter at least 1cm, H-zone location or aggressive histological subtype) primary BCCs (pBCCs) and 204 facial recurrent BCCs (rBCCs) were randomly allocated to treatment with either SE or MMS between 5th October 1999 and 27th February 2002. The primary outcome was recurrence of carcinoma. A modified intention to treat analysis was performed. FINDINGS: For primary BCC, the 10-year cumulative probabilities of recurrence were 4.4% after MMS and 12.2% after SE (Log-rank test χ(2) 2.704, p=0.100). For recurrent BCC, cumulative 10-year recurrence probabilities were 3.9% and 13.5% for MMS and SE, respectively (Log-rank χ(2) 5.166, p=0.023). A substantial proportion of recurrences occurred after more than 5years post-treatment: 56% for pBCC and 14% for rBCC. INTERPRETATION: Fewer recurrences occurred after treatment of high risk facial BCC with MMS compared to treatment with SE. The proportion of recurrences occurring more than 5years post-treatment was especially high for pBCC, stressing the need for long-term follow-up in patients with high risk facial pBCC.
RCT Entities:
BACKGROUND:Basal cell carcinoma (BCC) is the most common form of cancer among Caucasians and its incidence continues to rise. Surgical excision (SE) is considered standard treatment, though randomised trials with long-term follow-up are rare. We now report the long-term results of a randomised trial comparing surgical excision with Mohs' micrographic surgery (MMS) for facial BCC. METHODS: 408 facial, high risk (diameter at least 1cm, H-zone location or aggressive histological subtype) primary BCCs (pBCCs) and 204 facial recurrent BCCs (rBCCs) were randomly allocated to treatment with either SE or MMS between 5th October 1999 and 27th February 2002. The primary outcome was recurrence of carcinoma. A modified intention to treat analysis was performed. FINDINGS: For primary BCC, the 10-year cumulative probabilities of recurrence were 4.4% after MMS and 12.2% after SE (Log-rank test χ(2) 2.704, p=0.100). For recurrent BCC, cumulative 10-year recurrence probabilities were 3.9% and 13.5% for MMS and SE, respectively (Log-rank χ(2) 5.166, p=0.023). A substantial proportion of recurrences occurred after more than 5years post-treatment: 56% for pBCC and 14% for rBCC. INTERPRETATION: Fewer recurrences occurred after treatment of high risk facial BCC with MMS compared to treatment with SE. The proportion of recurrences occurring more than 5years post-treatment was especially high for pBCC, stressing the need for long-term follow-up in patients with high risk facial pBCC.
Authors: C Murray; D Sivajohanathan; T P Hanna; S Bradshaw; N Solish; B Moran; R Hekkenberg; A C Wei; T Petrella Journal: Curr Oncol Date: 2019-02-01 Impact factor: 3.677
Authors: Sarah E Stuart; Patrick Schoen; Chengshi Jin; Rupa Parvataneni; Sarah Arron; Eleni Linos; W John Boscardin; Mary-Margaret Chren Journal: J Am Acad Dermatol Date: 2017-03-29 Impact factor: 11.527
Authors: Ganesh M Shankar; Joshua M Francis; Mikael L Rinne; Shakti H Ramkissoon; Franklin W Huang; Andrew S Venteicher; Elliot H Akama-Garren; Yun Jee Kang; Nina Lelic; James C Kim; Loreal E Brown; Sarah K Charbonneau; Alexandra J Golby; Chandra Sekhar Pedamallu; Mai P Hoang; Ryan J Sullivan; Andrew D Cherniack; Levi A Garraway; Anat Stemmer-Rachamimov; David A Reardon; Patrick Y Wen; Priscilla K Brastianos; William T Curry; Fred G Barker; William C Hahn; Brian V Nahed; Keith L Ligon; David N Louis; Daniel P Cahill; Matthew Meyerson Journal: JAMA Oncol Date: 2015-08 Impact factor: 31.777