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我父亲肺鳞癌的治疗贴(2014年3月1日驾鹤西去)

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1180661 1620 老马 发表于 2011-10-27 08:05:18 | 置顶 |
老马  博士一年级 发表于 2012-4-27 18:50:42 | 显示全部楼层 来自: 浙江温州
Pooled Analysis of S-1 Trials in Non-Small Cell Lung Cancer According to Histological Type$ {7 O# L9 |/ I
NOBUYUKI YAMAMOTO1, TAKEHARU YAMANAKA2, YUKITO ICHINOSE3, KAORU KUBOTA4, HIROSHI SAKAI5, AKIHIKO GEMMA6, NAGAHIRO SAIJO7, MASAHIRO FUKUOKA8 and HISANOBU NIITANI9 7 g2 o( Q" V# ^: h8 r
+ Author Affiliations( u$ k: `" c+ x$ X

1 F1 Y( U  E9 \) X% a/ D1Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka 411-8777, Japan
- N; v" T1 `6 J$ M9 O+ f2Cancer Biostatistics Laboratory, Institute for Clinical Research, National Kyushu Cancer Center, Fukuoka 811-1395, Japan
# K1 ^# l3 T  a# u4 W: `3Department of Thoracic Oncology, National Kyushu Cancer Center, Fukuoka 811-1395, Japan 9 G' o0 d8 e( ^6 R4 B. z
4Division of Thoracic Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan 9 N, n: o; N% _1 X- i* N1 o- e& @
5Division of Thoracic Oncology, Saitama Cancer Center, Saitama 362-0806, Japan ( m$ g4 z  r/ {* Q
6Division of Pulmonary Medicine, Infectious Diseases, and Oncology Department of Internal Medicine, Nippon Medical School, Tokyo 113-8603, Japan / d; V; ]# _# x6 m- M! [
7Kinki University School of Medicine, Osaka 589-8511, Japan
, ]$ y9 l" R! A( G1 Z8Izumi Municipal Hospital, Osaka 594-0071, Japan 0 |% f. k9 [& }! h: P* k. L, {
9Tokyo Cooperative Oncology Group, Tokyo 105-0013, Japan
) r' w, D( z5 L; n7 ~# aCorrespondence to: Nobuyuki Yamamoto, Division of Thoracic Oncology, Shizuoka Cancer Center, 1007 Shimonagakubo, Nagaizumi-cho, Sunto-gun, Shizuoka 411-8777, Japan. Tel: +81 559895222, Fax: +81 559895783, e-mail: n.yamamoto@scchr.jp . _+ m0 ]. S6 A1 O
AbstractBackground: The antimetabolic agent S-1 inhibits thymidylate synthase similar to pemetrexed, but through a different mechanism of action. Whether the antitumour activity of S-1 depends on histological type remains unclear. We analysed pooled data from 2 phase II clinical studies of cisplatin and S-1 in patients with previously untreated advanced non-small cell lung cancer. Patients and Methods: We comprised 110 patients with stage IIIB or IV non–small cell lung cancer. Univariate and multivariate analyses were performed to determine the effects of histological type on progression-free survival and response rates. Results: On pooled analysis of the data, according to histological type, median progression-free survival was 3.8 months in patients with squamous cell carcinoma and 4.4 months in those with non-squamous cell carcinoma. Both analyses showed that progression-free survival and response rate did not differ significantly. Conclusion: Unlike molecular targeted agents and pemetrexed, a combination of cisplatin and S-1 may be no difference in response according to histological type. ( t5 {' w% t5 L" f7 }

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个人公众号:treeofhope
老马  博士一年级 发表于 2012-4-27 18:52:43 | 显示全部楼层 来自: 浙江温州
S-1 monotherapy for previously treated non-small cell lung cancer: A retrospective analysis by age and histopathological type
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Authors: Yuki Tomita, Tetsuya Oguri, Osamu Takakuwa, Makoto Nakao, Eiji Kunii, Takehiro  Uemura, Hiroaki Ozasa, Mikinori Miyazaki, Ken Maeno, Shigeki Sato " G3 X& W' J0 G2 @8 k
) X, c, W2 S$ a
Affiliations: Department of Medical Oncology and Immunology, Nagoya City University Graduate School of Medical Sciences, Mizuho-cho, Mizuho-ku, Nagoya, Aichi 467-8601, Japan  
8 ]7 K, F% ]: N& S4 ~  Z# j8 U* T
Published online on: Thursday, December 1, 2011 0 @, J  \5 C/ ^6 s

* f, U8 u" S7 a! F8 D# ?. LDoi: 10.3892/ol.2011.507
' s3 _) c4 M3 a* m+ i0 D1 i% c9 }8 F& J
Pages: 405-410
( C. z; {+ z9 X3 m, f: ^  n/ T4 A; S& ^# L" C
Abstract:
4 ~) [; R" f4 a/ M+ uS-1, an oral fluoropyrimidine derivative, has been approved for the treatment of non-small cell lung cancer (NSCLC) in Japan. In the present study, the efficacy and safety of S-1 monotherapy for elderly patients with previously treated NSCLC were retrospectively evaluated, and the efficacy of S-1 monotherapy was compared by histopathological type. This retrospective study included 54 patients with advanced or recurrent NSCLC who had received S-1 monotherapy following the failure of previous chemotherapy regimens at our institutes. Patient outcomes were compared based on their age and histopathological type. S-1 was administered orally, twice daily, while the duration and interval were modified according to the medical condition of each patient. The default delivery schedule, the mean number of S-1 cycles, did not differ significantly between the two age groups (<70 and ≥70 years). The rate of therapy discontinuation, schedule modification or dose reduction due to intolerable toxicities or patient refusal was relatively frequent in the older group (40.7 and 55.6% for ages <70 and ≥70 years, respectively; p=0.414), and the incidence of grade 3 anemia was relatively high in the older group (3.7 and 18.5%, respectively; p=0.192). The response rates (13.0 and 4.8%, respectively; p=0.609) and disease control rates (39.1 and 33.3%, respectively; p=0.761) did not differ significantly between the two age groups. According to histopathological type, the disease control rate was significantly higher in adenocarcinoma (57.9%) compared to non-adenocarcinoma (20.0%, p=0.013). Thus, S-1 monotherapy may be equally effective and tolerated in patients <70 years and those ≥70 years. Additionally, adenocarcinoma may have a higher disease control rate than non-adenocarcinoma.; U  b2 L6 ^4 C" ^: u2 x

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个人公众号:treeofhope
老马  博士一年级 发表于 2012-4-27 18:57:27 | 显示全部楼层 来自: 浙江温州
Thymidylate synthase (TS) gene expression in primary lung cancer patients: a large-scale study in Japanese population
3 O- P% e2 u& vF. Tanaka1,*, H. Wada2, Y. Fukui3 and M. Fukushima3
" x0 P5 T3 s$ i# v1 _: _5 B% [+ Author Affiliations
4 ^0 D1 C( x7 N. R3 ^, y. v1Second Department of Surgery, University of Environmental and Occupational Health, Kitakakyushu & r  I+ ?0 w- r# }  S+ s" K
2Department of Thoracic Surgery, Kyoto University, Kyoto
( [0 i7 [* \* P9 ~" ?5 @3Tokushima Research Center, Taiho Pharmaceutical Co. Ltd, Tokushima, Japan / B! k$ z1 \3 c# E+ l9 k
&#8629;*Correspondence to: Dr F. Tanaka, Second Department of Surgery, University of Environmental and Occupational Health, 1-1 Isegaoka, Yahata-nishi, Kitakakyushu, 807-8555, Japan. Tel: +81-93-891-7442; Fax: +81-93-692-4004; E-mail: ftanaka@med.uoeh-u.ac.jp
8 N9 C8 y/ D$ G* [Received September 3, 2010.
4 X0 g* k+ ?* e4 N9 RRevision received November 11, 2010. ( o) M! S$ z9 i
Accepted November 17, 2010. 6 H2 ~9 Y! q# O7 G  E
Abstract) ?. G- Y; O- e" C* f7 s
Background: Previous small-sized studies showed lower thymidylate synthase (TS) expression in adenocarcinoma of the lung, which may explain higher antitumor activity of TS-inhibiting agents such as pemetrexed.
+ }+ \( G& u# Y/ W; wPatients and methods: To quantitatively measure TS gene expression in a large-scale Japanese population (n = 2621) with primary lung cancer, laser-captured microdissected sections were cut from primary tumors, surrounding normal lung tissues and involved nodes.
( B/ [& s& a2 I: `+ h3 w2 cResults: TS gene expression level in primary tumor was significantly higher than that in normal lung tissue (mean TS/β-actin, 3.4 and 1.0, respectively; P < 0.01), and TS gene expression level was further higher in involved node (mean TS/β-actin, 7.7; P < 0.01). Analyses of TS gene expression levels in primary tumor according to histologic cell type revealed that small-cell carcinoma showed highest TS expression (mean TS/β-actin, 13.8) and that squamous cell carcinoma showed higher TS expression as compared with adenocarcinoma (mean TS/β-actin, 4.3 and 2.3, respectively; P < 0.01); TS gene expression was significantly increased along with a decrease in the grade of tumor cell differentiation. There was no significant difference in TS gene expression according to any other patient characteristics including tumor progression.
% d" J0 F, ~+ k6 }4 \$ \) mConclusion: Lower TS expression in adenocarcinoma of the lung was confirmed in a large-scale study. 5 S3 R4 C5 @; p1 `4 F2 T* R
个人公众号:treeofhope
走在异乡  高中一年级 发表于 2012-4-28 00:30:22 | 显示全部楼层 来自: 四川成都
一直关注老马的帖子,前方的指明灯。祝福你爸好疗效
累计签到:1 天
连续签到:1 天
[LV.1]初来乍到
baiselianyi  初中二年级 发表于 2012-4-28 10:24:44 | 显示全部楼层 来自: 浙江台州
一直得到老马帮助,祝福老马爸爸
老马  博士一年级 发表于 2012-4-28 18:00:37 | 显示全部楼层 来自: 浙江温州
26日吃了12片地米(0.75mg一片),27日吃了22片地米(0.75mg 一片),28日吃了12片地米(0.75mg一片),都分二次吃。
/ Y3 L* s  J- u8 T; \2 M今天为止没有任何反应,每天吃VC,VB2,还有漱口水,就怕口腔溃疡。
个人公众号:treeofhope
bishop_cn  大学一年级 发表于 2012-4-28 23:16:11 | 显示全部楼层 来自: 中国
副作用如何,单药反应很小吧?
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老马  博士一年级 发表于 2012-4-29 00:20:00 | 显示全部楼层 来自: 浙江温州
LUX-Lung 8: A Phase III Trial of Afatinib (BIBW 2992) Versus Erlotinib for the Treatment of Squamous Cell Lung Cancer After at Least One Prior Platinum Based Chemotherapy
+ `/ d+ |2 ], K: Hhttp://clinicaltrials.gov/ct2/show/NCT01523587
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8 H! j+ w0 R3 Q" k6 C* B7 WBIBW 2992 Plus Simvastatin vs. BIBW 2992 in Previously Treated Patients With Advanced Non-adenocarcinomatous NSCLC
7 I7 d" I0 B9 G) Ahttp://clinicaltrials.gov/ct2/show/NCT01156545
个人公众号:treeofhope
老马  博士一年级 发表于 2012-4-29 20:53:58 | 显示全部楼层 来自: 浙江温州
本帖最后由 老马 于 2012-4-30 09:33 编辑
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从4月24日开始到4月28日,打了5天的舒普深(注射用头孢哌酮钠舒巴坦钠),效果非常好。
+ O  I: w0 V- x2 V至今为止,未出现化疗副作用。
个人公众号:treeofhope
英雄武松  大学四年级 发表于 2012-4-30 01:37:05 | 显示全部楼层 来自: 哈萨克斯坦
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没有副作用是第一追求,效果显著是第二追求。
/ H) q3 _- c$ l# i- Q4 P0 K不错。

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